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Louis Dallaire

Research Profile

Physiology

Pregnancy

Procedures

Anatomy

Chemicals & Drugs

Concepts & Ideas

Second Pregnancy Trimester

Disorders

Living Beings

Infants

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Publications

TOP 3
Martin DesGroseilliers; Emmanuelle Lemyre; Louis Dallaire; Nicole Lemieux
Tetrasomy Y by structural rearrangement: clinical report.
Frédérique Tihy; Emmanuelle Lemyre; Louis Dallaire; Nicole Lemieux
Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p.
Frédérique Tihy; Emmanuelle Lemyre; Nicole Lemieux; Louis Dallaire
De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype.

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All Publications

2002: Martin DesGroseilliers; Emmanuelle Lemyre; Louis Dallaire; Nicole Lemieux
Tetrasomy Y by structural rearrangement: clinical report.
American journal of medical genetics 2002;111(4):401-4.
2000: Frédérique Tihy; Emmanuelle Lemyre; Louis Dallaire; Nicole Lemieux
Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p.
American journal of medical genetics 2000;91(5):383-6.
1999: Frédérique Tihy; Emmanuelle Lemyre; Nicole Lemieux; Louis Dallaire
De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype.
American journal of medical genetics 1999;87(4):302-5.
1999: Emmanuelle Lemyre; C Infante-Rivard; Louis Dallaire
Prevalence of congenital anomalies at birth among offspring of women at risk for a genetic disorder and with a normal second-trimester ultrasound.
Teratology 1999;60(4):240-4.
1999: L Caron; Frédérique Tihy; Louis Dallaire
Frequencies of chromosomal abnormalities at amniocentesis: over 20 years of cytogenetic analyses in one laboratory.
American journal of medical genetics 1999;82(2):149-54.
1997: N Lepage; N McDonald; Louis Dallaire; M Lambert
Age-specific distribution of plasma amino acid concentrations in a healthy pediatric population.
Clinical chemistry 1997;43(12):2397-402.
1997: Alexey V Pshezhetsky; C Richard; L Michaud; Suleiman A Igdoura; S Wang; MA Elsliger; J Qu; Daniel Leclerc; Roy A Gravel; Louis Dallaire; M Potier
Cloning, expression and chromosomal mapping of human lysosomal sialidase and characterization of mutations in sialidosis.
Nature genetics 1997;15(3):316-20.
1996: M Boutouil; raouf fetni; J Qu; Louis Dallaire; Chantal Richer; Nicole Lemieux
Fragile site and interstitial telomere repeat sequences at the fusion point of a de novo (Y;13) translocation.
Human genetics 1996;98(3):323-7.
1996: T C Hunter; S B Melancon; Louis Dallaire; S Taft; Thomas R Skopek; Richard J Albertini; J Patrick O'Neill
Germinal HPRT splice donor site mutation results in multiple RNA splicing products in T-lymphocyte cultures.
Somatic cell and molecular genetics 1996;22(2):145-50.
1996: Juan Carlos Feoli-Fonseca; Marie Lambert; G Mitchell; SB Melançon; Louis Dallaire; D S Millington; Ijaz Qureshi
Chronic sodium benzoate therapy in children with inborn errors of urea synthesis: effect on carnitine metabolism and ammonia nitrogen removal.
Biochemical and molecular medicine 1996;57(1):31-6.
1995: Louis Dallaire; G Mitchell; R Giguère; F Lefebvre; SB Melançon; M Lambert
Prenatal diagnosis of Smith-Lemli-Opitz syndrome is possible by measurement of 7-dehydrocholesterol in amniotic fluid.
Prenatal diagnosis 1995;15(9):855-8.
1995: Grant A Mitchell; C Jakobs; K M Gibson; MF Robert; A Burlina; Carlo Dionisi Vici; Louis Dallaire
Molecular prenatal diagnosis of 3-hydroxy-3-methylglutaryl CoA lyase deficiency.
Prenatal diagnosis 1995;15(8):725-9.
1995: J Michaud; D Filiatrault; Louis Dallaire; Marie Lambert
New autosomal recessive form of amelia.
American journal of medical genetics 1995;56(2):164-7.
1995: Louis Dallaire; G Lortie; M Des Rochers; R Clermont; C Vachon
Parental reaction and adaptability to the prenatal diagnosis of fetal defect or genetic disease leading to pregnancy interruption.
Prenatal diagnosis 1995;15(3):249-59.
1994: J Michaud; P Russo; A Grignon; Louis Dallaire; D Bichet; D Rosenblatt; E Lamothe; Marie Lambert
Autosomal dominant polycystic kidney disease in the fetus.
American journal of medical genetics 1994;51(3):240-6.
1993: MA Elsliger; Louis Dallaire; M Potier
Fetal intestinal and renal origins of trehalase activity in human amniotic fluid.
Clinica chimica acta; international journal of clinical chemistry 1993;216(1-2):91-102.
1992: J Qu; Louis Dallaire; raouf fetni; Chantal Richer
Prenatal identification of a 45,X/46,Xder(Y) mosaicism and confirmation by high resolution cytogenetics and fluorescence in situ hybridization.
Prenatal diagnosis 1992;12(11):909-17.
1991: Louis Dallaire; J Michaud; S B Melancon; M Potier; M Lambert; G Mitchell; J Boisvert
Prenatal diagnosis of fetal anomalies during the second trimester of pregnancy: their characterization and delineation of defects in pregnancies at risk.
