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Curriculum Vitae

Prof Sarar Hamza Elhassan Mohamed

MBBS, FRCPCH(UK), MRCP(UK), MRCPCH(UK), DCH(Ire), CPTP(Ire), CCST(Ire), CSD (Ire), MD (Sud)

Personal Data

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Name: Sarar Hamza Elhassan Mohamed

Nationality Irish

Marital Status: Married.

Address: 45 Liffey Terrace, Lucan, Co Dublin, Ireland

E-mail: [email protected], [email protected]

[email protected]

Telephone: Mobile:00966541235272, Home: 0096614842990,

Present Post Professor and Consultant Pediatric Endocrinologist and Metabolic Physician, King Saud University Medical City, King

Saud University, Riyadh, Saudi Arabia..

QualificationsOct 2014 Certificate of Specialist Doctor ( a certificate allows candidate to

work as a Specialist doctor in all Europe), Irish Medical Council

Feb 2006 FRCPCH (Fellowship of the Royal College of Paediatrics and Child

Health, (UK)

June 2004 CCST (Certificate of Completion of Specialist Training, accredited by Royal College of Physicians, Ireland. (This is a five years postgraduate

. . training as Specialist Registrar (Senior Fellow) in Pediatics, Metabolic

diseases and Endocrinology started after completion of membership of

Royal College (MRCP).

March 2003: MRCPCH (UK), Membership of the Royal College of Paediatrics and

Child Health (UK)

Jan 2000 CPTP (Certificate of Professional Training in Paediatrics), two years

Training program, accredited by Royal College of Physician of Ireland

July 1999: MRCP (UK), Membership of the Royal College of Physicians (UK)

September1998: DCH (Diploma in Child Health, Royal College of Physicians of Ireland March 1994-1997: MD in Paediatrics, University of Khartoum, Sudan(three years .

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mailto:[email protected]

mailto:[email protected]

postgraduate course both clinical and research)

March 1992: MBBS, University of Khartoum, Sudan.

Life Support Courses

Basic life support course: Re-certified Nov 2014

Neonatal Resuscitation Course: Re-certified December 2007

Paediatrics Advanced Life Support Course: Re-certified Nov 2010

Professional Registration General Medical Council, UK, in specialist register no 7499250, 2015

Irish Medical Council, in specialist register no 2205 since Sept 2004

Full registration with the Irish Medical Council, no 22057 since 2002

Consultant registration with Saudi Medical Council since 2005

Full registration with Sudan Medical Council since 1994

Consultant registration with Sudan Medical Council since 1997

Membership of Professional Bodies

Royal College of Paediatrics and Child Health (UK)

Royal College of Physician (UK)

European Society of Pediatric Endocrinology

American Endocrine Society

Society for the Study of Inborn Error of Metabolism (SSIEM), (UK)

British Metabolic Diseases Group (BMDG)

International Society for Newborn Screening (ISNS)

Society for the Study of Inborn Error of Metabolism, Middle East

Saudi Genetic Society

Irish Paediatrics Association (Ireland)

Arab Society of Pediatric Endocrinology

Saudi Society of Endocrinology and Metabolism

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Sudanese Diabetes Society

Sudanese Pediatrics Society

Sudan Medical Association

Sudanese Group of Pediatric Endocrinologists

Awards & Prizes

1.Awarded Registrar Prize for a paper entitled, Magnesium sulphate improves outcome in

Persistent Pulmonary Hypertension of the Newborn, Irish Paediatric Association meeting 2002 2.Awarded Kamal Elsalmabi Prize and distinction in Paediatrics & Child Health, March 1992,

University of Khartoum, Sudan

3.Awarded Prof. Daud Prize in Medicine March 1992, University of Khartoum

4.Awarded El Bagdadi Prize for best student during 5 years study in the Faculty of Medicine,

March 1992, University of Khartoum 5.Awarded Distinction & Prize in Community Medicine, Feb 1991, University of Khartoum.

Thesis

1 -Sarar Mohamed , G Satti, S Ibrahim. Efficacy of Artemether versus Quinine in the treatment

Of cerebral malaria in Sudanese children. A randomised controlled trial,

MD Thesis, University of Khartoum1997.

2- Sarar Mohamed , M Elfatih. Acute respiratory tract infection in children under 5 in Kosti,

Sudan.Thesis, Department of community medicine, university of Khartoum, 1991.

3. Sarar Mohamed. Molecular study of Glycogen Storage Disease type 3, Molecular laboratory,

Metabolic Unit, Children’s University Hospital, Dublin, Ireland, 2003-2004.

Teaching and Academic Experience

Examiner, Royal College of Paediatrics and Child Health:

Examiner for MRCPCH

Professor of Paediatrics Department of Paediatrics, College of Medicine, King Saud

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University, Riyadh, Saudi Arabia. March 2012 to dateAssociate Professor of Paediatrics Department of Paediatrics, College of Medicine, King Saud

University, Riyadh, Saudi Arabia. April 2012 to Feb 2016

Assistant Professor of Paediatrics Department of Paediatrics, College of Medicine, King Saud

University, Riyadh, Saudi Arabia. May 2010 to April 2012

Assistant Professor of Paediatrics Department of Paediatrics, Faculty of Medicine, University of

Khartoum, March1997_December 1999Tutor, Trinity College, Dublin, Ireland, Jan 2001-July 2001

Tutor, Teaching and Research Assistant in Pediatrics

Department of Paediatrics, Faculty of Medicine

University of Khartoum, Sudan. July. '93 - Feb ‘97

Consultant Experience

May 2010 up to date Consultant Pediatric Endocrinologist and Metabolic Physician,

King Khalid University Hospital, Riyadh, Saudi Arabia. Feb 2010-May 2010 Consultant Metabolic Physician and Pediatric Endocrinologist,

Shagalneel Modern Hospital, Khartoum, Sudan. Feb 2005- Feb 2010 Consultant Metabolic Physician and Pediatric Endocrinologist

Saad Specialist Hospital (SSH), AlKhobar, Saudi Arabia

June 2004_Jan 2005 Consultant, Pediatric Metabolic Medicine,

University Hospital, Temple Street, Dublin, Ireland.

March. '97 – 1998 Consultant Pediatrician with special interest in Pediatric

Endocrinology and Metabolic Diseases, Department of Pediatrics, University of Khartoum/ Ahmed Gasim Children's Hospital, Khartoum

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Specialist Registrar (Senior Fellow) Experience. (This is a five years postgraduate . .

training as Specialist Registrar (Senior Fellow) in Pediatics, Metabolic

diseases and Endocrinology started after completion of membership of

Royal College (MRCP).

