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Evidence for aerobic ATP synthesis in isolated myelin vesicles

The international journal of biochemistry & cell biology, 2009-07, Vol.41 (7), p.1581-1591

2009

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A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

Neuron (Cambridge, Mass.), 2011-10, Vol.72 (2), p.257-268

2011

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Early abnormalities in sciatic nerve function and structure in a rat model of Charcot-Marie-Tooth type 1A disease

Experimental neurology, 2004-11, Vol.190 (1), p.213-223

2004

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TBK1 is associated with ALS and ALS-FTD in Sardinian patients

Neurobiology of aging, 2016-07, Vol.43, p.180.e1-180.e5

2016

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In vitro VLA-4 blockade results in an impaired NK cell-mediated immune surveillance against melanoma

Immunology letters, 2017-01, Vol.181, p.109-115

2017

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CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients

Neurobiology of aging, 2015-04, Vol.36 (4), p.1767.e3-1767.e6

2015

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C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population

Neurobiology of aging, 2012-08, Vol.33 (8), p.1848.e15-1848.e20

2012

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ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry

Neurobiology of aging, 2015-10, Vol.36 (10), p.2906.e1-2906.e5

2015

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Short-term accrual of gray matter pathology in patients with progressive multiple sclerosis: an in vivo study using diffusion tensor MRI

NeuroImage (Orlando, Fla.), 2005-02, Vol.24 (4), p.1139-1146

2005

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HFE p.H63D polymorphism does not influence ALS phenotype and survival

Neurobiology of aging, 2015-10, Vol.36 (10), p.2906.e7-2906.e11

2015

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α-Lipoic acid is effective in prevention and treatment of experimental autoimmune encephalomyelitis

Journal of neuroimmunology, 2004-03, Vol.148 (1), p.146-153

2004

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Mechanisms of the adaptive immune response inside the central nervous system during inflammatory and autoimmune diseases

Pharmacology & therapeutics (Oxford), 2006-09, Vol.111 (3), p.555-566

2006

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Experimental Charcot–Marie–Tooth type 1A: A cDNA microarrays analysis

Molecular and cellular neuroscience, 2005-04, Vol.28 (4), p.703-714

2005

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Corrigendum to “Computer-aided retraining of memory and attention in people with multiple sclerosis: a randomized, double-blind controlled trial” [J. Neurol. Sci. 222 (2004) 99–104]

Journal of the neurological sciences, 2004-09, Vol.224 (1), p.113-113

2004

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Restricted immune responses lead to CNS demyelination and axonal damage

Journal of neuroimmunology, 2000-07, Vol.107 (2), p.178-183

2000

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Formic acid treatment exposes hidden neurofilament and tau epitopes in abnormal cytoskeletal filaments from patients with progressive supranuclear palsy and Alzheimer's disease

Neuroscience letters, 1990-07, Vol.115 (2), p.351-355

1990

Volltextzugriff (PDF)

Comments on Davar et al., PAIN, 67 (1996) 135-139: PAIN 3433

Pain (Amsterdam), 1997-08, Vol.72 (1), p.287

1997

Volltextzugriff (PDF)

Use of cosH1 probe in hereditary neuropathy with liability to pressure palsies: A reliable genetic test for demonstration of identical size of 17p11.2 deletion in unrelated patients

Neuroscience letters, 1996-07, Vol.213 (1), p.71-73

1996

Volltextzugriff (PDF)

Molecular analysis of three cases with hereditary motor and sensory neuropathy with myelin outfolding

Neuroscience letters, 1995-07, Vol.194 (1), p.136-138

1995

Volltextzugriff (PDF)

Tau-reactive neurofibrillary tangles in cerebellar cortex from patients with Alzheimer's disease

Neuroscience letters, 1989-09, Vol.103 (3), p.259-262

1989

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Evidence for aerobic ATP synthesis in isolated myelin vesicles

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

Early abnormalities in sciatic nerve function and structure in a rat model of Charcot-Marie-Tooth type 1A disease

TBK1 is associated with ALS and ALS-FTD in Sardinian patients

In vitro VLA-4 blockade results in an impaired NK cell-mediated immune surveillance against melanoma

CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients

C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population

ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry

Short-term accrual of gray matter pathology in patients with progressive multiple sclerosis: an in vivo study using diffusion tensor MRI

ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion

HFE p.H63D polymorphism does not influence ALS phenotype and survival

α-Lipoic acid is effective in prevention and treatment of experimental autoimmune encephalomyelitis

Mechanisms of the adaptive immune response inside the central nervous system during inflammatory and autoimmune diseases

Experimental Charcot–Marie–Tooth type 1A: A cDNA microarrays analysis

Corrigendum to “Computer-aided retraining of memory and attention in people with multiple sclerosis: a randomized, double-blind controlled trial” [J. Neurol. Sci. 222 (2004) 99–104]

Restricted immune responses lead to CNS demyelination and axonal damage

Formic acid treatment exposes hidden neurofilament and tau epitopes in abnormal cytoskeletal filaments from patients with progressive supranuclear palsy and Alzheimer's disease

Comments on Davar et al., PAIN, 67 (1996) 135-139: PAIN 3433

Use of cosH1 probe in hereditary neuropathy with liability to pressure palsies: A reliable genetic test for demonstration of identical size of 17p11.2 deletion in unrelated patients

Molecular analysis of three cases with hereditary motor and sensory neuropathy with myelin outfolding

Tau-reactive neurofibrillary tangles in cerebellar cortex from patients with Alzheimer's disease

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