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TREATMENT OF SICKLE CELL ANEMIACHARACHE S.1981; ANNU. REV. MED.; ISSN 0066-4219; USA; DA. 1981; VOL. 32; PP. 195-206; BIBL. 55 REF.Article

Hydroxyurea as treatment for sickle cell anemiaCHARACHE, S.Hematology/oncology clinics of North America. 1991, Vol 5, Num 3, pp 571-583, issn 0889-8588Article

COMPARISON OF THE EFFECTS OF LOWER MONOHYDRIC ALCOHOLS AND INOSITA, HEXAPHOSPHATE ON THE OXIDATION OF HEMOGLOBIN BY MENADIONEMCDONALD VW; CHARACHE S.1982; BIOCHIMICA ET BIOPHYSICA ACTA; ISSN 0006-3002; NLD; DA. 1982; VOL. 705; NO 1; PP. 48-54; BIBL. 22 REF.Article

THE EFFECT OF HEMOGLOBIN F-CHESAPEAKE (ALPHA ₂^92ARG->LEUGAMMA ²) ON FETAL OXYGEN AFFINITY AND ERYTHROPOIESISJONES CM; CHARACHE S; HATHAWAY PJ et al.1979; PEDIATR. RES.; USA; DA. 1979; VOL. 13; NO 7; PP. 851-853; BIBL. 23 REF.Article

POLYCYTHEMIA PRODUCED BY HEMOGLOBIN OSLER (B145 CHC2) TYR->ASP.CHARACHE S; BRIMHALL B; JONES RT et al.1975; JOHNS H,OPKINS MED. J.; U.S.A.; DA. 1975; VOL. 136; NO 3; PP. 132-136; BIBL. 17REF.Article

Pregnancy in sickle cell diseaseCHARACHE, S; NIEBYL, J. R.Clinics in haematology. 1985, Vol 14, Num 3, pp 729-746, issn 0308-2261Article

HUMAN HEMOGLOBINS AND HEMOGLOBINOPATHIES: A REVIEW TO 1981SCHNEIDER RG ED; CHARACHE S ED; SCHROEDER WA ED et al.1980; TEX. REP. BIOL. MED.; ISSN 0040-4675; USA; DA. 1980-1981; VOL. 40; 504 P.Serial Issue

COMPARISON OF MICROCHROMATOGRAPHY AND ELECTROPHORESIS WITH ELUTION FOR HEMOGLOBIN A₂ (HBA₂) QUANTITATIONHAMILTON SR; MILLER ME; JESSOP M et al.1979; AMER. J. CLIN. PATHOL.; USA; DA. 1979; VOL. 71; NO 4; PP. 368-396; BIBL. 29 REF.Article

EVALUATION OF EXTRACORPOREAL ALKYLATION OF RED CELLS AS A POTENTIAL TREATMENT FOR SICKLE CELL ANEMIA.CHARACHE S; DREYER R; ZIMMERMAN I et al.1976; BLOOD; U.S.A.; DA. 1976; VOL. 47; NO 3; PP. 481-488; BIBL. 1 P. 1/2Article

OXYGEN AFFINITY AND STABILITY OF HEMOGLOBIN DUNN (ALPHA 6 (A4) ASP->ASN): USE OF ISOELECTRIC FOCUSING IN RECOGNITION OF A NEW ABNORMAL HEMOGLOBINCHARACHE S; BRIMHALL B; ZAATARI G et al.1980; AM. J. HEMATOL.; ISSN 0361-8609; USA; DA. 1980; VOL. 9; NO 2; PP. 151-160; BIBL. 25 REF.Article

Hzmochromatosis and diabetesSAUDEK, C. D; CHARACHE, S.Baillière's clinical endocrinology and metabolism. 1992, Vol 6, Num 4, pp 807-817, issn 0950-351XArticle

Differences in the reaction sequences associated with drug-induced oxidation of hemoglobins E, S, A, and FMACDONALD, V. W; CHARACHE, S.The Journal of laboratory and clinical medicine. 1983, Vol 102, Num 5, pp 762-772, issn 0022-2143Article

