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Bulletin De L'Academie Nationale De Medecine|September 2, 2009
[Ultrastructural lesions of axonal mitochondria in patients with childhood-onset Charcot-Marie-Tooth disease due to MFN2 mutations]Benoît Funalot, Corinne Magdelaine, Franck Sturtz, et al.
Journal of Neurosurgery. Pediatrics|January 3, 2012
Primary nerve repair following resection of a neurenteric cyst of the oculomotor nerveScott J Turner, Mark A Dexter, James E H Smith, et al.
Developmental Medicine and Child Neurology|June 6, 2003
Peripheral neuropathies of infancyJo M Wilmshurst, John D Pollard, Garth Nicholson, et al.
Journal of the Peripheral Nervous System : JPNS|November 23, 2006
Expression of the antioxidant enzyme peroxiredoxin 5 in the human peripheral nervous systemJun Lan Lu, Jean-Michel Vallat, John D Pollard, et al.
Pediatrics|June 3, 2005
Congenital central hypoventilation syndrome and Hirschsprung's disease in an extremely preterm infantRamesh Bajaj, Janine Smith, Delphine Trochet, et al.
Developmental Medicine and Child Neurology|February 27, 2016
Auditory neuropathy in Brown-Vialetto-Van Laere syndrome due to riboflavin transporter RFVT2 deficiencyManoj P Menezes, Katherine O'Brien, Mandy Hill, et al.
European Journal of Human Genetics : EJHG|September 15, 2017
Mutations in RARS cause a hypomyelination disorder akin to Pelizaeus-Merzbacher diseaseMichael Nafisinia, Nara Sobreira, Lisa Riley, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 21, 2015
Pathophysiology of motor dysfunction in a childhood motor neuron disease caused by mutations in the riboflavin transporterManoj P Menezes, Michelle A Farrar, Richard Webster, et al.
European Journal of Medical Genetics|August 6, 2013
NKX2-1 mutation in a family diagnosed with ataxic dyskinetic cerebral palsyGai McMichael, Eric Haan, Alison Gardner, et al.
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