GENERIC 2679583

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026896, umls-concept:C0314603, umls-concept:C0376315
pubmed:issue	4
pubmed:dateCreated	1989-12-21
pubmed:abstractText	Myasthenia in newborns and infants is usually genetic and not mediated by antibodies to the acetylcholine receptor. Several different pre- and postsynaptic defects are responsible for early-onset myasthenia. This review presents a classification of these syndromes based upon knowledge of their pathophysiologic bases and a plan for the evaluation of new patients.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8508183
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0887-8994
pubmed:author	pubmed-author:FenichelG MGM, pubmed-author:MisulisK EKE
pubmed:issnType	Print
pubmed:volume	5
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	205-10
pubmed:dateRevised	2006-5-23
pubmed:meshHeading	pubmed-meshheading:2679583-Humans, pubmed-meshheading:2679583-Infant, pubmed-meshheading:2679583-Infant, Newborn, pubmed-meshheading:2679583-Myasthenia Gravis
pubmed:articleTitle	Genetic forms of myasthenia gravis.
pubmed:affiliation	Department of Neurology; Vanderbilt University Medical Center, Nashville, Tennessee 37212.
pubmed:publicationType	Journal Article, Review