author-photo

André Lescault

Laval University

9

Papers

295

Citations

Citation Trend

Filter By

Papers (9) Sort By

Journal Conference Others

Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansions

2006 Neurology
Show All
- Source
- Cite
- Save
Citations (73)
Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I).

1990 American Journal of Human Genetics
Show All
- Source
- Cite
- Save
Citations (80)
Oral loading of homogentisic acid in controls and in obligate heterozygotes for hereditary tyrosinemia type I.

1990 American Journal of Human Genetics
Show All
- Source
- Cite
- Save
Citations (6)
Myotonic dystrophy: linkage with apolipoprotein E and estimation of the gene carrier status with genetic markers.

1989 Canadian Journal of Neurological Sciences
Show All
- Source
- Cite
- Save
Citations (7)
A NEW VISTA ON TYROSINE TOXICITY AND CANCER

1986
Show All
- Source
- Cite
- Save
Citations (0)
Hereditary Tyrosinemias (Type I): A New Vista on Tyrosine Toxicity and Cancer

1986 Advances in Experimental Medicine and Biology
Show All
- Source
- Cite
- Save
Citations (24)
Prenatal diagnosis of hereditary tyrosinaemia confirmed.

1982 Prenatal Diagnosis
Show All
- Source
- Cite
- Save
Citations (4)
Detection of succinylacetone and the use of its measurement in mass screening for hereditary tyrosinemia

1982 Clinica Chimica Acta
Show All
- Source
- Cite
- Save
Citations (64)
Prenatal diagnosis of hereditary tyrosinaemia: Measurement of succinylacetone in amniotic fluid

1982 Prenatal Diagnosis
Show All
- Source
- Cite
- Save
Citations (37)