(Q45298869)

11 December 2017

Problems and pitfalls in the diagnosis of ALS. (English)

1 reference

amyotrophic lateral sclerosis

11 December 2017

1 reference

Ludolph AC

1

1 reference

PubMed ID

10448976

11 December 2017

Knirsch U

series ordinal

2

1 reference

11 December 2017

1 June 1999

1 reference

Journal of the Neurological Sciences

11 December 2017

1 reference

11 December 2017

165 Suppl 1

1 reference

11 December 2017

S14-20

1 reference

Avoiding false positive diagnoses of motor neuron disease: lessons from the Scottish Motor Neuron Disease Register

11 December 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases a

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Prognosis in familial amyotrophic lateral sclerosis: progression and survival in patients with glu100gly and ala4val mutations in Cu,Zn superoxide dismutase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Cu/Zn superoxide dismutase gene mutations in amyotrophic lateral sclerosis: correlation between genotype and clinical features

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Inclusion body myositis. Observations in 40 patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Electrophysiologic findings in multifocal motor neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Multifocal motor neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

AAEM case report #30: multifocal motor neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Magnetic resonance imaging of the brachial plexus in patients with multifocal motor neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Age-dependent penetrance of disease in a transgenic mouse model of familial amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Progressive motor neuron impairment in an animal model of familial amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Massive mitochondrial degeneration in motor neurons triggers the onset of amyotrophic lateral sclerosis in mice expressing a mutant SOD1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

A controlled trial of riluzole in amyotrophic lateral sclerosis. ALS/Riluzole Study Group

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Dose-ranging study of riluzole in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis/Riluzole Study Group II

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

An analysis of extended survival in patients with amyotrophic lateral sclerosis treated with riluzole

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Benefit of vitamin E, riluzole, and gabapentin in a transgenic model of familial amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

The copper chelator d-penicillamine delays onset of disease and extends survival in a transgenic mouse model of familial amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Bcl-2: prolonging life in a transgenic mouse model of familial amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Clinicopathological study of 35 cases of multiple system atrophy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Toward earlier diagnosis of amyotrophic lateral sclerosis: revised criteria. rhCNTF ALS Study Group

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

Chronic inflammatory polyneuritis and neuropathies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900021-0

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-510X(99)00021-0

1 reference

11 December 2017

1 reference

PubMed ID

10448976