Jan 2000-June 2004 Specialist Registrar (Senior fellow) in Metabolic Medicine/

Biochemical Genetics lab/ Metabolic and newborn screening lab, Paediatric Endocrinology

and Diabetes, Paediatric ICU, Neonatal ICU, and Pediatric Emergency in the 3 Dublin

Children Hospitals ( The Children’s Hospital, Temple St, Our Lady Hospital for Sick

Children, The National Children’s Hospital) and Rotunda Maternity Hospital.

July 1999-Dec 1999 Senior Houseofficer/ Acting Registrar in the Neonatal ICU, Rotunda Hospital, Dublin.

Jan 1999-June1999 Registrar in Paediatric Accident and Emergency, Our Lady’s Hospital for Sick Children, Crumlin, Dublin.

July 1998-Dec1998 Senior Houseofficer in Paediatrics.

Letterkenny General Hospital, Letterkenny, Ireland

Feb 1998-June 1998 Senior Houseofficer in Paediatrics and Metabolic unit. The Children’s

Hospital, Temple St, Dublin

Registrar Experience in Pediatrics, Diabetes, Endocrinology and Metabolic diseases: May 1994-Feb 1997Children's Emergency Hospital (Khartoum), and Soba University Hospital (2 years under supervision of Prof Abdulaziz Elamin, Pediatric Endocrinologist and Metabolic Physician).

Senior House officer ( Resident) Experience

May 1992-April 1994 2 years rotation in Pediatrics, General Medicine, Obse & Gynae, and Surgery.

Editorial board Membership

Assistant Editor in Chief

Sudanese Journal of Pediatrics, (published by Sudanese Association

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of Pediatricians), Jan 2009 till date

Member of Editorial board

Sudanese Journal of Pediatrics, since Jan 2007

Administration and committee contribution in department of paediatrics,

King Saud University

1. Head, Metabolic unit and Newborn Screening Service, March 2013-August 2015.

2. Acting Head, Pediatric Endocrinology Unit, May 2010-Jan 2012

3. Head of Clinical Practice Guidelines Committee: contributed to development and

implementation of 10 clinical guidelines including Diabetic Ketoacidosis, septic shock,

Bronchial Asthma, and bronchiolitis with auditing.

4. Member of Quality improvement Committee.

5. Member of Examination committee

6. Member of Undergraduate committee

7. Member of Pediatric department board

Academic & Carreer development courses & workshops

Academic & Carreer development courses & workshops attended at King Saud University

1. Systematic review longitudinal 1 year course. King Saud University, Riyadh,

Saudi Arabia. April 2012

2. Clinical guidelines development: evidence base tool. Evidence based chair,

King Saud University, Riyadh, Saudi Arabia. December 2010

3. Biostatistics, SPSS & Research methodology, Department of Medical Education,

King Saud University, Riyadh, Saudi Arabia. January 2011

4. Multiple Choice Questions workshop, Department of Medical Education,

King Saud University, Riyadh, Saudi Arabia. November 2011

5. Rehabilitation Medicine, Department of Rehabilitation, King Saud University, Riyadh, Saudi Arabia. November 2011

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6. Implementation of clinical guidelines workshop. Department of Quality

improvement, King Saud University, Riyadh, Saudi Arabia. December 2011

7. How to become a small group facilitator, Medical education department, March 2012

8. Problem Based Learning workshop, March 2011

Administration, Leadership and Management courses

9- Joint Commission Accreditation (JCI) Training workshop, May 2005, SSH, Saudi

10-Leadership and Management course. Royal college of surgeons, Ireland, Oct 2003.

11-Health management and administration. Intensive 2 weeks course, World Health

Organization, Sudan, Jan 1997.

12- Statistical Methods in Medicine course, 20th April-8th June 2004. Trinity College Dublin.

13-A Focus on Primary Health Care. Ministry of Health, Sudan, 1997.

Endocrine/Metabolic Courses and meetings

14. Neonatal Endocrinology course. Apocrates organization, UK, held in Riyadh, March 2011

15. Growth and puberty workshop, Khartoum, Sudan, October 2011

16. Insulin pump: practical course, Irish diabetes association, Dublin, June 2009.

17. Growth and Growth hormone workshop, Dubai, April 2013

18. Middle East Metabolic Group conference, American University of Beirut, Lebanon,

Feb2009

19. Middle East Metabolic Group conference, University of Ghase, Turkey, October 2009

20. Annual conference of Middle East Metabolic Group conference, Bahrain, October 2010

21. Annual conference of Middle East Metabolic Group conference, American University of

Beirut, Lebanon, October 2011.

22. Annual conference of Middle East Metabolic Group conference, American University of Beirut, Lebanon, October 2012.

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13. Middle East Metabolic Group conference, University of Ghase, Turkey, October 2009

14. Middle East Metabolic Group conference, Marakish, Moroco, Oct 2014.

15. Arab Society of Pediatric Endocrinology, first meeting, Kwait 2013

16. Arab Society of Pediatric Endocrinology, first meeting, Abu Dhbi Nov 2014

17. European Society of Pediatric Endocrinology meeting, Milan, Italy, September 2013

18. European Society of Pediatric Endocrinology meeting, Dublin, Ireland, September 2014

19. The American Endocrine Society conference, San Fransisco, June 2013.

20. Saudi Endocrine conference, Riyadh, November 2012

21. Saudi Endocrine conference, Riyadh, November 2014

22. SSIEM International metabolic meeting, Germany, September 2007

23. Metabolic disorders in Newborn, Orphan Academy Europe, Qatar, 2007

24. SSIEM International metabolic meeting, Japan, September 2006

25. International Society of Newborn screening conference, Japan 2006

26. Neurotransmitter Disorders, Paris, Orphan Academy, September 2005

27. SSIEM International metabolic meeting, Paris, September 2005

28. Insulin Pump and continuous glucose monitoring certified course, SSH, Saudi, September 2005

29. Thyroid update meeting, Royal College of Physicians of Ireland, 14-15 May 2004.

30. SSIEM International metabolic meeting, Amsterdam, September 2004

31. Metabolic Dietetic Meeting, London, March 2004

32. Intensive Metabolic Course, Paris, Orphan Academy, November 2004

33. Peroxisomal Biogenesis Disorders Course, Amsterdam, Orphan Academy; September 2004

34. Spring meeting of the royal college of paediatrics and child health, metabolic section, April 2004

35. SSIEM (Society for Study of Inborn Error of Metabolism) meeting, Dublin, September 2002

36. study day on Diabetes of the young, Irish Paediatric Federation, Dublin, April 2000.

