Filosa S - 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. 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

Genetic heterogeneity at the glucose-6-phosphate dehydrogenase locus in southern Italy: a study on a population from the Matera district.

Calabrò V, Giacobbe A, Vallone D, Montanaro V, Cascone A, Filosa S, Battistuzzi G. Calabrò V, et al. Among authors: filosa s. Hum Genet. 1990 Nov;86(1):49-53. doi: 10.1007/BF00205171. Hum Genet. 1990. PMID: 2253938

3

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: filosa s. Hum Hered. 1994 Sep-Oct;44(5):279-86. doi: 10.1159/000154230. Hum Hered. 1994. PMID: 7927357

4

Glucose 6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemia.

Alfinito F, Calabro V, Cappellini MD, Fiorelli G, Filosa S, Iolascon A, Miraglia del Giudice E, Perrotta S, Migliorati R, Vallone D, et al. Alfinito F, et al. Among authors: filosa s. Br J Haematol. 1994 May;87(1):148-52. doi: 10.1111/j.1365-2141.1994.tb04885.x. Br J Haematol. 1994. PMID: 7947239

5

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. Hum Genet. 1994 Nov;94(5):560-2. doi: 10.1007/BF00211027. Hum Genet. 1994. PMID: 7959695

6

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. Genomics. 1993 Jul;17(1):6-14. doi: 10.1006/geno.1993.1276. Genomics. 1993. PMID: 8104869

7

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: filosa s. Am J Hum Genet. 1993 Mar;52(3):527-36. Am J Hum Genet. 1993. PMID: 8447319 Free PMC article.

8

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. Am J Hum Genet. 1996 Oct;59(4):887-95. Am J Hum Genet. 1996. PMID: 8808605 Free PMC article.

9

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: filosa s. 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.

10

[Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Han and Li nationalities in Hainan, China and identification of a new mutation in human G6PD gene].

Cai W, Filosa S, Martini G, Zhou Y, Zhou D, Cai L, Kuang Y. Cai W, et al. Among authors: filosa s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2001 Apr;18(2):105-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2001. PMID: 11295127 Chinese.

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