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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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Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis

Nature genetics, 2008-01, Vol.40 (1), p.29-31

2008

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Recombinant human insulin-like growth factor I (rhIGF-I) for the treatment of amyotrophic lateral sclerosis/motor neuron disease

Cochrane database of systematic reviews, 2012-11, Vol.11, p.CD002064

2012

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Magnesium treatment for patients with refractory status epilepticus due to POLG1-mutations

Journal of neurology, 2011-02, Vol.258 (2), p.218-222

2011

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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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Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype–phenotype correlation study

Brain (London, England : 1878), 2008-05, Vol.131 (5), p.1217-1227

2008

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Drug treatment for spinal muscular atrophy types II and III

Cochrane database of systematic reviews, 2012-04 (4), p.CD006282

2012

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Multifocal motor neuropathy

Lancet neurology, 2005-05, Vol.4 (5), p.309-319

2005

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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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Euthanasia and Physician-Assisted Suicide among Patients with Amyotrophic Lateral Sclerosis in the Netherlands

The New England journal of medicine, 2002-05, Vol.346 (21), p.1638-1644

2002

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Increased expression of rapsyn in muscles prevents acetylcholine receptor loss in experimental autoimmune myasthenia gravis

Brain (London, England : 1878), 2005-10, Vol.128 (10), p.2327-2337

2005

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Drug treatment for spinal muscular atrophy type I

Cochrane database of systematic reviews, 2012-04 (4), p.CD006281

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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Spastin mutations in sporadic adult-onset upper motor neuron syndromes

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

2005

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Drug treatment for spinal muscular atrophy type I

Cochrane database of systematic reviews, 2011-12 (12), p.CD006281

2011

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Immunosuppressive treatment for non-systemic vasculitic neuropathy

Cochrane database of systematic reviews, 2007-01 (1), p.CD006050

2007

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AChR deficiency due to ε-subunit mutations: two common mutations in the Netherlands

Journal of neurology, 2009-10, Vol.256 (10), p.1719-1723

2009

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Drug treatment for spinal muscular atrophy types II and III

Cochrane database of systematic reviews, 2011-12 (12), p.CD006282

2011

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

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

2009

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Genes, trials, and care: the dynamics of neuromuscular disease

Lancet neurology, 2004, Vol.3 (1), p.16-16

Wokke, John HJ

2004

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Physician-assisted death: dying with dignity?

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

2003

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Diagnosis of multifocal motor neuropathy – Authors' reply

Lancet neurology, 2005-07, Vol.4 (7), p.393-393

2005

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Riluzole

The Lancet (British edition), 1996-12, Vol.348 (9042), p.1660-1661

Wokke, John HJ

1996

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RESEARCH REPORT: Functional health status of patients with chronic inflammatory neuropathies

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

2005

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

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

Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis

Recombinant human insulin-like growth factor I (rhIGF-I) for the treatment of amyotrophic lateral sclerosis/motor neuron disease

Magnesium treatment for patients with refractory status epilepticus due to POLG1-mutations

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

Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype–phenotype correlation study

Drug treatment for spinal muscular atrophy types II and III

Multifocal motor neuropathy

Cold paresis in multifocal motor neuropathy

Euthanasia and Physician-Assisted Suicide among Patients with Amyotrophic Lateral Sclerosis in the Netherlands

Increased expression of rapsyn in muscles prevents acetylcholine receptor loss in experimental autoimmune myasthenia gravis

Drug treatment for spinal muscular atrophy type I

Entrapment in anti myelin-associated glycoprotein neuropathy

Spastin mutations in sporadic adult-onset upper motor neuron syndromes

Drug treatment for spinal muscular atrophy type I

Immunosuppressive treatment for non-systemic vasculitic neuropathy

AChR deficiency due to ε-subunit mutations: two common mutations in the Netherlands

Drug treatment for spinal muscular atrophy types II and III

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

Genes, trials, and care: the dynamics of neuromuscular disease

Physician-assisted death: dying with dignity?

Diagnosis of multifocal motor neuropathy – Authors' reply

Riluzole

RESEARCH REPORT: Functional health status of patients with chronic inflammatory neuropathies

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