(Q44591915)

4 December 2017

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title

Diagnosis of amyotrophic lateral sclerosis. (English)

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amyotrophic lateral sclerosis

4 December 2017

main subject

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author name string

Rowland LP

series ordinal

1

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4 December 2017

publication date

1 October 1998

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Journal of the Neurological Sciences

4 December 2017

published in

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4 December 2017

volume

160 Suppl 1

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4 December 2017

page(s)

S6-24

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The amyotrophic lateral sclerosis (ALS) patient perspective on misdiagnosis and its repercussions

4 December 2017

cites work

1 reference

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Misdiagnosis in patients with amyotrophic lateral sclerosis

7 January 2021

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

7 January 2021

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Diagnosis of motor neuron disease by neurologists: a study in three countries

7 January 2021

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Clinical features and associations of 560 cases of motor neuron disease

7 January 2021

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Reversible forms of motor neuron disease. Lead "neuritis".

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

An EMG case report of lead neuropathy 19 years after a shotgun injury

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Chronic motor neuron disease possibly related to intoxication with organochlorine insecticides.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Subacute, reversible motor neuron disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Reversible motor neuron disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Motor neuron disease, lymphoproliferative disease, and bone marrow biopsy

7 January 2021

1 reference

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Lymphoproliferative disorders and motor neuron disease: an update

7 January 2021

1 reference

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Progressive dysphagia due to adult Chiari I malformation mimicking amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Intramedullary astrocytoma presenting as spinal muscular atrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

AAEM case report #28: monomelic amyotrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Idiopathic generalized myokymia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

A quantitative study of intermediolateral column cells in motor neuron disease and the Shy-Drager syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Pure autonomic failure with motor neuron disease: report of a clinical study and postmortem examination of a patient

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Motor neuron disease with pallido-luysio-nigral atrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Neurodegenerative 'overlap' syndrome: Clinical and pathological features of Parkinson's disease, motor neuron disease, and Alzheimer's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Parkinsonism in motor neuron disease: case report and literature review.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Macroglobulinemia with peripheral neuropathy simulating motor neuron disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Anterior horn changes of motor neuron disease associated with demyelinating radiculopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Multifocal demyelinating neuropathy with persistent conduction block

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Multifocal acquired demyelinating neuropathy masquerading as motor neuron disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Gammopathy with proximal motor axonopathy simulating motor neuron disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Neuropathies with prolonged conduction block, single and grouped fasciculations, localized limb myokymia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Slow resolution of multifocal weakness and fasciculation: a reversible motor neuron syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

A treatable multifocal motor neuropathy with antibodies to GM1 ganglioside

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

IgM deposits at nodes of Ranvier in a patient with amyotrophic lateral sclerosis, anti-GM1 antibodies, and multifocal motor conduction block

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Multifocal motor neuropathy human sera block distal motor nerve conduction in mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Electrophysiologic findings in multifocal motor neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Motor nerve biopsy studies in motor neuropathy and motor neuron disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Motor conduction block and high titres of anti-GM1 ganglioside antibodies: pathological evidence of a motor neuropathy in a patient with lower motor neuron syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Multifocal demyelinating motor neuropathy: pathologic evidence of 'inflammatory demyelinating polyradiculoneuropathy'

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Pathological findings in a patient with amyotrophic lateral sclerosis and multifocal motor neuropathy with conduction block

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

The neurological manifestations of cervical spondylosis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Upper limb involvement in cervical spondylosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

CERVICAL MYELOPATHY WITH FASCICULATIONS IN THE LOWER EXTREMITIES

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Cervical Spondylotic Myelopathy With Reversible Fasciculations in the Lower Extremities

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

High cervical myelopathy presenting with the numb clumsy hand syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Denervation in wasted hand muscles in a case of primary cerebellar ectopia without syringomyelia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Hand wasting due to mid-cervical spinal cord compression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Cervical myelopathy secondary to movement disorders: case report

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Myelopathy hand characterized by muscle wasting. A different type of myelopathy hand in patients with cervical spondylosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Hand wasting in spondylotic high cord compression: an electromyographic study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Surgical treatment of cervical spondylotic myelopathy: time for a controlled trial

