Search filters

List of works by Louis Dallaire

A syndrome of generalized elastic fiber deficiency with leprechaunoid features: a distinct genetic disease with an autosomal recessive mode of inheritance

scientific article published on 01 July 1976

Amniotic fluid alpha-galactosidase activity: an indicator of gestational age.

scientific article

Amniotic-fluid disaccharidases in the prenatal detection of cystic fibrosis

scientific article published on September 10, 1983

Antenatal diagnosis of neural tube defects in Canada: extension of a collaborative study

scientific article published on March 17, 1979

Autoimmunity and chromosomal aberrations: serological studies in mothrs of childern with Down's syndrome

scientific article

Autosomal dominant polycystic kidney disease in the fetus.

scientific article published on July 1994

Bilateral aniridia, multiple webs and severe mental retardation in a 47,XXY-48,XXXY mosaic.

scientific article published in January 1973

Biochemical approach to prenatal diagnosis of inborn errors of metabolism and congenital malformations

scientific article published on 01 December 1975

Canadian multicenter randomized clinical trial of chorion villus sampling and amniocentesis. List of all cytogenetic abnormalities detected

scientific article published on 01 May 1992

Canadian multicenter randomized clinical trial of chorion villus sampling and amniocentesis. chromosome mosaicism in CVS and amniocentesis samples

scientific article published on 01 May 1992

Chronic sodium benzoate therapy in children with inborn errors of urea synthesis: effect on carnitine metabolism and ammonia nitrogen removal

scientific article published on 01 February 1996

Clinical heterogeneity in cobalamin C variant of combined homocystinuria and methylmalonic aciduria

scientific article published on 01 March 1986

Cloning, expression and chromosomal mapping of human lysosomal sialidase and characterization of mutations in sialidosis

scientific article

Club foot, an adverse outcome of early amniocentesis: disruption or deformation? CEMAT. Canadian Early and Mid-Trimester Amniocentesis Trial.

scientific article

Comparative behavioral, biochemical and pigmentary effects of MPTP, MPP+ and paraquat in Rana pipiens

scientific article published in October 1985

Comparative study of urine and serum organic acids in newborn infants using gas chromatography

scientific article published on April 1, 1974

Confirmation of regional assignment of nucleoside phosphorylase (NP) on chromosome 14 by gene dosage studies

scientific article published on December 18, 1978

Correlation between serum lipoamide dehydrogenase activity and phosphatidylcholine therapy in Friedreich's ataxia.

scientific article

Cystinuria: increased prevalence in patients with mental disease

scientific article published in October 1970

Cytogenetic aspects of the Canadian early and mid-trimester amniotic fluid trial (CEMAT)

scientific article (publication date: July 1999)

Date of conception and prevention of neural tube defects.

scientific article published on October 1984

De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype

scientific article

Developmental patterns of intestinal disaccharidases in human amniotic fluid

scientific article published on May 1, 1978

Dicarboxylic Amino Acid Uptake in Normal, Friedreich's Ataxia, and Dicarboxylic Aminoaciduria Fibroblasts

scientific article published on 01 May 1979

Dicarboxylic aminoaciduria: an inborn error of amino acid conservation

scientific article published in September 1977

Differential stabilities of fetal intestinal disaccharidases determine their relative amounts released into amniotic fluid

scientific article published on 01 January 1984

Early treatment of severe infantile glycine encephalopathy (nonketotic hyperglycinemia) with strychnine and sodium benzoate

scientific article published on January 1, 1979

Effect of nitisinone (NTBC) treatment on the clinical course of hepatorenal tyrosinemia in Québec

scientific article published on July 13, 2012

Fetal congenital diaphragmatic hernia: accuracy of sonography in the diagnosis and prediction of the outcome after birth

