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I Moroni

Showing results (1-10 of 34) with videos related to

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Neuromuscular Disorders : NMD|December 28, 2016
Intrafamilial phenotypic variability in Andersen-Tawil syndrome: A diagnostic challenge in a potentially treatable conditionA Ardissone, V Sansone, L Colleoni, et al.
Pediatric Neurology|November 1, 1995
Riboflavin-responsive glutaric aciduria type II presenting as a leukodystrophyG Uziel, B Garavaglia, E Ciceri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 11, 2000
Clinical, biochemical and neuroradiological findings in L-2-hydroxyglutaric aciduriaI Moroni, L D'Incerti, L Farina, et al.
Neuroradiology|December 22, 1998
L-2-Hydroxyglutaric aciduria: MRI in seven casesL D'Incerti, L Farina, I Moroni, et al.
Neurology|March 29, 2006
Childhood-onset multifocal motor neuropathy with conduction blocksI Moroni, M Bugiani, C Ciano, et al.
Neuropediatrics|June 21, 2002
Cerebral white matter involvement in children with mitochondrial encephalopathiesI Moroni, M Bugiani, A Bizzi, et al.
Clinical Dysmorphology|October 25, 2000
Costello syndrome: a cancer predisposing syndrome?I Moroni, F Bedeschi, R Luksch, et al.
Neuropediatrics|September 16, 2003
Consciousness disturbances in megalencephalic leukoencephalopathy with subcortical cystsM Bugiani, I Moroni, A Bizzi, et al.
Current Molecular Medicine|October 18, 2014
Mitochondrial Diseases in ChildhoodA Ardissone, E Lamantea, F Invernizzi, et al.
Neuromuscular Disorders : NMD|October 1, 1996
Mild clinical phenotype in a 12-year-old boy with partial merosin deficiency and central and peripheral nervous system abnormalitiesM Mora, I Moroni, G Uziel, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Neuromuscular Disorders : NMD|December 28, 2016
Intrafamilial phenotypic variability in Andersen-Tawil syndrome: A diagnostic challenge in a potentially treatable conditionA Ardissone, V Sansone, L Colleoni, et al.
Pediatric Neurology|November 1, 1995
Riboflavin-responsive glutaric aciduria type II presenting as a leukodystrophyG Uziel, B Garavaglia, E Ciceri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 11, 2000
Clinical, biochemical and neuroradiological findings in L-2-hydroxyglutaric aciduriaI Moroni, L D'Incerti, L Farina, et al.
Neuroradiology|December 22, 1998
L-2-Hydroxyglutaric aciduria: MRI in seven casesL D'Incerti, L Farina, I Moroni, et al.
Neurology|March 29, 2006
Childhood-onset multifocal motor neuropathy with conduction blocksI Moroni, M Bugiani, C Ciano, et al.
Neuropediatrics|June 21, 2002
Cerebral white matter involvement in children with mitochondrial encephalopathiesI Moroni, M Bugiani, A Bizzi, et al.
Clinical Dysmorphology|October 25, 2000
Costello syndrome: a cancer predisposing syndrome?I Moroni, F Bedeschi, R Luksch, et al.
Neuropediatrics|September 16, 2003
Consciousness disturbances in megalencephalic leukoencephalopathy with subcortical cystsM Bugiani, I Moroni, A Bizzi, et al.
Current Molecular Medicine|October 18, 2014
Mitochondrial Diseases in ChildhoodA Ardissone, E Lamantea, F Invernizzi, et al.
Neuromuscular Disorders : NMD|October 1, 1996
Mild clinical phenotype in a 12-year-old boy with partial merosin deficiency and central and peripheral nervous system abnormalitiesM Mora, I Moroni, G Uziel, et al.
Pageof 4