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FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients

Journal of medical genetics, 2004-04, Vol.41 (4), p.e50-e50

2004

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Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS

Neurology, 2004-08, Vol.63 (4), p.724

2004

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Occurrence and characterization of peripheral nerve involvement in neurofibromatosis type 2

Brain (London, England : 1878), 2002-05, Vol.125 (Pt 5), p.996-1004

2002

Volltextzugriff (PDF)

Lithium in patients with amyotrophic lateral sclerosis (LiCALS): a phase 3 multicentre, randomised, double-blind, placebo-controlled trial

Lancet neurology, 2013-04, Vol.12 (4), p.339-345

2013

Volltextzugriff (PDF)

Development and validation of Spasticity Index—Amyotrophic Lateral Sclerosis

Acta neurologica Scandinavica, 2018-07, Vol.138 (1), p.47-54

2018

Volltextzugriff (PDF)

Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy region

Annals of neurology, 1997-09, Vol.42 (3), p.364-368

1997

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The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication

Nature genetics, 1992-06, Vol.1 (3), p.171-175

1992

Volltextzugriff (PDF)

Spinal Neurofibromatosis without Café-au-Lait Macules in Two Families with Null Mutations of the NF1 Gene

American journal of human genetics, 2001-12, Vol.69 (6), p.1395-1400

2001

Volltextzugriff (PDF)

Neurofibromatosis type 1 with involvement of the enteric nerves

Journal of neurology, neurosurgery and psychiatry, 2007-10, Vol.78 (10), p.1163-1164

2007

Volltextzugriff (PDF)

Axon damage in CMT due to mutation in myelin protein P0

Neuromuscular disorders : NMD, 2001-11, Vol.11 (8), p.753-756

2001

Volltextzugriff (PDF)

An Essential Role for the Tumor-Suppressor Merlin in Regulating Fatty Acid Synthesis

Cancer research (Chicago, Ill.), 2017-09, Vol.77 (18), p.5026-5038

2017

Volltextzugriff (PDF)

Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A

Nature genetics, 1992-06, Vol.1 (3), p.176-179

1992

Volltextzugriff (PDF)

Lack of immune responses to immediate or delayed implanted allogeneic and xenogeneic Schwann cell suspensions

Glia, 1997-11, Vol.21 (3), p.299-314

1997

Volltextzugriff (PDF)

A novel nonsense mutation in the ABC1 gene causes a severe syringomyelia‐like phenotype of Tangier disease

Brain (London, England : 1878), 2003-04, Vol.126 (4), p.920-927

2003

Volltextzugriff (PDF)

Balo's concentric sclerosis followed by MRI and positron emission tomography

Neuroradiology, 1993-10, Vol.35 (8), p.578-580

1993

Volltextzugriff (PDF)

Long-term culture and characterization of human neurofibroma-derived Schwann cells

Journal of neuroscience research, 2000-09, Vol.61 (5), p.524-532

2000

Volltextzugriff (PDF)

Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD

Annals of neurology, 2005-11, Vol.58 (5), p.777-780

2005

Volltextzugriff (PDF)

Peripheral compound odontoma erupting in the gingiva

Head & face medicine, 2013-06, Vol.9 (1), p.15-15, Article 15

2013

Volltextzugriff (PDF)

MR-Pathologic Comparison of the Upper Spinal Cord in Different Motor Neuron Diseases

European neurology, 2005-01, Vol.53 (2), p.74-77

2005

Volltextzugriff (PDF)

Complicated hereditary spastic paraplegia with thin corpus callosum: variation of phenotypic expression over time

Journal of neurology, 2004-10, Vol.251 (10), p.1285-1287

2004

Volltextzugriff (PDF)

Transient, recurrent, white matter lesions in X-linked Charcot-Marie-Tooth disease with novel connexin 32 mutation

Archives of neurology (Chicago), 2003-04, Vol.60 (4), p.605

2003

Volltextzugriff (PDF)

Pathogenesis of Charcot–Marie–Tooth 1A (CMT1A) neuropathy

Trends in neurosciences (Regular ed.), 1998-07, Vol.21 (7), p.282-286

1998

Volltextzugriff (PDF)

Recurrent hematomas following craniotomy for traumatic intracranial mass

Journal of neurosurgery, 1990-01, Vol.72 (1), p.9

1990

Volltextzugriff (PDF)

Safety and efficacy of diaphragm pacing in patients with respiratory insufficiency due to amyotrophic lateral sclerosis (DiPALS): a multicentre, open-label, randomised controlled trial

Lancet neurology, 2015-09, Vol.14 (9), p.883-892

Anon

2015

Volltextzugriff (PDF)

DiPALS: Diaphragm Pacing in patients with Amyotrophic Lateral Sclerosis - a randomised controlled trial

Health technology assessment (Winchester, England), 2016-06, Vol.20 (45), p.1-186

2016

Volltextzugriff (PDF)

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FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients

Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS

Occurrence and characterization of peripheral nerve involvement in neurofibromatosis type 2

Lithium in patients with amyotrophic lateral sclerosis (LiCALS): a phase 3 multicentre, randomised, double-blind, placebo-controlled trial

Development and validation of Spasticity Index—Amyotrophic Lateral Sclerosis

Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy region

The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication

Spinal Neurofibromatosis without Café-au-Lait Macules in Two Families with Null Mutations of the NF1 Gene

Neurofibromatosis type 1 with involvement of the enteric nerves

Axon damage in CMT due to mutation in myelin protein P0

An Essential Role for the Tumor-Suppressor Merlin in Regulating Fatty Acid Synthesis

Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A

Lack of immune responses to immediate or delayed implanted allogeneic and xenogeneic Schwann cell suspensions

A novel nonsense mutation in the ABC1 gene causes a severe syringomyelia‐like phenotype of Tangier disease

Balo's concentric sclerosis followed by MRI and positron emission tomography

Long-term culture and characterization of human neurofibroma-derived Schwann cells

Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD

Peripheral compound odontoma erupting in the gingiva

MR-Pathologic Comparison of the Upper Spinal Cord in Different Motor Neuron Diseases

Complicated hereditary spastic paraplegia with thin corpus callosum: variation of phenotypic expression over time

Transient, recurrent, white matter lesions in X-linked Charcot-Marie-Tooth disease with novel connexin 32 mutation

Pathogenesis of Charcot–Marie–Tooth 1A (CMT1A) neuropathy

Recurrent hematomas following craniotomy for traumatic intracranial mass

Safety and efficacy of diaphragm pacing in patients with respiratory insufficiency due to amyotrophic lateral sclerosis (DiPALS): a multicentre, open-label, randomised controlled trial

DiPALS: Diaphragm Pacing in patients with Amyotrophic Lateral Sclerosis - a randomised controlled trial

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