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Pain and the Guillain-Barré syndrome in children under 6 years old.
Nguyen DK, Agenarioti-Bélanger S, Vanasse M. Nguyen DK, et al. J Pediatr. 1999 Jun;134(6):773-6. doi: 10.1016/s0022-3476(99)70297-0. J Pediatr. 1999. PMID: 10356150
Intermittent peripheral weakness as the presenting feature of pyruvate dehydrogenase deficiency.
Debray FG, Lambert M, Vanasse M, Decarie JC, Cameron J, Levandovskiy V, Robinson BH, Mitchell GA. Debray FG, et al. Eur J Pediatr. 2006 Jul;165(7):462-6. doi: 10.1007/s00431-006-0104-5. Epub 2006 Mar 22. Eur J Pediatr. 2006. PMID: 16552546
Acute combined central and peripheral nervous system demyelination in children.
Adamovic T, Riou EM, Bernard G, Vanasse M, Décarie JC, Poulin C, Gauvin F. Adamovic T, et al. Pediatr Neurol. 2008 Nov;39(5):307-16. doi: 10.1016/j.pediatrneurol.2008.07.022. Pediatr Neurol. 2008. PMID: 18940553
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. 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
Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: neurologic, ophthalmologic, and neuropsychologic examination of six patients.
Lemay JF, Lambert MA, Mitchell GA, Vanasse M, Valle D, Arbour JF, Dubé J, Flessas J, Laberge M, Lafleur L, et al. Lemay JF, et al. J Pediatr. 1992 Nov;121(5 Pt 1):725-30. doi: 10.1016/s0022-3476(05)81900-6. J Pediatr. 1992. PMID: 1432421
Congenital axonal neuropathy and encephalopathy.
Chau V, Clément JF, Robitaille Y, D'Anjou G, Vanasse M. Chau V, et al. Pediatr Neurol. 2008 Apr;38(4):261-6. doi: 10.1016/j.pediatrneurol.2007.11.005. Pediatr Neurol. 2008. PMID: 18358405
Critical illness polyneuromyopathy in a child with severe demyelinating myelitis.
Adamovic T, Willems A, Vanasse M, D'Anjou G, Robitaille Y, Litalien C, Gauvin F. Adamovic T, et al. J Child Neurol. 2009 Jun;24(6):758-62. doi: 10.1177/0883073808330166. Epub 2009 Mar 4. J Child Neurol. 2009. PMID: 19264734
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. N Engl J Med. 1990 Feb 15;322(7):432-7. doi: 10.1056/NEJM199002153220704. N Engl J Med. 1990. PMID: 2153931
Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansion.
Montermini L, Richter A, Morgan K, Justice CM, Julien D, Castellotti B, Mercier J, Poirier J, Capozzoli F, Bouchard JP, Lemieux B, Mathieu J, Vanasse M, Seni MH, Graham G, Andermann F, Andermann E, Melançon SB, Keats BJ, Di Donato S, Pandolfo M. Montermini L, et al. Ann Neurol. 1997 May;41(5):675-82. doi: 10.1002/ana.410410518. Ann Neurol. 1997. PMID: 9153531
Efficacy and safety of lacosamide as an adjunctive therapy for refractory focal epilepsy in paediatric patients: a retrospective single-centre study.
Toupin JF, Lortie A, Major P, Diadori P, Vanasse M, Rossignol E, D'Anjou G, Perreault S, Larbrisseau A, Carmant L, Birca A. Toupin JF, et al. Among authors: vanasse m. Epileptic Disord. 2015 Dec;17(4):436-43. doi: 10.1684/epd.2015.0782. Epileptic Disord. 2015. PMID: 26609635 Free article.
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