scientific article published on 01 May 1996

Fetal intestinal and renal origins of trehalase activity in human amniotic fluid

scientific article published on 01 July 1993

Fetal intestinal disaccharidases in human amniotic fluid

scientific article published on July 1, 1976

Fetal intestinal microvilli in human amniotic fluid

scientific article published on 01 November 1986

Feto-maternal amino acid metabolism

scientific article published on 01 October 1974

Fluorometric assay of neuraminidase with a sodium (4-methylumbelliferyl-alpha-D-N-acetylneuraminate) substrate

scientific article published on April 1979

Fragile site and interstitial telomere repeat sequences at the fusion point of a de novo (Y;13) translocation

scientific article published on 01 September 1996

Frequencies of chromosomal abnormalities at amniocentesis: over 20 years of cytogenetic analyses in one laboratory

scientific article

Friedreich's ataxia: malic enzyme activity in cellular fractions of cultured skin fibroblasts

scientific article published on 01 November 1984

Genetic aspects of tyrosinemia

scientific article published on October 1967

Genetic aspects of tyrosinemia in the Chicoutimi region

scientific article

Germinal HPRT splice donor site mutation results in multiple RNA splicing products in T-lymphocyte cultures

scientific article published on 01 March 1996

Hereditary multiple intestinal atresia

scientific article published on January 1, 1974

Hyperargininemia: intellectual and motor improvement related to changes in biochemical data

scientific article

Hypocarnitinemia in patients affected by a primary defect of ammonia metabolism treated with sodium benzoate

scientific article published on May 1990

Integration of prenatal diagnosis of genetic diseases into medical practice

scientific article published on October 1976

Is selective abortion for a genetic disease an issue for the medical profession? A comparative study of Quebec and France

scientific article published in August 1993

Lesch-Nyhan syndrome: molecular investigation of three French Canadian families using a hypoxanthine-guanine phosphoribosyltransferase cDNA probe

scientific article published on 01 December 1988

Lipoamide dehydrogenase in Friedreich's ataxia fibroblasts

scientific article published on February 1, 1978

Lipoamide dehydrogenase in cultured human skin fibroblasts

scientific article published in July 1978

Maternal alphafetoproteln screening by the polypropylene tube immunoradiometric assay on dried blood

scientific article published on 01 October 1982

Molecular analyses of a Lesch-Nyhan syndrome mutation (hprtMontreal) by use of T-lymphocyte cultures

scientific article

Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sex

scientific article published on January 6, 1998

N-acetyl-β-hexosaminidase isoenzymes of amniotic fluid and maternal serum. Their relevance to prenatal diagnosis of the GM2 gangliosidoses

scientific article published on May 2, 1977

Neuraminidase activity in the mucolipidoses (types I, II and III) and the cherry-red spot myoclonus syndrome

scientific article published on December 3, 1979

Neuraminidase in Cultured Fibroblasts and Leucocytes of Homozygotes and Heterozygotes for the Mucolipidosis II Gene (I-Cell Disease)

scientific article published on 01 January 1979

New amphibian models for the study of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP).

scientific article published in March 1985

New autosomal recessive form of amelia.

scientific article published on March 1995

Occurrence and Properties of Fetal Intestinal Glycosidases (Disaccharidases) in Human Amniotic Fluid

scientific article published on January 1, 1975

Oral and dental development in X chromosome aneuploidy

scientific article published on 01 February 1985

Oral lecithin and linoleic acid in Friedreich's ataxia: I. Design of the study, material and methods

scientific article published on 01 May 1982

Oral lecithin and linoleic acid in Friedreich's ataxia: II. Clinical results

scientific article published on May 1982

Oral lecithin and linoleic acid in Friedreich's ataxia: III. Biochemical results

scientific article published on 01 May 1982

Origin and developmental patterns of lactase and other glycosidases in sheep amniotic and allantoic fluid

scientific article published on September 1, 1979

Parental reaction and adaptability to the prenatal diagnosis of fetal defect or genetic disease leading to pregnancy interruption

scientific article published on March 1995

Physiological limitation of benzoic acid detoxification by glycine-n-acylase in the normal human being (child and adult)

