Vanasse M - Search Results

1

Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability.

Hamdan FF, Gauthier J, Araki Y, Lin DT, Yoshizawa Y, Higashi K, Park AR, Spiegelman D, Dobrzeniecka S, Piton A, Tomitori H, Daoud H, Massicotte C, Henrion E, Diallo O; S2D Group; Shekarabi M, Marineau C, Shevell M, Maranda B, Mitchell G, Nadeau A, D'Anjou G, Vanasse M, Srour M, Lafrenière RG, Drapeau P, Lacaille JC, Kim E, Lee JR, Igarashi K, Huganir RL, Rouleau GA, Michaud JL. Hamdan FF, et al. Among authors: vanasse m. Am J Hum Genet. 2011 Mar 11;88(3):306-16. doi: 10.1016/j.ajhg.2011.02.001. Epub 2011 Mar 3. Am J Hum Genet. 2011. PMID: 21376300 Free PMC article.

2

Intellectual disability without epilepsy associated with STXBP1 disruption.

Hamdan FF, Gauthier J, Dobrzeniecka S, Lortie A, Mottron L, Vanasse M, D'Anjou G, Lacaille JC, Rouleau GA, Michaud JL. Hamdan FF, et al. Among authors: vanasse m. Eur J Hum Genet. 2011 May;19(5):607-9. doi: 10.1038/ejhg.2010.183. Epub 2011 Mar 2. Eur J Hum Genet. 2011. PMID: 21364700 Free PMC article.

3

Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy.

Cossette P, Liu L, Brisebois K, Dong H, Lortie A, Vanasse M, Saint-Hilaire JM, Carmant L, Verner A, Lu WY, Wang YT, Rouleau GA. Cossette P, et al. Among authors: vanasse m. Nat Genet. 2002 Jun;31(2):184-9. doi: 10.1038/ng885. Epub 2002 May 6. Nat Genet. 2002. PMID: 11992121

4

Long-term outcome of Leigh syndrome caused by the NARP-T8993C mtDNA mutation.

Debray FG, Lambert M, Lortie A, Vanasse M, Mitchell GA. Debray FG, et al. Among authors: vanasse m. Am J Med Genet A. 2007 Sep 1;143A(17):2046-51. doi: 10.1002/ajmg.a.31880. Am J Med Genet A. 2007. PMID: 17663470 Review.

5

Single-strand conformational polymorphisms (SSCP): detection of useful polymorphisms at the dystrophin locus.

Zietkiewicz E, Sinnett D, Richer C, Mitchell G, Vanasse M, Labuda D. Zietkiewicz E, et al. Among authors: vanasse m. Hum Genet. 1992 Jun;89(4):453-6. doi: 10.1007/BF00194322. Hum Genet. 1992. PMID: 1618495

6

Autosomal dominant juvenile myoclonic epilepsy and GABRA1.

Cossette P, Lortie A, Vanasse M, Saint-Hilaire JM, Rouleau GA. Cossette P, et al. Among authors: vanasse m. Adv Neurol. 2005;95:255-63. Adv Neurol. 2005. PMID: 15508928 Review. No abstract available.

7

A newborn with spinal muscular atrophy type 0 presenting with a clinicopathological picture suggestive of myotubular myopathy.

Nadeau A, D'Anjou G, Debray G, Robitaille Y, Simard LR, Vanasse M. Nadeau A, et al. Among authors: vanasse m. J Child Neurol. 2007 Nov;22(11):1301-4. doi: 10.1177/0883073807307105. J Child Neurol. 2007. PMID: 18006961

8

Evolution and treatment of childhood chronic inflammatory polyneuropathy.

Rossignol E, D'Anjou G, Lapointe N, Haddad E, Vanasse M. Rossignol E, et al. Among authors: vanasse m. Pediatr Neurol. 2007 Feb;36(2):88-94. doi: 10.1016/j.pediatrneurol.2006.09.012. Pediatr Neurol. 2007. PMID: 17275659

9

Congenital axonal neuropathy and encephalopathy.

Chau V, Clément JF, Robitaille Y, D'Anjou G, Vanasse M. Chau V, et al. Among authors: vanasse m. Pediatr Neurol. 2008 Apr;38(4):261-6. doi: 10.1016/j.pediatrneurol.2007.11.005. Pediatr Neurol. 2008. PMID: 18358405

10

Transient creatine phosphokinase elevations in children: a single-center experience.

Perreault S, Birca A, Piper D, Nadeau A, Gauvin F, Vanasse M. Perreault S, et al. Among authors: vanasse m. J Pediatr. 2011 Oct;159(4):682-5. doi: 10.1016/j.jpeds.2011.03.045. Epub 2011 May 17. J Pediatr. 2011. PMID: 21592501

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

92 results

Search Page