Michaud J - Search Results

1

Neurologic crises in hereditary tyrosinemia.

Mitchell G, Larochelle J, Lambert M, Michaud J, Grenier A, Ogier H, Gauthier M, Lacroix J, Vanasse M, Larbrisseau A, et al. Mitchell G, et al. Among authors: michaud j. N Engl J Med. 1990 Feb 15;322(7):432-7. doi: 10.1056/NEJM199002153220704. N Engl J Med. 1990. PMID: 2153931 Free article.

2

Nutritional vitamin B12 deficiency: two cases detected by routine newborn urinary screening.

Michaud JL, Lemieux B, Ogier H, Lambert MA. Michaud JL, et al. Eur J Pediatr. 1992 Mar;151(3):218-20. doi: 10.1007/BF01954389. Eur J Pediatr. 1992. PMID: 1601016

3

Population history and its impact on medical genetics in Quebec.

Laberge AM, Michaud J, Richter A, Lemyre E, Lambert M, Brais B, Mitchell GA. Laberge AM, et al. Among authors: michaud j. Clin Genet. 2005 Oct;68(4):287-301. doi: 10.1111/j.1399-0004.2005.00497.x. Clin Genet. 2005. PMID: 16143014 Review.

4

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. Dallaire L, et al. Among authors: michaud j. Prenat Diagn. 1991 Aug;11(8):629-35. doi: 10.1002/pd.1970110821. Prenat Diagn. 1991. PMID: 1837356

5

Intraoperative cardiac arrest due to the oculocardiac reflex and subsequent death in a child with occult Epstein-Barr virus myocarditis.

Fayon M, Gauthier M, Blanc VF, Ahronheim GA, Michaud J. Fayon M, et al. Among authors: michaud j. Anesthesiology. 1995 Sep;83(3):622-4. doi: 10.1097/00000542-199509000-00024. Anesthesiology. 1995. PMID: 7661365 Free article. No abstract available.

6

Stroke-like episodes in autosomal recessive cytochrome oxidase deficiency.

Morin C, Dubé J, Robinson BH, Lacroix J, Michaud J, De Braekeleer M, Geoffroy G, Lortie A, Blanchette C, Lambert MA, Mitchell GA. Morin C, et al. Among authors: michaud j. Ann Neurol. 1999 Mar;45(3):389-92. Ann Neurol. 1999. PMID: 10072055

7

New autosomal recessive form of amelia.

Michaud J, Filiatrault D, Dallaire L, Lambert M. Michaud J, et al. Am J Med Genet. 1995 Mar 27;56(2):164-7. doi: 10.1002/ajmg.1320560210. Am J Med Genet. 1995. PMID: 7625439 Review.

8

Strand-separating conformational polymorphism analysis: efficacy of detection of point mutations in the human ornithine delta-aminotransferase gene.

Michaud J, Brody LC, Steel G, Fontaine G, Martin LS, Valle D, Mitchell G. Michaud J, et al. Genomics. 1992 Jun;13(2):389-94. doi: 10.1016/0888-7543(92)90258-t. Genomics. 1992. PMID: 1612597

9

A progressive neurological syndrome associated with an isolated vitamin E deficiency.

Laplante P, Vanasse M, Michaud J, Geoffroy G, Brochu P. Laplante P, et al. Among authors: michaud j. Can J Neurol Sci. 1984 Nov;11(4 Suppl):561-4. doi: 10.1017/s0317167100035046. Can J Neurol Sci. 1984. PMID: 6509402

10

Effect of human recombinant leptin on lipid handling by fully differentiated Caco-2 cells.

Stan S, Levy E, Bendayan M, Zoltowska M, Lambert M, Michaud J, Asselin C, Delvin EE. Stan S, et al. Among authors: michaud j. FEBS Lett. 2001 Nov 9;508(1):80-4. doi: 10.1016/s0014-5793(01)03032-0. FEBS Lett. 2001. PMID: 11707272 Free article.

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