Prenatal diagnosis 1991;11(8):629-35.
1991: M A Lambert; B Marescau; Michel Desjardins; M Laberge; J L Dhondt; Louis Dallaire; P P De Deyn; Ijaz Qureshi
Hyperargininemia: intellectual and motor improvement related to changes in biochemical data.
The Journal of pediatrics 1991;118(3):420-4.
1990: Thomas R Skopek; Leslie Recio; D Simpson; Louis Dallaire; S B Melancon; H Ogier; J Patrick O'Neill; M T Falta; Janice A Nicklas; Richard J Albertini
Molecular analyses of a Lesch-Nyhan syndrome mutation (hprtMontreal) by use of T-lymphocyte cultures.
Human genetics 1990;85(1):111-6.
1990: A Michalak; M A Lambert; Louis Dallaire; S B Melançon; R Laframboise; Bernard Lemieux; Ijaz Qureshi
[Hypocarnitinemia in patients affected by a primary defect of ammonia metabolism treated with sodium benzoate].
Diabète & métabolisme 1990;16(3):226-33.
1988: Daniel Sinnett; L Lavergne; SB Melançon; Louis Dallaire; M Potier; Damian Labuda
Lesch-Nyhan syndrome: molecular investigation of three French Canadian families using a hypoxanthine-guanine phosphoribosyltransferase cDNA probe.
Human genetics 1988;81(1):4-8.
1987: P R Morin; S B Melançon; Louis Dallaire; M Potier
Prenatal detection of intestinal obstructions, aneuploidy syndromes, and cystic fibrosis by microvillar enzyme assays (disaccharidases, alkaline phosphatase, and glutamyltransferase) in amniotic fluid.
American journal of medical genetics 1987;26(2):405-15.
1986: M Potier; J Cousineau; L Michaud; M Zolinger; S B Melançon; Louis Dallaire
Fetal intestinal microvilli in human amniotic fluid.
Prenatal diagnosis 1986;6(6):429-36.
1986: L Lavergne; SB Melançon; Louis Dallaire; M Potier; Daniel Sinnett; C Hours; Damian Labuda
Prenatal diagnosis using DNA probes in twins at risk for Duchenne muscular dystrophy.
Lancet 1986;2(8500):216-7.
1986: G A Mitchell; D Watkins; SB Melançon; D S Rosenblatt; G Geoffroy; J Orquin; M B Homsy; Louis Dallaire
Clinical heterogeneity in cobalamin C variant of combined homocystinuria and methylmalonic aciduria.
The Journal of pediatrics 1986;108(3):410-5.
1985: P Farge; Louis Dallaire; M Potier; S B Melançon
Prenatal diagnosis of trisomy 10 p in a twin pregnancy.
Prenatal diagnosis 1985;5(3):199-203.
1985: P Farge; Louis Dallaire; G Albert; S B Melançon; M Potier; G Leboeuf
Oral and dental development in X chromosome aneuploidy.
Clinical genetics 1985;27(2):122-6.
1984: Louis Dallaire; S B Melançon; M Potier; J P Mathieu; G Ducharme
Date of conception and prevention of neural tube defects.
Clinical genetics 1984;26(4):304-7.
1984: P R Morin; M Potier; Louis Dallaire; S B Melançon
Prenatal detection of the congenital nephrotic syndrome (Finnish type) by trehalase assay in amniotic fluid.
Prenatal diagnosis 1984;4(4):257-60.
1984: M Potier; P R Morin; S B Melançon; Louis Dallaire
Differential stabilities of fetal intestinal disaccharidases determine their relative amounts released into amniotic fluid.
Biology of the neonate 1984;45(5):257-60.
1983: P R Morin; M Potier; R LaSalle; S B Melançon; Louis Dallaire
Amniotic-fluid disaccharidases in the prenatal detection of cystic fibrosis.
Lancet 1983;2(8350):621-2.
1982: J Cousineau; M Potier; Louis Dallaire; S B Melançon
Separation of amniotic fluid cell types in primary culture by Percoll density gradient centrifugation.
Prenatal diagnosis 1982;2(4):241-9.
1982: Louis Dallaire; A Grenier; G Ducharme; S B Melancon; M Potier; M Des Rochers
Maternal alphafetoprotein screening by the polypropylene tube immunoradiometric assay on dried blood.
Prenatal diagnosis 1982;2(4):265-71.
1982: G Beauregard; S B Melançon; Louis Dallaire; M Potier
[Studies on sialidosis and mucolipidosis. Properties of neuraminidase in cultured skin fibroblasts].
Biochimica et biophysica acta 1982;706(2):212-20.
1982: R Gagné; A Lescault; A Grenier; C Laberge; S B Mélançon; Louis Dallaire
Prenatal diagnosis of hereditary tyrosinaemia: measurement of succinylacetone in amniotic fluid.
Prenatal diagnosis 1982;2(3):185-8.
1982: Louis Dallaire; S B Melançon; M Potier; M Gagnon; J Boisvert; G Lortie
[Prenatal diagnosis of genetic diseases during the second trimester of pregnancy, II: results].
L'unión médicale du Canada 1982;111(4):299-310.
1982: Louis Dallaire; S B Melançon; M Potier; M Gagnon; J Boisvert; G Lortie
[Prenatal diagnosis of genetic diseases. I: indications].
L'unión médicale du Canada 1982;111(3):189-202.
1981: P R Morin; M Potier; Louis Dallaire; S B Melançon; J Boisvert
Prenatal detection of the autosomal recessive type of polycystic kidney disease by trehalase assay in amniotic fluid.
Prenatal diagnosis 1981;1(1):75-9.
1980: P R Morin; M Potier; Louis Dallaire; S B Melançon; A Milunsky
Prenatal detection of intestinal obstruction: deficient amniotic fluid disaccharidases in affected fetuses.
Clinical genetics 1980;18(3):217-22.