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G Tamagnini

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Articles 18
Citations 119
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Recent Articles
1.
Tamagnini G, Bourguignon T, Rega F, Verbrugghe P, Lamberigts M, Langenaeken T, et al.
Expert Rev Med Devices . 2021 Feb; 18(3):239-244. PMID: 33583313
Introduction: The Inspiris Resilia tissue valve was recently introduced into clinical practice. This review summarizes the pre-clinical and clinical studies leading to this new bioprosthesis. Areas Covered: The novel Resilia...
2.
Manco L, Ribeiro M, Maximo V, Almeida H, Costa A, Freitas O, et al.
Br J Haematol . 2000 Oct; 110(4):993-7. PMID: 11054094
Mutations in the PKLR gene responsible for pyruvate kinase (PK)-deficient anaemia are mainly located in the coding regions: 11 are in the splicing sites and, recently, three mutations have been...
3.
Ribeiro M, Alloisio N, Almeida H, Gomes C, Texier P, Lemos C, et al.
Blood . 2000 Aug; 96(4):1602-4. PMID: 10942416
Absence of band 3, associated with the mutation Coimbra (V488M) in the homozygous state, caused severe hereditary spherocytosis in a young child. Although prenatal testing was made available to the...
4.
Bento M, Ribeiro M, Cunha E, Goncalves P, Martin-Nunez G, Tamagnini G
Haematologica . 2000 Apr; 85(4):443-4. PMID: 10756381
No abstract available.
5.
Moriniere M, Ribeiro L, Dalla Venezia N, Deguillien M, Maillet P, Cynober T, et al.
Blood . 2000 Feb; 95(5):1834-41. PMID: 10688845
Early biochemical studies defined 4 functional domains of the erythroid protein 4.1 (4.1R). From amino-terminal to carboxy-terminal, these are 30 kd, 16 kd, 10 kd, and 22/24 kd in size....
6.
Marques J, Tamagnini G, Humberto J
Acta Med Port . 1999 Sep; 12(4-6):227-9. PMID: 10481327
The authors present a case of a boy, aged 8 years and 11 months, yellow race, with dyserythropoietic anemia type II, diagnosed at two months of age. Screening for partial...
7.
Amaral O, Lacerda L, Marcao A, Pinto E, Tamagnini G, Sa Miranda M
Clin Genet . 1999 Aug; 56(1):100-2. PMID: 10466427
No abstract available.
8.
Manco L, Ribeiro M, Almeida H, Freitas O, Abade A, Tamagnini G
Br J Haematol . 1999 Jun; 105(3):591-5. PMID: 10354117
In nine unrelated Portuguese patients with pyruvate kinase (PK) deficient anaemia, whose symptoms ranged from a mild chronic haemolytic anaemia to a severe anaemia presenting at birth and requiring multiple...
9.
Mcvey J, Boswell E, Takamiya O, Tamagnini G, Valente V, Fidalgo T, et al.
Blood . 1998 Jul; 92(3):920-6. PMID: 9680360
We have studied a family with homozygous lethal, blood coagulation factor VII (FVII) deficiency. To identify the mutation responsible for the deficiency, exons 2 to 8 and the intron-exon junctions...
10.
Alloisio N, Texier P, Vallier A, Ribeiro M, Morle L, Bozon M, et al.
Blood . 1997 Jul; 90(1):414-20. PMID: 9207478
We present two novel alleles of the anion-exchanger 1 (AE1) gene, allele Coimbra and allele Mondego. Allele Coimbra (V488M, GTG --> ATG) affects a conserved position in the putative second...