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Yves Robitaille

Showing results (11-20 of 28) with videos related to

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Journal of Child Neurology|January 15, 2011
Neuropathological homology in true Galloway-Mowat syndromeJulia Keith, Victoria A Fabian, Peter Walsh, et al.
Muscle & Nerve|July 30, 2013
An atypical case of SCN9A mutation presenting with global motor delay and a severe pain disorderInge Anita Meijer, Michel Vanasse, Sonia Nizard, et al.
Journal of Child Neurology|November 17, 2007
A newborn with spinal muscular atrophy type 0 presenting with a clinicopathological picture suggestive of myotubular myopathyAmelie Nadeau, Guy D'Anjou, Guillaume Debray, et al.
The Journal of Pediatrics|January 15, 2004
Sudden death in growth hormone-treated children with Prader-Willi syndromeGuy Van Vliet, Cheri L Deal, Patricia A Crock, et al.
Journal of Child Neurology|March 7, 2009
Critical illness polyneuromyopathy in a child with severe demyelinating myelitisTanja Adamovic, Ariane Willems, Michel Vanasse, et al.
Epilepsia|February 13, 2003
Bilateral Rasmussen encephalitis: postmortem documentation in a five-year-oldSharon M Tobias, Yves Robitaille, William F Hickey, et al.
Developmental Medicine and Child Neurology|July 17, 2015
The histopathology of polymicrogyria: a series of 71 brain autopsy studiesAnna C Jansen, Yves Robitaille, Mrinalini Honavar, et al.
Carcinogenesis|April 11, 2009
c-Met activation in medulloblastoma induces tissue factor expression and activity: effects on cell migrationMathieu Provençal, David Labbé, Ryan Veitch, et al.
Epilepsia|February 16, 2011
The clinical spectrum of nodular heterotopias in children: report of 31 patientsMyriam Srour, Marie-France Rioux, Caroline Varga, et al.
Pediatrics|April 4, 2007
Long-term outcome and clinical spectrum of 73 pediatric patients with mitochondrial diseasesFrançois-Guillaume Debray, Marie Lambert, Isabelle Chevalier, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Journal of Child Neurology|January 15, 2011
Neuropathological homology in true Galloway-Mowat syndromeJulia Keith, Victoria A Fabian, Peter Walsh, et al.
Muscle & Nerve|July 30, 2013
An atypical case of SCN9A mutation presenting with global motor delay and a severe pain disorderInge Anita Meijer, Michel Vanasse, Sonia Nizard, et al.
Journal of Child Neurology|November 17, 2007
A newborn with spinal muscular atrophy type 0 presenting with a clinicopathological picture suggestive of myotubular myopathyAmelie Nadeau, Guy D'Anjou, Guillaume Debray, et al.
The Journal of Pediatrics|January 15, 2004
Sudden death in growth hormone-treated children with Prader-Willi syndromeGuy Van Vliet, Cheri L Deal, Patricia A Crock, et al.
Journal of Child Neurology|March 7, 2009
Critical illness polyneuromyopathy in a child with severe demyelinating myelitisTanja Adamovic, Ariane Willems, Michel Vanasse, et al.
Epilepsia|February 13, 2003
Bilateral Rasmussen encephalitis: postmortem documentation in a five-year-oldSharon M Tobias, Yves Robitaille, William F Hickey, et al.
Developmental Medicine and Child Neurology|July 17, 2015
The histopathology of polymicrogyria: a series of 71 brain autopsy studiesAnna C Jansen, Yves Robitaille, Mrinalini Honavar, et al.
Carcinogenesis|April 11, 2009
c-Met activation in medulloblastoma induces tissue factor expression and activity: effects on cell migrationMathieu Provençal, David Labbé, Ryan Veitch, et al.
Epilepsia|February 16, 2011
The clinical spectrum of nodular heterotopias in children: report of 31 patientsMyriam Srour, Marie-France Rioux, Caroline Varga, et al.
Pediatrics|April 4, 2007
Long-term outcome and clinical spectrum of 73 pediatric patients with mitochondrial diseasesFrançois-Guillaume Debray, Marie Lambert, Isabelle Chevalier, et al.
Pageof 3