메뉴 건너뛰기




Volumn 17, Issue 2, 2002, Pages 132-134

Pontocerebellar hypoplasia type 2 and Reye-like syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CEREBELLUM HYPOPLASIA; CLINICAL FEATURE; CLINICAL OBSERVATION; COGNITIVE DEVELOPMENT; DEGENERATIVE DISEASE; DIFFERENTIAL DIAGNOSIS; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; DISEASE SEVERITY; DYSKINESIA; DYSTONIA; EXTRAPYRAMIDAL SYMPTOM; FEMALE; HUMAN; LIMB MOVEMENT; MALFORMATION SYNDROME; METABOLIC DISORDER; MICROCEPHALY; MOTOR DEVELOPMENT; NUCLEAR MAGNETIC RESONANCE IMAGING; PRESCHOOL CHILD; PRIORITY JOURNAL; REYE SYNDROME;

EID: 0036257420     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/088307380201700208     Document Type: Article
Times cited : (6)

References (19)
  • 1
    • 0027771377 scopus 로고
    • Pontocerebellar hypoplasia: An overview of a group of inherited neurodegenerative disorders with fetal onset
    • (1993) Brain Dev , vol.15 , pp. 411-422
    • Barth, P.G.1
  • 2
    • 0028872285 scopus 로고
    • The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, and extrapyramidal dyskinesia (pontocerebellar hypoplasia type 2): Compiled data from 10 pedigrees
    • (1995) Neurology , vol.45 , pp. 311-317
    • Barth, P.G.1    Blennow, G.2    Lenard, H.G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.