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- ABIODUN P.O., FATUNDE O.J., FLACH K.H., BUCK T.
Increased incidence of hepatitis B markers in children with sickle-cell anemia.
Blut 1989; 58 : 147-50.
- AKINYANJU O.O.
A profile of sickle cell disease in Nigeria.
Ann Acad Sci (New York) 1989; 565 : 126-36.
- ALLISON A.C.
Protection afforded by sickle-cell trait against subtertian malarial infection.
Br Med J 1954; 290-4.
- ARENA J.M.
Vascular accident and hemiplegia in sickle cell anemia.
Am J dis Child 1935; 49 : 722-3.
- ASAKURA T., ONISHI T., FRIEDMAN S., SCHWARTZ E.
Abnormal precipitation of oxyhemoglobin S by mechanical shaking.
Proc Natl Acad Sci USA 1974; 71 : 1594-8.
- BACHIR D., GALACTEROS F.
Prise en charge des maladies drépanocytaires.
Rev Prat 1989; 71 : 53-65.
- BACHIR D., BEAUVAIS P.
Prise en charge des patients drépanocytaires.
Rev Prat (Paris) 1989; 71 : 1900- 7.
- BERCHEL C., DIARA J.P., LORET A., FOUCAN L., LE TURDU C., SAMUEL Y.
Histoire naturelle de la drépanocytose.
Rev Prat (Paris) 1992; 42 : 1885-91.
- BERNARD J., LEVY J.P., VARET B., CLAUDEL J.P., RAIN J.D., SULTAN Y.
Hématologie.
Masson éditeur. 1983; ed 6 : 47.
- BERTRAND E.
Drépanocytose et cœur.
Arch Mal Cœur 1989; 82 : 1881-4.
- BEURLING-HARBURY.C., SCHADE S.G.
Platelet activation during pain crisis in sickle cell anemia patients.
Am J Hematol 1989; 31 : 237-41.
- BEUZARD Y.
Perspectives thérapeutiques de la drépanocytose.
Rev Prat (Paris) 1992; 42 : 1908-14.
- BUNN H.F. McDONOUGH M.
Asymetrical hemoglobin hybrids. An approach to the study of subunit interctions.
Biochemistry 1974; 13 : 988-93.
- ÇETINER S., AKOGLU T.F., KILINÇ Y., AKOGLU E., KÜMI M.
Immunological studies in sickle cell disease: comparison of homozygote mild and severe variants.
Clin Immunol Immunopathol 1989; 53 : 32-9.
- CHRISTAKIS J., VAVATSI N., HASSAPOPOULOU H., PAPADOPOULOU M., MANDRAVELI K., LOUKOPOULOS D., MORRIS J.S., SERJEANT B.E., SERJEANT G.R.
Comparition of homozygous sickle cell disease in Northern Greece and Jamaica.
The Lancet 1990; 335 : 637-40.
- DEISSEROTH A., NIENHUIS A., LAWRENCE J., GILES R., TURNER P.
Chromozomal localization of human b globin gene on human chromosome 11 in somatic cell hybrids.
Proc Natl Acad Sci USA. 1978; 75 : 1456-60.
- De LAGAUSIE P., EYMERI J.C., TAVAKOLI D.
Intérêt de la cholécystectomie réglée chez l'enfant drépanocytaire homozygote.
Ann Chir 1989; 43 : 361-2.
- DIALLO J.S., WADE A., N'DIAYE R.
Manifestations oculaires de la drépanocytose.
Sandoz éd 1984; 173-9.
- 19DUROSINMI M.A., OGUNSEYINDE A.O., OLATUNJI P.O. ESAN G.J.F.
Prevalence of cholelithiasis in Nigerians with sickle cell disease.
Afr J Med Sci. 1989; 18 : 223-7.
- EBOMOYI E. ADEDOYEN M.A., OGUNLESI O.
A comparative study of growth status of children with and without SS disease at Ilorin, Kwara state, Nigeria.
