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kw.\*:("Hemoglobina D")

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Cystic fibrosis in a black child with hemoglobin S-D diseaseAMENDOLA, G; GARVIN, J; PIOMELLI, S et al.The American journal of pediatric hematology/oncology. 1990, Vol 12, Num 3, pp 340-342, issn 0192-8562, 3 p.Article

Hb D Los Angeles (D-Punjab) and Hb presbyterian: analysis of the defect at the DNA levelSCHNEE, J; AULEHLA-SCHOLZ, C; EIGEL, A et al.Human genetics. 1990, Vol 84, Num 4, pp 365-367, issn 0340-6717Article

Le point sur les nouvelles insulines = Update on new insulinsPHILIPS, Jean-Christophe; RADERMECKER, Régis.Revue médicale suisse. 2005, Vol 1, Num 30, pp 1936-1941, issn 1660-9379, 5 p.Article

An infant with homozygous hemoglobin D-IranTHORNBURG, Courtney D; ZIMMERMAN, Sherri A; SCHULTZ, William H et al.Journal of pediatric hematology/oncology. 2001, Vol 23, Num 1, pp 67-68, issn 1077-4114Article

Pneumococcal septicemia and meningitis in an infant with HB S/D-LOS Angeles disease : a failure of neonatal hemoglobinopathy screeningABHYANKAR, S. H; MILLER, S. T; RAO, S. P et al.Hemoglobin. 1991, Vol 15, Num 1-2, pp 119-123, issn 0363-0269, 5 p.Article

Co-inheritance of Hemoglobin D and β-thalassemia Traits in Three Iranian Families: Clinical RelevanceMARYAM TAGHAVI BASMANJ; KARIMIPOOR, Morteza; AMIRIAN, Azam et al.Archives of Iranian medicine. 2011, Vol 14, Num 1, pp 61-63, 3 p.Article

Molecular exclusion of Haemoglobin SD disease by prenatal diagnosisFODOR, F. H; ENG, C. M.Prenatal diagnosis. 1999, Vol 19, Num 1, pp 58-60, issn 0197-3851Article

Co-inheritance of Hb D-PUNJAB (CODON 121; GAA→CAA) and β0-thalassemia (IVS-II-1; G→A)ADEKILE, A. D; KAZANETZ, E. G; LEONOVA, J. YE et al.Journal of pediatric hematology/oncology. 1996, Vol 18, Num 2, pp 151-153, issn 1077-4114Article

Expression of Hemoglobin Variant Migration by Capillary Electrophoresis Relative to Hemoglobin A2 Improves PrecisionKEREN, David F; SHALHOUB, Renee; GULBRANSON, Ronald et al.American journal of clinical pathology. 2012, Vol 137, Num 4, pp 660-664, issn 0002-9173, 5 p.Article

Hemoglobin D/β-thalassemia and β-thalassemia major in a Saudi familyOWAIDAH, Tarek M; AL-SALEH, Mahasen M; AL-HELLANI, Ali M et al.Saudi medical journal. 2005, Vol 26, Num 4, pp 674-677, issn 0379-5284, 4 p.Article

Neonatal screening for haemoglobinopathies : the results of a 10-year programme in an English Health RegionALMEIDA, Antonio M; HENTHORN, Joan S; DAVIES, Sally C et al.British journal of haematology. 2001, Vol 112, Num 1, pp 32-35, issn 0007-1048Article

Mean cell haemoglobin concentration in subjects with haemoglobin C, D, E and S traitsHINCHLIFFE, R. F; NORCLIFFE, D; FARRAR, L. M et al.Clinical and laboratory haematology. 1996, Vol 18, Num 4, pp 245-248, issn 0141-9854Article

Mécanisme potentiel de la pénétration de l'hémoglobine conjuguée au dextrane dans la paroi artérielle = Potential mechanism of dextran-conjugated hemoglobin penetration inside arterial wallSMANI, Y; FAIVRE, B; FRIES, I et al.Archives des maladies du coeur et des vaisseaux. 2006, Vol 99, Num 7-8, pp 722-726, issn 0003-9683, 5 p.Article