scientific article published in April 1974

Prenatal detection of intestinal obstruction by disaccharidase assay in amniotic fluid

scientific article published on 01 November 1977

Prenatal detection of intestinal obstruction: deficient amniotic fluid disaccharidases in affected fetuses

scientific article published on 01 September 1980

Prenatal detection of intestinal obstructions, aneuploidy syndromes, and cystic fibrosis by microvillar enzyme assays (disaccharidases, alkaline phosphatase, and glutamyltransferase) in amniotic fluid

scientific article published on 01 February 1987

Prenatal detection of the autosomal recessive type of polycystic kidney disease by trehalase assay in amniotic fluid

scientific article published on 01 January 1981

Prenatal detection of the congenital nephrotic syndrome (Finnish type) by trehalase assay in amniotic fluid

scientific article published on 01 July 1984

Prenatal diagnosis in medical genetics

scientific article published on 01 November 1971

Prenatal diagnosis of Smith-Lemli-Opitz syndrome is possible by measurement of 7-dehydrocholesterol in amniotic fluid

scientific article published on 01 September 1995

Prenatal diagnosis of fetal anomalies during the second trimester of pregnancy: Their characterization and delineation of defects in pregnancies at risk

scientific article published on 01 August 1991

Prenatal diagnosis of genetic disease in Canada: report of a collaborative study

scientific article published on October 1976

Prenatal diagnosis of genetic diseases during the second trimester of pregnancy, II: results

scientific article published on 01 April 1982

Prenatal diagnosis using DNA probes in twins at risk for Duchenne muscular dystrophy

scientific article published on 01 July 1986

Prenatal diagnosis: data on the cell viability and alpha fetoproteins of the amniotic fluid

scientific article published on December 1, 1975

Prenatal identification of a 45,X/46,Xder(Y) mosaicism and confirmation by high resolution cytogenetics and fluorescence in situ hybridization

scientific article published on 01 November 1992

Prevention in obstetrics: role of medical genetics

scientific article published on 01 October 1975

Proceedings: Dicarboxylic aminoaciduria: a new metabolic disease involving the transport of glutamic and aspartic acids

scientific article published on 01 September 1975

Purification and some properties of liver and brain beta-N-acetyl-hexosaminidase S.

scientific article

Pyruvate Dehydrogenase, Lipoamide Dehydrogenase and Citrate Synthase Activity in Fibroblasts from Patients with Friedreich's and Charlevoix-Saguenay Ataxia

scientific article published on 01 May 1979

Recent data and future perspectives in cytogenetics

scientific article published on August 1969

Recommendations on the use of folic acid supplementation to prevent the recurrence of neural tube defects. Clinical Teratology Committee, Canadian College of Medical Geneticists

scientific article

Selective abortion: a new moral order? Consensus and debate in the medical community

scientific article published on January 1995

Separation of amniotic fluid cell types in primary culture by Percoll density gradient centrifugation

scientific article published on 01 October 1982

Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p.

scientific article published on April 2000

Synchronization of amniotic fluid cells for high resolution cytogenetics

scientific article published on 01 January 1989

Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance.

scientific article

Taurine and Beta-Alanine Uptake in Cultured Human Skin Fibroblasts from Patients with Friedreich's Ataxia

scientific article published on May 1, 1979

Tetrasomy Y by structural rearrangement: clinical report

scientific article

The beta-amino acid transport system in Friedreich's ataxia

scientific article published on 01 November 1980

Thyroid antibodies in relation to infectious hepatitis and Down's syndrome.

scientific article

Trisomy recurrence: a reconsideration based on North American data

scientific article

[Medical genetics and its goals]

scientific article published on 01 December 1972

[Prenatal diagnosis of genetic diseases. I: indications]

scientific article published on 01 March 1982

[Sandhoff's disease: clinical and genetic study of a French-Canadian child]

scientific article published on 01 July 1974

[Studies on sialidosis and mucolipidosis. Properties of neuraminidase in cultured skin fibroblasts]

scientific article published on 01 September 1982