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Axonal damage markers in cerebrospinal fluid are increased in ALS

Neurology, 2006-03, Vol.66 (6), p.852

2006

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Patients with elevated triglyceride and cholesterol serum levels have a prolonged survival in amyotrophic lateral sclerosis

Journal of neurology, 2011-04, Vol.258 (4), p.613-617

2011

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Small-fiber neuropathy in patients with ALS

Neurology, 2011-06, Vol.76 (23), p.2024

2011

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Alcohol withdrawal syndrome: mechanisms, manifestations, and management

Acta neurologica Scandinavica, 2017-01, Vol.135 (1), p.4-16

2017

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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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Novel missense and truncating mutations in FUS/TLS in familial ALS

Neurology, 2010-08, Vol.75 (9), p.815

2010

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Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect

Neurology, 2011-09, Vol.77 (10), p.959

2011

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Truncating mutations in FUS/TLS give rise to a more aggressive ALS-phenotype than missense mutations: a clinico-genetic study in Germany

European journal of neurology, 2013-03, Vol.20 (3), p.540-546

2013

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Topography of cerebral atrophy in early Huntington’s disease: a voxel based morphometric MRI study

Journal of neurology, neurosurgery and psychiatry, 2004-02, Vol.75 (2), p.213-220

2004

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CSF glial markers correlate with survival in amyotrophic lateral sclerosis

Neurology, 2010-03, Vol.74 (12), p.982

2010

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Optical coherence tomography does not support optic nerve involvement in amyotrophic lateral sclerosis

European journal of neurology, 2013-08, Vol.20 (8), p.1170-1176

2013

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Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the −2578AA genotype

Journal of medical genetics, 2009-12, Vol.46 (12), p.840-846

2009

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Targeted antioxidative and neuroprotective properties of the dopamine agonist pramipexole and its nondopaminergic enantiomer SND919CL2x [(+)2-amino-4,5,6,7-tetrahydro-6-Lpropylamino-benzathiazole dihydrochloride]

The Journal of pharmacology and experimental therapeutics, 2006-01, Vol.316 (1), p.189

2006

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TDP-43 in amyotrophic lateral sclerosis - is it a prion disease?

European journal of neurology, 2015-05, Vol.22 (5), p.753-761

2015

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High dose vitamin E therapy in amyotrophic lateral sclerosis as add-on therapy to riluzole: results of a placebo-controlled double-blind study

Journal of Neural Transmission, 2005-05, Vol.112 (5), p.649-660

2005

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Diffusion tensor imaging analysis of sequential spreading of disease in amyotrophic lateral sclerosis confirms patterns of TDP-43 pathology

Brain (London, England : 1878), 2014-06, Vol.137 (Pt 6), p.1733-1740

2014

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Dopamine transporter: involvement in selective dopaminergic neurotoxicity and degeneration

Journal of Neural Transmission, 2004-10, Vol.111 (10-11), p.1267-1286

2004

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Optical coherence tomography-based assessment of retinal vascular pathology in cerebral small vessel disease

Neurological research and practice, 2020-05, Vol.2 (1), p.13-13, Article 13

2020

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Fully Automated Atlas-Based MR Imaging Volumetry in Huntington Disease, Compared with Manual Volumetry

American journal of neuroradiology : AJNR, 2011-08, Vol.32 (7), p.1328-1332

2011

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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

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The TUDCA trial - innovative trial designs for amyotrophic lateral sclerosis drugs?

European journal of neurology, 2016-01, Vol.23 (1), p.11-12

Ludolph, A. C.

2016

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Statins, diabetes mellitus and prognosis of amyotrophic lateral sclerosis: data from 501 patients of a population‐based registry in southwest Germany

European journal of neurology, 2020-08, Vol.27 (8), p.1405-1414

2020

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Recent silent infarcts do not increase the risk of haemorrhage after intravenous thrombolysis

European journal of neurology, 2020-12, Vol.27 (12), p.2483-2490

2020

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CSF filtration is an effective treatment of Guillain-Barré syndrome: a randomized clinical trial

Neurology, 2001-09, Vol.57 (5), p.774

2001

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Formation and characterisation of neuromuscular junctions between hiPSC derived motoneurons and myotubes

Stem cell research, 2015-09, Vol.15 (2), p.328-336

2015

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Axonal damage markers in cerebrospinal fluid are increased in ALS

Patients with elevated triglyceride and cholesterol serum levels have a prolonged survival in amyotrophic lateral sclerosis

Small-fiber neuropathy in patients with ALS

Alcohol withdrawal syndrome: mechanisms, manifestations, and management

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

Novel missense and truncating mutations in FUS/TLS in familial ALS

Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect

Truncating mutations in FUS/TLS give rise to a more aggressive ALS-phenotype than missense mutations: a clinico-genetic study in Germany

Topography of cerebral atrophy in early Huntington’s disease: a voxel based morphometric MRI study

CSF glial markers correlate with survival in amyotrophic lateral sclerosis

Optical coherence tomography does not support optic nerve involvement in amyotrophic lateral sclerosis

Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the −2578AA genotype

Targeted antioxidative and neuroprotective properties of the dopamine agonist pramipexole and its nondopaminergic enantiomer SND919CL2x [(+)2-amino-4,5,6,7-tetrahydro-6-Lpropylamino-benzathiazole dihydrochloride]

TDP-43 in amyotrophic lateral sclerosis - is it a prion disease?

High dose vitamin E therapy in amyotrophic lateral sclerosis as add-on therapy to riluzole: results of a placebo-controlled double-blind study

Diffusion tensor imaging analysis of sequential spreading of disease in amyotrophic lateral sclerosis confirms patterns of TDP-43 pathology

Dopamine transporter: involvement in selective dopaminergic neurotoxicity and degeneration

Optical coherence tomography-based assessment of retinal vascular pathology in cerebral small vessel disease

Fully Automated Atlas-Based MR Imaging Volumetry in Huntington Disease, Compared with Manual Volumetry

Occurrence and characterization of peripheral nerve involvement in neurofibromatosis type 2

The TUDCA trial - innovative trial designs for amyotrophic lateral sclerosis drugs?

Statins, diabetes mellitus and prognosis of amyotrophic lateral sclerosis: data from 501 patients of a population‐based registry in southwest Germany

Recent silent infarcts do not increase the risk of haemorrhage after intravenous thrombolysis

CSF filtration is an effective treatment of Guillain-Barré syndrome: a randomized clinical trial

Formation and characterisation of neuromuscular junctions between hiPSC derived motoneurons and myotubes

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