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Bibliography
153
BIBLIOGRAPHY
A. I. Juwah, E. U. Nlemadim, W. Kaine. Types of anaemic crisis in
paediatric patients with sickle cell anaemia seen in Enugu, Nigeria.
Arch Dis Child. 2004; 89: 572-576.
A. V. Shrikhande, A. A. Dani, J. R. Tijare, A. K. Agrawal. Hematological
profile of sickle cell disease in central India. Indian J. Hematol. Blood
Transfus. 2003; (3–4): 92–98.
A. M. Emokpae, P. O. Uadia, and A. Kuliya-Gwarzo. Antioxidant enzymes
and acute phase proteins correlate with marker of lipid peroxide in
adult Nigerian sickle cell disease patients. Iranian Journal of Basic
Medical Sciences. 2010; 13(4): 177–182.
A.J. Duits, H. Ten Cate, and D.P.M. Brandjes. Protein C and S and
Inflammation in Sickle Cell Disease. American Journal of Hematology .
2004; 76: 26–32
Abhay Bhave, V.K. Kulkarni, D.N. Bhattad, D.P. Upase, Aarti Mane, Colah
Roshan, Khushnuma. Microcytic Hypochromic Anaemia in Sickle Cell
disease- Think again. JAPI. 2009; 57: 479-480.
Adelekan D.A., Thurnham D.I., Adekile A.D. Reduced antioxidant
capacity in pediatric patients with homozygous sickle cell disease. Eur J
Clin Nutr. 1989; 43: 609-14.
Aebi H. Catalase in vitro. Methods Enzymolgy. 1984; 105: 121-126.
Bibliography
154
Afonja O.A. Osteoblastic activity in sickle cell disease. Clin Chem
Newsletter. 1982; 3: 161-163.
Agil A., Sadrzadeh S.M. Hydroxy-urea protects erythrocytes against
oxidative damage. Redox Rep. 2000; 5: 29–34.
Agrawal M.B. The burden of haemoglobinopathies in India- time to
wake up. J Acad Phys Ind. 2005; 53: 1017-1018.
Akinsegun Akinbami, Adedoyin Dosunmu, Adewumi Adediran .Steady
state hemoglobin concentration and packed cell volume in homozygous
sickle cell disease patients in Lagos, Nigeria. Caspian J Intern Med
2012; 3(2): 405-409
Akohoue S.A., Shankar S., Milne G.L. morrow J., Chen Y. K., Ajay U.W.,
Buschowski S.M., Energy expenditure, inflammation, and oxidative
stress in steady state adolescents with sickle cell anemia. Pediatr Res.
2007; 61(2): 233-238.
Alsultan A. I., Seif M. A., Amin T. T., Naboli, M., Alsuliman A. M.
Relationship between oxidative stress, ferritin and insulin resistance in
sickle cell disease. Eur. Rev. Med. Pharmacol. Sci. 2010; 14: 527–538.
Ames, Cathcart, Schwiers, Hochstein. Uric acid provides antioxidant
defense in humans against radical caused ageing, cancer: A hypothesis.
1981; 78(11): 6858-6862.
Bibliography
155
Amstad P., Peskin A., Shah G., Mirault E.M., Moret R., Zbiden I., Cerutti P.
The balance between Cu,Zn-superoxide dismutase and catalase affects
the sensitivity of mouse epidermal cell to oxidative stress.
Biochemistry. 1991; 30: 9305-9313.
Angela D. Burnette, Shahid M. Nimjee, Milena Batchvarova, Rahima
Zennadi, Marilyn J. Telen, Jun-ichi Nishimura, and Bruce A. Sullenger,
.RNA Aptamer Therapy for Vaso-Occlusion in Sickle Cell Disease.
Nucleic acid therapeutics. 2011; 21(4):18.
Anil Pathare, Salam Al Kindi, Adel Alwan Alnaqdy, Shahina Daar, Huxley
Knox-Macaulay, and David Dennison. Cytokine profile of sickle cell
disease in Oman .American journal of Hematology 2004; 77: 323-328.
Anna Bogdanova, Asya Makhro, Jue Wang, Peter Lipp and Lars Kaestner
. Calcium in Red Blood Cells—A Perilous Balance. Int. J. Mol. Sci. 2013;
14: 9848-9872.
Antunes F., Salvador A., Marinho H.S., Alves R., Pinto R.E. Lipid
peroxidation in mitochondrial inner membranes. An integrative kinetic
model. Free Radic Biol Med. 1996; 21: 917-943.
Arlet J.B., Ribeil J.A., Chatellier G., Pouchot J.E., Montalembert M., Prie D.,
Courbebaisse M. hyperuricemia in sickle cell disease in France. Rev
Meed interne. 2012 ; 33(1): 13-7.
Bibliography
156
Ashfaq S., Abramson J.L., Jones D.P.,Rhodes D.S., Weintraub S.W>,
Hooper C.W., Vaccarino V., Harrison G. D., Qauumi A.A. The
relationship between plasma levels of oxidized and reduced thiols and
early atherosclerosis in healthy adults. J Am Coll Cardiol. 2006; 47(5):
1005-1011.
Ayekyaw. A simple colorimetric method for ascorbic acid
determination in blood plasma. Clin Chim Acta. 1978; 86: 153-157.