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Short Pediatrics courses in Europe

37. .Neonatal Resuscitation Course, American Heart Association, Dublin 1998. Re-certified 2005

38. Neonatal Transport Course, Dublin, Oct 2000.

39. Neonatal Ventilation Course, London, UK, Oct 2001

40. Training course on Cardiology of the Young, Great Ormond Street Hospital, London,April2002.

41. A workshop on Neonatal Screening for Hearing Loss, Belfast, Feb 2000.

42. A course on Update on Neonatology, Dublin, Sep 1999.

43. Second annual Cystic Fibrosis clinical meeting, The Killarney Park Hotel, Ireland, Feb 2002.

44. Spring meeting of the Royal College of Physcians and Child Health, University of York, April 2003

45. Spring meeting of the Royal College of Physicians and Child Health, University of York, April 2004.

46. Paediatric Advance Life Support Course (PALS), UK Resuscitation Council, April 1999.

Short Courses in Sudan

47. Molecular Biology Techniques in Research and Diagnosis of

Infectious Diseases - Applied Course, Sudan, Jan 1996.

48. Training course on Human-immuno deficiency Virus (HIV). Ministry of Health, Sudan,

Feb1997.

49. Training course on Breast Feeding. Ministry of Health, Sudan Feb 1996.

50. Training course on Malaria. Ministry of Health, Sudan Dec 1995.

51. Training course on: Proper use of essential drugs. World Health Organisation. Sudan , Nov 1995.

52. Diarrhoea case management, training of trainers course. World Health Organisation.

Programme for Control of Diarrhoeal Diseases, May 1995.

53. Acute Respiratory infection (ARI) training of trainers course. Ministry of Health - Sudan, Oct 1997.

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Hand Books in English compiled by Sarar Mohamed

1. Pediatric Diabetes: Educational Handbook

2. Pediatric Endocrinology and diabetes protocols and guidelines

3. Protocols for the management of acute metabolic disorders

A Book translated from English to Arabic by Sarar Mohamed:

Oxford Specialist Handbooks in Paediatrics: Paediatric Endocrinology and

Diabetes by: Gary Butler and Jeremy Kirk, Oxford University Press

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Publications: Articles Published in Peer Reviwed Medical Journals

.1. Mohamed S, Roche EF, Hoey HM. Mode of initial presentation and chromosomal

abnormalities in Irish patients with Turner syndrome: a single-centre experience. J

Pediatr Endocrinol Metab. 2014 Nov 6. pii: /j/jpem.ahead-of-print/jpem-2014-

0287/jpem-2014-0287.xml. doi: 10.1515/jpem-2014-0287.

2. Mohamed S, Roche EF, Hoey HM. High Prevalence of Spontaneous Puberty in

Patients with Turner Syndrome in Tertiary Referral Center in Ireland. Acta Endo

(Buc) 2015 11: 60-63 doi: 10.4183/aeb.2015.60

3. Mohamed S, El-Kholy S, Al-Juryyan N, Al-Nemri AM, Abu-Amero KK.

A CYP21A2 gene mutation in patients with congenital adrenal hyperplasia.

Molecular genetics report from Saudi Arabia.

Saudi Med J. 2015 Jan;36(1):113-6.

4. Mohamed S, Elkholy S, El-Meleagy E, Abu-Amero K, Hellani AM. Clinical and

molecular characterization of maturity onset-diabetes of the young caused by

hepatocyte nuclear factor-4 alpha mutation: red flags for prediction of the

diagnosis. Ann Saudi Med. 2014 May-Jun;34(3):217-21. doi: 10.5144/0256-

4947.2014.217.

5. Mohamed S, Hussein MD. Prevalence of Thinness, Stunting and Anemia Among

Rural School-aged Sudanese Children: A Cross-sectional Study.

J Trop Pediatr. 2015 Apr 20.

6. Mohamed S. From Concept to Bedside: What Pediatricians Should Know about

Synthesis of Clinical Practice Guidelines?. Iranian Journal of Pediatrics, Volume

24 (Number 5), October 2014, Pages: 557-564.

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http://www.ncbi.nlm.nih.gov/pubmed/25896992









7. Mohamed S, Adi Y, AlFaleh K. Oxandrolone for growth-hormone treated children and

adolescents with Turner syndrome (Protocol). Cochrane Database of Systematic Reviews

2013, Issue 9. Art. No.: CD010736. DOI: 10.1002/14651858.CD010736.

8. Hussein M, Mohamed S. Prevalence of anaemia in preschool children in Karma Albalad

area, Northern State, Sudan. EMHJ 2014. 20 (1): 33-38.

9. Mohamed S. Hussein MD. Prevalence of acute malnutrition in pre-school children in a

rural area of Northern Sudan. East African Medical Journal 2014. Vol. 91 No. 1 :8-13

10. Alharbi KK, Kashour TS, Al-Hussaini W, Al-Nbaheen MS, Mohamed S, Hasanato RM,

Tamimi W, Al-Naami MY, Khan IA. Association of angiotensin converting enzyme gene

insertion/deletion polymorphism and familial hypercholesterolemia in the Saudi

population. Lipids Health Dis. 2013 Dec 1;12:177. doi: 10.1186/1476-511X-12-177.

11. Mohamed S, Hamad MH, Abu-Amero KK. Identification of 2 novel homozygous

mutations in the methylmalonyl-CoA mutase gene in Saudi patients. Saudi Med J. 2015

Sep;36(9):1110-4. doi: 10.15537/smj.2015.9.12118

12. Alharbi KK, Kashour TS, Al-Hussaini W, Nbaheen MS, Hasanato RM, Mohamed S,

Tamimi W, Khan IA. Screening for genetic mutations in LDLR gene with familial

hypercholesterolemia patients in the Saudi population. Acta Biochim Pol. 2015 Sep 8.

13. Salih MA, Bosley TM, Alorainy IA, Sabry MA, Rashed MS, Al-Yamani EA, El-Akoum

S, Mohamed SH, Abu-Amero KK, Hellani AM. Preimplantation genetic diagnosis in

isolated sulfite oxidase deficiency. Canadian J Neurol Sci. 2013 Jan;40(1):109-12.

14. Al-Saadi MM, Meo SA, Al-Drees AM, Mohamed S, Shaikh SA, Al-Rubeaan K. Lung

functions in poorly controlled type 1 Saudi diabetic children and adolescents. Saudi Med J.

2011 Aug;32(8):778-83.

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15. Sarar Mohamed, Ebtessam M. El Melegy, Iman Talaat, Amany Hosny, Khaled K. Abu-

Amero. Neurometabolic Disorders Related Early Childhood epilepsy: A Single Center

Experience in Saudi Arabia. Pediatric and Neonatology Journal 2015

16. Hassanato R, Mohamed S, et al. Vitamin D status among female medical students in

Saudi Arabia. Acta Endocrinologica 2015 (11): 257-261.

