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Volumn 11, Issue 3, 2012, Pages 377-379

A novel finding in MNGIE (Mitochondrial Neurogastrointestinal Encephalomyopathy): Hypergonadotropic hypogonadism

Author keywords

Hypergonadotropic hypogonadism; Mitochondrial myopathy; MNGIE

Indexed keywords

INFUSION FLUID;

EID: 84864859207     PISSN: 11093099     EISSN: None     Source Type: Journal    
DOI: 10.14310/horm.2002.1368     Document Type: Article
Times cited : (11)

References (6)
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    • 77957684211 scopus 로고    scopus 로고
    • Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Case report with a new mutation
    • Bariş Z, Eminoǧlu T, Dalgiç B, Tümer L, Hasanoǧlu A, 2010 Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): case report with a new mutation. Eur J Pediatr 169: 1375-1378.
    • (2010) Eur J Pediatr , vol.169 , pp. 1375-1378
    • Bariş, Z.1    Eminoǧlu, T.2    Dalgiç, B.3    Tümer, L.4    Hasanoǧlu, A.5
  • 2
    • 34247126028 scopus 로고    scopus 로고
    • Cognitive dysfunction and hypogonadotrophic hypogonadism in a Brazilian patient with mitochondrial neurogastrointestinal encephalomyopathy and a novel ECGF1 mutation
    • Carod-Artal FJ, Herrero MD, Lara MC, et al, 2007 Cognitive dysfunction and hypogonadotrophic hypogonadism in a Brazilian patient with mitochondrial neurogastrointestinal encephalomyopathy and a novel ECGF1 mutation. Eur J Neurol 14: 581-585.
    • (2007) Eur J Neurol , vol.14 , pp. 581-585
    • Carod-Artal, F.J.1    Herrero, M.D.2    Lara, M.C.3
  • 3
    • 0033613865 scopus 로고    scopus 로고
    • Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder
    • Nishino I, Spinazzola A, Hirano M, 1999 Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. Science 283: 689-692.
    • (1999) Science , vol.283 , pp. 689-692
    • Nishino, I.1    Spinazzola, A.2    Hirano, M.3
  • 4
    • 6844249406 scopus 로고    scopus 로고
    • A case of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes associated with diabetes mellitus and hypothalamo-pituitary dysfunction
    • Joko T, Iwashige K, Hashimoto T, et al, 1997 A case of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes associated with diabetes mellitus and hypothalamo-pituitary dysfunction. Endocr J 44: 805-809.
    • (1997) Endocr J , vol.44 , pp. 805-809
    • Joko, T.1    Iwashige, K.2    Hashimoto, T.3
  • 5
    • 0030770750 scopus 로고    scopus 로고
    • Sporadic heteroplasmic single 5.5 kb mitochondrial DNA deletion associated with cerebellar ataxia, hypogonadotropic hypogonadism, choroidal dystrophy, and mitochondrial respiratory chain complex I deficiency
    • Barrientos A, Casademont J, Genis D, et al, 1997 Sporadic heteroplasmic single 5.5 kb mitochondrial DNA deletion associated with cerebellar ataxia, hypogonadotropic hypogonadism, choroidal dystrophy, and mitochondrial respiratory chain complex I deficiency. Hum Mutat 10: 212-216.
    • (1997) Hum Mutat , vol.10 , pp. 212-216
    • Barrientos, A.1    Casademont, J.2    Genis, D.3
  • 6
    • 0026585685 scopus 로고
    • Endocrine abnormalities in mitochondrial myopathy with external ophthalmoplegia
    • Quade A, Zierz S, Klingmüller D, 1992 Endocrine abnormalities in mitochondrial myopathy with external ophthalmoplegia. Clin Investig 70: 396-402.
    • (1992) Clin Investig , vol.70 , pp. 396-402
    • Quade, A.1    Zierz, S.2    Klingmüller, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.