Zobrazeno 1 - 10 of 205 pro vyhledávání: '"B, Ringelhann"'
2
Molecular characterization of beta-thalassemia in Hungary
Autor: J. G. Szelenyi, B. Ringelhann, V. Divoky, S. Hollân, Karel Indrák, M. Svobodova, A. Marosi, M. Horanyi, Titus H.J. Huisman, M. Laub
Publikováno v: Human genetics. 92(4)
We have identified seven different beta-thalassemia mutations and one delta beta-thalassemia determinant (the Sicilian type) in 32 members of 17 Hungarian families. The most common mutation is the IVS-I-1 (G--A) change; its high frequency is comparab
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::188afbc2917e4aeaa0a7c200f53c7a63
https://pubmed.ncbi.nlm.nih.gov/8225319
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5
Hemoglobin Lepore Washington and Hemochromatosis in a Hungarian Patient
Autor: G. D. Efremov, A. Reviczky, B. Ringelhann, E. Csak
Publikováno v: Hemoglobin. 3:193-204
A Hungarian family with four heterozygotes for Hb Lepore Washington is described. One, a 43-year-old male, had high levels of serum iron, saturated iron-binding capacity, and ferritin, and normal levels of folic acid and vitamin B12. Liver biopsy sho
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8913ceaf0978dc44bdaf6ac0f27cdfd
https://doi.org/10.3109/03630267908998914
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6
Homozygotes for the hereditary persistence of fetal hemoglobin: The ratio of G? to A? chains and biosynthetic studies
Autor: Walter A. Schroeder, C. T. A. Acquaye, F.I.D. Konotey-Ahulu, B. Ringelhann, Titus H.J. Huisman, P. K. Sukumaran, G. Yawson, J. H. Oldham
Publikováno v: Biochemical Genetics. 15:1083-1096
Two sons of a previously reported Ghanaian homozygote for the hereditary persistence of fetal hemoglobin (HPFH) (Ringelhann et al., 1970) also are HPFH homozygotes. In addition, another unrelated adult Ghanaian homozygote has been detected. All of th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7264f19735dd2b309111d0b06af1e741
https://doi.org/10.1007/bf00484499
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7
Further Investigations of the γ-Chain in a Ghanaian Adult, Homozygous for Hereditary Persistence of Fetal Haemoglobin
Autor: B. Ringelhann, H. Kamuzora, H. Lehmann, F.I.D. Konotey-Ahulu, P.A. Lorkin
Publikováno v: Acta Haematologica. 53:315-320
The γ chain in a Ghanaian homozygous for hereditary persistence of fetal haemoglobin was considered to be of the Gγ type on the basis of the amino acid
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::74539630bb47427cde371b1b9f9c09e6
https://doi.org/10.1159/000208198
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8
The γ-Chain in a Ghanaian Adult, Homozygous for Hereditary Persistence of Fetal Haemoglobin
Autor: F.I.D. Konotey-Ahulu, B. Ringelhann, P.A. Lorkin, H. Lehmann, H. Kamuzora
Publikováno v: Acta Haematologica. 51:179-184
Fetal haemoglobin consists of α - and γ-chains. There are two types of human γ-chains:one, (Gγ) in which residue 136 is one of glycine, and another (Aγ), in which that position is oc
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30ed244fa2dc9ad199122f775454f60a
https://doi.org/10.1159/000208291
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10
Haemoglobin K Woolwich (α2β2132 Lysine → Glutamine) in Ghana
Autor: H. Lehmann, B. Ringelhann, Francis K. Nkrumah, Barbar G. Wiltshire, N.C. Talapatra, F.I.D. Konotey-Ahulu
Publikováno v: Acta Haematologica. 45:250-258
A fast moving haemoglobin, K Woolwich, was found in patients admitted to Korle Bu Teaching Hospital, Accra, and in members of 2 tribes which live in different regions of Ghana and differ linguisticall
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b5ad6d40b336224d81d14b68ea7adbae
https://doi.org/10.1159/000208632
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