Afr J Med Med Sci 1989; 18 : 69-74.
- EDINGTON G.M., LEHMANN H.
Expression of the sickle-cell gene in Africa.
Br Med J 1955; 1308-11.
- EL HAZMI M.A., RAMIA S.
Frequencies of hepatitis B, delta and human immune deficiency virus markers in multitransfused Saudi patients with thalassemia and sickle-cell disease.
J Trop Med and Hyg 1989; 92:1-5.
- EL MOUZAN M.I., AL AWAMI B.H., AL TORKI M.T.
Clinical features of sickle cell disease in Eastern Arab children.
Am J Pediatr Hematol Oncol 1990; 12 : 51-5.
- ESTRADE G., POITRINEAU O., BERNASCONI F., GARNIER D., DONATIIN Y.
Fonction ventriculaire gauche et drépanocytose: étude échographique.
Arch Mal Coeur 1989; 82 : 1975-81.
- EVERSON G.T., NEMETH A., KOUROURIAN S., ZOGG D., BERGER LEFF N., DIXON D., GITHENS J.H., PRETORIUS D.
Gallblader functions is alterated in sickle hemoglobinopathy.
Gastroenterology 1989; 96 : 1307-16.
- FALUSI A.G., ESAN J.F.
Foetal hemoglobin levels in sickle-cell anemia in Nigerians.
AfrJ Med Sci 1989; 18 : 145-9.
- FEVZI OZKAYNAK M., ORTEGA J.A.
Reversibility of anatomical and functional asplenia by chronic transfusion in child with sickle cell anemia.
Am J Pediatric Hematol Oncol 1989; 11 : 445-6.
- FLEMING A.F.
The presentation, management and prevention of crisis in sickle cell disease in Africa.
Blood Rev 1989; 3 : 18-28.
- FOX P.D., DUNN D.T., MORRIS J.S., SERJEANT G.R.
Risk factors for proliferative sickle retinopathy.
Br J Ophthalmol 1990; 74 : 172-6.
- FRIEDMAN M.J.
Ultrastructural damage to the malaria parasite in the sickle-cell.
J Protozool 1979; 26 : 195-9.
- GALACTEROS F.
Drépanocytose, la maladie capitale.
JIM 1991; 208 : 37-45.
- GALACTEROS F.
Diagnostic néonatal des hémoglobinopathies.
Rev Prat (Paris) 1992; 42 : 1893-5.
- GENDREL D., KOMBILA M., NARDOU M., GENDREL C., DJOUBA F., MARTZ M., RICHARD-LENOBLE D.
Paludisme et hémoglobine : interactions chez l'enfant africain.
Presse Med 1992; 21 : 887-90.
- GINI E.K., KALUILA M., MUKUNA K., MANZOMBI M., KABAKELE K.
Hémoglobine A2 comme facteur modérateur de la gravité de la drépanocytose.
Médecine d'Afrique Noire 1989; 36 : 596-8.
- GIROT R.
Traitement de la thalassémie et de la drépanocytose chez l'enfant.
Ann Pediat 1978; 25 : 277-84.
- GOLDBERG M.A., BRUGNARA C., DOVER G.J., SCHAPIRA L., CHARACHE S., BUNN F.
Treatment of sickle cell anemia with hydroxyurea and eythropoïetin.
New Engl J Med. 1990; 323 : 366-72.
- GOLDCHER A.
Conseil génétique et drépanocytose.
Rev Prat 1992; 42 : 1896-9.
- HIGGS D.R., OLD J.M., CLEGG J.B., PRESSLEY L., HUNT D.M., WEATHERALL D.J., SERJEANT G.R.
Negro α-thalassemia is caused by deletion of a single a-globin gene.
The Lancet 1979; 1 : 272-6.
- HOFFRICHTER J., PHILIP P.D., EATON W.A.
Kinetics and mechanism of desoxyhemoglobin S gelation: a new approach to understanding sickle cell disease.
Proc Nat Acad Sci USA 1974; 71 : 4864-8.