Ayodele Adelakun, Olumide Ajani, Temitope Ogunleye, Elizabeth Disu,
Ayokulehin Kosoko and Ganiyu Arinola. Respiratory Burst Enzymes
and Oxidantantioxidant Status in Nigerian Children with Sickle Cell
Disease. British Biotechnology Journal. 2014; 4(3):270-278.
Baker H. Frank O. Warley’s practical Clinical Biochemistry 1968 ; sixth
edition chapter 35 : 902-905.
Benkerrou M., Delarche C., Brahimi L., Fay M., Vimlma E. Elion J.,
Gougerot- Pocidalo M.A., Elbim C. Hydroxyurea corrects the
dysregulated L-selectin expression and increased H2O2 production of
polymorphonuclear neutrophils from patients with sickle cell anemia.
Blood. 2002; 99(7): 2297–303.
Beutler E., Duron O. & Kefly B. M. Improved method for the
determination of blood glutathione. J. Lab. Clin. Med. 1963; 61: 882-8.
Bibliography
157
Bradley And Hornbeck, Warley’s practical Clinical Biochemistry 1968 ;
1: sixth edition chapter 35.
Brugnara C. Reticulocyte cellular indices: A new approach in the
diagnosis of anemias and monitoring of erythropoietic function. Crit.
Rev Clin Lab Sci. 200; 37(2): 93-130.
Bunn H.F. Pathogenesis and treatment of sickle cell disease. N Engl J
Med. 1997; 337: 762 - 769.
Capo C., Bongrand P. Benoliel AM, Depieds R: Non-specific recognition
in phagocytosis: Ingestion of alde-hyde-treated erythrocytes by rat
peritoneal macro-phages. Immunology 1979; 36: 501-508.
Carlo Bruagnara. Red cell dehydration in pathophysiology and
treatment of sickle cell disese. HMS boston. December 2000.
Cerqueira B.A., Boas W.V., Zanette A.D., Reis M.G., Goncalves M.S.
Increased concentrations of IL-18 and uric acid in sickle cell anemia:
contribution of hemolysis, endothelial activation and the
inflammasome. Cytokine. Nov. 2011; 56 (2): 471-6.
Chen, Wilfred U. Ajayi, and Maciej S. Buchowski. Energy Expenditure,
Inflammation, and oxidative stress in steady-state adolescents with
Sickle Cell Anemia. Pediatr Res 2007; 61: 233–238.
Chirico, E. N.; Pialoux, V. Role of oxidative stress in the pathogenesis of
sickle cell disease. IUBMB Life. 2012; 64: 72–80.
Bibliography
158
Charache S., Lubin B.L., Reid C.D. . Management and therapy of sickle cell
disease. U.S. department of health and nutrition services, public health
service, National institute of health, NIH publication. 92:2117.
Claudia R. Morris, Gregory J. Kato, Mirjana Poljakovic, Xunde Wang
William C. Blackwelder, Vandana Sanchdev, M, Stanley L. Hazen, Elliott
P. Vichinsky, Sidney M. Morris Jr., Mark T. Gladwin. Dysregulated
Arginine Metabolism, Hemolysis-Associated Pulmonary Hypertension
and Mortality in Sickle Cell Disease. JAMA. 2005; 294(1): 81–90.
Clayton Natta, and Lawrence Machlin Clayton Natta,, and Lawrence
Machlin.. Plasma levels of tocopherol in sickle cell anemia subjects. The
American Journal of Clinical Nutrition. 1979; 32: 1359-1362.
Coletta M., Hofrichter J., Ferrone F.A., Eaton W.A. Kinetics of sickle
haemoglobin polymerization in single red cells. Nature
.1982;300(5888):194-197.
Creary M., Williamson D., & Kulkarini R. Sickle cell disease: current
Acivities, public health, implication and future direction . Journal of
women’s health.2007;16(5): 575-578.
D. Koracevic, G. Koracevic, V. Djordjevic, S. Andrejevic, V. Cosic .
Method for the measurement of antioxidant activity in human fluids. J
Clin Pathol 2001; 54: 356–361.
Bibliography
159
D. G. Hafeman, R. A. Sunde andw. G. Hoekstra. Effect of Dietary
Selenium on Erythrocyte and Liver Glutathione Peroxidase in the Rat. J.
Nutr. 1974; 104: 580-587.
Darcielle Bruna Dias Elias, ronelia Pinhiro Goncolvet. Evaluation of the
concentration of Malondialdehyde and nitrite in patients with sickle
cell anemia treated or not with hydroxyurea einstein. 2010; 8(4 Pt 1):
414-8.
Das, S. K., Nair, R. C. . Superoxide dismutase, glutathione peroxidase,
Catalase and lipid peroxidation of normal and sickled erythrocytes. Br.
J. Haematol. 1980; 44: 87–92.
Dasgupta, T., Hebbel, R. P., Kaul, D. K. Protective effect of arginine on
oxidative stress in transgenic sickle mouse models. Free Radic. Biol.
Med. 2006; 41: 1771–1780.
Debes Ray, Pradeep Deshmukh, Kalayan Goswani, Neelam Garg,
Antioxidant Vitamin levels in sickle cell disoeder. Natl. Med J India,
2007; 20: 11-13.
