Diagnosis of amyotrophic lateral sclerosis (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

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

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7 January 2021

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

7 January 2021

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A treatable multifocal motor neuropathy with antibodies to GM1 ganglioside

7 January 2021

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

7 January 2021

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

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Motor nerve biopsy studies in motor neuropathy and motor neuron disease

7 January 2021

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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

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

7 January 2021

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

7 January 2021

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The neurological manifestations of cervical spondylosis

7 January 2021

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Upper limb involvement in cervical spondylosis

7 January 2021

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CERVICAL MYELOPATHY WITH FASCICULATIONS IN THE LOWER EXTREMITIES

7 January 2021

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Cervical Spondylotic Myelopathy With Reversible Fasciculations in the Lower Extremities

7 January 2021

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High cervical myelopathy presenting with the numb clumsy hand syndrome

7 January 2021

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

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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

7 January 2021

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7 January 2021

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7 January 2021

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Clinical and electrodiagnostic features of X-linked recessive bulbospinal neuronopathy

7 January 2021

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

7 January 2021

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Androgen receptor gene polymorphisms in amyotrophic lateral sclerosis

7 January 2021

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

7 January 2021

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

7 January 2021

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The clinical spectrum of hexosaminidase deficiency diseases

7 January 2021

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Juvenile spinal muscular atrophy: a new hexosaminidase deficiency phenotype

7 January 2021

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

7 January 2021

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Cramp,fasciculation syndrome: A treatable hyperexcitable peripheral nerve disorder

7 January 2021

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Not-so-benign fasciculation

7 January 2021

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MUSCLE FASCICULATIONS IN A HEALTHY POPULATION

7 January 2021

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From benign fasciculations and cramps to motor neuron disease

7 January 2021

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

7 January 2021

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

7 January 2021

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The origin of muscle fasciculations and cramps

7 January 2021

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

7 January 2021

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7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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7 January 2021

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

7 January 2021

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

7 January 2021

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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

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The central nervous system in motor neurone disease

7 January 2021

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

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

7 January 2021

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

7 January 2021

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

7 January 2021

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Primary lateral sclerosis. Clinical features, neuropathology and diagnostic criteria

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Primary lateral sclerosis: a neuropsychological study.

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The open opercular sign: diagnosis and significance.

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

7 January 2021

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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

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

7 January 2021

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

7 January 2021

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Diffuse Lewy body disease as substrate of primary lateral sclerosis

7 January 2021

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

7 January 2021

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A case of Machado-Joseph disease presenting with spastic paraparesis

7 January 2021

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Infantile onset of hereditary ascending spastic paralysis with bulbar involvement

7 January 2021

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Amyotrophic cervical myelopathy in adolescence

7 January 2021

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7 January 2021

Monomelic muscle atrophy

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

7 January 2021

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

7 January 2021

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Early and late losses of motor units after poliomyelitis

7 January 2021

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

7 January 2021

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7 January 2021

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Human immunodeficiency virus-associated motor axonal polyradiculoneuropathy

7 January 2021

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Lower motor neuron dysfunction associated with human immunodeficiency virus infection

7 January 2021

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

7 January 2021

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Immunologic reactivity against Borrelia burgdorferi in patients with motor neuron disease

7 January 2021

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

7 January 2021

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

7 January 2021

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Transmissible agent in the amyotrophic form of Creutzfeldt-Jakob disease

7 January 2021

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Inclusion body myositis (IBM): Myopathy or neuropathy?

7 January 2021

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Inclusion body myositis and myopathies

7 January 2021

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Inclusion body myositis. Observations in 40 patients

7 January 2021

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

7 January 2021

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Inclusion body myositis, a review

7 January 2021

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7 January 2021

Inclusion body myositis

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Inclusion body myositis: clinical and pathological boundaries

7 January 2021

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Inclusion body myositis: no evidence for a neurogenic component

7 January 2021

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The role of quantitative electromyography in inclusion body myositis

7 January 2021

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Primary sensory neuropathy with muscular changes associated with carcinoma

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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Pure motor neuropathy complicating carcinoma of bronchus recovered after surgery

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NEUROMUSCULAR DISORDERS ASSOCIATED WITH MALIGNANT NEOPLASTIC DISEASE

7 January 2021

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Subacute motor neuronopathy: a remote effect of lymphoma

7 January 2021

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Motor neuron syndromes in cancer patients

7 January 2021

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

7 January 2021

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Anti-neurone antibodies are not characteristic of amyotrophic lateral sclerosis

7 January 2021

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

7 January 2021

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Primary lateral sclerosis. A clinical diagnosis reemerges

7 January 2021

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

7 January 2021

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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