- HUISSMAN T.H.J.
Trimodaly in the percentages of β chain variants in heterozygotes: the effect of active HBα structural loci.
Hemoglobin 1977; 1 : 349-382.
- JACKSON J.F., ODOM J.L., BELL W.N., JACKSON, Miss.
Amelioration of sickle cell disease by persistent fetal hemoglob in.
JAMA 1961; 177 : 867-9.
- KAN Y.W., DOZY A.M.
Polymorphism of DNA sequence adjacent to human β-globin structural gen: relationship to sickle mutation.
Proc Natl Acad Sci USA 1978; 75 : 5631-5.
- KARAYALCIN G., LANZKOWSKY P.
Plasma protein C levels in children with sickle cell disease.
Int J Pediatr Hematol Oncol; 1989, 11 : 320-3.
- KENNY M.W., MEAKIN M., WORTHINGTON D.J., STUART J.
Erythrocyte deformability in sickel-cell crisis.
Br J Hæmatol 1981; 49 : 103-9.
- LAB1F D.
Histoire génétique de la drépanocytose.
Rev. Prat. (Paris) 1992; 45 : 1879-81.
- LABIE D., SRINIVAS R., DUNDA O., DODE C., LAPOUMEROULi C.
Haplotypes in tribal indians bearing the sickle gen: evidence for the unicentric origine of the bs mutation and the unicentric origin of the tribal populations of India.
Human Biology 1989; 61 : 479-91.
- LENA-RUSSO D., NORTH M.L., GIROT R..
Épidemiologie des maladies génétiques de l'hémoglobine en France métropolitaine.
Rev Prat (Paris) 1992; 42 : 1867-72.
- LUX S.E., JOHN K.M.
The membrane defect in irreversibly sickled cell: irreversible deformation of the spectrin-actin lattice.
Blood 1975; 46 : 1052.
- MALPANI A.R., RAMANT S.K., SUNDARAM M.
Case report 558.
Skeletal Radiol 1989; 18 : 399-401.
- MEARS G., LACHMAN H., CABANNES R., AMEGNIZIN K. P. E., LAB1F D., NAGEL R. L.
Sickle gene: its origin and diffusion from West Africa.
J Clin Inves 1981; 68 : 606-10.
- NAGEL R.L., ROTH E.F. Jr.
Malaria and red cell genetic defects.
Blood 1989; 74 : 1213-9.
- NOGUCHI C.T., SCHECHTER A.N.
The intracellular polymerization of sikle cell hemoglobin and its relevance to sickle cell disease.
Blood 1981; 58 : 1057-68.
- OMANGA U., MUGANGA N., KAPEPELA.
Septicémies bactériennes de l'enfant drépanocytaire homozygote.
Semaine des Hopitaux de Paris 1990; 66 : 30-3.
- PATEL R.B., RAMANT S., PARMAR B.
Klebsielle pneumonie osteomyelytis in sickle cell anemia.
Indian J Pediatr 1989; 56 : 145-9.
- PERRINE R.P., PEMBREY M.E., JOHN P., PERRINE S., SHOUP F.
Natural history of sickle cell anemia in Saudi Arabs. A studv of 270 subjects.
Ann Intern Med. 1978; 88:1-6.
- POWARS D., WILSON B., IMBUS C., PEGELOW C., ALLEN J.
The natural history of stroke in sickle cell disease.
Am J Med 1978; 65 : 461-471.
- PROHOVNIK S.G., PAVLAKIS S., PIOMELLI J., BELLO J., MOHR J.P., HILAL S., DE VIVO D.C.
Cerebral hyperemia, stroke, and transfusion in sickle cell disease.
Neurology 1989; 39 : 344-8.
- RICHARDSON S.G.N., MATTHEWS K.B., STUART J., GEDDES A.M., WILCOX R.M.
Serial changes in coagulation and voscosity during sickle-cell crisis.
Br J Hmatol 1979; 41 : 95-103.
