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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

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

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

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

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

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

SYNDROMES ALPHA ET BETA THALASSEMIQUES HETEROZYGOTES EN TOURAINE. A PROPOS DE 7 CAS.OTHMANI LARBI.1977; ; S.L.; DA. 1977; PP. (96P.); BIBL. 7 P. 1/2; (THESE DOCT. MED.; TOURS)Thesis

ALPHA -THALASSEMIA AND BETA -THALASSEMIA IN A TURKISH FAMILY.ALTAY C; SAY B; YETGIN S et al.1977; AMER. J. HEMATOL.; U.S.A.; DA. 1977; VOL. 2; NO 1; PP. 1-15; BIBL. 26 REF.Article

THE BETA THALASSAEMIASFESSAS P; LOUKOPOULOS D.1974; CLIN. IN HAEMATOL.; G.B.; DA. 1974; VOL. 3; NO 2; PP. 411-435; BIBL. 2P.1/2Article

SCREENING FOR THALASSEMIA TRAIT BY ELECTRONIC MEASUREMENT OF MEAN CORPUSCULE VOLUME = DEPISTAGE DU TRAIT THALASSEMIQUE PAR MESURE ELECTRONIQUE DU VOLUME CORPUSCULAIRE MOYENPEARSON HA; O'BRIEN RT; MCINTOSH S et al.1973; NEW ENGL. J. MED.; U.S.A.; DA. 1973; VOL. 288; NO 7; PP. 351-353; BIBL. 13REF.Serial Issue

ALPHA GLOBIN GENE ANALYSIS IN A SARDINIAN FAMILY WITH INTERACTING ALPHA AND BETA THALASSAEMA GENESMELIS MA; GALANELLO R; CAO A et al.1983; BRITISH JOURNAL OF HAEMATOLOGY; ISSN 0007-1048; GBR; DA. 1983; VOL. 53; NO 4; PP. 667-671; BIBL. 12 REF.Article

THE INTERACTION OF ALPHA THALASSAEMIA WITH HETEROZYGOUS BETA THALASSAEMIAKANAVAKIS E; WAINSCOAT JS; WOOD WG et al.1982; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1982; VOL. 52; NO 3; PP. 465-473; BIBL. 1 P.Article

THE EFFECT OF ALPHA -THALASSEMIA ON THE EXPRESSION OF THE BETA -THALASSEMIA/HPFH HETEROZYGOTE IN A BLACK FAMILYBEUTLER E; TURNER E; KUHL W et al.1981; BLOOD; ISSN 0006-4971; USA; DA. 1981; VOL. 57; NO 6; PP. 1132-1134; BIBL. 8 REF.Article

BETA -AND NON-BETA -THALASSAEMIA IN SARDINIA AND THEIR FREQUENCIES = LES THALASSEMIES BETA ET NON BETA EN SARDAIGNE ET LEURS FREQUENCESTERRENATO L.1973; ANN. HUM. GENET.; G.B.; DA. 1973; VOL. 36; NO 3; PP. 285-295; BIBL. 23 REF.Serial Issue

KINETIC ALTERATIONS OF THE RED CELL MEMBRANE PHOSPHATASE IN ALPHA - AND BETA -THALASSEMIAMORLE L; DORLEAC E; ALLOISIO N et al.1982; AM. J. HEMATOL.; ISSN 0361-8609; USA; DA. 1982; VOL. 13; NO 4; PP. 269-282; BIBL. 26 REF.Article

INTERACTION OF ALPHA - AND DELTA BETA O-THALASSAEMIA: HAEMATOLOGICAL FEATURES AND GLOBIN CHAIN SYNTHESIS ANALYSISGALANELLO R; FU BETTA M; MELIS MA et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 1; PP. 40-42; BIBL. 18 REF.Article

HEMOGLOBIN G SAN JOSE (BETA 27(A4) GLU->GLY ALPHA 2), BETA THALASSEMIA, AND ALPHA THALASSEMIA IN A SILICIAN FAMILYMUSUMECI S; SCHILIRO G; PIZZARELLI G et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 52; NO 2; PP. 239-247; BIBL. 1 P.Article

INTERACTION OF ALPHA AND BETA THALASSAEMIA GENES IN TWO SARDINIAN FAMILIESFURBETTA M; GALANELLO R; XIMENES A et al.1979; BRIT. J. HAEMATOL.; GBR; DA. 1979; VOL. 41; NO 2; PP. 203-210; BIBL. 22 REF.Article

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