Dehghan A., Kardys I., DeMaat M.P., Uitterlinden A.G., Sijbrands E.J.,
Bootsma A.H., Stijnen T., Hofman A., Scram M.T. and Witteman J.C.
Genetic variation, C-reactive protein levels and incidence of diabetes.
Diabetes. 2008 56(3): 872-878.
Bibliography
160
Droge W. Free radicals in the physiological control of cell function.
Physiol Rev 2002; 82(1): 47-95.
E. S. Klings and H. W. Farber. Role of free radicals in the pathogenesis of
acute chest syndrome in sickle cell disease. Respiratory Research.
2001; 2(5): 280–285.
E.M. Isoa. Current event in the management of sickle cell disease : an
review . Benin Journal of Postgraduate Medicine . 2009; 11( suppl.
Dec).
Edis belini junior , Danilo Griling humberto da Silva, Lidiane de Spouza
Torres, Eduardo Alves de Almeida, Rodalfo Delfini Cancado, carlos
Chiattone Claudia Regina Bonini Domingos. Oxidative stress and
antioxidants capacity in sickle cell anemia patients receiving different
treatment and medication for different periods of time. Ann hematol
.2012; 91: 479-489.
Elizabeth M. Barden, Deborah A. Kawchak, Kwaku Ohene-Frempong,
Virginia A. Stallings, and Babette S. Zemel. Body composition in
children with sickle cell disease. Am J Clin Nutr 2002; 76: 218–25.
Enika Nagababu, Mary E. Fabry, Ronald L. Nagel, and Joseph M. Rifkind.
Heme Degradation and Oxidative Stress in Murine Models for
Hemoglobinopathies: Thalassemia, Sickle Cell Disease and Hemoglobin
C Disease. Blood Cells Mol Dis. 2008; 41(1): 60-66.
Bibliography
161
Erfan Nur , Bart J. Biemond, Hans-Martin Otten, Dees P. Brandjes, John-
John B. Schnog. Oxidative stress in sickle cell disease: pathophysiology
andpotential implications for disease management. Am. J. Hematol.
2011; 86:484–489.
Essien E.U.. Plasma levels of retinol, ascotbic acid and alfa- Tocopherol
in sickle cll anemia. Cent Afr J Med. 1995; 41(2): 48-50.
Ezeiruaku, F.C., Eze, E. M. and Ukaji, D. C. Activity Levels of Some
Erythrocyte Enzymes (Glutathione STransferase, Nadh Ferricyanide
Reductase) and Serum Lactate Dehydrogenase in the Three Human
Genotype (Hbss, Hbaa And Hbas) in southern Nigeria. JETEAS.
2(2):314-317.
Filiz Simsek, Gulyuz Ozturk, Sabri Kemahlı, Deniz Erbas, Alev
Hasanoglu. Oxidant and antioxidant status in beta thalassemia major
patients. Ankara Üniversitesi Tıp Fakültesi Mecmuası 2005; 58: 34-38.
Foluke Fasola,Kayode Adedapo,John Anetor, and Modupe Kuti, .Total
Antioxidants Status and SomemHematological Values in Sickle Cell
Disease Patients in Steady State . Journal of the national medical
association. 2007; 99(8): 891.
Bunn H.F. Pathogenesis and treatment of sickle cell disease. N Engl J
Med 1997; 337:762-769.
Bibliography
162
G. Wu, Y.Z. Fang, S. Yang, J. R. Lupton, and N. D. Turner, Glutathione
Metabolism and Its Implications for Health. Journal of Nutrition. 2004;
134(3): 489–492.
Gizi A., Papasstiriou I., Apostolakou F., Lazaropoulou C., Papastamataki
M., Kanaski I., Kalotychou V., Gousstis E., Kattamis A. , Rombos I.,
Kanavakis E. . Assessment of oxidative stress in patients with sickle
cell disease: the glutathione system and oxidant- antioxidant status.
Blood cells Mil Djs. 2011; 46(3): 220-5.
Halliwell B, Gutteridge J.M. Lipid peroxidation, oxygen radicals, cell
damage, and antioxidant therapy. Lancet 1984; 1(83): 1396-1397.
Halliwell B. and Gutteridge J. M. C. Oxygen free radicals and iron in
relation to biology and medicine: Some problems and conceptsArch.
Biochem. Biophys. 1986 ; 246: 501-514.
Harper’s illustrated Biochmeistry 28th Edition . Mc Gra Hill.
Haynes J. Jr, Obiako B. . Activated polymorphonuclear cells increase
sickle red blood cell retention in lung: Role of phospholipids. Am. J.
Physiol. Heart Circ. Physiol. 2002; 282: H122–30.
Hebbel R.P., Eaton I.W., Balasingam M., Steinberg M.H. . Spontaneous
oxygen radical generation by sickle eryth-rocytes. J Clin Invest. 1982;
70: 1253-1259.
Bibliography
163
Hebbel R.P., Miller W.J. Phagocytosis of sickle erythrocytes:
immunologic and oxidative determinants of hemolytic anemia. Blood.
1984; 64: 733.
Hebbel R.P., Morgan W.T., Eaton J.W., Hedlund B.E.. Accelerated
autoxidation and heme loss due to instability of sickle hemoglobin.
