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B Chadefaux-Vekemans

Showing results (1-10 of 23) with videos related to

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The New England Journal of Medicine|July 25, 1996
Thrombophilia, homocystinuria, and mutation of the factor V geneI Quéré, H Lamarti, B Chadefaux-Vekemans
Clinical Chemistry|July 27, 2001
Urinary sulfur compounds in Down syndromeM C Belardinelli, A Chabli, B Chadefaux-Vekemans, et al.
Clinical Biochemistry|April 27, 2007
Measurement of cystine in granulocytes using liquid chromatography-tandem mass spectrometryA Chabli, J Aupetit, M Raehm, et al.
Journal of Inherited Metabolic Disease|December 31, 1998
Four novel mutations at the cystathionine beta-synthase locus causing homocystinuriaM Coudé, J Aupetit, M T Zabot, et al.
Prenatal Diagnosis|May 1, 1994
Prenatal diagnosis of combined methylmalonic aciduria and homocystinuria (cobalamin CblC or CblD mutant)B Chadefaux-Vekemans, M O Rolland, S Lyonnet, et al.
Kidney International|December 14, 1999
Effective correction of hyperhomocysteinemia in hemodialysis patients by intravenous folinic acid and pyridoxine therapyM Touam, J Zingraff, P Jungers, et al.
Clinical Chemistry|November 1, 1995
Free amino acids in amniotic fluid and the prenatal diagnosis of homocystinuria with methylmalonic aciduriaP Parvy, J Bardet, B Chadefaux-Vekemans, et al.
Prenatal Diagnosis|July 13, 2002
Improving the prenatal diagnosis of citrullinemia using citrulline/ornithine+arginine ratio in amniotic fluidB Chadefaux-Vekemans, D Rabier, A Chabli, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1996
[Hyperhomocysteinemia in coronary artery diseases. Apropos of a study on 102 patients]J Blacher, G Montalescot, A Ankri, et al.
Prenatal Diagnosis|July 6, 2006
Prenatal diagnosis of some metabolic diseases using early amniotic fluid samples: report of a 15 years, experienceB Chadefaux-Vekemans, D Rabier, N Cadoudal, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
The New England Journal of Medicine|July 25, 1996
Thrombophilia, homocystinuria, and mutation of the factor V geneI Quéré, H Lamarti, B Chadefaux-Vekemans
Clinical Chemistry|July 27, 2001
Urinary sulfur compounds in Down syndromeM C Belardinelli, A Chabli, B Chadefaux-Vekemans, et al.
Clinical Biochemistry|April 27, 2007
Measurement of cystine in granulocytes using liquid chromatography-tandem mass spectrometryA Chabli, J Aupetit, M Raehm, et al.
Journal of Inherited Metabolic Disease|December 31, 1998
Four novel mutations at the cystathionine beta-synthase locus causing homocystinuriaM Coudé, J Aupetit, M T Zabot, et al.
Prenatal Diagnosis|May 1, 1994
Prenatal diagnosis of combined methylmalonic aciduria and homocystinuria (cobalamin CblC or CblD mutant)B Chadefaux-Vekemans, M O Rolland, S Lyonnet, et al.
Kidney International|December 14, 1999
Effective correction of hyperhomocysteinemia in hemodialysis patients by intravenous folinic acid and pyridoxine therapyM Touam, J Zingraff, P Jungers, et al.
Clinical Chemistry|November 1, 1995
Free amino acids in amniotic fluid and the prenatal diagnosis of homocystinuria with methylmalonic aciduriaP Parvy, J Bardet, B Chadefaux-Vekemans, et al.
Prenatal Diagnosis|July 13, 2002
Improving the prenatal diagnosis of citrullinemia using citrulline/ornithine+arginine ratio in amniotic fluidB Chadefaux-Vekemans, D Rabier, A Chabli, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1996
[Hyperhomocysteinemia in coronary artery diseases. Apropos of a study on 102 patients]J Blacher, G Montalescot, A Ankri, et al.
Prenatal Diagnosis|July 6, 2006
Prenatal diagnosis of some metabolic diseases using early amniotic fluid samples: report of a 15 years, experienceB Chadefaux-Vekemans, D Rabier, N Cadoudal, et al.
Pageof 3