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Items: 1 to 50 of 139

1.

Interdisciplinary teaching in family medicine teaching units: the residents' points of view.

Dallaire LF, Rhéaume C, Vézina L.

Can Med Educ J. 2018 Jul 27;9(3):e25-e40. eCollection 2018 Jul.

2.

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

Larochelle J, Alvarez F, Bussières JF, Chevalier I, Dallaire L, Dubois J, Faucher F, Fenyves D, Goodyer P, Grenier A, Holme E, Laframboise R, Lambert M, Lindstedt S, Maranda B, Melançon S, Merouani A, Mitchell J, Parizeault G, Pelletier L, Phan V, Rinaldo P, Scott CR, Scriver C, Mitchell GA.

Mol Genet Metab. 2012 Sep;107(1-2):49-54. doi: 10.1016/j.ymgme.2012.05.022. Epub 2012 Jul 13.

PMID:
22885033
3.

Identifying mobility heterogeneity in very frail older adults. Are frail people all the same?

Montero-Odasso M, Bergman H, Béland F, Sourial N, Fletcher JD, Dallaire L.

Arch Gerontol Geriatr. 2009 Sep-Oct;49(2):272-277. doi: 10.1016/j.archger.2008.09.010. Epub 2008 Nov 4.

PMID:
18986718
4.

Integrated services for frail elders (SIPA): a trial of a model for Canada.

Béland F, Bergman H, Lebel P, Dallaire L, Fletcher J, Contandriopoulos AP, Tousignant P.

Can J Aging. 2006 Spring;25(1):5-42. English, French.

PMID:
16770746
5.

A system of integrated care for older persons with disabilities in Canada: results from a randomized controlled trial.

Béland F, Bergman H, Lebel P, Clarfield AM, Tousignant P, Contandriopoulos AP, Dallaire L.

J Gerontol A Biol Sci Med Sci. 2006 Apr;61(4):367-73.

PMID:
16611703
6.

Trisomy recurrence: a reconsideration based on North American data.

Warburton D, Dallaire L, Thangavelu M, Ross L, Levin B, Kline J.

Am J Hum Genet. 2004 Sep;75(3):376-85. Epub 2004 Jul 8.

7.

Tetrasomy Y by structural rearrangement: clinical report.

DesGroseilliers M, Lemyre E, Dallaire L, Lemieux N.

Am J Med Genet. 2002 Sep 1;111(4):401-4.

PMID:
12210299
8.

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

Tihy F, Lemyre E, Dallaire L, Lemieux N.

Am J Med Genet. 2000 Apr 24;91(5):383-6.

PMID:
10767003
9.

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

Tihy F, Lemyre E, Lemieux N, Dallaire L.

Am J Med Genet. 1999 Dec 3;87(4):302-5. Review.

PMID:
10588834
10.

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

Farrell SA, Summers AM, Dallaire L, Singer J, Johnson JA, Wilson RD.

J Med Genet. 1999 Nov;36(11):843-6.

11.
12.

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

Winsor EJ, Tomkins DJ, Kalousek D, Farrell S, Wyatt P, Fan YS, Carter R, Wang H, Dallaire L, Eydoux P, Welch JP, Dawson A, Lin JC, Singer J, Johnson J, Wilson RD.

Prenat Diagn. 1999 Jul;19(7):620-7.

PMID:
10419609
13.
14.

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

Costa T, Lambert M, Teshima I, Ray PN, Richer CL, Dallaire L.

Am J Med Genet. 1998 Jan 6;75(1):40-4. Review.

PMID:
9450855
15.

Age-specific distribution of plasma amino acid concentrations in a healthy pediatric population.

Lepage N, McDonald N, Dallaire L, Lambert M.

Clin Chem. 1997 Dec;43(12):2397-402.

16.

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

Pshezhetsky AV, Richard C, Michaud L, Igdoura S, Wang S, Elsliger MA, Qu J, Leclerc D, Gravel R, Dallaire L, Potier M.

Nat Genet. 1997 Mar;15(3):316-20.

PMID:
9054950
17.

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

Boutouil M, Fetni R, Qu J, Dallaire L, Richer CL, Lemieux N.

Hum Genet. 1996 Sep;98(3):323-7.

PMID:
8707303
18.

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

Guibaud L, Filiatrault D, Garel L, Grignon A, Dubois J, Miron MC, Dallaire L.

AJR Am J Roentgenol. 1996 May;166(5):1195-202.

PMID:
8615269
19.

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

Hunter TC, Melancon SB, Dallaire L, Taft S, Skopek TR, Albertini RJ, O'Neill JP.

Somat Cell Mol Genet. 1996 Mar;22(2):145-50.

PMID:
8782493
20.

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

Feoli-Fonseca JC, Lambert M, Mitchell G, Melançon SB, Dallaire L, Millington DS, Qureshi IA.

Biochem Mol Med. 1996 Feb;57(1):31-6.

PMID:
8812724
21.

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

Dallaire L, Mitchell G, Giguère R, Lefebvre F, Melançon SB, Lambert M.

Prenat Diagn. 1995 Sep;15(9):855-8.

PMID:
8559757
22.

Molecular prenatal diagnosis of 3-hydroxy-3-methylglutaryl CoA lyase deficiency.

Mitchell GA, Jakobs C, Gibson KM, Robert MF, Burlina A, Dionisi-Vici C, Dallaire L.

Prenat Diagn. 1995 Aug;15(8):725-9.

PMID:
7479590
23.

New autosomal recessive form of amelia.

Michaud J, Filiatrault D, Dallaire L, Lambert M.

