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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
1988-10-27
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pubmed:abstractText |
We report an autopsied patient who initially presented signs of cerebellar ataxia. After seven months, small cell carcinoma of the lung was revealed. Electromyography on repetitive stimulation and autopsy findings proved that the neurological disorders were due to Eaton-Lambert syndrome and subacute cerebellar degeneration, as forms of carcinomatous neuromyopathy.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0021-5120
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
27
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
203-6
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:3418988-Adult,
pubmed-meshheading:3418988-Autopsy,
pubmed-meshheading:3418988-Brain,
pubmed-meshheading:3418988-Carcinoma, Bronchogenic,
pubmed-meshheading:3418988-Cerebellar Ataxia,
pubmed-meshheading:3418988-Cerebellar Diseases,
pubmed-meshheading:3418988-Humans,
pubmed-meshheading:3418988-Lung Neoplasms,
pubmed-meshheading:3418988-Male,
pubmed-meshheading:3418988-Myasthenia Gravis,
pubmed-meshheading:3418988-Syndrome,
pubmed-meshheading:3418988-Tomography, X-Ray Computed
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pubmed:year |
1988
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pubmed:articleTitle |
Bronchogenic carcinoma with subacute cerebellar degeneration and Eaton-Lambert syndrome; an autopsy case.
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pubmed:affiliation |
Department of Pulmonary Medicine, Jichi Medical School, Tochigi, Japan.
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pubmed:publicationType |
Journal Article,
Case Reports
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