Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("Thalassémie")

Filter

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Language

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Origin

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 5780

  • Page / 232
Export

Selection :

  • and

GLOBIN CHAIN SYNTHESIS IN THE MARROW AND RETICULOCYTES OF BETA THALASSEMIA, HEMOGLOBIN H DISEASE, AND BETA DELTA THALASSEMIA = SYNTHESE DES CHAINES DE GLOBINE DANS LA MOELLE ET LES RETICULOCYTES AU COURS DE LA BETA THALASSEMIE, DE L'HEMOGLOBINOSE H ET DE LA BETA DELTA THALASSEMIESHCHORY M; RAMOT B.1972; BLOOD; U.S.A.; DA. 1972; VOL. 40; NO 1; PP. 105-111; BIBL. 21REF.Serial Issue

NORMAL AND ABNORMAL HUMAN HEMOGLOBINS1972; ADV. CLIN. CHEM.; U.S.A.; DA. 1972; VOL. 15; PP. 149-253; BIBL. 29P.Serial Issue

δ-thalassemia caused by disruption of the site for an erythroid-specific transcription factor, GATA-1, in the δ-globin gene promoterMATSUDA, M; SAKAMOTO, N; FUKUMAKI, Y et al.Blood. 1992, Vol 80, Num 5, pp 1347-1351, issn 0006-4971Article

Hematological phenotype of the double heterozygous state for alpha and beta thalassemiaROSATELLI, C; FALCHI, A. M; SCALAS, M. T et al.Hemoglobin. 1984, Vol 8, Num 1, pp 25-35, issn 0363-0269Article

Gene analysis in δβ and δ° thalassemiaBAIRD, M; DRISCOLL, M. C; BEN-BASSAT, I et al.The Journal of biological chemistry (Print). 1984, Vol 259, Num 1, pp 512-515, issn 0021-9258Article

TWO FAMILIES WITH HAEMOGLOBINOPATHIES RARELY OBSERVED IN ITALY (HBC AND HBDPI UNJAB CONTIENT = DEUX FAMILLES PRESENTANT UNE HEMOGLOBINOPATHIE RAREMENT OBSERVEE EN ITALIE (HBC ET HBDPI UNJAB CONTIENT LAMEDICA GM; LAMEDICA G; CERRUTI MAINARDI P et al.1972; PANMINERVA MED.; ITAL.; DA. 1972; VOL. 14; NO 9; PP. 270-275; BIBL. 28 REF.Serial Issue

ABNORMAL GLOBIN SYNTHESIS IN THALASSEMIC RED CELLS = SYNTHESE DE GLOBINE ANORMALE DANS LES HEMATIES THALASSEMIQUESSCHWARTZ E.1974; SEMINARS HEMATOL.; U.S.A.; DA. 1974; VOL. 11; NO 4; PP. 549-567; BIBL. 3P.Article

HEMATOLOGICAL EVALUATION OF PATIENTS WITH VARIOUS COMBINATIONS OF ALPHA -THALASSEMIAALTAY C; GURGEY A; TUNCBILEK E et al.1980; AM. J. HEMATOL.; ISSN 0361-8609; USA; DA. 1980; VOL. 9; NO 3; PP. 261-267; BIBL. 19 REF.Article

LABORATORY DIAGNOSIS OF HB CC-ALPHA -THALASSEMIAWONG SC; ALI MAM.1979; CLIN. BIOCHEM.; CAN; DA. 1979; VOL. 12; NO 5; PP. 157-158; BIBL. 9 REF.Article

Nomenclature of the α-thalassaemiasLEHMANN, H; CARRELL, R. W.Lancet (British edition). 1984, Num 8376, pp 552-553, issn 0140-6736Article

Thalassemia minor: routine erythrocyte measurements and differentiation from iron deficiencyJOHNSON, C. S; TEGOS, C; BEUTLER, E et al.American journal of clinical pathology. 1983, Vol 80, Num 1, pp 31-36, issn 0002-9173Article

Multiple mutations produce δβ0 thalassemia in sardiniaPIRASTU, M; YUET WAI KAN; GALANELLO, R et al.Science (Washington, D.C.). 1984, Vol 223, Num 4639, pp 929-930, issn 0036-8075Article

ThalassemiaPONCZ, M; COHEN, A; SCHWARTZ, E et al.Advances in pediatrics. 1984, Vol 31, pp 43-86, issn 0065-3101Article

HbA2 Victoria δ24(B6) Gly→Asp a nex δ chain variant occurring with β-thalassemiaBRENNAN, S. O; WILLIAMSON, D; SMITH, M. B et al.Hemoglobin. 1984, Vol 8, Num 2, pp 163-168, issn 0363-0269Article

