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Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients

BMC genomics, 2009-08, Vol.10 (1), p.405-405, Article 405

2009

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Clinical features of late-onset Pompe disease: A prospective cohort study

Muscle & nerve, 2008-10, Vol.38 (4), p.1236-1245

2008

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Randomized sequential trial of valproic acid in amyotrophic lateral sclerosis

Annals of neurology, 2009-08, Vol.66 (2), p.227-234

2009

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Cold paresis in multifocal motor neuropathy

Journal of neurology, 2011-02, Vol.258 (2), p.212-217

2011

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A randomized sequential trial of creatine in amyotrophic lateral sclerosis

Annals of neurology, 2003-04, Vol.53 (4), p.437-445

2003

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Clinical features and predictors for disease natural progression in adults with Pompe disease: a nationwide prospective observational study

Orphanet journal of rare diseases, 2012-11, Vol.7 (1), p.88-88

2012

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Entrapment in anti myelin-associated glycoprotein neuropathy

Journal of neurology, 2009-04, Vol.256 (4), p.620-624

2009

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Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen

Lancet neurology, 2008-04, Vol.7 (4), p.319-326

2008

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Spastin mutations in sporadic adult-onset upper motor neuron syndromes

Annals of neurology, 2005-12, Vol.58 (6), p.865-869

2005

Volltextzugriff (PDF)

Effect of enzyme therapy and prognostic factors in 69 adults with Pompe disease: an open-label single-center study

Orphanet journal of rare diseases, 2012-09, Vol.7 (1), p.73-73, Article 73

2012

Volltextzugriff (PDF)

Seipin/BSCL2 mutation screening in sporadic adult-onset upper motor neuron syndromes

Journal of neurology, 2009-05, Vol.256 (5), p.824-826

2009

Volltextzugriff (PDF)

Subtle involvement of the sympathetic nervous system in amyotrophic lateral sclerosis

Muscle & nerve, 2002-03, Vol.25 (3), p.402-408

2002

Volltextzugriff (PDF)

Progressive idiopathic axonal neuropathy: A comparative clinical and histopathological study with vasculitic neuropathy

Journal of neurology, 2004-03, Vol.251 (3), p.269-278

2004

Volltextzugriff (PDF)

FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands

Archives of neurology (Chicago), 2010-02, Vol.67 (2), p.224

2010

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Ganglioside-specific IgG and IgA recruit leukocyte effector functions in Guillain–Barré syndrome

Journal of neuroimmunology, 2007-01, Vol.182 (1), p.177-184

2007

Volltextzugriff (PDF)

Functional health status of patients with chronic inflammatory neuropathies

Journal of the peripheral nervous system, 2005-06, Vol.10 (2), p.181-189

2005

Volltextzugriff (PDF)

Severity of Guillain–Barré syndrome is associated with Fcγ Receptor III polymorphisms

Journal of neuroimmunology, 2005-05, Vol.162 (1), p.157-164

2005

Volltextzugriff (PDF)

Riluzole

The Lancet (British edition), 1996-09, Vol.348 (9030), p.795-799

Wokke, John

1996

Volltextzugriff (PDF)

Physician-assisted death: dying with dignity?

Lancet neurology, 2003-10, Vol.2 (10), p.637-643

2003

Volltextzugriff (PDF)

Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromes

Archives of neurology (Chicago), 2009-04, Vol.66 (4), p.509

2009

Volltextzugriff (PDF)

MRI of the brachial plexus in polyneuropathy associated with monoclonal gammopathy

Muscle & nerve, 2001-10, Vol.24 (10), p.1312-1318

2001

Volltextzugriff (PDF)

Development of weakness in patients with chronic inflammatory demyelinating polyneuropathy and only sensory symptoms at presentation : a long-term follow-up study

Journal of neurology, 1999-12, Vol.246 (12), p.1134-1139

1999

Volltextzugriff (PDF)

Cytogenetic aberrations in neuropathy associated with IgM monoclonal gammopathy

Journal of the neurological sciences, 2007-09, Vol.260 (1), p.124-131

2007

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Mycophenolate mofetil as adjunctive therapy for MMN patients: a randomized, controlled trial

Brain (London, England : 1878), 2007-08, Vol.130 (8), p.2004-2010

2007

Volltextzugriff (PDF)

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Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients

Clinical features of late-onset Pompe disease: A prospective cohort study

Randomized sequential trial of valproic acid in amyotrophic lateral sclerosis

Cold paresis in multifocal motor neuropathy

A randomized sequential trial of creatine in amyotrophic lateral sclerosis

Clinical features and predictors for disease natural progression in adults with Pompe disease: a nationwide prospective observational study

Entrapment in anti myelin-associated glycoprotein neuropathy

ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study

Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen

Spastin mutations in sporadic adult-onset upper motor neuron syndromes

Effect of enzyme therapy and prognostic factors in 69 adults with Pompe disease: an open-label single-center study

Seipin/BSCL2 mutation screening in sporadic adult-onset upper motor neuron syndromes

Subtle involvement of the sympathetic nervous system in amyotrophic lateral sclerosis

Progressive idiopathic axonal neuropathy: A comparative clinical and histopathological study with vasculitic neuropathy

FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands

Ganglioside-specific IgG and IgA recruit leukocyte effector functions in Guillain–Barré syndrome

Functional health status of patients with chronic inflammatory neuropathies

Severity of Guillain–Barré syndrome is associated with Fcγ Receptor III polymorphisms

Riluzole

Physician-assisted death: dying with dignity?

Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromes

MRI of the brachial plexus in polyneuropathy associated with monoclonal gammopathy

Development of weakness in patients with chronic inflammatory demyelinating polyneuropathy and only sensory symptoms at presentation : a long-term follow-up study

Cytogenetic aberrations in neuropathy associated with IgM monoclonal gammopathy

Mycophenolate mofetil as adjunctive therapy for MMN patients: a randomized, controlled trial

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