- RODGERS G.P.
Approches nouvelles du traitement de la drépanocytose.
JAMA 1991; 16 : 811-8.
- ROGERS Z.R., POWARS D.R., KINNEY T.R., WILLIAMS W.D., SCHROEDER W.A.
Nonblack patients with sickle cell disease have african βs gene cluster haplotypes.
JAMA 1989; 261 : 2991-4.
- SALAMAH M.M., MALLOUH A.A., HAMDAN J.A
Acute splenic sequestration crises in Saudi children with sickle-cell disease.
Ann Trop Pædiatr 1989; 9 : 115-7.
- SCHNEIDER R.G.
Review of hemoglobin variants studied in southwestern U.S.A.
Hemoglobin 1980; 4 : 363-71.
- SEELER R.A.
Deaths in children with sickle cell anemia: a clinical analysis of 19 fatal instances in Chicago.
Clin Pediatr 1972; 11 : 634-7.
- SHAFER F.E., HASTINGS C., VICHINSKY E.P.
The pathophysiolog of sickle tell disease: factors contributing to variable severity.
Int J Pediatr Hematol Oncol 1994; 1 : 359-78.
- SMITH J.A.
The natural history of sickle tell disease.
Ann Acad Sci (New York) 1989; 565 : 104-8.
- SOWEMIMO-COKER S.O., MEISELMAN H.J., FRANCIS R.B. Jr.
Increased circulating endothelial cells in sickle cell crisis.
Am J Hematol 1989; 31 : 263-5.
- SYDENSTRICKED V.P., MULHERIN W.A., HOUSEAL R.W.
Sickle cell anemia.
Am J Dis in Child 1923; 26 : 132-54.
- TANGNEY C.C., PHILLIPS G., FERNANDES P., HOPKINS R, WU S.-M.
Selected indices of micronutriment status in adults patients with sickle cell anemia.
Am J Hematol 1989; 32 : 161-6.
- TOMLISON W.J.
Abdominal crises in uncomplicated sickle cell anemia.
Am J Med 1945; 209 : 722.
- VILELA M.M.S., SAMPAIO M.S.C., COSTA F.F., BRANDALISE S.R.
Reduce phagocytic activity mediated by C3b Fc monocyte receptors from children with sickle-cell disease.
Brazilian J Med Biol Res 1989; 22 : 725-8.
- WAJKMAN H., LABIE D.
Facteurs biologiques modulant la gravité de la drépanocytose.
Ann Pédiatr (Paris) 1985; 32 : 813-8.
- WARKENTIN T.E., BARR R.D., ALI M.A.M., MOHANDAS N.
Recurrent acute sequestration crisis due to interacting genetic defect : hemoglobin SC disease and hereditary spherocytis.
Blood 1990; 75 : 266-70.
- WEATHERALL D.J.
Abnormal hemoglobin in the neonatal period and their relationship to thalassemia.
Br J Hoematol 1963; 9 : 265-77.
- WEBB D.K.H., SERJEANT G.R.
Systemic salmonella infection in sickle cell anaemia.
Ann Trop Pædiatr 1989; 3 : 169-72.
- WILSON J.P., WATERER R.R., WOFFORD J., CHAPMAN S.W.
Serious infections with Edwarsiella tarda.
Arch Inter Med 1989; 149 208-12.
- ZITTHOUN R., SAIVIAMA M., MARIE J.P.
Manuel d'hématologie
Doin éditeurs - Paris.4e éd 1993; 103.
SOMMAIRE | HISTORIQUE | RAPPELS | ÉPIDÉMIOLOGIE |ÉTUDE CLINIQUE | DIAGNOSTIC POSITIF DE LA DRÉPANOCYTOSE | DIAGNOSTIC ANTE ET NÉONATAL | TRAITEMENT DE LA DRÉPANOCYTOSE | LES PERSPECTIVES THÉRAPEUTIQUES DE LA DRÉPANOCYTOSE | CONCLUSION | BIBLIOGRAPHIE