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Volumn 172, Issue 3, 2005, Pages 355-358

Glycogen storage disease type III in Inuit children

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHILD; CLINICAL ARTICLE; DISEASE SEVERITY; ENZYME DEGRADATION; ESKIMO; FEMALE; GLYCOGEN STORAGE DISEASE TYPE 3; HIGH RISK POPULATION; HUMAN; HYPOGLYCEMIA; INFANT; LIVER CIRRHOSIS; MALE; MUSCLE WEAKNESS; PATIENT CARE; POPULATION RESEARCH;

EID: 13444287964     PISSN: 08203946     EISSN: None     Source Type: Journal    
DOI: 10.1503/cmaj.1031589     Document Type: Article
Times cited : (14)

References (14)
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    • Coleman, R.A.1    Winter, H.S.2    Wolf, B.3    Gilchrist, J.M.4    Chen, Y.T.5
  • 2
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    • Glycogen storage diseases: Phenotypic, genetic, and biochemical characteristics, and therapy
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    • Wolfsdorf, J.I.1    Holm, I.A.2    Weinstein, D.A.3
  • 3
    • 0027057809 scopus 로고
    • Glycogen debranching enzyme deficiency: Long-term study of serum enzyme activities and clinical features
    • Coleman RA, Winter HS, Wolf B, Chen YT. Glycogen debranching enzyme deficiency: long-term study of serum enzyme activities and clinical features. J Inherit Metab Dis 1992;15: 869-81.
    • (1992) J Inherit Metab Dis , vol.15 , pp. 869-881
    • Coleman, R.A.1    Winter, H.S.2    Wolf, B.3    Chen, Y.T.4
  • 4
    • 0031056445 scopus 로고    scopus 로고
    • Type IIIb glycogen storage disease associated with end-stage cirrhosis and hepatocellular carcinoma
    • The Liver Transplant Group
    • Haagsma EB, Smit GP, Niezen-Koning KE, Gouw AS, Meennan L, Slooff MJ. Type IIIb glycogen storage disease associated with end-stage cirrhosis and hepatocellular carcinoma. The Liver Transplant Group. Hepatology 1997;25(3):537-40.
    • (1997) Hepatology , vol.25 , Issue.3 , pp. 537-540
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  • 7
    • 13444279319 scopus 로고    scopus 로고
    • Ottawa: Census Division, Statistics Canada
    • Statistics Canada. 2001 Aboriginal population profile. Ottawa: Census Division, Statistics Canada; 2001.
    • (2001) 2001 Aboriginal Population Profile
  • 8
    • 0030689829 scopus 로고    scopus 로고
    • A single-base deletion in the 3′-coding region of glycogen-debranching enzyme is prevalent in glycogen storage disease type III in a population of North African Jewish patients
    • Parvari R, Moses S, Shen J, Hershkovitz E, Lerner A, Chen YT. A single-base deletion in the 3′-coding region of glycogen-debranching enzyme is prevalent in glycogen storage disease type III in a population of North African Jewish patients. Eur J Hum Genet 1997;5(5):266-70.
    • (1997) Eur J Hum Genet , vol.5 , Issue.5 , pp. 266-270
    • Parvari, R.1    Moses, S.2    Shen, J.3    Hershkovitz, E.4    Lerner, A.5    Chen, Y.T.6
  • 9
    • 0031055330 scopus 로고    scopus 로고
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  • 10
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  • 13
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    • Yang, B.Z.1    Stewart, C.2    Ding, J.H.3    Chen, Y.T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.