17. Mohamed S. Sanfilippo syndrome, glucose-6-phosphate dehydrogenase deficiency and

sickle cell/β+ thalassemia in a child: the burden of consanguinity. Am J Med Genet A.

2014 Jan;164A(1):267-9. doi: 10.1002/ajmg.a.36180.

18. Mohamed S, El-Meleagy E, Nasr A, Ebberink MS, Wanders RJ, Waterham HR.

A mutation in PEX19 causes a severe clinical phenotype in a patient with . peroxisomal

biogenesis disorder. Am J Med Genet A. 2010 Sep;152A(9):2318-21. doi:

10.1002/ajmg.a.33560.

19. Mohamed S, Ahmed W, Al-Jurayyan N, Faqeih E, Al-Nemri A, Al-Ghamdi M.

Infantile Systemic Hyalinosis Complicated with Right Atrial Thrombus and

Pericardial Effusion in an Infant. Pediatr Neonatol. 2014 Nov 21. pii: S1875-

9572(14)00162-4. doi: 10.1016/j.pedneo.2014.01.008.

20. Mohamed S, Osman A, Al Jurayyan NA, Al Nemri A, Salih MA.

Congenital toxoplasmosis presenting as central diabetes insipidus in an infant: a .

case report. BMC Res Notes. 2014 Mar 28;7:184. doi: 10.1186/1756-0500-7-184.

21. Mohamed S, Kambal MA, Al Jurayyan NA, Al-Nemri A, Babiker A, Hasanato R, Al-

Jarallah AS. Tyrosinemia type 1: a rare and forgotten cause of reversible hypertrophic

cardiomyopathy in infancy. BMC Res Notes. 2013 Sep 9;6:362. doi: 10.1186/1756-0500-

6-362.

22. Hellani A, Mohamed S, Al-Akoum S, Bosley TM, Abu-Amero KK.

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A t(5;16)(p15.32;q23.3) generating 16q23.3 --> qter duplication and 5p15.32 --> pter

deletion in two siblings with mental retardation, dysmorphic features, and speech. delay.

Am J Med Genet A. 2010 Jun;152A(6):1555-60. doi: 10.1002/ajmg.a.33400.

23. Al-Owain M, Mohamed S, Kaya N, Zagal A, Matthijs G, Jaeken J.

A novel mutation and first report of dilated cardiomyopathy in ALG6-CDG (CDG-Ic): a

case report. Orphanet J Rare Dis. 2010 Apr 16;5:7. doi: 10.1186/1750-1172-5-7.

24. Ismail AF, Mohamed S, Ezz-Elregal M, Talat I, Muthurajan S, Fouda A.

Associations with hypoglycemia are useful: a case report of Allgrove syndrome.

Turk J Gastroenterol. 2012;23(5):608-9. No abstract available.

25. Sarar Mohamed . Newborn screening for Glucose-6-Phosphate Dehydrogenase

Deficiency in Eastern Province, Saudi Arabia. Curr Pediatr Res 2012; 16 (1).

26. Sarar Mohamed. A clinical and DNA study on patients with Neuronal ceroid

lipofuscinosis in Eastern Province, Saudi Arabia. Curr Pediatr Res 2012; 16 (1).

27. Sarar Mohamed. Cat eye syndrome: A mild phenotype with isolated growth hormone

Deficiency. Curr Pediatr Res 2012; 16 (1).

28. Mohamed S. An Infant with Leprechaunism, Ambiguous Genitalia and Poor Glycemic

Control: A Management Chalenge. Acta Endo (Buc) 2014 10: 134-139 doi:

10.4183/aeb.2014.134

29. Abulrahman AlNemri, Rashid AlJurayyan, Sarar Mohamed, Hessah AlOtaibi, Sharifa

AlEissa. Nair Al Jurayyan. Neonatal Hyperbilirubinemia and elevated liver enzymes

associated with thyroid hormone deficiency. Curr Pediatr Res 2012; 16(1).

30. Hessah AlOtaibi, Nair Al Jurayyan, Sarar Mohamed, Mustafa A Salih. Osteomalacia

in Adolescents Presenting as Proximal Myopathy. Curr Pediatr Res 2012; 16(1).

31. Nasir A.M. Al-Jurayyan, Sarar Mohamed, Munir Faiz Saad Uddin, Abdulaziz N.A. Al-

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Jurayyan. Pseudohypoparathyroidism Type 1b; a Rare Cause of Femoral Neck Fracture.

Journal of Taibah University Medical Sciences 2011; 6(1): 43-47

32. Mohamed S . Recognition and diagnostic approach to acute metabolic disorders in the

neonatal period. Sudan J Paediatr 2011;11(1): 20-28.

33. Mohamed S . Treatment strategies for acute metabolic disorders in neonates. Sudan J Paediatr 2011;11(2):6- 13.

34. Sarar Mohamed , Hadi El-Khodary, Nawal M. Khalifa, Ali Hellani, Susan El-Kholy,

Ebtessam El-Melegy, Amal A. El-Menshay. Pattern of Metabolic Disorders Presenting to

Pediatric and Metabolic Clinics in Developing Countries. Research Journal of Medicine

and Medical Sciences, 4(1): 14-19, 2009

35. Ebtisam ElMelegy, Sarar Mohamed, Ostopetrosis presenting with hypocalcemic seizure

early in the neonatal period. Med J Cairo Univ 2009;77: 115-118

36. Sarar Mohamed , Mohamed Ezz-Regal, Ashraf Fouda. Achalasia in Children:

keep your eye open for adrenal insufficiency. S J Pediatrics 2009;9:76-80

37. Sarar Mohamed, Ali Hellani, Ebtisam ElMelegy. New Mutation at BTD Gene:

Biotinidase deficiency presenting with status epilepticus resistant to conventional anti-

epileptics. Med. J. Cairo Univ 2009;77: 111-113

38. Sarar Mohamed , EP. Treacy. Severe Glycogen Storage Disease type 111 a:

lack of response to dietary intervention. S J Pediatrics 2009;9:89-92

39. Ebtisam ElMelegy, Sarar Mohamed . Menkes Disease presenting with subdural fluid

collection and fractures mimicking non-accidental injury. Med J Cairo Univ 2009;77: 119-121-

40. Sarar Mohamed, Ebtisam Elmeleagy, Umair Khan, Ali Hellani. Classical

Phenylketonuria and Antley-Bixler syndrome co-exist in a patient. Med J Cairo Univ

2008,4: 165-167.

