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The New England Journal of Medicine
|
July 25, 1996
Thrombophilia, homocystinuria, and mutation of the factor V gene
I Quéré, H Lamarti, B Chadefaux-Vekemans
Clinical Chemistry
|
July 27, 2001
Urinary sulfur compounds in Down syndrome
M C Belardinelli, A Chabli, B Chadefaux-Vekemans, et al.
Clinical Biochemistry
|
April 27, 2007
Measurement of cystine in granulocytes using liquid chromatography-tandem mass spectrometry
A 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 homocystinuria
M 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 therapy
M 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 aciduria
P 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 fluid
B 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, experience
B Chadefaux-Vekemans, D Rabier, N Cadoudal, et al.
Page
of 3
Search research articles
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Showing results (1-10 of 23) with videos related to
Sort By:
Page
of 3
The New England Journal of Medicine
|
July 25, 1996
Thrombophilia, homocystinuria, and mutation of the factor V gene
I Quéré, H Lamarti, B Chadefaux-Vekemans
Clinical Chemistry
|
July 27, 2001
Urinary sulfur compounds in Down syndrome
M C Belardinelli, A Chabli, B Chadefaux-Vekemans, et al.
Clinical Biochemistry
|
April 27, 2007
Measurement of cystine in granulocytes using liquid chromatography-tandem mass spectrometry
A 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 homocystinuria
M 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 therapy
M 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 aciduria
P 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 fluid
B 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, experience
B Chadefaux-Vekemans, D Rabier, N Cadoudal, et al.
Page
of 3