Search research articles
Contact Us
Filters
Showing results (11-20 of 48) with videos related to
Page
of 5
Sort By:
American Journal of Human Genetics
|
January 1, 1988
Screening of the Philadelphia variant of galactokinase in racially unmixed black Africans: first results
T Soni, M Brivet, M Blanc, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
January 1, 1989
[Metabolic cooperation in cocultures of fibroblasts from patients with various abnormalities of galactose metabolism]
N Kadhom, M Brivet, J Baptista, et al.
Annals of Clinical Biochemistry
|
March 1, 1995
Rapid diagnosis of long chain and medium chain fatty acid oxidation disorders using lymphocytes
M Brivet, A Slama, J M Saudubray, et al.
Digestive Diseases and Sciences
|
March 1, 1987
Upper gastrointestinal endoscopy. An unrecognized cause of hyperamylasemia
G Pelletier, N Nee, M Brivet, et al.
Biochemical Genetics
|
April 1, 1991
Normal expression of thymidine kinase and O6-methylguanine-DNA methyltransferase in cultured fibroblasts from individuals with hereditary galactokinase deficiency
C Stephenson, M Brivet, M Gautier, et al.
Revue Neurologique
|
February 1, 1995
[Late neurologic complications of galactosemia: study of 3 cases]
P A Bohu, D Hannequin, C Hemet, et al.
Pediatric Research
|
October 1, 1996
Complementation analysis of carnitine palmitoyltransferase I and II defects
A Slama, M Brivet, A Boutron, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica
|
June 1, 1992
Enhancement of normal polymorphonuclear cells respiratory burst in ascitic fluid by fibronectin. Comparison between cirrhotic and malignant ascitic fluids
L Lebrun, G Pelletier, M J Briantais, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 11, 2002
[Severe Reye syndrome: report of 14 cases managed in a pediatric intensive care unit over 11 years]
F Thabet, P Durand, L Chevret, et al.
The Journal of Pediatrics
|
November 5, 1997
Very long chain acyl-coenzyme A dehydrogenase deficiency in two siblings: evolution after prenatal diagnosis and prompt management
T Sluysmans, D Tuerlinckx, C Hubinont, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 48) with videos related to
Sort By:
Page
of 5
American Journal of Human Genetics
|
January 1, 1988
Screening of the Philadelphia variant of galactokinase in racially unmixed black Africans: first results
T Soni, M Brivet, M Blanc, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
January 1, 1989
[Metabolic cooperation in cocultures of fibroblasts from patients with various abnormalities of galactose metabolism]
N Kadhom, M Brivet, J Baptista, et al.
Annals of Clinical Biochemistry
|
March 1, 1995
Rapid diagnosis of long chain and medium chain fatty acid oxidation disorders using lymphocytes
M Brivet, A Slama, J M Saudubray, et al.
Digestive Diseases and Sciences
|
March 1, 1987
Upper gastrointestinal endoscopy. An unrecognized cause of hyperamylasemia
G Pelletier, N Nee, M Brivet, et al.
Biochemical Genetics
|
April 1, 1991
Normal expression of thymidine kinase and O6-methylguanine-DNA methyltransferase in cultured fibroblasts from individuals with hereditary galactokinase deficiency
C Stephenson, M Brivet, M Gautier, et al.
Revue Neurologique
|
February 1, 1995
[Late neurologic complications of galactosemia: study of 3 cases]
P A Bohu, D Hannequin, C Hemet, et al.
Pediatric Research
|
October 1, 1996
Complementation analysis of carnitine palmitoyltransferase I and II defects
A Slama, M Brivet, A Boutron, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica
|
June 1, 1992
Enhancement of normal polymorphonuclear cells respiratory burst in ascitic fluid by fibronectin. Comparison between cirrhotic and malignant ascitic fluids
L Lebrun, G Pelletier, M J Briantais, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 11, 2002
[Severe Reye syndrome: report of 14 cases managed in a pediatric intensive care unit over 11 years]
F Thabet, P Durand, L Chevret, et al.
The Journal of Pediatrics
|
November 5, 1997
Very long chain acyl-coenzyme A dehydrogenase deficiency in two siblings: evolution after prenatal diagnosis and prompt management
T Sluysmans, D Tuerlinckx, C Hubinont, et al.
Page
of 5