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41. Sarar Mohamed, Ahmad Alzagal, Ebtisam Elmelegy. Complex 1 Respiratory Chain

Disorder presenting with severe dilated cardiomyopathy and severe renal tubular acidosis.

Med. J. Cairo Univ 2008;76: 359-361

42. Sarar Mohamed, T Matthews, D Corcoran, T Clarke. Magnesium Sulphate improves the

outcome in Persistant Pulmonary Hypertension of the newborn. S J Pediatrics 2007;8,102-113.

43. G Satti, Sarar Mohamed , S Ibrahim. Treatment of Cerebral malaria using Artemether.

Eg J Microb 2002, 74;211-221

44. Mohamed S, Ibrahim F, Kamil K, Satti SA. Meckel- Gruber syndrome: Antenatal diagnosis and

ethical perspectives. Sudan J Paediatr 2012;12(2):70-72.

45. Al-Jurayyan NA, Mohamed S, Al Otaibi HM, Al Issa ST, Omer HG. Short stature in children:

pattern and frequency in a pediatric clinic, Riyadh, Saudi Arabia. Sudan J Paediatr 2012;12(1):79-

83.

46. Jurayyan NA, Jurayyan RNA, Mohamed S, Babiker AM, Al Otaibi HMN, Radiological

Imaging of Disorders of Sex Development (DSD). Sudan J Paediatr 2013; 13(2):10-16.

47. M.Kheir AE, Abozied EE, Mohamed S, Salih AA. The pattern of anthropometric

measurements among term newborn infants in Khartoum state in relation to

maternal factors. Sudan J Paediatr2013; 13 (2):31-36.

48. Al Jurayyan NAM, Mohamed S, Al Issa SDA, Al Jurayyan ANA. Rickets and osteomalacia in

Saudi children and adolescents attending endocrine clinic, Riyadh, Saudi Arabia. Sudan J Paediatr

2012;12(1):56-63.

49. Babiker AM, Jurayyan NA, Mohamed S, Abdullah MA. Overview of diagnosis, management and

outcome of congenital hypothyroidism: a call for a national screening programme in Sudan. Sudan

J Paediatr 2012; 12(2):7-16.

50. Amir M.I. Babiker, Shariefa D.A. Issa, Sarar Mohamed, Hessah M.N. Al Otaibi,

Nasir A.A. Al Jurayyan. Screening for autoimmune diseases in type 1 diabetes:

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Low incidence of adrenal insufficiency. Journal of Taibah University Medical

Sciences (2014) 9(3), 224e227

51. Babikir AA, Mohamed S. Loss of a Stethoscope: Ebola memoires. Sudan J

Paediatr 2014; 14(2):112 -123.

52. Al-Jurayyan N, Al-Jurayyan A, Al Issa S, Mohamed S, Al Otaibi H, Babiker A. 5

alfa reductase deficiency syndrome: An experience from a referral university

hospital in Saudi Arabia. PNCO 2015. 3 (1): 113-117.

53. Sarar Mohamed, MD, FRCPCH, Muddathir H. Hamad, MD, Hamdy H. Hassan, MD,

Mustafa A. Salih, MD, FAAN. Glutaric aciduria type 1 as a cause of dystonic cerebral

palsy. Saudi Med J 2015; Vol. 36 (11): 1354-1357

54. Iman M. Talaat, Naglaa M. Kamal, Ebtessam H.K. El Melegy ,

Hamed A. Alghamdi , Mohammed F. Aljabri , Enas A.A. Abdallah , Mohammed

Sarar , Mohamed A. Alshahrani. First report of co-morbidity of pantothenate kinase-associated

neurodegeneration and three types of chronic hemolytic anemias. Annals of Medicine and

Surgery 5 (2016) 11-13.

55.Sarar Mohamed, Muddathir H. A. Hamad, Altaf A. Kondkar, Khaled

K.Abu-Amero. A novel mutation in Ornithine transcarbamyalse (OTC) gene

causing mild intermittent hyperammonemia. Saudi Medical Journal, 36 (10), 2015.

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Manuscripts submitted for publication

1. Substantial reduction in hospital stay of children and adolescents with

diabetic ketoacidosis after implementation of clinical practice guidelines

in a university hospital in Saudi Arabia.

Sarar Mohamed, FRCPCH, Hala Omer, MD, Amir M Babiker, FRCPCH, Hessah

. Al Otaibi, MD, Shaikh M Iqbal, FRCPCH, Mohamed E Osman, MD, Ayman Al- . . .

. Eyadhy, MD, Mohamed Al-Othman, MD, Abdulrahman A Al Nemri, MD, Yasser

S . . Amer, MD, Lubna Alansary, MD, Rana Hasanato, MD, Nasir Al-Juryyan, MD.

In Round 2 Review by Saudi Medical Journal.

2. New Observations Regarding the Retinopathy of Genetically-Confirmed

Kearns Sayre Syndrome

Igor Kozak, MD,PhD, Darren T. Oystreck, MMedSci,,

Khaled K. Abu-Amero, PhD, Sawsan R. Nowilaty, MD,

Hisham Alkhalidi, FRCPC, Sahar M. Elkhamary, MD,

Sarar Mohamed, MD, Muddathir H. A. Hamad, MD,

Mustafa A.M. Salih, MD, Emma L. Blakely, PhD,

Robert Taylor, PhD FRCPath, and Thomas M. Bosley, MD

Submitted to Retina Journal.

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Publications: Abstracts published in Medical Journals

1-Mohamed S, Hellani A, Elkholy S. Mutation in Hepatocyte Nuclear factor 4 α gene in

Saudi family with Maturity onset Dibetes. J Inherit Metab Dis (2008) Abs 31:39

2-Mohamed S, Nasr A, Abdeljaber M. Cat Eye Syndrome associated with severe growth failure

caused by isolated growth hormone deficiency in a Saudi male. J Inhert Met Dis (2006) Abs

29;143.

3-Mohamed S, Khaunizi M, Nasr A, Dossary S, Greally MT. Leprechaunism syndrome: An

exaggerated hyperglycaemic response to ACTH challenge. J Inhert Met Dis (2006) Abs 29;142.

4- Mohamed S, Rezvi S, Treacy E, Monavari AA. Short Chain Hydroxyacyl CoA

Dehydrogenase deficiency associated with hyperinsulinism in a young child. Inhert Met Dis

(2006) Abs,29;113

5- Mohamed S, Nasr A, Abu Sibah A Oestopetrosis presenting with hypocalcemic seizure early

in the neonatal period. J Inhert Met Dis (2006) Abs 29;143

6-S Mohamed , K Reddy , S Yap , C O’Neill , PD Mayne , EP Treacy . Galactosaemia/Duarte

individuals: Is dietary intervention necessary beyond the first few month of life? Arch Dis Child

2004; Abs89: 59.