Proc Natl Acad Sci U S A. 1988; 85(1): 237-241.
Hebbel R.P., Osarogiagbon R., Kaul D. The endothelial biology of sickle
cell disease: inflammation and a chronic vasculopathy. Microcirculation
.2004; 11: 129-51.
Hebbel R.P. Beyond hemoglobin polymerization: The red blood cell
membrane and sickle disease pathophysiology.Blood.1991;77: 214–37.
Hebbel R.P. The systems biology-based argument for taking a bold step
in chemoprophylaxis of sickle vasculopathy. Am J Hematol 2009; 84(9):
543-545.
Horn H.D., Bergmeyer H.U. Glutathione reductase: Methods of
Enzymatic Analysis. New York: Academic Press. 1963: 875-81.
Imoru Momodu, kabiru Sulelman, Shehu Abdullahi, Umar A. Shehu.
Haematological values in Nigerian children with steady state
homozygous sickle cell disease. Intenational journal of academic
research. 2011; 3(1).
Bibliography
164
Inwald D.P., Kirkham F.J., Peters M.J., Lane R., Wade A., Evans J.P., Klein
N.J. Platelet and leucocyte activation in childhood sickle cell disease:
association with nocturnal hypoxaemia. Br J Haematol 2000; 111: 474-
81.
J.B. Schnog, M.R. Mac Gillavry, A.P. van Zanten, J.C.M. Meijers, R.A. Rojer,
J.B.Harlan, Martin F Goldberg. Management and therapy of eye related
disorder in sickle cell disese. 2000.
Jaonne Thompson, Marvin Reid, Ian Hambleton, Graham R. Serjeant.
Albuminuria and renal function in homogyzous sickle cell disease. Arch
intern Med. 2007; 167: 701-708,
Jean C.D., Maryse T., Marie J.F. . Plasma M.alondialdehyde levels during
myocardial infarction. Clin Chim Acta 1983; 129: 319-22.
Jison M.L., Munson P.J., Barb J.J., Sufredini A.F., Talwar S., Logun
C., Raghavachari N., Beigel J.H., Shelhamer J.H., Danner R.L., Gladwin
M.T. Blood mononuclear cell gene expression profiles characterize the
oxidant, hemolytic, and inflammatory stress of sickle cell disease. Blood
2004; 104: 270–80.
Joan Schall, Babette I.S. Zemel , Deborah A. Kawchak M.S., Kwaku Ohene-
Frempong , Virginia. Vitamin A status, hospitalizations, and other
outcomes in young children with sickle cell disease. JPDES. 2004; 03:
51.
Bibliography
165
Johnkennedy Nnodim, Meludu Samuel C., Dioka C.E., Ihim Augustine,
Jones D.P.. Redox potential of GSH/GSSG couple: assay and biological
significance. Methods Enzymol 2002; 348: 93-112.
Joy Okpuzor, Olumide Adebesin, Henriatta Ogbunugafor, Ifeanyi Amadi.
The potential of medicinal plants in sickle cell disease control: A
review. International journal of Biomedical and health science 2008;
4(2): 47-55.
Jyoti Titus, Suresh Chari, Madhur Gupta, and Nitin Parekh . Pro-oxidant
and anti-oxidant status in patients of sickle cell anaemia, Indian Journal
of Clinical Biochemistry, 2004; 19 (2) 168-172.
Kalyan Goswami and Debes Ray. Putative pathogenic effect of oxidative
effect of oxidative stress in sickle cell disorder. Biomedical research,
2011; 22(1): 33-37.
Karl A. Nath, Joseph P. Grande, Jill J. Haggard, Anthony J. Croatt,
Zvonimir S. Katusic, Anna Solovey, and Robert P. Hebbel. Oxidative
Stress and Induction of Heme Oxygenase-1 in the Kidney in Sickle Cell
Disease. American Journal of Pathology. 2001;158(3): 893-903.
Kassab-Chekir, S. Laradi, S. Ferchichi. Oxidant, antioxi-dant status and
metabolic data in patientswith beta-thalassemia. ClinChimActa, vol.
2003. 338: 79-86.
Bibliography
166
Katherine C. Wood and D. Neil Granger. Sickle cell disease: Role of
reactive oxygen and nitrogen metabolites. Clinical and experimental
pharmacology and physiology 2007; 34: 926-932.
Kaul, D.K, Liu, X.D., Zhang, X., Ma, L., Hsia, C.J., Nagel, R.L. Inhibition of
sickle red cell adhesion and vasoocclusion in the microcirculation by
antioxidants. Am. J. Physiol. Heart Circ. Physiol. 2006; 291: 167-175.
Kaul, D.K. and Hebbel, R.P. Hypoxia/reoxygenation causes inflammatory
response in transgenic sickle mice but not in normal mice. J. Clin.
Invest, 2000; 106: 411-420.
Kenneth I. Ataga,Charity G. Moore,Cheryl A. Hillery,Susan Jones,Herbert
C. Whinna,Dell Strayhorn,Cathy Sohier, Alan Hinderliter,Leslie V.
Parise, and Eugene P. Orringer. Coagulation activation and
inflammation in sickle cell disease associated pulmonary hypertension.
