Gilsanz F - Search Results

1

Frequency of congenital dyserythropoietic anemias in Europe.

Heimpel H, Matuschek A, Ahmed M, Bader-Meunier B, Colita A, Delaunay J, Garcon L, Gilsanz F, Goede J, Högel J, Kohne E, Leichtle R, Munoz J, Perrotta S, Piscopo C, Renella R, Schwarz K, Smolenska-Sym G, Wickramasinghe S, Zanella A, Iolascon A. Heimpel H, et al. Among authors: gilsanz f. Eur J Haematol. 2010 Jul;85(1):20-5. Eur J Haematol. 2010. PMID: 20665989

2

The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulum.

Alloisio N, Texier P, Denoroy L, Berger C, Miraglia del Giudice E, Perrotta S, Iolascon A, Gilsanz F, Berger G, Guichard J. Alloisio N, et al. Among authors: gilsanz f. Blood. 1996 May 15;87(10):4433-9. Blood. 1996. PMID: 8639805 Free article.

3

A markedly disrupted skeletal network with abnormally distributed intramembrane particles in complete protein 4.1-deficient red blood cells (allele 4.1 Madrid): implications regarding a critical role of protein 4.1 in maintenance of the integrity of the red blood cell membrane.

Yawata A, Kanzaki A, Gilsanz F, Delaunay J, Yawata Y. Yawata A, et al. Among authors: gilsanz f. Blood. 1997 Sep 15;90(6):2471-81. Blood. 1997. PMID: 9310500 Free article.

4

4.1R-deficient human red blood cells have altered phosphatidylserine exposure pathways and are deficient in CD44 and CD47 glycoproteins.

Jeremy KP, Plummer ZE, Head DJ, Madgett TE, Sanders KL, Wallington A, Storry JR, Gilsanz F, Delaunay J, Avent ND. Jeremy KP, et al. Among authors: gilsanz f. Haematologica. 2009 Oct;94(10):1354-61. doi: 10.3324/haematol.2009.006585. Haematologica. 2009. PMID: 19794081 Free PMC article.

5

Evidence that red blood cell protein p55 may participate in the skeleton-membrane linkage that involves protein 4.1 and glycophorin C.

Alloisio N, Dalla Venezia N, Rana A, Andrabi K, Texier P, Gilsanz F, Cartron JP, Delaunay J, Chishti AH. Alloisio N, et al. Among authors: gilsanz f. Blood. 1993 Aug 15;82(4):1323-7. Blood. 1993. PMID: 8353290 Free article.

6

Homozygous 4.1(-) hereditary elliptocytosis associated with a point mutation in the downstream initiation codon of protein 4.1 gene.

Dalla Venezia N, Gilsanz F, Alloisio N, Ducluzeau MT, Benz EJ Jr, Delaunay J. Dalla Venezia N, et al. Among authors: gilsanz f. J Clin Invest. 1992 Nov;90(5):1713-7. doi: 10.1172/JCI116044. J Clin Invest. 1992. PMID: 1430200 Free PMC article.

7

Life-threatening nonspherocytic hemolytic anemia in a patient with a null mutation in the PKLR gene and no compensatory PKM gene expression.

Diez A, Gilsanz F, Martinez J, Pérez-Benavente S, Meza NW, Bautista JM. Diez A, et al. Among authors: gilsanz f. Blood. 2005 Sep 1;106(5):1851-6. doi: 10.1182/blood-2005-02-0555. Epub 2005 May 3. Blood. 2005. PMID: 15870173 Free article.

8

G6PD deficiency: the genotype-phenotype association.

Mason PJ, Bautista JM, Gilsanz F. Mason PJ, et al. Among authors: gilsanz f. Blood Rev. 2007 Sep;21(5):267-83. doi: 10.1016/j.blre.2007.05.002. Epub 2007 Jul 3. Blood Rev. 2007. PMID: 17611006 Review.

9

Clinical significance of Gata-1, Gata-2, EKLF, and c-MPL expression in acute myeloid leukemia.

Ayala RM, Martínez-López J, Albízua E, Diez A, Gilsanz F. Ayala RM, et al. Among authors: gilsanz f. Am J Hematol. 2009 Feb;84(2):79-86. doi: 10.1002/ajh.21332. Am J Hematol. 2009. PMID: 19097174 Free article.

10

Erythroid membrane protein defects in hereditary spherocytosis. A study of 62 Spanish cases.

Ricard MP, Gilsanz F, Millan I. Ricard MP, et al. Among authors: gilsanz f. Haematologica. 2000 Sep;85(9):994-5. Haematologica. 2000. PMID: 10980645 No abstract available.

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