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A Lescault

Showing results (1-10 of 13) with videos related to

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L'Union Medicale Du Canada|March 1, 1974
[Effects of methionine poisoning on energy metabolism in the guinea pig liver]A Lescault, C Laberge
L'Union Medicale Du Canada|December 1, 1974
[In vitro study of hepatic adenyl cyclase in cases of hereditary tyrosinemia]A Lescault, C Laberge
Advances in Experimental Medicine and Biology|January 1, 1986
Hereditary tyrosinemias (type I): a new vista on tyrosine toxicity and cancerC Laberge, A Lescault, R M Tanguay
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 4, 1982
Detection of succinylacetone and the use of its measurement in mass screening for hereditary tyrosinemiaA Grenier, A Lescault, C Laberge, et al.
Prenatal Diagnosis|October 1, 1982
Prenatal diagnosis of hereditary tyrosinaemia confirmedR Gagné, A Lescault, A Grenier, et al.
L'Union Medicale Du Canada|July 1, 1981
["Succinylacetone effect' after oral homogentisate loading]C Laberge, A Lescault, A Grenier, et al.
Canadian Journal of Physiology and Pharmacology|June 1, 1977
Red blood cell catechol O-methyltransferase activity in thyroid dysfunctionP Coulombe, J H Dussault, A Lescault, et al.
Prenatal Diagnosis|July 1, 1982
Prenatal diagnosis of hereditary tyrosinaemia: measurement of succinylacetone in amniotic fluidR Gagné, A Lescault, A Grenier, et al.
Neurology|April 26, 2006
Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansionsM-E Arsenault, C Prévost, A Lescault, et al.
American Journal of Human Genetics|August 1, 1990
Oral loading of homogentisic acid in controls and in obligate heterozygotes for hereditary tyrosinemia type IC Laberge, A Lescault, A Grenier, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
L'Union Medicale Du Canada|March 1, 1974
[Effects of methionine poisoning on energy metabolism in the guinea pig liver]A Lescault, C Laberge
L'Union Medicale Du Canada|December 1, 1974
[In vitro study of hepatic adenyl cyclase in cases of hereditary tyrosinemia]A Lescault, C Laberge
Advances in Experimental Medicine and Biology|January 1, 1986
Hereditary tyrosinemias (type I): a new vista on tyrosine toxicity and cancerC Laberge, A Lescault, R M Tanguay
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 4, 1982
Detection of succinylacetone and the use of its measurement in mass screening for hereditary tyrosinemiaA Grenier, A Lescault, C Laberge, et al.
Prenatal Diagnosis|October 1, 1982
Prenatal diagnosis of hereditary tyrosinaemia confirmedR Gagné, A Lescault, A Grenier, et al.
L'Union Medicale Du Canada|July 1, 1981
["Succinylacetone effect' after oral homogentisate loading]C Laberge, A Lescault, A Grenier, et al.
Canadian Journal of Physiology and Pharmacology|June 1, 1977
Red blood cell catechol O-methyltransferase activity in thyroid dysfunctionP Coulombe, J H Dussault, A Lescault, et al.
Prenatal Diagnosis|July 1, 1982
Prenatal diagnosis of hereditary tyrosinaemia: measurement of succinylacetone in amniotic fluidR Gagné, A Lescault, A Grenier, et al.
Neurology|April 26, 2006
Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansionsM-E Arsenault, C Prévost, A Lescault, et al.
American Journal of Human Genetics|August 1, 1990
Oral loading of homogentisic acid in controls and in obligate heterozygotes for hereditary tyrosinemia type IC Laberge, A Lescault, A Grenier, et al.
Pageof 2