Michaud J - Search Results

1

Neuronal expression of human immunodeficiency virus type 1 env proteins in transgenic mice: distribution in the central nervous system and pathological alterations.

Berrada F, Ma D, Michaud J, Doucet G, Giroux L, Kessous-Elbaz A. Berrada F, et al. Among authors: michaud j. J Virol. 1995 Nov;69(11):6770-8. doi: 10.1128/JVI.69.11.6770-6778.1995. J Virol. 1995. PMID: 7474088 Free PMC article.

2

Neuropathology of NFHgp160 transgenic mice expressing HIV-1 env protein in neurons.

Michaud J, Fajardo R, Charron G, Sauvageau A, Berrada F, Ramla D, Dilhuydy H, Robitaille Y, Kessous-Elbaz A. Michaud J, et al. J Neuropathol Exp Neurol. 2001 Jun;60(6):574-87. doi: 10.1093/jnen/60.6.574. J Neuropathol Exp Neurol. 2001. PMID: 11398834

3

Homozygous deletion of Tenascin-R in a patient with intellectual disability.

Dufresne D, Hamdan FF, Rosenfeld JA, Torchia B, Rosenblatt B, Michaud JL, Srour M. Dufresne D, et al. J Med Genet. 2012 Jul;49(7):451-4. doi: 10.1136/jmedgenet-2012-100831. Epub 2012 Jun 22. J Med Genet. 2012. PMID: 22730557 Free PMC article.

4

Effects of basic fibroblast growth factor on the differentiation, growth, and viability of a new human medulloblastoma cell line (UM-MB1).

Kenigsberg RL, Hong Y, Yao H, Lemieux N, Michaud J, Tautu C, Théorêt Y. Kenigsberg RL, et al. Among authors: michaud j. Am J Pathol. 1997 Sep;151(3):867-81. Am J Pathol. 1997. PMID: 9284836 Free PMC article.

5

Intracranial hemorrhage in a newborn with hemophilia following elective cesarean section.

Michaud JL, Rivard GE, Chessex P. Michaud JL, et al. Am J Pediatr Hematol Oncol. 1991 Winter;13(4):473-5. doi: 10.1097/00043426-199124000-00014. Am J Pediatr Hematol Oncol. 1991. PMID: 1785675

6

Alterations of visual and auditory evoked potentials in fragile X syndrome.

Knoth IS, Vannasing P, Major P, Michaud JL, Lippé S. Knoth IS, et al. Int J Dev Neurosci. 2014 Aug;36:90-7. doi: 10.1016/j.ijdevneu.2014.05.003. Epub 2014 May 27. Int J Dev Neurosci. 2014. PMID: 24875778

7

The clinical spectrum of nodular heterotopias in children: report of 31 patients.

Srour M, Rioux MF, Varga C, Lortie A, Major P, Robitaille Y, Décarie JC, Michaud J, Carmant L. Srour M, et al. Among authors: michaud j. Epilepsia. 2011 Apr;52(4):728-37. doi: 10.1111/j.1528-1167.2010.02975.x. Epub 2011 Feb 14. Epilepsia. 2011. PMID: 21320118 Free article.

8

Disruption of TBC1D7, a subunit of the TSC1-TSC2 protein complex, in intellectual disability and megalencephaly.

Capo-Chichi JM, Tcherkezian J, Hamdan FF, Décarie JC, Dobrzeniecka S, Patry L, Nadon MA, Mucha BE, Major P, Shevell M, Bencheikh BO, Joober R, Samuels ME, Rouleau GA, Roux PP, Michaud JL. Capo-Chichi JM, et al. Among authors: michaud jl. J Med Genet. 2013 Nov;50(11):740-4. doi: 10.1136/jmedgenet-2013-101680. Epub 2013 May 17. J Med Genet. 2013. PMID: 23687350

9

De novo mutations in moderate or severe intellectual disability.

Hamdan FF, Srour M, Capo-Chichi JM, Daoud H, Nassif C, Patry L, Massicotte C, Ambalavanan A, Spiegelman D, Diallo O, Henrion E, Dionne-Laporte A, Fougerat A, Pshezhetsky AV, Venkateswaran S, Rouleau GA, Michaud JL. Hamdan FF, et al. PLoS Genet. 2014 Oct 30;10(10):e1004772. doi: 10.1371/journal.pgen.1004772. eCollection 2014 Oct. PLoS Genet. 2014. PMID: 25356899 Free PMC article.

10

Dysfunction of the Cerebral Glucose Transporter SLC45A1 in Individuals with Intellectual Disability and Epilepsy.

Srour M, Shimokawa N, Hamdan FF, Nassif C, Poulin C, Al Gazali L, Rosenfeld JA, Koibuchi N, Rouleau GA, Al Shamsi A, Michaud JL. Srour M, et al. Am J Hum Genet. 2017 May 4;100(5):824-830. doi: 10.1016/j.ajhg.2017.03.009. Epub 2017 Apr 20. Am J Hum Genet. 2017. PMID: 28434495 Free PMC article.

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