7-S Mohamed, P Mulhair, C O’Neill, E Naughten, S Yap, EP Treacy, PD Mayne. Is high-risk

screening for Classical Galactosaemia in Ireland effective? J Inher Met Dis 2004 Abs, 27 :196.

8-S Mohamed , P Mulhair , C O’Neill , E Naughten , EP Treacy, S Yap, PD Mayne. The

outcome of high risk screening for galactosaemia in Ireland, 1989-2003. Arch Dis Child 2004;

Abs 89, 59.

9-S Mohamed, K Reddy, S Yap, C O’Neill, Y Rogers, PD Mayne, EP Treacy. Long-term Dietary

Management and outcome of Galactosaemia/Duarte (D/G) cases. J Inher Met Dis 2004 Abs:206

10-Chew HB, Walsh O, Hughes JAF, Mohamed S, Irranca M, Clark A, O’Neill C, Monavari A,

20

Treacy E, Manning R. Fertility and pregnancy in patients with galactosemia.Inhert Met Dis (2006)

Abs, 29;124

11. Mohamed S, khan U, El Melegy E, et al.

Mutation Screening of high-risk patients with Neuronal ceroid lipofuscinoses-a

convenient way of diagnosis? Inhert Met Dis (2007) Abs,30:102

12. Crushell E, Beauchamp NJ, O’Neill, Murhy AM, Mohamed S, Monavari A, Treacy

EP. Glycogen Storage Disease Type 3: Genotype Phenotype Correlation in the Irish

population.Inhert Met Dis (2007) Abs,30:59

13-Mohamed S, Hamasha M, Shanaa A, Ritmiller R, Khodery H. Hospital based

expanded newborn metabolic screening in a developing country: challenges and outcome.

J Inherit Metab Dis (2008) Abs 31:151

14-Mohamed S, Hassan A, Dossary S, Sarkis P, El-Khodery H, Nasr A. Newborn screening for

Glucose-6-Phosphatase Dehydrogenase Deficiency: high incidence in Saudi infants. J Inher Met

Dis (2006) Abs, 29;85

15- Mohamed S, Nasr A, ElFiki M, Hassan A Thalassemia/Sickle Cell syndrome, Glucose-6-

Phosphate Dehydrogenase deficiency, and Mucopolysachridosis type 3 expressed in one child.

J Inhert Met Dis (2006) Abs 29;150

16-S Mohamed, U Hendroff, M O’Regan, C O’Neill, E P Treacy. Severe Glycogen Storage

Disease Type 111a in three siblings: Lack of response to dietary interventions? J Inher Met Dis

2004, Abs 27: 20017-El-Melegy E, Hassan A, El-Khodery H, Greally M, Nasr A, Mohamed S. Peroxisomal

Disorders. Neuropediatrics Journal, 2006 Abs.

18-Mohamed S, Al Zaghal A. Complex 1 respiratory chain deficiency presenting with severe

dilated cardiomyopathy and severe renal tubular acidosis in a Saudi boy. J Inher Met Dis (2006)

Abs 29;118

21

19-Mohamed S, Hassan A, El-Melegy, Alzagal A. Congenital Disorder of Glycosylation type 1a

presenting with dilated cardiomyopathy in a Saudi boy. J Inhert Met Dis (2006) Abs 29;123

20- Mohamed S, Monavari AA. Hunter syndrome in a girl caused by balanced translocation. J

Inhert Met Dis (2006) Abs,29;150

21. Mohamed S, Hellani, et al. Pre-implantation Genetic Diagnosis:

Preventive tool for Nonketotic Hyperglycinaemia. Inhert Met Dis (2007) Abs,30:2

22. Mohamed S, El-Melegy E, et al. Biotidinase Deficiency Presenting As Status

Epilepticus Resistant To Conventional Anti-Epileptics Inhert Met Dis (2007) Abs,30:41

23. Mohamed S, El-Melegy E, et al. Don't

forget Menkes disease in the differential diagnosis of Non-accidental injury presenting

with subdural fluid collection and fractures. Inhert Met Dis (2007) Abs, 30:129.

24. Mohamed S, Khan U, et al. Classical Phenylketonuria and Antley- Bixler Syndrome in

one Saudi boy Inhert Met Dis (2007), Abs 30:22.

25-Mohamed S, Khodery H, Elshwaf A, Belushi S, Hellani A, Elkholy S, Elmelegy E.

Pattern of metabolic disorders presenting to a metabolic clinic in a developing country

over two years. J Inherit Metab Dis (2008) Abs 31:150

22

Oral presentations in national and international conferences and courses

1-Sarar Mohamed. Update on hyponatremia and Syndrome of Inappropriate

secretion of antidiuretic hormone. Saudi Pediatric Nephrology conference, King

Saud University, Riyadh, March 2011

2- Sarar Mohamed. Approach to metabolic acidosis, Saudi Pediatric Nephrology

conference, King Saud University, Riyadh, March 2011.

3. Sarar Mohamed. Update on Congenital Adrenal Hyperplasia. Saudi Pediatric

Conference, Jazan, March 2011

4- Sarar Mohamed. Update on management of type 1 diabetes. Saudi Pediatric

Conference, Jazan, March 2011

5- Sarar Mohamed. Ketoacidosis in children without diabetes. Saudi Association

of Endocrinology and Metabolism symposium, Riyadh, 19 Sept 2011.

6-. Calcium sensing receptors: new advances. Sudanese Pediatric Association

Conference, Khartoum, Sudan, October 2011.

7- Sarar Mohamed. Diagnostic approach to IEM in acutely sick neonates..

Sudanese Pediatric Association Conference, Khartoum, Sudan, October 2011.

8- Sarar Mohamed. Management of precocious puberty, Endocrine workshop.


9- Sarar Mohamed. Management of delayed puberty, Endocrine workshop.


10- Sarar Mohamed. Puberty Disorders: practical pearls, Endocrine workshop.


23

11- Sarar Mohamed. Diagnostic Pearls in IEM. Sudanese Pediatric Association,

guest lecture, July 2011.

12. Sarar Mohamed. Management Pearls in IEM. Sudanese Pediatric Association,

guest lecture, July 2011.

13-sarar Mohamed. Newborn screening for congenital hypothyroidism: it high

time to start in Sudan. Sudanese Pediatrics Association conference, Khartoum,2009

14- Sarar mohamed. Newborn Metabolic screening from the spot to diagnosis and

management. The 15th Congress of Pan Arab Pediatrics Association, Khartoum,

Nov 2007.

