Gilsanz F - Search Results

1

Fetal anaemia due to pyruvate kinase deficiency.

Gilsanz F, Vega MA, Gómez-Castillo E, Ruiz-Balda JA, Omeñaca F. Gilsanz F, et al. Arch Dis Child. 1993 Nov;69(5 Spec No):523-4. doi: 10.1136/adc.69.5_spec_no.523. Arch Dis Child. 1993. PMID: 8285758 Free PMC article.

2

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.

3

Hemolytic anemia in chronic large granular lymphocytic leukemia of natural killer cells: cytotoxicity of natural killer cells against autologous red cells is associated with hemolysis.

Gilsanz F, De La Serna J, Moltó L, Alvarez-Mon M. Gilsanz F, et al. Transfusion. 1996 May;36(5):463-6. doi: 10.1046/j.1537-2995.1996.36596338025.x. Transfusion. 1996. PMID: 8693514

4

Improvement in the erythropoiesis of chronic haemodialysis patients with desferrioxamine.

de la Serna FJ, Praga M, Gilsanz F, Rodicio JL, Ruilope LM, Alcazar JM. de la Serna FJ, et al. Among authors: gilsanz f. Lancet. 1988 May 7;1(8593):1009-11. doi: 10.1016/s0140-6736(88)91839-9. Lancet. 1988. PMID: 2896866 Clinical Trial.

5

[Reference values in the diagnosis of anemia in the elderly].

Gilsanz F, Gómez-Tabera C, Torres M, Barredo M, Esténoz J, López-Carbajo A, Millán I. Gilsanz F, et al. Rev Clin Esp. 1996 May;196(5):289-92. Rev Clin Esp. 1996. PMID: 8768027 Spanish.

6

Chronic ethanol abuse and membrane fluidity changes in liver disease.

Gilsanz F, Diez E, Gomez-Tabera C, del Pozo AM. Gilsanz F, et al. Drug Alcohol Depend. 1992 Feb;29(3):237-43. doi: 10.1016/0376-8716(92)90097-v. Drug Alcohol Depend. 1992. PMID: 1559429

7

Diagnosis of hereditary spherocytosis with dual-angle differential light scattering.

Gilsanz F, Ricard MP, Millan I. Gilsanz F, et al. Am J Clin Pathol. 1993 Aug;100(2):119-22. doi: 10.1093/ajcp/100.2.119. Am J Clin Pathol. 1993. PMID: 8356943

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

Acquired pure red cell aplasia: a study of six cases.

Gilsanz F, Garcia Vela J, Vargas JA, Ibañez J, Oña F, López J, Roggendorf M. Gilsanz F, et al. Ann Hematol. 1995 Oct;71(4):181-3. doi: 10.1007/BF01910315. Ann Hematol. 1995. PMID: 7578524

10

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.

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