Am J Med Genet. 1995 Mar 27;56(2):164-7. Review.

PMID:
7625439
24.

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

Dallaire L, Lortie G, Des Rochers M, Clermont R, Vachon C.

Prenat Diagn. 1995 Mar;15(3):249-59.

PMID:
7784383
25.

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

Bouchard L, Renaud M, Kremp O, Dallaire L.

Int J Health Serv. 1995;25(1):65-84.

PMID:
7729967
26.

Autosomal dominant polycystic kidney disease in the fetus.

Michaud J, Russo P, Grignon A, Dallaire L, Bichet D, Rosenblatt D, Lamothe E, Lambert M.

Am J Med Genet. 1994 Jul 1;51(3):240-6.

PMID:
8074152
27.
28.

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

Renaud M, Bouchard L, Kremp O, Dallaire L, Labadie JF, Bisson J, Trugeon A.

Prenat Diagn. 1993 Aug;13(8):691-706.

PMID:
8284288
29.

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

Elsliger MA, Dallaire L, Potier M.

Clin Chim Acta. 1993 Jul 16;216(1-2):91-102.

PMID:
8222277
30.

Phosphate transport in capillaries of the blood-brain barrier.

Béliveau R, Dallaire L, Giroux S.

Adv Exp Med Biol. 1993;331:75-80. No abstract available.

PMID:
8333350
31.

Phosphate transport by capillaries of the blood-brain barrier.

Dallaire L, Béliveau R.

J Biol Chem. 1992 Nov 5;267(31):22323-7.

32.
33.

Regulation of phosphate transport by second messengers in capillaries of the blood-brain barrier.

Dallaire L, Giroux S, Béliveau R.

Biochim Biophys Acta. 1992 Sep 21;1110(1):59-64.

PMID:
1382598
34.

Familial chromosomal aberrations and metabolic disorders.

Hamerton JL, Dallaire L, Tomkins D, Lippman A.

Prenat Diagn. 1992 May;12(5):473-6. No abstract available.

PMID:
1523213
35.

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

Teshima IE, Kalousek DK, Vekemans MJ, Markovic V, Cox DM, Dallaire L, Gagne R, Lin JC, Ray M, Sergovich FR, et al.

Prenat Diagn. 1992 May;12(5):443-66.

PMID:
1523211
36.

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

Tomkins DJ, Vekemans MJ, Teshima IE, Cox DM, Dallaire L, Gagne R, Kalousek DK, Lin JC, Markovic VD, Ray M, et al.

Prenat Diagn. 1992 May;12(5):439-41. No abstract available.

PMID:
1523210
37.

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

Dallaire L, Michaud J, Melancon SB, Potier M, Lambert M, Mitchell G, Boisvert J.

Prenat Diagn. 1991 Aug;11(8):629-35.

PMID:
1837356
38.

Purification and characterization of metabolically active capillaries of the blood-brain barrier.

Dallaire L, Tremblay L, Béliveau R.

Biochem J. 1991 Jun 15;276 ( Pt 3):745-52.

39.

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

Lambert MA, Marescau B, Desjardins M, Laberge M, Dhondt JL, Dallaire L, De Deyn PP, Qureshi IA.

J Pediatr. 1991 Mar;118(3):420-4. No abstract available.

PMID:
1999785
40.

Screening for trisomy 21 with ultrasonographic determination of biparietal diameter/femur length ratio.

Marquette GP, Boucher M, Desrochers M, Dallaire L.

Am J Obstet Gynecol. 1990 Nov;163(5 Pt 1):1604-5.

PMID:
2146880
41.

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

Skopek TR, Recio L, Simpson D, Dallaire L, Melancon SB, Ogier H, O'Neill JP, Falta MT, Nicklas JA, Albertini RJ.

Hum Genet. 1990 Jun;85(1):111-6.

PMID:
2358296
42.

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

Michalak A, Lambert MA, Dallaire L, Melançon SB, Laframboise R, Lemieux B, Qureshi IA.

Diabete Metab. 1990 May-Jun;16(3):226-33. French.

PMID:
2210018
43.

A new program for reducing patient falls.

Dallaire LB, Burke EV.

Nursing. 1989 Jan;19(1):65. No abstract available.

PMID:
2909933
44.

Synchronization of amniotic fluid cells for high resolution cytogenetics.

Qu J, Dallaire L, Lemieux N, Drouin R, Richer CL.

Prenat Diagn. 1989 Jan;9(1):49-56.

PMID:
2748550
45.

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

Sinnett D, Lavergne L, Melançon SB, Dallaire L, Potier M, Labuda D.

Hum Genet. 1988 Dec;81(1):4-8.

PMID:
2904404
46.

Total parenteral nutrition in the newborn: amino acids-energy interrelationships.

Pineault M, Chessex P, Bisaillon S, Lepage D, Dallaire L.

Am J Clin Nutr. 1988 Oct;48(4):1065-9.

PMID:
3138906
48.

mRNA characterization of human fetal enamel matrix.

Farge P, Couble P, Magloire H, Dallaire L.

Arch Oral Biol. 1987;32(9):655-8.

PMID:
3481967
49.

Fetal intestinal microvilli in human amniotic fluid.

Potier M, Cousineau J, Michaud L, Zolinger M, Melançon SB, Dallaire L.

Prenat Diagn. 1986 Nov-Dec;6(6):429-36.

PMID:
3027683
50.

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

Lavergne L, Melançon SB, Dallaire L, Potier M, Sinnett D, Hours C, Labuda D.

Lancet. 1986 Jul 26;2(8500):216-7. No abstract available.

PMID:
2873456

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