The β-globin genotype E121Q/W15X (cd121GAA→CAA/cd15TGG→TGA) underlines Hb D/β-(0) thalassaemia marked by domination of haemoglobin DAHMED, M; STUHRMANN, M; BASHAWRI, L et al.Annals of hematology (Print). 2001, Vol 80, Num 11, pp 629-633, issn 0939-5555Article

Sample dilution to resolve mistaken identification of haemoglobin D as haemoglobin E using the variant automated systemTHOMAS, S.Journal of clinical pathology. 1998, Vol 51, Num 3, pp 253-254, issn 0021-9746Article

Hemoglobin D Ibadan-β° thalassemia : detection by neonatal screening and confirmation by electrospray-ionization mass spectrometryLANE, P. A; WITKOWSKA, H. E; FALICK, A. M et al.American journal of hematology. 1993, Vol 44, Num 3, pp 158-161, issn 0361-8609Article

Baisse visuelle: quand le fond d'œil n'explique pas tout = Visual loss: when the dilated fundus examination does not explain the featuresLAZRAK, Z; TITAH, C; BOK, C et al.Images en ophtalmologie. 2011, Vol 5, Num 1, pp 6-8, issn 1961-3172, 3 p.Article

L'Hb Charlieu [α1 Cd 106 (G13) Leu > Pro]: un nouveau variant alpha-thalassémique de l'hémoglobine découvert au décours d'une microcytose inexpliquée = Hb Charlieu [α1 Cd106 (G 13) Leu > Pro]: A new alpha-thalassemic hemoglobin variant found during an unexplained microcytosisJOLY, P; SZYMANOWICZ, A; NEYRON, M.-J et al.Immuno analyse & biologie spécialisée. 2010, Vol 25, Num 2, pp 104-109, issn 0923-2532, 6 p.Article

Influence du taux d'hémoglobine foetale (HBF) sur le stress oxydant chez le drépanocytaire homozygote vivant à Abidjan, Cote-d'Ivoire = Influence of fetal haemoglobin rate (FHb) on the oxidizing stress in homozygote sickle cell patient living in Abidjan, Côte-d'IvoireNACOULMA, E. W. C; SAWADOGO, D; SAKANDE, J et al.Bulletin de la Société de pathologie exotique. 2006, Vol 99, Num 4, pp 241-244, issn 0037-9085, 4 p.Article

Taux d'hémoglobine record pour une carence vitaminique ! = Severe anemia with vitamin deficiency !GAUBERT, Marie Line; ONEN, Fannie; LIEBERHERR, Déborah et al.La Revue de gériatrie. 2005, Vol 30, Num 10, pp 739-742, issn 0397-7927, 3 p.Article

La cause d'une anémie normocytaire chez les sujets âgés doit-elle être systématiquement recherchée quelle que soit la valeur de la concentration d'hémoglobine ? = Normocytic anemia in the eldery. Should the cause of anemia systematically investigated independently of hemoglobin concentration?CHASSAGNE, P; VERDONCK, A; DRUESNE, L et al.La Revue de médecine interne (Paris). 2004, Vol 25, Num 3, pp 189-194, issn 0248-8663, 6 p.Article

mRNA analysis in reticulocytes of subjects with Hb D, Hb Porto Alegre, Hb E, and different types of unstable hemoglobin variantsSMETANINA, N. S; HUISMAN, T. H. J.American journal of hematology. 1996, Vol 52, Num 4, pp 258-263, issn 0361-8609Article

A swedish family with α1-antitrypsin deficiency, haemochromatosis, haemoglobinopathy D and early death in liver cirrhosisERIKSSON, S; LINDMARK, B; HANIK, L et al.Journal of hepatology. 1986, Vol 2, Num 1, pp 65-72, issn 0168-8278Article

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