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Volumn 42, Issue 5, 2011, Pages 194-196

Bowel obstruction in patients with Alpers-Huttenlocher syndrome

Author keywords

Alpers Huttenlocher syndrome (AHS); constipation; EEG; gastrointestinal dysmotility; ketogenic diet; lacosamide; MRI; refractory convulsive status; urinary retention

Indexed keywords

ANALGESIC AGENT; DNA DIRECTED DNA POLYMERASE GAMMA; DOMPERIDONE; ERYTHROMYCIN; HARKOSERIDE; MACROGOL; METOCLOPRAMIDE; TOPIRAMATE;

EID: 81855172277     PISSN: 0174304X     EISSN: 14391899     Source Type: Journal    
DOI: 10.1055/s-0031-1287812     Document Type: Article
Times cited : (13)

References (14)
  • 1
    • 67649354905 scopus 로고    scopus 로고
    • Frequency of mitochondrial defects in patients with chronic intestinal pseudo-obstruction
    • Amiot A, Tchikviladze M, Joly F et al. Frequency of mitochondrial defects in patients with chronic intestinal pseudo-obstruction. Gastroenterology: 2009; 137 101 109
    • (2009) Gastroenterology , vol.137 , pp. 101-109
    • Amiot, A.1    Tchikviladze, M.2    Joly, F.3
  • 2
    • 77952540309 scopus 로고    scopus 로고
    • Compound heterozygous gamma gene mutation in a patient with Alpers disease
    • Cardena J F, Amato R S. Compound heterozygous gamma gene mutation in a patient with Alpers disease. Sem Pediatr Neurol: 2010; 17 62 64
    • (2010) Sem Pediatr Neurol , vol.17 , pp. 62-64
    • Cardena, J.F.1    Amato, R.S.2
  • 3
    • 7044253112 scopus 로고    scopus 로고
    • Paralytic ileus in MELAS with phenotypic features of MNGIE
    • Chang T M, Chi C S, Tsai C R et al. Paralytic ileus in MELAS with phenotypic features of MNGIE. Pediatr Neurol: 2004; 31 374 377
    • (2004) Pediatr Neurol , vol.31 , pp. 374-377
    • Chang, T.M.1    Chi, C.S.2    Tsai, C.R.3
  • 4
    • 81855192225 scopus 로고
    • University of Washington, Seattle, Pagon RA, Bird TD, Dolan CR, Stephens K (eds.). Source GeneReviews [Internet]. Seattle (WA): 2010 Mar 16
    • Cohen B H, Chinnery P F, Copeland W C. POLG-Related Disorders. In: Pagon RA, Bird TD, Dolan CR, Stephens K (eds.). Source GeneReviews [Internet]. Seattle (WA): University of Washington, Seattle: 1993; 2010 Mar 16
    • (1993) POLG-Related Disorders
    • Cohen, B.H.1    Chinnery, P.F.2    Copeland, W.C.3
  • 7
    • 53149083738 scopus 로고    scopus 로고
    • Gastrointestinal dysmotility in mitochondrial neurogastrointestinal encephalomyopathy is caused by mitochondrial DNA depletion
    • Giordano C, Sebastiani M, De Giorgio R et al. Gastrointestinal dysmotility in mitochondrial neurogastrointestinal encephalomyopathy is caused by mitochondrial DNA depletion. Am J Pathol: 2008; 173 1120 1128
    • (2008) Am J Pathol , vol.173 , pp. 1120-1128
    • Giordano, C.1    Sebastiani, M.2    De Giorgio, R.3
  • 8
    • 67349274524 scopus 로고    scopus 로고
    • Heteroplasmic mutation in the anticodon-stem of mitochondrial tRNA(Val) causing MNGIE-like gastrointestinal dysmotility and cachexia
    • Horvth R, Bender A, Abicht A et al. Heteroplasmic mutation in the anticodon-stem of mitochondrial tRNA(Val) causing MNGIE-like gastrointestinal dysmotility and cachexia. J Neurol: 2009; 256 810 815
    • (2009) J Neurol , vol.256 , pp. 810-815
    • Horvth, R.1    Bender, A.2    Abicht, A.3
  • 9
    • 62149091063 scopus 로고    scopus 로고
    • Ketogentic diet in Alpers-Huttenlocher syndrome
    • Joshi C N, Greenberg C R, Mhanni A A et al. Ketogentic diet in Alpers-Huttenlocher syndrome. Pediatr Neurol: 2009; 40 314 316
    • (2009) Pediatr Neurol , vol.40 , pp. 314-316
    • Joshi, C.N.1    Greenberg, C.R.2    Mhanni, A.A.3
  • 10
    • 79954856406 scopus 로고    scopus 로고
    • Gastrointestinal neuromuscular pathology in Alpers disease
    • Kapur R P, Fligner C, Maghsoodi B et al. Gastrointestinal neuromuscular pathology in Alpers disease. Am J Surg Pathol: 2011; 35 714 722
    • (2011) Am J Surg Pathol , vol.35 , pp. 714-722
    • Kapur, R.P.1    Fligner, C.2    Maghsoodi, B.3
  • 11
    • 76149087433 scopus 로고    scopus 로고
    • A novel POLG gene mutation in 4 children with Alpers-like hepatocerebral syndromes
    • Kurt B, Jaeken J, Van Hove J et al. A novel POLG gene mutation in 4 children with Alpers-like hepatocerebral syndromes. Arch Neurol: 2010; 67 239 244
    • (2010) Arch Neurol , vol.67 , pp. 239-244
    • Kurt, B.1    Jaeken, J.2    Van Hove, J.3
  • 12
    • 53249111329 scopus 로고    scopus 로고
    • 2+ waves in freshly dispersed interstitial cells of Cajal from the rabbit urethra
    • 2+ waves in freshly dispersed interstitial cells of Cajal from the rabbit urethra. J Physiol: 2008; 586 Pt 19 4631 4642
    • (2008) J Physiol , vol.586 , Issue.PART 19 , pp. 4631-4642
    • Sergeant, G.P.1    Bradley, E.2    Thornbury, K.D.3
  • 13
    • 0034943967 scopus 로고    scopus 로고
    • Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions
    • DOI 10.1038/90034
    • Van Goethem G, Dermaut B, Lfgren A et al. Mutation of POLG is associated with progressive external opthalmoplegia characterized by mtDNA deletions. Nat Genet: 2001; 28 211 212 (Pubitemid 32626018)
    • (2001) Nature Genetics , vol.28 , Issue.3 , pp. 211-212
    • Van Goethem, G.1    Dermaut, B.2    Lofgren, A.3    Martin, J.-J.4    Van Broeckhoven, C.5
  • 14
    • 65949104596 scopus 로고    scopus 로고
    • Absence of the interstitial cell of Cajal network in mitochondrial neurogastrointestinal encephalomyopathy
    • Zimmer V, Feiden W, Becker G et al. Absence of the interstitial cell of Cajal network in mitochondrial neurogastrointestinal encephalomyopathy. Neurogastroenterol Motil: 2009; 21 627 631
    • (2009) Neurogastroenterol Motil , vol.21 , pp. 627-631
    • Zimmer, V.1    Feiden, W.2    Becker, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.