Altisent C - Search Results

1

Rapid hemophilia A molecular diagnosis by a simple DNA sequencing procedure: identification of 14 novel mutations.

Vidal F, Farssac E, Altisent C, Puig L, Gallardo D. Vidal F, et al. Among authors: altisent c. Thromb Haemost. 2001 Apr;85(4):580-3. Thromb Haemost. 2001. PMID: 11341489

2

Implications of gene sequencing in the direct diagnosis of hemophilia by PCR-RFLP.

Vidal F, Farssac E, Altisent C, Puig L, Gallardo D. Vidal F, et al. Among authors: altisent c. Haematologica. 2002 Jan;87(1):109-10. Haematologica. 2002. PMID: 11801473 No abstract available.

3

Von Willebrand gene tracking by single-tube automated fluorescent analysis of four short tandem repeat polymorphisms.

Vidal F, Julià A, Altisent C, Puig L, Gallardo D. Vidal F, et al. Among authors: altisent c. Thromb Haemost. 2005 May;93(5):976-81. doi: 10.1160/TH04-10-0699. Thromb Haemost. 2005. PMID: 15886817

4

A versatile strategy for preimplantation genetic diagnosis of haemophilia A based on F8-gene sequencing.

Sánchez-García JF, Gallardo D, Navarro J, Márquez C, Gris JM, Sánchez MA, Altisent C, Vidal F. Sánchez-García JF, et al. Among authors: altisent c. Thromb Haemost. 2006 Dec;96(6):839-45. Thromb Haemost. 2006. PMID: 17139381

5

Rapid molecular diagnosis of von Willebrand disease by direct sequencing. Detection of 12 novel putative mutations in VWF gene.

Corrales I, Ramírez L, Altisent C, Parra R, Vidal F. Corrales I, et al. Among authors: altisent c. Thromb Haemost. 2009 Mar;101(3):570-6. doi: 10.1160/th08-08-0500. Thromb Haemost. 2009. PMID: 19277422

6

A novel mutation (2409delT) in exon 14 of the factor VIII gene causes severe haemophilia A.

Vidal F, Farssac E, Altisent C, Puig L, Gallardo D. Vidal F, et al. Among authors: altisent c. Hum Hered. 2000 Jul-Aug;50(4):266-7. doi: 10.1159/000022928. Hum Hered. 2000. PMID: 10782022 No abstract available.

7

Factor IX gene sequencing by a simple and sensitive 15-hour procedure for haemophilia B diagnosis: identification of two novel mutations.

Vidal F, Farssac E, Altisent C, Puig L, Gallardo D. Vidal F, et al. Among authors: altisent c. Br J Haematol. 2000 Nov;111(2):549-51. doi: 10.1046/j.1365-2141.2000.02389.x. Br J Haematol. 2000. PMID: 11122099 Free article.

8

Unraveling the Influence of Common von Willebrand factor variants on von Willebrand Disease Phenotype: An Exploratory Study on the Molecular and Clinical Profile of von Willebrand Disease in Spain Cohort.

Borràs N, Garcia-Martínez I, Batlle J, Pérez-Rodríguez A, Parra R, Altisent C, López-Fernández MF, Costa Pinto J, Batlle-López F, Cid AR, Bonanad S, Cabrera N, Moret A, Mingot-Castellano ME, Navarro N, Pérez-Montes R, Marcellini S, Moreto A, Herrero S, Soto I, Fernández-Mosteirín N, Jiménez-Yuste V, Alonso N, de Andrés-Jacob A, Fontanes E, Campos R, Paloma MJ, Bermejo N, Berrueco R, Mateo J, Arribalzaga K, Marco P, Palomo Á, Castro Quismondo N, Iñigo B, Del Mar Nieto M, Vidal R, Martínez MP, Aguinaco R, Tenorio M, Ferreiro M, García-Frade J, Rodríguez-Huerta AM, Cuesta J, Rodríguez-González R, García-Candel F, Dobón M, Aguilar C, Corrales I, Vidal F. Borràs N, et al. Among authors: altisent c. Thromb Haemost. 2020 Mar;120(3):437-448. doi: 10.1055/s-0040-1702227. Epub 2020 Mar 5. Thromb Haemost. 2020. PMID: 32135566

9

Common Genetic Variants in ABO and CLEC4M Modulate the Pharmacokinetics of Recombinant FVIII in Severe Hemophilia A Patients.

Garcia-Martínez I, Borràs N, Martorell M, Parra R, Altisent C, Ramírez L, Álvarez-Román MT, Nuñez R, Megias-Vericat JE, Corrales I, Alonso S, Vidal F. Garcia-Martínez I, et al. Among authors: altisent c. Thromb Haemost. 2020 Oct;120(10):1395-1406. doi: 10.1055/s-0040-1714214. Epub 2020 Jul 29. Thromb Haemost. 2020. PMID: 32726853

10

Treatment with interferon plus ribavirin in anti-HIV negative patients with congenital coagulation disorders and chronic hepatitis C.

Sauleda S, Esteban JI, Altisent C, Puig L, Esteban R, Guardia J. Sauleda S, et al. Among authors: altisent c. Thromb Haemost. 2000 Jun;83(6):807-10. Thromb Haemost. 2000. PMID: 10896229

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