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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

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

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

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

Compound heterozygote state for GγAγ(δβ)°-thalassemia and hereditary persistence of fetal hemoglobinFUCHAROEN, Supan; PANYASAI, Sitthichai; SURAPOT, Satja et al.American journal of hematology. 2005, Vol 80, Num 2, pp 119-123, issn 0361-8609, 5 p.Article

Insertion of common mutations into the human β-globin locus using GET Recombination and an EcoRI endonuclease counterselection cassetteJAMSAI, Duangporn; NEFEDOV, Mikhail; NARAYANAN, Kumaran et al.Journal of biotechnology. 2003, Vol 101, Num 1, pp 1-9, issn 0168-1656, 9 p.Article

Pitfalls in genetic counselling for β-thalassemia: an individual with 4 different thalassemia mutationsGALANELLO, R; PAGLIETTI, M. E; ADDIS, M et al.Clinical genetics. 1988, Vol 33, Num 3, pp 151-155, issn 0009-9163Article

Thalassemia intermedia in two patients with Hb Lepore-β°-thalassemia (frameshift codon 8, -AA)BOZKURT, G; BAYSAL, E; GU, L.-H et al.Hemoglobin. 1994, Vol 18, Num 3, pp 247-250, issn 0363-0269Article

Interaction of heterozygous β°-thalassemia with single functional α-globulin geneGALANELLO, R; PAGLIETTI, E; MELIS, M. A et al.American journal of hematology. 1988, Vol 29, Num 2, pp 63-66, issn 0361-8609Article

The design of an information system on thalassemiaROSSI-MORI, A; RICCI, F. L; ZAMBON, G et al.Médecine et informatique. 1984, Vol 9, Num 1, pp 15-24, issn 0307-7640Article

Skelettveränderungen bei der Thalassämie = Modifications osseuses dans la thalassémie = Skeletal changes in thalassemiaALAIYAN, H; MITTELMEIER, H; GRAF, N et al.Zeitschrift für Orthopädie und ihre Grenzgebiete. 1988, Vol 126, Num 4, pp 437-447, issn 0044-3220Article

Avidity of radiogallium for bone in thalassemiaGRIMMOND, A. P; SPENCER, R. P.Clinical nuclear medicine. 1987, Vol 12, Num 9, pp 758-759, issn 0363-9762Article

A study of the mechanisms and sites of action of desferrioxamine in thalassaemia majorBIANCO, I; GRAZIANI, B; LERONE, M et al.Acta haematologica. 1984, Vol 71, Num 2, pp 100-105, issn 0001-5792Article

Feasibility of antenatal diagnosis of β thalassaemia by DNA polymorphisms in Asian Indian and Cypriot populationsOLD, J. M; PETROU, M; MODELL, B et al.British journal of haematology. 1984, Vol 57, Num 2, pp 255-263, issn 0007-1048Article

Malays with thalassaemia in West MalaysiaGEORGE, E; KHUZIAH, R.Tropical and geographical medicine. 1984, Vol 36, Num 2, pp 123-125, issn 0041-3232Article

Molecular heterogeneity of beta thalassaemia in the Italian populationGIAMPAOLO, A; MAVILIO, F; MASSA, A et al.British journal of haematology. 1984, Vol 56, Num 1, pp 79-85, issn 0007-1048Article

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

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

Transfusion regimen in beta thalassemia major using magnetic measurement techniquesSAKHNINI, Lama; KHUZAIE, Rula.World journal of microbiology & biotechnology. 2003, Vol 19, Num 5, pp 451-454, issn 0959-3993, 4 p.Article

The β- and δ-Thalassemia repositoryHUISMAN, T. H. J.Hemoglobin. 1992, Vol 16, Num 4, pp 237-358, issn 0363-0269Article

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

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