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Volumn 19, Issue 2, 2010, Pages 195-197

Chronic intestinal pseudo-obstruction and neurological manifestations in early adulthood: Considering MNGIE syndrome in differential diagnosis

Author keywords

Intestinal pseudo obstruction; MNGIE syndrome; Neurologic symptoms

Indexed keywords

BARIUM; GENOMIC DNA;

EID: 77954672579     PISSN: 18418724     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (12)

References (8)
  • 1
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    • Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome
    • Papadimitriou A, Comi GP, Hadjigeorgiou GM, et al. Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome. Neurology 1998; 51: 1086-1092.
    • (1998) Neurology , vol.51 , pp. 1086-1092
    • Papadimitriou, A.1    Comi, G.P.2    Hadjigeorgiou, G.M.3
  • 2
    • 0028301915 scopus 로고
    • Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Clinical, biochemical and genetic features of an autosomal recessive mitochondrial disorder
    • Hirano M, Silvestri G, Blake DM, et al. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical and genetic features of an autosomal recessive mitochondrial disorder. Neurology 1994; 44: 721-727.
    • (1994) Neurology , vol.44 , pp. 721-727
    • Hirano, M.1    Silvestri, G.2    Blake, D.M.3
  • 3
    • 0037265642 scopus 로고    scopus 로고
    • Four novel thymidine phosphorylase gene mutations in mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) patients
    • Kocaefe YC, Erdem S, Ozgüç M, Tan E. Four novel thymidine phosphorylase gene mutations in mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) patients. Eur J Hum Genet 2003; 11: 102-104.
    • (2003) Eur J Hum Genet , vol.11 , pp. 102-104
    • Kocaefe, Y.C.1    Erdem, S.2    Ozgüç, M.3    Tan, E.4
  • 4
    • 0032231702 scopus 로고    scopus 로고
    • Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qter
    • Hirano M, Garcia-de-Yebenes J, Jones AC, et al. Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qter. Am J Hum Genet 1998; 63: 526-533.
    • (1998) Am J Hum Genet , vol.63 , pp. 526-533
    • Hirano, M.1    de Garcia-Yebenes, J.2    Jones, A.C.3
  • 5
    • 0033613865 scopus 로고    scopus 로고
    • Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder
    • Nishino I, Spinazzola A, Hirano M. Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder. Science 1999; 283: 689-692.
    • (1999) Science , vol.283 , pp. 689-692
    • Nishino, I.1    Spinazzola, A.2    Hirano, M.3
  • 6
    • 16244391425 scopus 로고    scopus 로고
    • Neurologic presentation of celiac disease
    • Bushara KO. Neurologic presentation of celiac disease. Gastroenterology 2005; 128 (4 Suppl 1): S92-97.
    • (2005) Gastroenterology , vol.128 , Issue.1-4 SUPPL.
    • Bushara, K.O.1
  • 8
    • 33750306390 scopus 로고    scopus 로고
    • Allogeneic stem cell transplantation corrects biochemical derangements in MNGIE
    • Hirano M, Martí R, Casali C, at al. Allogeneic stem cell transplantation corrects biochemical derangements in MNGIE. Neurology 2006; 67: 1458-1460.
    • (2006) Neurology , vol.67 , pp. 1458-1460
    • Hirano, M.1    Martí, R.2    Casali, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.