Haematologica. 2008; 93(1): 20-26.
Kibileri Williams, Maria Rios, Nicole Dottin, Shani Hughes, Danielle
Strachan, Gershwin Davis, Kenneth S. Charles and Terence A.R.
Seemungal. Lung Function and Inflammation in Adult Sickle Cell
Disease in a West Indian Sickle Cell Cohort. J Pulmon Resp Med. 2012:
2: 5
Bibliography
167
Klings E.S., Farber H.W. Role of free radicals in the pathogenesis of
acute chest syndrome in sickle cell disease. Respir Res. 2001; 2(5):
280-285.
Kootathep S., Situnayake R.D., Thurnham D.I.,Chirico S, Lunec J, Davis
M, McConkey B. Chain breaking antioxidant status in rheumatoid
arthritis: clinical and laboratory correlates. Ann Rheum Dis. 1991; 50:
81-6.
L.M.S. Viana-Baracioli1, N.C. Tukamoto Junior, O. Ricci Junior, L.C. Matto,
I.L. Ângulo and C.R. Bonini-Domingo. Comparison of oxidative stress
and the frequency of polymorphisms in the HFE gene between
hemoglobin S trait blood donors and sickle cell disease patients.
Genetics and Molecular Research. 2011; 10(4): 3446-3454.
M. A. Emokpae, P. O. Uadia, and A. A. Gadzama. Correlation of oxidative
stress and inflammatory markers with the severity of sickle cell
nephropathy. Annals of African Medicine.2010; 9(3) 141–146.
Macy , E.M. , Hayes, T.E. & Tracy, R.P. variability in the measurement of
C- reactive protein in healthy subjects. Implications for reference
inrtervals and epidemiological applicatios. Clinical chemistry. 1997; 43:
52-58.
Manfredini V., Lazzaretti L.L., Griebeler I.H., Santin A.P., Brandão
V.D., Wagner S., Castro S.M., Peralba M.D.C., Benfato M.S. . Blood
Bibliography
168
antioxidant parameter in sickle anemia in steady state. J natl. Med.
Assoc. 2008; 100(8): 897-902.
Mariane D.E. Montalembert,Yacine Aggoun, Assa Niakate, Isabelle
Szezepanski, Damien Bonnet. Endothelial-dependent vasodilation is
impaired in children with sickle cell disease. The hematology journal,
2007; 92(12): 1709.
Mayes P.A., Murray R.K., Granner D.K., Mayes P.A., Rodwell V.W. (eds).
Structure and function of the water-soluble vitamins. In Harper’s
biochemistry. 25th ed. Stamford, Connecticut: Appleton and Lange.
2000: 642–52.
Mohammed F.A., Mahdi N., Sater M.A., Al-Ola K., Almawi W.Y. . The
relation of C-reactive protein to vasoocclusive crisis in children with
sickle cell disease. Blood Cells Mol Dis. 2010; 45: 293–6.
Mohsen A. F. El-Hazmi, Arjumand S. Warsy. The clinical, hematological
and biochemical expression of hemoglobin S (Hb S) in the Eastern
Saudi Arabia, journal of islamic academy of sciences. 1991; 4(2): 149-
158,
Morris, C. R. Suh, J. H. Hagar, W. Larkin, S.Bland, D. A. Steinberg, M. H.
Vichinsky, E. P. Shigenaga, M. Ames, B. Kuypers, F. A, Klings, E. S.
Erythrocyte glutamine depletion, altered redox environment, and
Bibliography
169
pulmonary hypertension in sickle cell disease. Blood. 2008; 111: 402–
410.
Mrtinn H. Steinberg , Donald H. Moharey, Jennifer S. Tirnaur. Sickle
Hemoglobin structure and functional properties. Walters Kulwer july
2013.
Muscari M.E. Paediatric nursing; 4th edition .USA: Lippinctt Williams &
Wilkins. 2005.
Mutay Aslan, Thomas M. Ryan, Brian Adler, Tim M. Townes, Dale A.
Parks, J. Anthony Thompson, Albert Tousson, Mark T. Gladwin, Rakesh
P. Patel, Margaret M. Tarpey Ines Batinic-Haberle,C. Roger White, and
Bruce A. Freeman. Oxygen radical inhibition of nitric oxide-dependent
vascular function in sickle cell disease. PNAS. 2001; 98(2):15215–1522.
Myriam Taverna, Anne-Lise Marie, Jean-Paul Mira, and Bertrand
Guidet.Specific antioxidant properties of human serum albumin. Annals
of Intensive Care. 2013; 3: 4
Nagababu E., Fabry M.E., Nagel R.L., Rifkind J.M. Heme degradation and
oxidative stress in murine models for hemoglobinopathies:
Thalassemia, sickle cell disease and hemoglobin C disease. Blood Cells.
2008; 41: 61-66.
Bibliography
170
Nath K.A., Grande J.P., Croatt A.J., Frank E, Caplice NM, Hebbel
RP, Katusic ZS. Transgenic sickle mice are markedly sensitive to renal
ischemiareperfusion injury. Am J Pathol 2005; 166(4): 963-972.
Natta C. L., Chen L. C., Chow C. K. Selenium and glutathione peroxidase
levels in sickle cell anemia. Acta Haematol. 1990; 83: 130–132;.
