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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 families
G Uziel, I Moroni, E Lamantea, et al.
Neuroradiology
|
January 7, 1999
Congenital muscular dystrophy with merosin deficiency: MRI findings in five patients
L Farina, L Morandi, I Milanesi, et al.
Revue Neurologique
|
January 1, 1991
Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathies
G Scarlato, N Bresolin, I Moroni, et al.
Italian Journal of Neurological Sciences
|
August 10, 2000
X-linked adrenoleukodystrophy: first report of the Italian Study Group
A Di Biase, S Salvati, C Avellino, et al.
Journal of Neurology
|
February 1, 1995
Ryanodine receptor gene point mutation and malignant hyperthermia susceptibility
I 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 glycosylation
S 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 disease
M 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 trial
N Bresolin, C Doriguzzi, C Ponzetto, et al.
Neurology
|
May 19, 2006
GJA12 mutations in children with recessive hypomyelinating leukoencephalopathy
M Bugiani, S Al Shahwan, E Lamantea, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 34) with videos related to
Sort By:
Page
of 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 families
G Uziel, I Moroni, E Lamantea, et al.
Neuroradiology
|
January 7, 1999
Congenital muscular dystrophy with merosin deficiency: MRI findings in five patients
L Farina, L Morandi, I Milanesi, et al.
Revue Neurologique
|
January 1, 1991
Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathies
G Scarlato, N Bresolin, I Moroni, et al.
Italian Journal of Neurological Sciences
|
August 10, 2000
X-linked adrenoleukodystrophy: first report of the Italian Study Group
A Di Biase, S Salvati, C Avellino, et al.
Journal of Neurology
|
February 1, 1995
Ryanodine receptor gene point mutation and malignant hyperthermia susceptibility
I 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 glycosylation
S 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 disease
M 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 trial
N Bresolin, C Doriguzzi, C Ponzetto, et al.
Neurology
|
May 19, 2006
GJA12 mutations in children with recessive hypomyelinating leukoencephalopathy
M Bugiani, S Al Shahwan, E Lamantea, et al.
Page
of 4