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Variable responses to rituximab treatment in neuromyelitis optica (Devic's disease)

Neurological sciences, 2007-08, Vol.28 (4), p.209-211

2007

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Sporadic vascular dementia as clinical presentation of a new missense mutation within exon 7 of NOTCH3 gene

Journal of the neurological sciences, 2008-08, Vol.271 (1), p.207-210

2008

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Mutations in the ryanodine receptor gene in central core disease and malignant hyperthermia

Nature genetics, 1993-09, Vol.5 (1), p.51-55

1993

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Variable responses to rituximab treatment in neuromyelitis optica (Devic’s disease)

Neurological sciences, 2007-08, Vol.28 (4), p.209-211

2007

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A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency

Neurology, 2000-04, Vol.54 (8), p.1693-1696

2000

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Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study

Journal of neurology, neurosurgery and psychiatry, 2011-07, Vol.82 (7), p.740-746

2011

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Positive effects of tertiary centres for amyotrophic lateral sclerosis on outcome and use of hospital facilities

Journal of neurology, neurosurgery and psychiatry, 2006-08, Vol.77 (8), p.948-950

2006

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Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuria

Neuropediatrics, 2002-04, Vol.33 (2), p.109-111

2002

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Dystrophinopathy expressing as either cardiomyopathy or Becker dystrophy in the same family

Neurology, 2000-01, Vol.54 (2), p.529-529

2000

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Extensive genetics of ALS: a population-based study in Italy

Neurology, 2012-11, Vol.79 (19), p.1983-1989

2012

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Ubidecarenone in the treatment of mitochondrial myopathies: a multi-center double-blind trial

Journal of the neurological sciences, 1990-12, Vol.100 (1), p.70-78

1990

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ALS clinical trials: do enrolled patients accurately represent the ALS population?

Neurology, 2011-10, Vol.77 (15), p.1432-1437

2011

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Muscle apoptosis in humans occurs in normal and denervated muscle, but not in myotonic dystrophy, dystrophinopathies or inflammatory disease

Neurogenetics, 1997-11, Vol.1 (2), p.81-87

1997

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MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutation

Clinical neuropathology, 2002-03, Vol.21 (2), p.72

2002

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Non-invasive ventilation in amyotrophic lateral sclerosis: a 10 year population based study

Journal of neurology, neurosurgery and psychiatry, 2012-04, Vol.83 (4), p.377-381

2012

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Tracheostomy in amyotrophic lateral sclerosis: a 10-year population-based study in Italy

Journal of neurology, neurosurgery and psychiatry, 2010-10, Vol.81 (10), p.1141-1143

2010

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Late onset and very mild course of Xp21 Becker type muscular dystrophy

Clinical neuropathology, 2001-09, Vol.20 (5), p.196

2001

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Free cytoplasmic Ca++ at rest and after cholinergic stimulus is increased in cultured muscle cells from Duchenne muscular dystrophy patients

Neurology, 1988-03, Vol.38 (3), p.476-476

1988

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Myopathy in a patient with chromosome 22q11 deletion

Neuropediatrics, 2001-04, Vol.32 (2), p.107-109

2001

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Idiopathic chronic inflammatory demyelinating polyneuropathy: an epidemiological study in Italy

Journal of neurology, neurosurgery and psychiatry, 2007-12, Vol.78 (12), p.1349-1353

2007

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Variable histological expression of dystrophinopathy in two females

Acta neuropathologica, 1999-06, Vol.97 (6), p.657-660

1999

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Unusual Clinical Expression of Dystrophinopathy in a Female, Mimicking a Congenital Myopathy

European neurology, 1999-01, Vol.42 (4), p.221-224

1999

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Early symptom progression rate is related to ALS outcome: a prospective population-based study

Neurology, 2002-07, Vol.59 (1), p.99-103

2002

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Guillain-Barré syndrome: a prospective, population-based incidence and outcome survey

Neurology, 2003-04, Vol.60 (7), p.1146-1150

2003

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Systematic use of dystrophin testing in muscle biopsies: results in 201 cases

European journal of clinical investigation, 1997-04, Vol.27 (4), p.352-358

1997

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Variable responses to rituximab treatment in neuromyelitis optica (Devic's disease)

Sporadic vascular dementia as clinical presentation of a new missense mutation within exon 7 of NOTCH3 gene

Mutations in the ryanodine receptor gene in central core disease and malignant hyperthermia

Variable responses to rituximab treatment in neuromyelitis optica (Devic’s disease)

A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency

Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study

Positive effects of tertiary centres for amyotrophic lateral sclerosis on outcome and use of hospital facilities

Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuria

Dystrophinopathy expressing as either cardiomyopathy or Becker dystrophy in the same family

Extensive genetics of ALS: a population-based study in Italy

Ubidecarenone in the treatment of mitochondrial myopathies: a multi-center double-blind trial

ALS clinical trials: do enrolled patients accurately represent the ALS population?

Muscle apoptosis in humans occurs in normal and denervated muscle, but not in myotonic dystrophy, dystrophinopathies or inflammatory disease

MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutation

Non-invasive ventilation in amyotrophic lateral sclerosis: a 10 year population based study

Tracheostomy in amyotrophic lateral sclerosis: a 10-year population-based study in Italy

Late onset and very mild course of Xp21 Becker type muscular dystrophy

Free cytoplasmic Ca++ at rest and after cholinergic stimulus is increased in cultured muscle cells from Duchenne muscular dystrophy patients

Myopathy in a patient with chromosome 22q11 deletion

Idiopathic chronic inflammatory demyelinating polyneuropathy: an epidemiological study in Italy

Variable histological expression of dystrophinopathy in two females

Unusual Clinical Expression of Dystrophinopathy in a Female, Mimicking a Congenital Myopathy

Early symptom progression rate is related to ALS outcome: a prospective population-based study

Guillain-Barré syndrome: a prospective, population-based incidence and outcome survey

Systematic use of dystrophin testing in muscle biopsies: results in 201 cases

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