Isolated facial and bulbar paresis: a persistent manifestation of neonatal myasthenia gravis.

Détails

ID Serval
serval:BIB_C85B37774829
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Titre
Isolated facial and bulbar paresis: a persistent manifestation of neonatal myasthenia gravis.
Périodique
Neurology
Auteur(s)
Jeannet P.Y., Marcoz J.P., Kuntzer T., Roulet-Perez E.
ISSN
1526-632X[electronic]
Statut éditorial
Publié
Date de publication
01/2008
Peer-reviewed
Oui
Volume
70
Numéro
3
Pages
237-238
Langue
anglais
Notes
Publication types: Case Reports ; Journal Article - Publication Status: ppublish
Mots-clé
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
Création de la notice
10/02/2008 13:22
Dernière modification de la notice
03/03/2018 21:21
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