G P Tamagnini
Overview
Explore the profile of G P Tamagnini including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
44
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Recent Articles
1.
Bento M, Ribeiro M, Cunha E, Rebelo U, Granjo E, Granado C, et al.
Hemoglobin
. 2000 Mar;
24(1):59-63.
PMID: 10722117
No abstract available.
2.
Ribeiro M, Cunha E, Goncalves P, Martin Nunez G, Fernandez Galan M, Tamagnini G, et al.
Hum Genet
. 1997 May;
99(5):669-73.
PMID: 9150738
Hb Lepore is one of the most common abnormal haemoglobins in Caucasians in Central Portugal and in the Spanish Alta Extremadura (0.28% in a survey of school children). A group...
3.
4.
Ribeiro M, Goncalves P, Cunha E, Bento C, Almeida H, Pereira J, et al.
Hemoglobin
. 1997 May;
21(3):261-9.
PMID: 9140722
No abstract available.
5.
Tamagnini G, Goncalves P, Ribeiro M, Kaeda J, Kutlar F, Baysal E, et al.
Hemoglobin
. 1993 Feb;
17(1):31-40.
PMID: 8454469
We report the characterization of seven different beta-thalassemia mutations in 131 newly diagnosed Portuguese beta-thalassemia heterozygotes. Methodology included the detection of abnormal fragments by agar gel electrophoresis of PCR-amplified DNA...
6.
Ribeiro M, Baysal E, Kutlar F, Tamagnini G, Goncalves P, Lopes D, et al.
Br J Haematol
. 1992 Apr;
80(4):567-8.
PMID: 1581247
No abstract available.
7.
Oner R, Oner C, Wilson J, Tamagnini G, Ribeiro L, HUISMAN T
Br J Haematol
. 1991 Oct;
79(2):306-10.
PMID: 1659862
We have studied a Portuguese family with a dominant beta-thalassaemia trait that was present in one member of each of three generations. It was characterized by a moderate anaemia, microcytosis...
8.
Tamagnini G, Ribeiro M, Valente V, Ramachandran M, Wilson J, Baysal E, et al.
Hemoglobin
. 1991 Jan;
15(6):487-96.
PMID: 1814856
We have identified a new high oxygen affinity hemoglobin variant in members of a Portuguese family; it is characterized by an Asp----Glu replacement at codon 99 of the beta chain...
9.
Zhao W, Wilson J, Webber B, Kutlar A, Tamagnini G, Kuam B, et al.
Hemoglobin
. 1990 Jan;
14(6):627-35.
PMID: 1983218
Hb Hekinan, an alpha chain variant that is characterized by a Glu----Asp mutation at position alpha 27, was observed in three Chinese females attending a prenatal clinic in Macau. The...
10.
Tamagnini G, Kuam B, Fai W
Hemoglobin
. 1988 Jan;
12(5-6):637-43.
PMID: 3209406
The implementation of a Primary Health Care system in Macau has created the need to study the prevalence of Congenital Anemias in the population to facilitate the planning of measures...