15- Sarar mohamed. Clinical approach and management of acute Metabolic

emergencies in the neonatal period.The15th Congress of Pan Arab Pediatrics

Association, Khartoum, November 2007

16- Sarar Mohamed, H Hoey. Hormonal Profile in Turner Syndrome. Proceedings

of The Sudanese Paediatric Association Conference, July 2003.

17- Sarar Mohamed Update on metabolic disorders in the newborn. Neuroscience

club, Eastern province, Dammam, Saudi Arabia, March 2009

18- Sarar Mohamed , K Reddy , S Yap , C O’Neill , PD Mayne , EP Treacy .

Galactosaemia/Duarte individuals: Is dietary intervention necessary beyond the first

few month of life? Conference of the Royal College of Pediatrics, UK, 2004

19-Sarar Mohamed , P Mulhair , C O’Neill , E Naughten , EP Treacy, S Yap, PD

Mayne. The outcome of high risk screening for galactosaemia in Ireland.

Conference of the Royal College of Pediatrics, UK, 2004

24

20-Sarar Mohamed, E Roche, M Eltahir, C Duggan, H Ahmed, E Quinn, H Hoey.

Puberty and Pregnancy in 65 Irish girls with Turner Syndrome. The Irish Perinatal

Society Conference, Kilkenny, Sep 2001.

21-Sarar Mohamed, E Roche, M Eltahir, H Ahmed, E Quinn, H Hoey.

Cytogenetic abnormalities in Irish patients with Turner Syndrome. The Irish

Paediatric Association Conference, Royal college of Physicians, Dublin, Oct 2001.

22-. Sarar Mohamed , T Matthews, D Corcoran, T Clarke. Respiratory Syncital

Virus

Immunoglobulin in preterm infants. The Irish Perinatal Society Conference,

Mullingar, Ireland Sep 2000.

23-Sarar Mohamed, T Matthews, D Corcoran, T Clarke. Congenital

Cytomegalovirus Infection in preterm infants. The Irish American Society

Conference, Westport, Ireland, May 2000.

24-C O’conell, Sarar Mohamed , T Matthews, D Corcoran, T Clarke. Presence of a

paediatrician at Caeserean section, is it necessary? The Irish Perinatal Society

Conference, Wexford, Ireland, April 2000 .

25-Sarar Mohamed, T Matthews, D Corcoran, T Clarke. Treatment of Persistent

Pulmonary Hypertension with Magnesium sulphate: Rotunda experience. The Irish

Perinatal Conference, Antrim, North Ireland, April 2002.

26-Sarar Mohamed, E Roche, M Eltahir, H Ahmed, E Quinn, H Hoey. Middle ear

disease and hearing loss in Turner syndrome. The Irish Paediatric Association

meeting in Kilkenny, May 2002.

25

27- Sarar Mohamed , T Matthews, D Corcoran, T Clarke. Magnesium sulphate

improves outcome in Persistent Pulmonary Hypertension of the Newborn. The Irish

Paediatric Association conference in Kilkenny, May 2002.

28. Sarar Mohamed. Development and implementation of Clinical Practice

Guidelines in Pediatric Endocrinology: Challenges and opportunities. Presented in

The American Endocrine Society conference, San Fransisco, June 2013.

29. Sarar Mohamed. Inherited types of Rickets Presented in the Saudi Endocrine

Society monthly club meeting, Merriot Hotel. Riyadh, September 2013.

30. Sarar Mohamed. Ketoacidosis without Diabetes. Presented in the Saudi

Endocrine Society monthly club meeting, Merriot Hotel. Riyadh, June 2013

31. Sarar Mohamed. Tyrosinemia: An unusual cause of cardiomyopathy. Saudi

Society of Pediatrician monthly club, Holiday Inn, Riyadh, April 2013.

32. Sarar Mohamed. Diagnostic Evaluation and management of precocious

puberty. Sudanese Pediatric Association conference, Khartoum Sudan, November

2013.

33. Sarar Mohamed. Approach to delayed puberty. Sudanese Pediatric

Association conference, Khartoum Sudan, November 2013.

34. Sarar Mohamed. Growth disorders and growth hormone deficiency.

Sudanese Pediatric Association conference, Khartoum Sudan, November

2013

35. Sarar Mohamed. Approved Indications for growth hormone therapy.

Growth symposium, Saudi Endocrine Society, Riyadh, May 2013

26

36. Sarar Mohamed. Screening for Congenital hypothyroidism: what general

pediatrician should know? National Newborn Screening Program

symposium, Riyadh, September 2013.

37. Sarar Mohamed. Congenital Adrenal hyperplasia: an update. National

Newborn Screening Program symposium, Riyadh, September 2013.

38. Sarar Mohamed. Screening for Congenital hypothyroidism: an update.

National Newborn Screening Program workshop, Hail, April 2013.

39. Sarar Mohamed. Congenital Adrenal hyperplasia prevents death and

disability. National Newborn Screening Program workshop, Hail, April 2013.

40. Sarar Mohamed. Management of Diabetic Ketoacidosis: an update. Saudi

Society of Pediatrician Symposium, Tabuk, March 2014.

41. Sarar Mohamed. Approach to management of growth disorders in children.

Saudi Society of Pediatrician Symposium, Tabuk, March 2014.

42. Sarar Mohamed. Endocrine and metabolic emergencies in children. Saudi

Society of Pediatrician Symposium, Guryyat, April 2014.

43. Sarar Mohamed. Management of type 1 diabetes in children. Saudi Society

of Pediatrician Symposium, Guryyat, April 2014.

44. Sarar Mohamed. Endocrine review for Endocrine fellows. Pediatric

Endocrinology fellowship course. King Faisal Specialist Hospital, December

2013.

45. Sarar Mohamed. Interpretation of growth chart: Back to the basics.

Pediatric Update Symposium, Prince Salman Hospital, Riyadh, May 2014.

27

46. Sarar Mohamed. Approach to thyroid nodules. Clinical approach to

common Endocrine cases, Symposium at King Faisal specialist Hospital, 28

May 2014.

47. Sarar Mohamed. Genetics of disorders of sex development. Clinical

approach to common Endocrine cases, Symposium at King Faisal specialist

Hospital, 28 May 2014.

48. Sarar Mohamed. Genetics of Growth hormone disorders. Clinical approach

to common Endocrine cases, Symposium at King Faisal specialist Hospital,

28 May 2014.

49.Sarar Mohamed. Maturity onset diabetes of the young: when should we

suspect the diagnosis? Arab Society of Pediatric Endocrinology conference,

Abu Dhabi, November 2014-11-27.

50. Sarar Mohamed. Maturity onset diabetes of the young: red flags for

suspicion of the diagnosis. Sarar Mohamed. Saudi Endocrine Society

meeting. Riyadh, November 2014.

