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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1980-4-25
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pubmed:abstractText |
Patients with sickle cell disease are subject to a variety of neurologic complications. A patient with sickle cell disease and rarely noted features or complications is described. The association of abnormal (sickle-type) hemoglobin (Hgb S) with trigeminal and facial neuropathies and vascular headaches appeared to coincide with reactivation of the hematologic disease.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0028-3878
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
30
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
210-1
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:6243763-Adult,
pubmed-meshheading:6243763-Anemia, Sickle Cell,
pubmed-meshheading:6243763-Cranial Nerves,
pubmed-meshheading:6243763-Female,
pubmed-meshheading:6243763-Humans,
pubmed-meshheading:6243763-Peripheral Nervous System Diseases,
pubmed-meshheading:6243763-Trigeminal Neuralgia,
pubmed-meshheading:6243763-Vascular Headaches
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pubmed:year |
1980
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pubmed:articleTitle |
Multiple cranial neuropathies, trigeminal neuralgia, and vascular headaches in sickle cell disease, a possible common mechanism.
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pubmed:publicationType |
Journal Article,
Case Reports
|