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Management of cervical spondylotic myelopathy and radiculopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

X-linked spinal muscular atrophy (Kennedy's syndrome). A kindred with hypobetalipoproteinemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

X-linked recessive bulbospinal neuronopathy: a report of ten cases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

The characteristic electrodiagnostic features of Kennedy's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

X-linked recessive bulbospinal neuronopathy. A clinicopathological study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Clinical and electrodiagnostic features of X-linked recessive bulbospinal neuronopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Androgen receptor gene polymorphisms in amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Spinobulbar muscular atrophy can mimic ALS: the importance of genetic testing in male patients with atypical ALS.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

'Essential tremor' and CAG repeats in the androgen receptor gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

The clinical spectrum of hexosaminidase deficiency diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Juvenile spinal muscular atrophy: a new hexosaminidase deficiency phenotype

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Juvenile-onset spinal muscular atrophy caused by compound heterozygosity for mutations in the HEXA gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Cramp,fasciculation syndrome: A treatable hyperexcitable peripheral nerve disorder

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Not-so-benign fasciculation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

MUSCLE FASCICULATIONS IN A HEALTHY POPULATION

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

From benign fasciculations and cramps to motor neuron disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Long-term follow-up of 121 patients with benign fasciculations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

A benign motor neuron disorder: delayed cramps and fasciculation after poliomyelitis or myelitis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

The origin of muscle fasciculations and cramps

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

A patient with one limb interstitial myositis with localised lipoatrophy presenting with severe cramps and fasciculations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Molecular genetic basis of familial ALS.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

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%2898%2900193-2

Increased 3-nitrotyrosine in both sporadic and familial amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Do posttranslational modifications of CuZnSOD lead to sporadic amyotrophic lateral sclerosis?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Familial amyotrophic lateral sclerosis. Molecular pathology of a patient with a SOD1 mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Therapeutic horizons for amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

SMN gene analysis of the spinal form of Charcot-Marie-Tooth disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Mapping of a distal form of spinal muscular atrophy with upper limb predominance to chromosome 7p

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

The relationship of spinal muscular atrophy to motor neuron disease: investigation of SMN and NAIP gene deletions in sporadic and familial ALS

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

The central nervous system in motor neurone disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Chronic progressive spinobulbar spasticity (primary lateral sclerosis)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Clinicopathological features of primary lateral sclerosis are different from amyotrophic lateral sclerosis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Onset, natural history and outcome in idiopathic adult motor neuron disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Chronic progressive myelopathy: diagnostic analysis of cases with and without sensory involvement

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Motor neuron disease (amyotrophic lateral sclerosis) arising from longstanding primary lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Primary lateral sclerosis. Clinical features, neuropathology and diagnostic criteria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Primary lateral sclerosis: a neuropsychological study.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

The open opercular sign: diagnosis and significance.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Opercular syndrome without opercular lesions: Foix-Chavany-Marie syndrome in progressive supranuclear motor system degeneration

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Anterior opercular cortex lesions cause dissociated lower cranial nerve palsies and anarthria but no aphasia: Foix-Chavany-Marie syndrome and "automatic voluntary dissociation" revisited

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Slowly progressive anarthria with late anterior opercular syndrome: a variant form of frontal cortical atrophy syndromes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Motor neuron disease, parkinsonism and dementia. Report of a case with diffuse Lewy body-like intracytoplasmic inclusions

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Diffuse Lewy body disease as substrate of primary lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

A new inherited prion disease (PrP-P105L mutation) showing spastic paraparesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

A case of Machado-Joseph disease presenting with spastic paraparesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Infantile onset of hereditary ascending spastic paralysis with bulbar involvement

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Amyotrophic cervical myelopathy in adolescence

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

7 January 2021

Monomelic muscle atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Benign monomelic amyotrophy of lower limb: a rare entity with a characteristic muscular CT.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Post-polio muscle dysfunction 29th ENMC workshop 14-16 October 1994, Naarden, the Netherlands

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Early and late losses of motor units after poliomyelitis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Isolation of LAV/HTLV-III from a patient with amyotrophic lateral sclerosis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Human immunodeficiency virus-associated motor axonal polyradiculoneuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Lower motor neuron dysfunction associated with human immunodeficiency virus infection

