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Neurology

Volumn 79, Issue 15, 2012, Pages

Child Neurology: A case of PMM2-CDG (CDG 1a) presenting with unusual eye movements

(2) Coorg, Rohini a Lotze, Timothy E a

a UNIVERSITY OF CALIFORNIA (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANAMNESIS; CASE REPORT; CEREBELLAR ATAXIA; CEREBELLUM ATROPHY; CHILD; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1; EYE MOVEMENT DISORDER; FEMALE; GENE; GENE MUTATION; GENETIC ANALYSIS; HUMAN; INFANT; MISSENSE MUTATION; NEUROLOGIC EXAMINATION; NEWBORN; NOTE; NUCLEAR MAGNETIC RESONANCE IMAGING; OPTOKINETIC NYSTAGMUS; PHYSICAL EXAMINATION; PMM2 GENE; PRESCHOOL CHILD; PRIORITY JOURNAL; SMOOTH PURSUIT EYE MOVEMENT;

EID: 84867542313 PISSN: 00283878 EISSN: 1526632X Source Type: Journal
DOI: 10.1212/WNL.0b013e31826e2617 Document Type: Article

Times cited : (14)

References (8)

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3
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4
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.