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M J Barceló

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BJOG : an International Journal of Obstetrics and Gynaecology|November 28, 2002
Prenatal diagnosis for risk of spinal muscular atrophyI Cuscó, M J Barceló, C Soler, et al.
European Journal of Haematology|March 1, 1990
The deoxyuridine suppression test in peripheral lymphocytesA Remacha, M J Barceló, M Pastor, et al.
Blood Cells, Molecules & Diseases|March 7, 2006
Genotyping the HFE gene by melting point analysis with the LightCycler system: Pros and consV Bach, M J Barceló, A Altés, et al.
Haematologica|July 1, 1997
Serum erythropoietin in the diagnosis of polycythemia vera. A follow-up studyA F Remacha, I Montserrat, A Santamaria, et al.
Blood Cells, Molecules & Diseases|November 1, 2005
Autosomal dominant hereditary hemochromatosis associated with two novel Ferroportin 1 mutations in SpainV Bach, A Remacha, A Altés, et al.
Haematologica|December 13, 2000
The S65C mutation in Spain. Implications for iron overload screeningA F Remacha, M J Barceló, M P Sardà, et al.
European Journal of Haematology|April 1, 1996
The deoxyuridine suppression test in HIV-1 positive patients: the role of azydothymidine (AZT)F García-Die, A Remacha, J Cadafalch, et al.
Annals of Hematology|April 1, 1992
Congenital intrinsic factor deficiency in a Spanish patientA F Remacha, M A Sambeat, M J Barceló, et al.
Anales Espanoles De Pediatria|February 6, 2002
[Interest in the study of genetic variants of the promoter region of the UGT1A1 gene in neonatal jaundice]M L Seco, E del Río, M J Barceló, et al.
Medicina Clinica|June 20, 1992
[Influence of chronic renal failure and of its treatment on serum erythropoietin]A F Remacha, A Oliver, F Calero, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
BJOG : an International Journal of Obstetrics and Gynaecology|November 28, 2002
Prenatal diagnosis for risk of spinal muscular atrophyI Cuscó, M J Barceló, C Soler, et al.
European Journal of Haematology|March 1, 1990
The deoxyuridine suppression test in peripheral lymphocytesA Remacha, M J Barceló, M Pastor, et al.
Blood Cells, Molecules & Diseases|March 7, 2006
Genotyping the HFE gene by melting point analysis with the LightCycler system: Pros and consV Bach, M J Barceló, A Altés, et al.
Haematologica|July 1, 1997
Serum erythropoietin in the diagnosis of polycythemia vera. A follow-up studyA F Remacha, I Montserrat, A Santamaria, et al.
Blood Cells, Molecules & Diseases|November 1, 2005
Autosomal dominant hereditary hemochromatosis associated with two novel Ferroportin 1 mutations in SpainV Bach, A Remacha, A Altés, et al.
Haematologica|December 13, 2000
The S65C mutation in Spain. Implications for iron overload screeningA F Remacha, M J Barceló, M P Sardà, et al.
European Journal of Haematology|April 1, 1996
The deoxyuridine suppression test in HIV-1 positive patients: the role of azydothymidine (AZT)F García-Die, A Remacha, J Cadafalch, et al.
Annals of Hematology|April 1, 1992
Congenital intrinsic factor deficiency in a Spanish patientA F Remacha, M A Sambeat, M J Barceló, et al.
Anales Espanoles De Pediatria|February 6, 2002
[Interest in the study of genetic variants of the promoter region of the UGT1A1 gene in neonatal jaundice]M L Seco, E del Río, M J Barceló, et al.
Medicina Clinica|June 20, 1992
[Influence of chronic renal failure and of its treatment on serum erythropoietin]A F Remacha, A Oliver, F Calero, et al.
Pageof 2