Nayma Sultana, Noorzahan Begum, Shelina Begum, Sultana Ferdousi,
Taskina Ali. Oral supplementation of vitamin E reduces osmotic
Fragility of RBC in haemolytic anemic patients with G6PD deficiency.
Pak J Physiol. 2009; 5(1): 25-28.
Neil A., Warren D., Kouichi R. . Impaired pentose phosphate shunt
function in sickle cell disease: A potential mechanism for increased
Heinz body formation and membrane lipid peroxidation. 1983; 15 (1):
1-13.
Nitin John. A review of clinical Profile in sickle cell trait . OMJ. 2010; 25:
3-8.
Niki E., Noguchi N., Tsuchihashi H., Gotoh N. . Interaction among
vitamin C, Vitamin E, and beta carotene. Am J Clin Nutr. 1995; 62(suppl
6): 1322S-13226S.
Nur E., Brandjes D.P., Schnog J . Otten H.M., Fijnvandraat K., Schalkwijk
C.G., Biemond B.J. Plasma levels of advanced glycation end products are
Bibliography
171
associated with haemolysis-related organ complications in sickle cell
patients. Br J Haematol. 2010; 151: 62-69.
O. G. Arinola, J.A. Olaniyi, M.O. Akiibinu. Evaluation of Antioxidants
levels and trace elements status in Nigerian sickle cell disease patients
with plasmodium parasitaemia. Pakistan journal of Nutrition. 2008;
7(6): 766-169.
Oloopoenia L., Fredrick W., Greaves W., Adams R., Addo FE, Castro O..
Pneumococcal sepsis and meningitis in adults with sickle cell disease.
South Med J .1990; 83: 1002–1004.
Onyemailoh Obiageli Bridget and Obi Patrick Chinedu. Antioxidant
vitamins and glycatedhaemoglobin status in sickle cell anaemia. Al
Ameen J Med Sci. 2014; 7(2): 175-177.
Patrick B., Ellen B. Fung, David W. Killilea,Quig Jiang, Mark Hudes,
Jacquline, Madden, John Porter, Patricia Evansa, Elliott Vichinisky, and
Paul Harmatz. Oxidative stress and inflammation in iron-overloaded
patients with β-thalassaemia or sickle cell disease. Br J Haematol. 2006;
135(2): 254– 263.
Petra Niklowitz, Anka Sonnenschein, Bernd Janetzky, Werner Andler,
Platt O.S.. Sickle cell anemia as an inflammatory disease. J Clin Investig.
2000; 106: 337–8.
Bibliography
172
Prakash S. Hundekar, Aadinath N. Suryakar, Aarti C. Karnik, Rajesh
Valvi, Rahul A. Ghone, Sonali S. Bhagat The Effect of Antioxidant
Supplementation on the Oxidant And Antioxidant Status in Sickle
Cell Anaemia Journal of Clinical and Diagnostic Research. 2011
(Suppl-2); 5(7): 1339-1342.
R. Marouf, O. Mojiminiyi, N. Abdella, M. Kortom, A.L. Wazzan.
Comparision of renal function marker in Kuwaiti patients with sikle
cell disease.J Clin pathol. 2006; 59: 345-351.
R.B. Gupta Sickle Cell Disease in Central India - Need for Micro Level
Planning. 2004.
Raj N. verma, Vipul N. Mankind, Danna D., Lucy D., Robert M . Depressed
erythrocyte glutathione reductase activity in sickle cell disease. The
American journal of clinical nutrition. 1983; 38: 884-887.
Rana M.W. Hasanato . Zinc and antioxidant vitamin deficiency in
patients with severe sickle cell anemia, Ann Saudi Med. 2006; 26(1):
17-21.
Rdha Raghupathy , Henny H. Billett. Promising therapies in sickle cell
disease. Cardiovascular & haematological disorder drug targets. 2009;
9: 1-8.
Bibliography
173
Ren H., Ghebremeskel K., Okpala I., Lee A., Ibegbulam O., Crawford M.
Patients with sickle cell disease have reduced blood antioxidant
protection. Nt J Vitam Nutr Res. 2008; 78(3): 139-47.
Richard Rokyta, Anna Yamamotova, Rchard Sulc, Adislav Trefil, Jaroslav
Racek, Vladislav Treska. Assessment of biochemical markers in
patients with pain of vascular origin. Clin Exp Med. 2008; 8: 199-206.
Roche M., Rondeau P., Singh N.R., Tarnus E., Bourdon E. The antioxidant
properties of serum albumin. FEBS Lett. 2008; 582(1): 783–1787.
Ruchaneekorn W. Kalpravidh, Thongchai Tangjaidee, Suneerat
Hatairaktham, Ratiya Charoensakdi, Narumol Panichkul, Noppadol
Siritanaratkul, and Suthat Fucharoen. Glutathione Redox System in 𝛽-
Thalassemia/Hb E Patients. The Scientific World Journal. 2013: 7.
S. Richard, H.H. Billett. Liver function tests in sickle cell disease. Clin.
Lab. Haem. 2002; 24: 21-27.
