Barceló MJ - Search Results

1

[Influence of chronic renal failure and of its treatment on serum erythropoietin].

Remacha AF, Oliver A, Calero F, Barceló MJ, Doñate T, Ballarín JA, García-Die F. Remacha AF, et al. Among authors: barcelo mj. Med Clin (Barc). 1992 Jun 20;99(4):125-7. Med Clin (Barc). 1992. PMID: 1635404 Spanish.

2

Evaluation of erythropoietin in endurance runners.

Remacha AF, Ordoñez J, Barcelo MJ, Garcia-Die F, Arza B, Estruch A. Remacha AF, et al. Among authors: barcelo mj. Haematologica. 1994 Jul-Aug;79(4):350-2. Haematologica. 1994. PMID: 7806089 Clinical Trial.

3

Serum erythropoietin in the diagnosis of polycythemia vera. A follow-up study.

Remacha AF, Montserrat I, Santamaria A, Oliver A, Barceló MJ, Parellada M. Remacha AF, et al. Among authors: barcelo mj. Haematologica. 1997 Jul-Aug;82(4):406-10. Haematologica. 1997. PMID: 9299851

4

The deoxyuridine suppression test in HIV-1 positive patients: the role of azydothymidine (AZT).

García-Die F, Remacha A, Cadafalch J, Barceló MJ, Parellada MM, Arza B. García-Die F, et al. Among authors: barcelo mj. Eur J Haematol. 1996 Apr;56(4):208-12. doi: 10.1111/j.1600-0609.1996.tb01931.x. Eur J Haematol. 1996. PMID: 8641388

5

Congenital intrinsic factor deficiency in a Spanish patient.

Remacha AF, Sambeat MA, Barceló MJ, Mones J, García-Die J, Gimferrer E. Remacha AF, et al. Among authors: barcelo mj. Ann Hematol. 1992 Apr;64(4):202-4. doi: 10.1007/BF01696224. Ann Hematol. 1992. PMID: 1581408

6

The deoxyuridine suppression test in peripheral lymphocytes.

Remacha A, Barceló MJ, Pastor M, Ubeda J, Espadaler M, Gimferrer E. Remacha A, et al. Among authors: barcelo mj. Eur J Haematol. 1990 Mar;44(3):196-200. doi: 10.1111/j.1600-0609.1990.tb00376.x. Eur J Haematol. 1990. PMID: 2328792

7

[Interest in the study of genetic variants of the promoter region of the UGT1A1 gene in neonatal jaundice].

Seco ML, del Río E, Barceló MJ, Remacha A, Ginovart G, Moliner E, Baiget M. Seco ML, et al. Among authors: barcelo mj. An Esp Pediatr. 2002 Feb;56(2):139-43. An Esp Pediatr. 2002. PMID: 11827650 Spanish.

8

Autosomal dominant hereditary hemochromatosis associated with two novel Ferroportin 1 mutations in Spain.

Bach V, Remacha A, Altés A, Barceló MJ, Molina MA, Baiget M. Bach V, et al. Among authors: barcelo mj. Blood Cells Mol Dis. 2006 Jan-Feb;36(1):41-5. doi: 10.1016/j.bcmd.2005.09.001. Epub 2005 Oct 27. Blood Cells Mol Dis. 2006. PMID: 16257244

9

Genotyping the HFE gene by melting point analysis with the LightCycler system: Pros and cons.

Bach V, Barceló MJ, Altés A, Remacha A, Félez J, Baiget M. Bach V, et al. Among authors: barcelo mj. Blood Cells Mol Dis. 2006 Mar-Apr;36(2):288-91. doi: 10.1016/j.bcmd.2005.12.030. Epub 2006 Mar 2. Blood Cells Mol Dis. 2006. PMID: 16515868

10

[Plasma carriers of vitamin B 12 in normal controls and in the initial diagnosis of pernicious anemia].

Remacha A, Fornells J, Barceló MJ, Ubeda J, Gimferrer E. Remacha A, et al. Among authors: barcelo mj. Sangre (Barc). 1988 Oct;33(5):357-60. Sangre (Barc). 1988. PMID: 3247616 Spanish. No abstract available.

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