Isolated facial and bulbar paresis: a persistent manifestation of neonatal myasthenia gravis.
Details
Serval ID
serval:BIB_C85B37774829
Type
Article: article from journal or magazin.
Publication sub-type
Case report (case report): feedback on an observation with a short commentary.
Collection
Publications
Institution
Title
Isolated facial and bulbar paresis: a persistent manifestation of neonatal myasthenia gravis.
Journal
Neurology
ISSN
1526-632X[electronic]
Publication state
Published
Issued date
01/2008
Peer-reviewed
Oui
Volume
70
Number
3
Pages
237-238
Language
english
Notes
Publication types: Case Reports ; Journal Article - Publication Status: ppublish
Keywords
Bulbar Palsy, Progressive/genetics, Bulbar Palsy, Progressive/physiopathology, Chromosomes, Human, Pair 22/genetics, Cranial Nerves/physiopathology, DNA Mutational Analysis, Deglutition Disorders/genetics, Deglutition Disorders/physiopathology, Dysarthria/genetics, Dysarthria/physiopathology, Facial Paralysis/genetics, Facial Paralysis/physiopathology, Humans, Infant, Newborn, Male, Mobius Syndrome/complications, Mobius Syndrome/genetics, Muscle Hypotonia/complications, Muscle Hypotonia/genetics, Muscle, Skeletal/innervation, Muscle, Skeletal/physiopathology, Mutation, Myasthenia Gravis/complications, Myasthenia Gravis/genetics, Neuromuscular Junction/genetics, Neuromuscular Junction/physiopathology, Palatal Muscles/innervation, Palatal Muscles/physiopathology, Pharynx/innervation, Pharynx/physiopathology
Pubmed
Web of science
Create date
10/02/2008 12:22
Last modification date
20/08/2019 15:43
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