51. Sarar Mohamed. Characteristics of young children with metabolic epilepsy

in a tertiary hospital. Middle East Metabolic meeting, Marakesh, Moroco,

October 2014.

52. Sarar Mohamed. Newborn Screening from spot to diagnosis and

management, Grand round, Pediatric Department, College of Medicine, King

Saud University, April 13.

28

53. Sarar Mohamed. Implementation of Clinical Practice Guidelines, Grand

round, Pediatric Department, , College of Medicine, King Saud University,

April 2012.

54. Sarar Mohamed. Recent advances in management of type 1 diabetes in

children. Grand round, Pediatric Department, , College of Medicine, King

Saud University, April 2011.

55. Sarar Mohamed. Pediatric Endocrinology update. Pediatric postgraduate

course. King Saud University, Riyadh, December 2010.

56. Sarar Mohamed. Approach to management of metabolic emergencies in the

neonatal period. Guest lecture, neonatal unit, College of Medicine, King

Saud University, June 2011.

57. Sarar Mohamed. Management of Diabetic Ketoacidosis: role of clinical

pathway. Pediatric Emergency Unit. , College of Medicine, King Saud

University, May 2011.

58. Sarar Mohamed. Update on Diabetes. Pediatric Postgraduate half day

teaching, College of Medicine, King Saud University, February 2011.

59. Sarar Mohamed. Endocrine case scenarios. Pediatric Postgraduate half day

teaching, College of Medicine, King Saud University, April 2011.

60. Sarar Mohamed. Puberty disorders. Pediatric Postgraduate half day

teaching, College of Medicine, King Saud University, October 2011.

61. Sarar Mohamed. Metabolic Emergencies. Pediatric Postgraduate half day

teaching, College of Medicine, King Saud University, January 2011.

29

Papers presented as Poster in international conferences

1-S Mohamed, U Hendroff, M O’Regan, C O’Neill, E P Treacy. Severe Glycogen Storage

Disease Type 111a in three siblings: Lack of response to dietary interventions? SSIEM

Conference 2004, Amsterdam The Netherland

2-S Mohamed, P Mulhair, C O’Neill, E Naughten, S Yap, EP Treacy, PD Mayne. Is high-risk

screening for Classical Galactosaemia in Ireland effective? ? SSIEM


3-S Mohamed, K Reddy, S Yap, C O’Neill, Y Rogers, PD Mayne, EP Treacy. Long-term

Dietary Management and outcome of Galactosaemia/Duarte (D/G) cases. ? SSIEM


4-Mohamed S, Hassan A, Dossary S, Sarkis P, El-Khodery H, Nasr A. Newborn screening for

Glucose-6-Phosphatase Dehydrogenase Deficiency: high incidence in Saudi infants.

International Congress of Inborn Errors of Metabolism (ICIEM)Conference 2006, Tokyo, Japan

5-Mohamed S, Al Zaghal A. Complex 1 respiratory chain deficiency presenting with severe

dilated cardiomyopathy and severe renal tubular acidosis in a Saudi boy.


6-Mohamed S, Hassan A, El-Melegy, Alzagal A. Congenital Disorder of Glycosylation type 1a

presenting with dilated cardiomyopathy in a Saudi boy.


7-Mohamed S, Nasr A, Abdeljaber M. Cat Eye Syndrome associated with severe growth failure

caused by isolated growth hormone deficiency in a Saudi male.


8-Mohamed S, Khaunizi M, Nasr A, Dossary S, Greally MT. Leprechaunism syndrome: An

exaggerated hyperglycaemic response to ACTH challenge.


30

9- Mohamed S, Nasr A, ElFiki M, Hassan A Thalassemia/Sickle Cell syndrome, Glucose-6-

Phosphate Dehydrogenase deficiency, and Mucopolysachridosis type 3 expressed in one child.


10- Mohamed S, Nasr A, Abu Sibah A Oestopetrosis presenting with hypocalcemic seizure early

in the neonatal period. International Congress of Inborn Errors of Metabolism (ICIEM)Conference

2006, Tokyo, Japan

11- Mohamed S, Monavari AA. Hunter syndrome in a girl caused by balanced translocation.


12- Mohamed S, Rezvi S, Treacy E, Monavari AA. Short Chain Hydroxyacyl CoA

Dehydrogenase deficiency associated with hyperinsulinism in a young child.


16-Chew HB, Walsh O, Hughes JAF, Mohamed S, Irranca M, Clark A, O’Neill C, Monavari A,

Treacy E, Manning R. Fertility and pregnancy in patients with galactosemia International

Congress of Inborn Errors of Metabolism (ICIEM)Conference 2006, Tokyo, Japan



convenient way of diagnosis? SSIEM Conference 2007, Hamburg, Germany


Preventive tool for Nonketotic Hyperglycinaemia. SSIEM Conference 2007, Hamburg, Germany

15. Mohamed S, El-Melegy E, et al. Biotidinase Deficiency Presenting As Status

Epilepticus Resistant To Conventional Anti-Epileptics. SSIEM Conference 2007, Hamburg,

Germany

16. Mohamed S, El-Melegy E, et al. Don't

forget Menkes disease in the differential diagnosis of Non-accidental injury presenting

with subdural fluid collection and fractures. SSIEM Conference 2007, Hamburg,

Germany

31

17. Mohamed S, Khan U, et al. Classical Phenylketonuria and Antley- Bixler Syndrome in

one Saudi boy . SSIEM Conference 2007, Hamburg, Germany

18. Crushell E, Beauchamp NJ, O’Neill, Murhy AM, Mohamed S , Monavari A, Treacy

EP. Glycogen Storage Disease Type 3: Genotype Phenotype Correlation in the Irish

population. SSIEM Conference 2007, Hamburg, Germany



convenient way of diagnosis? SSIEM Conference 2008, Lisbon, Portegal


Preventive tool for Nonketotic Hyperglycinaemia. SSIEM Conference 2008, Lisbon, Portegal

21- Mohamed S, Hellani A, Elkholy S. Mutation in Hepatocyte Nuclear factor 4 α gene in

Saudi family with Maturity onset Dibetes. SSIEM Conference 2008, Lisbon, Portegal

22-EL- Meleagy, A Nasr, M Greally, A Hassan, S Mohamed . Peroxisomal Biogenesis

Disorders SSH experience. Neurology conference, Dubai, November 2005.

23- Mohamed S, Hassan A, Dossary S, Sarkis P, El-Khodery H, Nasr A.

High incidence of Glucose-6-Phosphatase Dehydrogenase Deficiency in Saudi infants screened

at birth. The international society of newborn screening conference, Chiba, Japan, 2006

32

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