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Volumn 62, Issue 1, 1999, Pages 40-45

Type 1 G(M1) gangliosidosis with basal ganglia calcification: A case report

Author keywords

galactosidase; Basal ganglia calcification; Cherry red spot; Hepatosplenomegaly; Skeletal dysplasia; Type 1 G(M1) gangliosidosis

Indexed keywords

ARTICLE; BLOOD SMEAR; BRAIN CALCIFICATION; CASE REPORT; CHERRY RED SPOT; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; GM1 GANGLIOSIDOSIS; HEPATOSPLENOMEGALY; HUMAN; INFANT; MALE; CALCINOSIS; EXTRAPYRAMIDAL SYNDROME;

EID: 0032999405     PISSN: 05781337     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (15)
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  • 5
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  • 6
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  • 7
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    • β-Galactosidase deficiency in juvenile and adult patients: Report of six Japanese cases and review of literature
    • Suzuki Y, Nakamura N, Fukuoka K, Shimada Y, Uono M. β-Galactosidase deficiency in juvenile and adult patients: report of six Japanese cases and review of literature. Hum Genet 1977;36:219-29.
    • (1977) Hum Genet , vol.36 , pp. 219-229
    • Suzuki, Y.1    Nakamura, N.2    Fukuoka, K.3    Shimada, Y.4    Uono, M.5
  • 10
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    • (1991) Am J Hum Genet , vol.49 , pp. 566-574
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    • Bilateral basal ganglia lesions: Pediatric differential considerations
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  • 15
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.