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Autopsy report of HTLV-I-associated myelopathy presenting with ALS-like manifestations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Immunologic reactivity against Borrelia burgdorferi in patients with motor neuron disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Generalised motor neuron disease as an unusual manifestation of Borrelia burgdorferi infection

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Syndromes of amyotrophic lateral sclerosis and dementia: relation to transmissible Creutzfeldt-Jakob disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Transmissible agent in the amyotrophic form of Creutzfeldt-Jakob disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Inclusion body myositis (IBM): Myopathy or neuropathy?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Inclusion body myositis and myopathies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Inclusion body myositis. Observations in 40 patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Inclusion body myositis: peripheral nerve involvement. Combined morphological and electrophysiological studies on peripheral nerves

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Inclusion body myositis, a review

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

7 January 2021

Inclusion body myositis

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Inclusion body myositis: clinical and pathological boundaries.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Inclusion body myositis: no evidence for a neurogenic component

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

The role of quantitative electromyography in inclusion body myositis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Primary sensory neuropathy with muscular changes associated with carcinoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Motor neurone disease as a manifestation of neoplasm (with a note on the course of classical motor neurone disease).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Amyotrophic lateral sclerosis. A study of its presentation and prognosis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Motor neuron disease with renal cell carcinoma and postoperative neurologic remission: A clinicopathologic report

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Paraneoplastic motor neuron disease and renal cell carcinoma: improvement after nephrectomy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Remission of a syndrome indistinguishable from motor neurone disease after resection of bronchial carcinoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Pure motor neuropathy complicating carcinoma of bronchus recovered after surgery

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

NEUROMUSCULAR DISORDERS ASSOCIATED WITH MALIGNANT NEOPLASTIC DISEASE

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Subacute motor neuronopathy: a remote effect of lymphoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Motor neuron syndromes in cancer patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Motor neuron disease: a paraneoplastic process associated with anti-hu antibody and small-cell lung carcinoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Anti-neurone antibodies are not characteristic of amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

A monoclonal IgA in a patient with amyotrophic lateral sclerosis reacts with neurofilaments and surface antigen on neuroblastoma cells.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Primary lateral sclerosis. A clinical diagnosis reemerges

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Intermittent cyclophosphamide and prednisone treatment of polyneuropathy associated with monoclonal gammopathy of undetermined significance.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Neurologic complications of hyperthyroidism: remission of spastic paraplegia, dementia, and optic neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Thyrotoxic neuropathy (Basedow's paraplegia)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Pyramidal tract deficits and polyneuropathy in hyperthyroidism, Combination clinically mimicking amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Reversible corticospinal tract disease due to hyperthyroidism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Generalised myokymia in thyrotoxicosis report of a case

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Motor neurone disease and hyperthyroid Graves' disease: a chance association?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Two cases of Graves' disease with signs of a pyramidal lesion. Improvement in neurologic signs during treatment with antithyroid drugs

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Amyotrophic lateral sclerosis associated with thyrotoxicosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Motor neuron syndrome in the arms after radiation treatment

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Delayed radiation-induced bulbar palsy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Myokymic discharges of the tongue after radiation to the head and neck

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Distinction between neoplastic and radiation-induced brachial plexopathy, with emphasis on the role of EMG

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

The post-irradiation lower motor neuron syndrome neuronopathy or radiculopathy?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

The neuropathology of chromosome 17-linked dementia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Familial progressive subcortical gliosis: presence of prions and linkage to chromosome 17

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Sporadic and familial parkinsonism and motor neuron disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Familial aggregation of amyotrophic lateral sclerosis, dementia, and Parkinson's disease: evidence of shared genetic susceptibility

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Neurologic sequelae of domoic acid intoxication due to the ingestion of contaminated mussels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

A neurological syndrome associated with orthostatic hypotension: a clinical-pathologic study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Multiple system atrophy: a review of 203 pathologically proven cases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

Fulminant multiple system atrophy in a young adult presenting as motor neuron disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900193-2

10.1016/S0022-510X(98)00193-2

7 January 2021

Identifiers

DOI

1 reference

4 December 2017

1 reference