CONFORMATION IN SOLUTION OF HEMOGLOBIN OSLER (ALPHA ₂ ^ABETA ₂^145TYR->ASP)BUCCI E; FRONTICELLI C; NICKLAS J et al.1979; J. BIOL. CHEM.; USA; DA. 1979; VOL. 254; NO 21; PP. 10811-10819; BIBL. 32 REF.Article

HEMOGLOBIN SC, SSG PHILADELPHIA AND SO_ARAB DISEASES. DIAGNOSTIC IMPORTANCE OF AN INTEGRATIVE ANALYSIS OF CLINICAL HEMATOLOGIC AND ELECTROPHORETIC FINDINGS.CHARACHE S; ZINKHAM WH; DICKERMAN JD et al.1977; AMER. J. MED.; U.S.A.; DA. 1977; VOL. 62; NO 3; PP. 439-446; BIBL. 29 REF.Article

PROPERTIES OF HEMOGLOBULIN A AND HEMOGLOBULIN ZURICH (BETA 63 HISTIDINE->ARGININE). QUANTITATIVE EVALUATION OF FUNCTIONAL ABNORMALITIES IN HEMOGLOBINS.WALLACE WJ; VOLPE JA; MAXWELL JC et al.1976; BIOCHEM. BIOPHYS. RES. COMMUNIC.; U.S.A.; DA. 1976; VOL. 68; NO 4; PP. 1379-1386; BIBL. 28 REF.Article

APLASTIC CRISIS DUE TO EXTENSIVE BONE MARROW NECROSIS IN SICKLE CELL DISEASEPARDOLL DM; RODEHEFFER RJ; SMITH RRL et al.1982; ARCHIVES OF INTERNAL MEDICINE (1960); ISSN 0003-9926; USA; DA. 1982; VOL. 142; NO 12; PP. 2223-2225; BIBL. 13 REF.Article

OXYGEN TRANSPORT IN A WOMAN WITH HEMOGLOBIN HOPE/BETA ⁺ THALASSEMIACHARACHE S; ACHUFF S; WINSLOW R et al.1979; J. LAB. CLIN. MED.; USA; DA. 1979; VOL. 93; NO 2; PP. 316-320; BIBL. 10 REF.Article

INDIVIDUAL VARIATION IN THE PRODUCTION AND SURVIVAL OF F CELLS IN SICKLE-CELL DISEASEDOVER GJ; BOYER SH; CHARACHE S et al.1978; NEW ENGL. J. MED.; USA; DA. 1978; VOL. 299; NO 26; PP. 1428-1435; BIBL. 26 REF.Article

PERIPHERAL AND OPTIC NEURITIS IN A PATIENT WITH HEMOGLOBIN SC DISEASE DURING TREATMENT OF SALMONELLA OSTEOMYELITIS WITH CHLORAMPHENICOL.CHARACHE S; FINKELSTEIN D; LIETMAN PS et al.1977; JOHNS HOPKINS MED. J.; U.S.A.; DA. 1977; VOL. 140; NO 3; PP. 121-124; BIBL. 19 REF.Article

Experimental therapyCHARACHE, S.Hematology/oncology clinics of North America. 1996, Vol 10, Num 6, issn 0889-8588, 8, 1373-1382 [11 p.]Article

Eye disease in sickling disordersCHARACHE, S.Hematology/oncology clinics of North America. 1996, Vol 10, Num 6, issn 0889-8588, 7,8, 1357-1362 [7 p.]Article

Induction of fetal hemoglobin production in subjects with sickle cell anemia by oral sodium phenylbutyrateDOVER, G. J; BRUSILOW, S; CHARACHE, S et al.Blood. 1994, Vol 84, Num 1, pp 339-343, issn 0006-4971Article

Approches to the therapy of sickle cell anemia = Approches thérapeutiques de la drépanocytoseBEUZARD, Y; CHARACHE, S.Approches to the therapy of sickle cell anemia. 1985, 569 p., isbn 2-855-98287-1Conference Proceedings

Iron deficiency anemia: mitochondrial α-glycerophosphate dehydrogenase in guinea pig skeletal muscleMACDONALD, V. W; CHARACHE, S; HATHAWAY, P. J et al.The Journal of laboratory and clinical medicine. 1985, Vol 105, Num 1, pp 11-18, issn 0022-2143Article