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I Moroni

Showing results (11-20 of 34) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: a clinical, biochemical, and molecular study in six familiesG Uziel, I Moroni, E Lamantea, et al.
Neuroradiology|January 7, 1999
Congenital muscular dystrophy with merosin deficiency: MRI findings in five patientsL Farina, L Morandi, I Milanesi, et al.
Revue Neurologique|January 1, 1991
Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathiesG Scarlato, N Bresolin, I Moroni, et al.
Italian Journal of Neurological Sciences|August 10, 2000
X-linked adrenoleukodystrophy: first report of the Italian Study GroupA Di Biase, S Salvati, C Avellino, et al.
Journal of Neurology|February 1, 1995
Ryanodine receptor gene point mutation and malignant hyperthermia susceptibilityI Moroni, E F Gonano, G P Comi, et al.
Neurology|May 26, 2004
L-2-hydroxyglutaric aciduria and brain malignant tumors: a predisposing condition?I Moroni, M Bugiani, L D'Incerti, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 5, 2013
A fourth case of POMT2-related limb girdle muscle dystrophy with mild reduction of α-dystroglycan glycosylationS Saredi, S Gibertini, A Ardissone, et al.
Journal of Inherited Metabolic Disease|July 10, 1999
3-Methylglutaconic aciduria and hypermethioninaemia in a child with clinical and neuroradiological findings of Leigh diseaseM Di Rocco, U Caruso, I Moroni, et al.
Journal of the Neurological Sciences|December 1, 1990
Ubidecarenone in the treatment of mitochondrial myopathies: a multi-center double-blind trialN Bresolin, C Doriguzzi, C Ponzetto, et al.
Neurology|May 19, 2006
GJA12 mutations in children with recessive hypomyelinating leukoencephalopathyM Bugiani, S Al Shahwan, E Lamantea, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: a clinical, biochemical, and molecular study in six familiesG Uziel, I Moroni, E Lamantea, et al.
Neuroradiology|January 7, 1999
Congenital muscular dystrophy with merosin deficiency: MRI findings in five patientsL Farina, L Morandi, I Milanesi, et al.
Revue Neurologique|January 1, 1991
Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathiesG Scarlato, N Bresolin, I Moroni, et al.
Italian Journal of Neurological Sciences|August 10, 2000
X-linked adrenoleukodystrophy: first report of the Italian Study GroupA Di Biase, S Salvati, C Avellino, et al.
Journal of Neurology|February 1, 1995
Ryanodine receptor gene point mutation and malignant hyperthermia susceptibilityI Moroni, E F Gonano, G P Comi, et al.
Neurology|May 26, 2004
L-2-hydroxyglutaric aciduria and brain malignant tumors: a predisposing condition?I Moroni, M Bugiani, L D'Incerti, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 5, 2013
A fourth case of POMT2-related limb girdle muscle dystrophy with mild reduction of α-dystroglycan glycosylationS Saredi, S Gibertini, A Ardissone, et al.
Journal of Inherited Metabolic Disease|July 10, 1999
3-Methylglutaconic aciduria and hypermethioninaemia in a child with clinical and neuroradiological findings of Leigh diseaseM Di Rocco, U Caruso, I Moroni, et al.
Journal of the Neurological Sciences|December 1, 1990
Ubidecarenone in the treatment of mitochondrial myopathies: a multi-center double-blind trialN Bresolin, C Doriguzzi, C Ponzetto, et al.
Neurology|May 19, 2006
GJA12 mutations in children with recessive hypomyelinating leukoencephalopathyM Bugiani, S Al Shahwan, E Lamantea, et al.
Pageof 4