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Showing results (81-90 of 143) with videos related to

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Pediatric Transplantation|February 28, 2006
Disseminated adenovirus infection with respiratory failure in pediatric liver transplant recipients: impact of intravenous cidofovir and inhaled nitric oxideM A Wallot, C Dohna-Schwake, M Auth, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
Introduction of a ketogenic diet in young infantsJ Klepper, B Leiendecker, R Bredahl, et al.
Neuropediatrics|August 18, 2001
Hydrocephalus internus in two patients with 5,10-methylenetetrahydrofolate reductase deficiencyM Baethmann, U Wendel, G F Hoffmann, et al.
Journal of Neuropathology and Experimental Neurology|January 1, 1992
Adult polyglucosan body myopathyH H Goebel, Y S Shin, F Gullotta, et al.
Journal of the Neurological Sciences|June 17, 1999
Secondary reduction of alpha7B integrin in laminin alpha2 deficient congenital muscular dystrophy supports an additional transmembrane link in skeletal muscleR D Cohn, U Mayer, G Saher, et al.
Neuromuscular Disorders : NMD|September 27, 2008
Towards harmonisation of outcome measures for DMD and SMA within TREAT-NMD; report of three expert workshops: TREAT-NMD/ENMC workshop on outcome measures, 12th--13th May 2007, Naarden, The Netherlands; TREAT-NMD workshop on outcome measures in experimental trials for DMD, 30th June--1st July 2007, Naarden, The Netherlands; conjoint Institute of Myology TREAT-NMD meeting on physical activity monitoring in neuromuscular disorders, 11th July 2007, Paris, FranceE Mercuri, A Mayhew, F Muntoni, et al.
American Journal of Human Genetics|January 1, 1995
Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneityS Gispert, N Santos, R Damen, et al.
Neuropediatrics|January 4, 2005
Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus: a rare brain malformation syndrome associated with mental retardation and seizuresG Mirzaa, N N Dodge, I Glass, et al.
Human Molecular Genetics|September 26, 2000
Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophyR Herrmann, V Straub, M Blank, et al.
American Journal of Human Genetics|March 21, 2000
Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42M Brockington, C A Sewry, R Herrmann, et al.
Pageof 15

Showing results (81-90 of 143) with videos related to

Sort By:
Pageof 15
Pediatric Transplantation|February 28, 2006
Disseminated adenovirus infection with respiratory failure in pediatric liver transplant recipients: impact of intravenous cidofovir and inhaled nitric oxideM A Wallot, C Dohna-Schwake, M Auth, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
Introduction of a ketogenic diet in young infantsJ Klepper, B Leiendecker, R Bredahl, et al.
Neuropediatrics|August 18, 2001
Hydrocephalus internus in two patients with 5,10-methylenetetrahydrofolate reductase deficiencyM Baethmann, U Wendel, G F Hoffmann, et al.
Journal of Neuropathology and Experimental Neurology|January 1, 1992
Adult polyglucosan body myopathyH H Goebel, Y S Shin, F Gullotta, et al.
Journal of the Neurological Sciences|June 17, 1999
Secondary reduction of alpha7B integrin in laminin alpha2 deficient congenital muscular dystrophy supports an additional transmembrane link in skeletal muscleR D Cohn, U Mayer, G Saher, et al.
Neuromuscular Disorders : NMD|September 27, 2008
Towards harmonisation of outcome measures for DMD and SMA within TREAT-NMD; report of three expert workshops: TREAT-NMD/ENMC workshop on outcome measures, 12th--13th May 2007, Naarden, The Netherlands; TREAT-NMD workshop on outcome measures in experimental trials for DMD, 30th June--1st July 2007, Naarden, The Netherlands; conjoint Institute of Myology TREAT-NMD meeting on physical activity monitoring in neuromuscular disorders, 11th July 2007, Paris, FranceE Mercuri, A Mayhew, F Muntoni, et al.
American Journal of Human Genetics|January 1, 1995
Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneityS Gispert, N Santos, R Damen, et al.
Neuropediatrics|January 4, 2005
Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus: a rare brain malformation syndrome associated with mental retardation and seizuresG Mirzaa, N N Dodge, I Glass, et al.
Human Molecular Genetics|September 26, 2000
Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophyR Herrmann, V Straub, M Blank, et al.
American Journal of Human Genetics|March 21, 2000
Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42M Brockington, C A Sewry, R Herrmann, et al.
Pageof 15