Sanjana Bhagat , Pradeep Kumar Patra , Amar Singh Thakur. Association
of Inflammatory Biomarker C-Reactive Protein, Lipid Peroxidation and
Antioxidant Capacity Marker with HbF Level in Sickle Cell Disease
Patients from Chattisgarh. Ind J Clin Biochem. 2012; 27(4): 394–399
Sanjeev Shyam Rao, Jagdish Prasad Goyal, S.V. Raghunath, Vijay B. Shah.
Hematological profile of sickle cell disease from South Gujarat, India.
Hematology Report. 2012; 4(2): 8.
Bibliography
174
Santos C.X.C., Anjos E.l., Augusto O. Uric acid oxidation by peroxynitrite:
multiple reactions, free radical formation, and amplification of lipid
oxidation. Arch Biochem Biophys. 1999; 372: 285-294.
Schall J. I. , Zemel B.S., Kawchak D.A., Ohene‑Frempong K., Stallings V.A.
Vitamin A status, hospitalizations, and other outcomes in young
children with sickle cell disease. J Pediatr. 2004; 145: 99‑106.
Schnog J.B., Mac Gillavry M.R., Van Zanten A.P., Meijers J.C., Rojer R.A.,
Duits A.J., Ten Cate H., Brandjes D.P. . Protein C and S and inflammation
in sickle cell disease. AmJ Hematol. 2004; 76: 26–32.
Schulz G. E., Schirmer R.H., Pai E. FAD- binding site of glutathione
reductase . J. Mol Bio. 1982; 160 : 287-308.
S.E. Cox , V. L. Esperance, J. Makani , D. Soka, C.M. Hill, F.J. Kirkham.
Nocturnal haemoglobin saturation variability is asoociated with
vitamin C deficiency in Tanzanian children with sickle cell anemia. Acta
peadiatrica. 2011 ;100: 594-597.
Seema Tripathi, Rakesh Dadsena, Anil Kumar. Study of certain
Biochemical parameters in patients of sickle cell anemia. Advance of
bioresearch. 2011; 2(2): 79-81.
Sen C. K. Oxidants and antioxidants in exercise. Journal of applied
physiology(Bethesda, Md. : 1985). 1995; 79(3): 675-86.
Bibliography
175
Serjeant G.R. The clinical features of sickle cell disease. In: Clinical
Studies, ed by Bearn AG, Black DAK, Hiatt HH. North-Holland
Publishing Company. 1974; 4: 59.
Serjeant G.R.. Sickle Cell Disease. Lancet. 1997; 350: 725-730.
Sevanian K.J., Davies and P. Hochstein. Serum urate as an antioxidant for
ascorbic acid. American Journal of Clinical Nutrition. 1991; 54: 1129S-
1134S.
Sheng K., Shariff M., Hebbel R.P. Comparative oxidation of hemoglobins
A and S. Blood. 1998; 91(9): 3467-3470.
Shuchismita Behera, Sujata Dixit, Gandham Bulliyya, Shatanu Kumar
Kar. Vitamin A status and hematological values in sickle cell disorder
cases. Indian Journal of Medical Sciences. 2012; 66 (7-8): 169-74.
Silvia Maria Meira Magalhães. Oxidative status in sickle cell anemia. Rev
Bras Hematol Hemoter. 2011; 33(3): 172-177.
Solovey A., Lin Y., Browne P., Choong S. Wayner E., Hebbel R.P.
Circulating activated endothelial cells in sickle cell anemia. N Engl J
Med. 1997; 337:1584.
Somjee S.S., Warrier R.P., Thomson J.L., Ory-Ascani J., Hempe J.M.
Advanced glycation end-products in sickle cell anaemia. Br J Haematol
2005; 128(1): 112-118.
Bibliography
176
Squadrito G.L., Cueto R., Splenser A.E., Valavanidis A., Zhang H., Uppu
R.M., Pryor W.A. .Reaction of uric acid with peroxynitrite and
implications for the mechanism of neuroprotection by uric acid. Arch
Biochem Biophys. 2000; 376(2): 333-7.
Stefan Marklund And Gudrun Marklund. Involvement of the Superoxide
Anion Radical in the Autoxidation of Pyrogallol and a Convenient Assay
for Superoxide Dismutase. Eur. J. Biochem. 1974; 47: 469-474.
Stephen C., Jerlinda G.C., Andre D., Lindsey B., Vered, Mojibade N., Dylan,
Sherraine Griffin, Tara, Malcolm, Micheal R. Sickle hemoglobiin normal
coupling amomg erythrocyte O2 content, glycolysis , and antioxidant
capacity. Blood. 2013; 121(9): 1651-1662.
Stuart M.J., Nagel R.L.. Sickle-cell disease. Lancet. 2004; 364 : 1343-60.
Stone W.L., Payne P.H., Adebonojo F.O. Plasma vitamin E and low plasma
lipoprotein levels in sickle cell anemia patients. J Assoc Acad Minor
Physician. 1990;1(2): 12-6.
Suba Krishnan, Yamaja Setty, Suhita G. Betal,Vaidyula Vijender, Koneti
Rao,Carlton Dampier and Marie Stuart. .Increased levels of the
inflammatory biomarker C-reactive protein at baseline are associated
with childhood sickle cell vasocclusive crises. British Journal of
Haematology. 2009; 148: 797–804.
