Extremely severe complicated spastic paraplegia 3A with neonatal onset

Pediatric Neurology

Volumn 51, Issue 5, 2014, Pages 726-729

  Yonekawa, Takahiro ^a,b   Oya, Yasushi ^a   Higuchi, Yujiro ^c   Hashiguchi, Akihiro ^c   Takashima, Hiroshi ^c   Sugai, Kenji ^a   Sasaki, Masayuki ^a  

^a NATIONAL INSTITUTE OF MENTAL HEALTH   (Japan)

^b NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

^c KAGOSHIMA UNIVERSITY   (Japan)

Author keywords

atlastin 1; axonal neuropathy; pseudobulbar palsy; spastic paraplegia

Indexed keywords

ARTICLE; ATLATSIN GTPASE 1 GENE; BRAIN ELECTROPHYSIOLOGY; CASE REPORT; CEREBRAL PALSY; CHILD; DISEASE SEVERITY; DYSPHAGIA; GENE; GENE MUTATION; HUMAN; HYPOKINESIA; MALE; MASTICATION; MUSCLE HYPERTONIA; MUSCLE WEAKNESS; NEWBORN PERIOD; PSEUDOBULBAR PALSY; QUADRIPLEGIA; SCHOOL CHILD; SPASTIC PARAPLEGIA; SPASTICITY; SPEECH DISORDER; ADOLESCENT; FEMALE; GENETICS; MUTATION; NERVE CONDUCTION; PARAPLEGIA; PATHOPHYSIOLOGY; SPASTIC PARAPLEGIA, HEREDITARY;

ATL1 PROTEIN, HUMAN; GUANINE NUCLEOTIDE BINDING PROTEIN; MEMBRANE PROTEIN;

ADOLESCENT; CHILD; FEMALE; GTP-BINDING PROTEINS; HUMANS; MALE; MEMBRANE PROTEINS; MUTATION; NEURAL CONDUCTION; PARAPLEGIA; SPASTIC PARAPLEGIA, HEREDITARY;

EID: 84908307519     PISSN: 08878994     EISSN: 18735150     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2014.07.027     Document Type: Article

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