Remacha AF - Search Results

1

Genomewide linkage analysis of soluble transferrin receptor plasma levels.

Remacha AF, Souto JC, Soria JM, Buil A, Sardà MP, Lathrop M, Blangero J, Almasy L, Fontcuberta J. Remacha AF, et al. Ann Hematol. 2006 Jan;85(1):25-8. doi: 10.1007/s00277-005-1092-7. Epub 2005 Aug 23. Ann Hematol. 2006. PMID: 16132911

2

Enhanced risk of thrombotic disease in patients with acquired vitamin B12 and/or folate deficiency: role of hyperhomocysteinemia.

Remacha AF, Souto JC, Rámila E, Perea G, Sarda MP, Fontcuberta J. Remacha AF, et al. Ann Hematol. 2002 Nov;81(11):616-21. doi: 10.1007/s00277-002-0560-6. Epub 2002 Nov 9. Ann Hematol. 2002. PMID: 12454698

3

Genetic determinants of platelet large-cell ratio, immature platelet fraction, and other platelet-related phenotypes.

Pujol-Moix N, Vázquez-Santiago M, Morera A, Ziyatdinov A, Remacha A, Nomdedeu JF, Fontcuberta J, Soria JM, Souto JC. Pujol-Moix N, et al. Thromb Res. 2015 Aug;136(2):361-6. doi: 10.1016/j.thromres.2015.06.016. Epub 2015 Jun 17. Thromb Res. 2015. PMID: 26148565

4

Vitamin B12 deficiency, hyperhomocysteinemia and thrombosis: a case and control study.

Remacha AF, Souto JC, Piñana JL, Sardà MP, Queraltó JM, Martí-Fabregas J, García-Moll X, Férnandez C, Rodriguez A, Cuesta J. Remacha AF, et al. Int J Hematol. 2011 Apr;93(4):458-464. doi: 10.1007/s12185-011-0825-8. Epub 2011 Apr 8. Int J Hematol. 2011. PMID: 21475950

5

Combined cobalamin and iron deficiency anemia: a diagnostic approach using a model based on age and homocysteine assessment.

Remacha AF, Sardà MP, Canals C, Queraltò JM, Zapico E, Remacha J, Carrascosa C. Remacha AF, et al. Among authors: remacha j. Ann Hematol. 2013 Apr;92(4):527-31. doi: 10.1007/s00277-012-1634-8. Epub 2012 Nov 25. Ann Hematol. 2013. PMID: 23183879

6

Erytrocyte-related phenotypes and genetic susceptibility to thrombosis.

Remacha AF, Vilalta N, Sardà MP, Millón J, Pujol-Moix N, Ziyatdinov A, Fontcuberta J, Nomdedeu J, Soria JM, Souto JC. Remacha AF, et al. Blood Cells Mol Dis. 2016 Jul;59:44-8. doi: 10.1016/j.bcmd.2016.04.006. Epub 2016 Apr 13. Blood Cells Mol Dis. 2016. PMID: 27282566 No abstract available.

7

The role of serum transferrin receptor in the diagnosis of iron deficiency.

Remacha AF, Sarda MP, Parellada M, Ubeda J, Manteiga R. Remacha AF, et al. Haematologica. 1998 Nov;83(11):963-6. Haematologica. 1998. PMID: 9864913

8

Role of serum holotranscobalamin (holoTC) in the diagnosis of patients with low serum cobalamin. Comparison with methylmalonic acid and homocysteine.

Remacha AF, Sardà MP, Canals C, Queraltò JM, Zapico E, Remacha J, Carrascosa C. Remacha AF, et al. Ann Hematol. 2014 Apr;93(4):565-9. doi: 10.1007/s00277-013-1905-z. Epub 2013 Sep 21. Ann Hematol. 2014. PMID: 24057896

9

Genetic determinants of iron metabolism plasma phenotypes and their relationship with risk of thrombosis.

Souto JC, Remacha A, Buil A, Almasy L, Blangero J, Fontcuberta J. Souto JC, et al. Haematologica. 2003 Dec;88(12):1436-8. Haematologica. 2003. PMID: 14688005 No abstract available.

10

Does the SLC40A1 gene modify HFE-related haemochromatosis phenotypes?

Altès A, Bach V, Ruiz A, Esteve A, Remacha AF, Sardà MP, Felez J, Baiget M. Altès A, et al. Among authors: remacha af. Ann Hematol. 2009 Apr;88(4):341-5. doi: 10.1007/s00277-008-0590-9. Epub 2008 Sep 27. Ann Hematol. 2009. PMID: 18820912

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