The effects of alpha-thalassaemia in HbSC diseaseSTEINBERG, M. H; COLEMAN, M. B; ADAMS, J. G et al.British journal of haematology. 1983, Vol 55, Num 3, pp 487-492, issn 0007-1048Article

LO STUDIO DELLA DISTRIBUZIONE VOLUMETRICA NELLE CELLULE EMATICHE QUALE SEMPLICE E RAPIDO SCREENING PER LE BETA ED ALFA-TALASSEMIE = L'ETUDE DE LA DISTRUBTION VOLUMETRIQUE DES CELLULES DU SANG EN TANT QUE DEPISTAGE SIMPLE ET RAPIDE POUR LES BETA ET ALPHA-THALASSEMIESBONANNI G; CIANCARELLI M; FIORITONI G et al.1979; HAEMATOLOGICA; ITA; DA. 1979; VOL. 64; NO 5; PP. 580-585; ABS. ENG; BIBL. 15 REF.Article

GLOBIN CHAIN SYNTHESIS IN VARIOUS ANEMIASRAMOT B; SHCHORY M; MOZEL M et al.1972; BIOCHIMIE; FR.; DA. 1972; VOL. 54; NO 5-6; PP. 669-673; ABS. FR.; BIBL. 11 REF.Serial Issue

(Aγδβ)° thalassaemia: similarity of phenotype in four different molecular defects, including one newly describedTRENT, R. J; JONES, R. W; CLEGG, J. B et al.British journal of haematology. 1984, Vol 57, Num 2, pp 279-289, issn 0007-1048Article

HEMATOLOGICAL AND BIOSYNTHETIC FEATURES OF BETA 0-THALASSEMIA WITH AN ASSOCIATED ALPHA -THALASSEMIA HETEROZYGOSITY IN SARDINIALONGINOTTI M; MASALA B; TIDORE M et al.1981; HEMOGLOBIN; ISSN 0363-0269; USA; DA. 1981; VOL. 5; NO 6; PP. 619-625; BIBL. 19 REF.Article

HUMAN GLOBIN GENE ANALYSIS FOR A PATIENT WITH BETA O/DELTA BETA O-THALASSEMIAOTTOLENGHI S; LANYON WG; WILLIAMSON R et al.1975; PROC. NATION. ACAD. SCI. U.S.A.; U.S.A.; DA. 1975; VOL. 72; NO 6; PP. 2294-2299; BIBL. 30 REF.Article

EARLY SPLENECTOMY IN THE MANAGEMENT OF THALASSEMIC CHILDREN IN DJAKARTA = SPLENECTOMIE PRECOCE DANS LE TRAITEMENT DE LA THALASSEMIE CHEZ LES ENFANTS A DJAKARTAWAHIDIJAT I; MARKUM AH; ADANG ZK et al.1972; ACTA HAEMATOL.; SUISSE; DA. 1972; VOL. 48; NO 1; PP. 28-33; BIBL. 20REF.Serial Issue

HEMOGLOBINE C-BETA -THALASSEMIE ET BETA -THALASSEMIE HOMOZYGOTE DANS UNE FAMILLE NOIRE AFRICAINEBASSET P; FALL M; OUDART JL et al.1975; NOUV. REV. FR. HEMATOL.; FR.; DA. 1975; VOL. 15; NO 3; PP. 343-355; ABS. ANGL.; BIBL. 1 P. 1/2Article

Double hétérozygotie HB O Arab/Beta+ thalassémie (dans une famille tunisienne) = Double heterozygot Hb O Arab/Beta+ thalassemia among a tunisian familyBEN ABDELADHIM, A; BEN OTHMAN, T; GRIRA, F et al.Tunisie médicale. 1988, Vol 66, Num 8-9, pp 631-635, issn 0041-4131Article

DOUBLE HETEROZYGOUS BETA DELTA -THALASSEMIA IN NEGROES = THALASSEMIE BETA DELTA BI-HETEROZYGOTE CHEZ DES NOIRSZELKOWITZ L; TORRES C; BHOOPALAM N et al.1972; ARCH. INTERN. MED.; U.S.A.; DA. 1972; VOL. 129; NO 6; PP. 975-979; BIBL. 30REF.Serial Issue

Actualités sur les thalassémies = Update on thalassemiaCOSTELLO, R.La Revue de médecine interne (Paris). 2009, Vol 30, issn 0248-8663, S22-S23, SUP2Conference Paper

  • Page / 232