Bibliography
177
Subhash Banerjee, Charles Owen, Sanjiv Chopra. Sickle cell hepatopathy.
Jhep.2001; 1021-1028.
Switzer J.A., Hess D.C., Nichols F.T., Adams R.J. Pathophysiology and
treatment of stroke in sickle-cell disease: present and future. Lancet
Neurol. 2006; 5: 501-512.
Sylvie A. Akohoue, Sadhna shankar, Ginger L. Milne, Jason Morrow, Kong
Y. Taiwo Kotila, Kayode Adedapo, Aduragbenro Adedapo, Olayiwola
Oluwasola, Eyitayo Fakunle, Biobele Brown. Liver dysfunction in
steady state sickle cell disease. Annals of Hepatology. 2005; 4(4): 261-
263.
Tanveer Jilani and Mohammad Perwaiz Iqbal. Does vitamin E have a
role in treatment and prevention of anemia’s?. Pak. J. Pharm. Sci. 2011;
Vol.24 (2) : 237-242.
Temme E.H.M., Zhang J., Schouten E.G., & Kesteloot H. Serum bilirubin
and 10-year mortality risk in a Belgian population. Cancer Causes and
Control. 2001; 12: 887-894.
Thakur S. Y. KHAN, G. P. LITTARRU. TBARS level in socioeconomical
poor rural sickle cell patients of bilaspur zone of chhattisgarh state.
2011; 2(3): 3.
Thomas Menke. Enrichment of coenzyme Q10 in plasma and blood cells:
defense against oxidative damage. Int. J. biol. Sci. 2007;3.
Bibliography
178
Trine Juul, Anna Malolepszy, Karen Dybkær, Rune Kidmose, Jan Trige
Rasmussen, Gregers Rom Andersen, Hans Erik Johnsen, Jan-Elo
Jørgensen, and Stig Uggerhoj Andersen. The in vivo toxicity of
hydroxyurea depends on its direct target Catalase. Journal of Biological
chemistry. 2010; 285: 28.
Van Beers E.J., Van Tuijn C.F., Mac Gillavry M.R., Vander G.A., Schnog J.J.,
Biemond B.J. . Sickle cell diseaserelated organ damage occurs
irrespective of pain rate: implications for clinical practice.
Haematologica. 2008; 93(5): 757-760.
Vanessa Cumming, Susanna Ali, Terrence Forrester, Karen Roye-Green
and Marvin Reid. Asymptomatic bacteriuria in sickle cell disease: a
cross-sectional study. BMC infectious diseases. 2006; 6: 46.
Vigusin D.M., Pepys, M.B. & Hawkins, P.N. .Metabolic and scintigraphic
studies of radioiodanated human C- reactive protein in health and
disease. Journal of Clinical investigation. 1993; 91: 1351-1357.
Viktoria Jeney, Jozsef Balla, Akihiro Yachie, Zsuzsa Varga, Gregory M.
Vercellotti, John W. Eaton and Gyorgy Balla. Pro-oxidant and cytotoxic
effects of circulating heme. Blood. 2002; 100: 879-887.
Wali U. , Yedu, M.H., samila B., And Jiya N.M. .Serum antioxidant vitamins
level in children with sickle cell anemia in Sokoto western Nigeria.
Bajopas. 2013; 6(1).
Bibliography
179
Wang W.C., Greer J.P., Foerster J., Lukens J.N., Rodgers G.M., Paraskevas
F., Glader B. (eds). .Sickle cell anemia and other sickling syndromes.
Wintrobe’s clinical hematology. 11th ed. Philadelphia: Lippincott
Williams and Wilkins; 2004:1264–1311.
Weatherall D.J., Clegg J.B., Blankson J., McNeil J.R. . A new sickling
disorder resulting from interaction of the genes of haemoglobin S and
alpha-thalassaemia. Br J Hematol. 1969; 17: 517-526.
Wood K. C. & Graner D. N. . sickle cell disease: role of reactive oxygen
species and nitrogen metabolites. Clinc exp pharmacol physiol. 2007;
34: 926-932.
Xiaomei Niu, Mehdi Nouraie, Andrew Campbell, Sohail Rana, Caterina P.
Minniti, Craig Sable, Deepika Darbari, Niti Dham, N. Scott Reading, Josef
T. Prchal, Gregory J. Kato, Mark T. Gladwin,Oswaldo L. Castro, Victor R.
Gordeuk. Angiogenic and Inflammatory Markers of Cardiopulmonary
Changes in Children and Adolescents with Sickle Cell Disease. 2009;
4(11): 7956.
Yoshihito Iuchi Yamaguchi University Japan. Anemia Caused by
Oxidative Stress. 2005.
Young I.S., Woodside J.V. Antioxidants in health and disease. J Clin
Pathol .2001; 54:176–186.
Bibliography
180
Yu B.P. Cellular defenses against damage from reactive oxygen
species. Physiological Reviews. 2007; 74: 139–162.
Yung G.L., Channick R.N., Fedullo P.F., Auger W.R., Kerr K.M., Jamieson
S.W., Successful pulmonary thromboendarterectomy in two patients
with sickle cell disease. Am J Respir Crit Care Med. 1998; 157: 1690-3.