Martini G - Search Results

1

Molecular basis of chronic non-spherocytic haemolytic anaemia: a new G6PD variant (393 Arg----His) with abnormal KmG6P and marked in vivo instability.

Filosa S, Calabrò V, Vallone D, Poggi V, Mason P, Pagnini D, Alfinito F, Rotoli B, Martini G, Luzzatto L, et al. Filosa S, et al. Among authors: martini g. Br J Haematol. 1992 Jan;80(1):111-6. doi: 10.1111/j.1365-2141.1992.tb06409.x. Br J Haematol. 1992. PMID: 1536798

2

A novel single-base mutation in the glucose 6-phosphate dehydrogenase gene is associated with chronic non-spherocytic haemolytic anaemia.

Filosa S, Cai W, Galanello R, Cao A, de Mattia D, Schettini F, Martini G. Filosa S, et al. Among authors: martini g. Hum Genet. 1994 Nov;94(5):560-2. doi: 10.1007/BF00211027. Hum Genet. 1994. PMID: 7959695

3

Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for glucose-6-phosphate dehydrogenase mutations causing severe enzyme deficiency.

Filosa S, Giacometti N, Wangwei C, De Mattia D, Pagnini D, Alfinito F, Schettini F, Luzzatto L, Martini G. Filosa S, et al. Among authors: martini g. Am J Hum Genet. 1996 Oct;59(4):887-95. Am J Hum Genet. 1996. PMID: 8808605 Free PMC article.

4

Molecular characterization of G6PD deficiency in Southern Italy: heterogeneity, correlation genotype-phenotype and description of a new variant (G6PD Neapolis).

Alfinito F, Cimmino A, Ferraro F, Cubellis MV, Vitagliano L, Francese M, Zagari A, Rotoli B, Filosa S, Martini G. Alfinito F, et al. Among authors: martini g. Br J Haematol. 1997 Jul;98(1):41-6. doi: 10.1046/j.1365-2141.1997.1512967.x. Br J Haematol. 1997. PMID: 9233561 Free article.

5

Discussion on pharmacogenetic interaction in G6PD deficiency and methods to identify potential hemolytic drugs.

Manganelli G, Fico A, Martini G, Filosa S. Manganelli G, et al. Among authors: martini g. Cardiovasc Hematol Disord Drug Targets. 2010 Jun;10(2):143-50. doi: 10.2174/187152910791292547. Cardiovasc Hematol Disord Drug Targets. 2010. PMID: 20350285 Review.

6

DNA haplotypes in the G6PD gene cluster studied in the Chinese Li population and their relationship to G6PDCanton.

Cai W, Filosa S, Martini G. Cai W, et al. Among authors: martini g. Hum Hered. 1994 Sep-Oct;44(5):279-86. doi: 10.1159/000154230. Hum Hered. 1994. PMID: 7927357

7

G6PD haplotypes spanning Xq28 from F8C to red/green color vision.

Filosa S, Calabrò V, Lania G, Vulliamy TJ, Brancati C, Tagarelli A, Luzzatto L, Martini G. Filosa S, et al. Among authors: martini g. Genomics. 1993 Jul;17(1):6-14. doi: 10.1006/geno.1993.1276. Genomics. 1993. PMID: 8104869

8

G6PD is indispensable for erythropoiesis after the embryonic-adult hemoglobin switch.

Paglialunga F, Fico A, Iaccarino I, Notaro R, Luzzatto L, Martini G, Filosa S. Paglialunga F, et al. Among authors: martini g. Blood. 2004 Nov 15;104(10):3148-52. doi: 10.1182/blood-2004-03-0835. Epub 2004 Jul 22. Blood. 2004. PMID: 15271799 Free article.

9

Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysis.

Calabrò V, Mason PJ, Filosa S, Civitelli D, Cittadella R, Tagarelli A, Martini G, Brancati C, Luzzatto L. Calabrò V, et al. Among authors: martini g. Am J Hum Genet. 1993 Mar;52(3):527-36. Am J Hum Genet. 1993. PMID: 8447319 Free PMC article.

10

Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia.

Vulliamy TJ, D'Urso M, Battistuzzi G, Estrada M, Foulkes NS, Martini G, Calabro V, Poggi V, Giordano R, Town M, et al. Vulliamy TJ, et al. Among authors: martini g. Proc Natl Acad Sci U S A. 1988 Jul;85(14):5171-5. doi: 10.1073/pnas.85.14.5171. Proc Natl Acad Sci U S A. 1988. PMID: 3393536 Free PMC article.

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