Gastrointestinal dysmotility in mitochondrial neurogastrointestinal encephalomyopathy is caused by mitochondrial DNA depletion
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Alpers-Huttenlocher syndrome: the role of a multidisciplinary health care teamMitochondrial vasculopathyAlpers-Huttenlocher syndromeMitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic optionsReview article: the assessment and management of chronic severe gastrointestinal dysmotility in adultsNucleotide salvage deficiencies, DNA damage and neurodegenerationLiver as a source for thymidine phosphorylase replacement in mitochondrial neurogastrointestinal encephalomyopathyEncephalomyopathies caused by abnormal nuclear-mitochondrial intergenomic cross-talkCoQ(10) deficiencies and MNGIE: two treatable mitochondrial disorders.Adult mitochondrial DNA depletion syndrome with mild manifestations.Biochemical abnormalities in a patient with thymidine phosphorylase deficiency with fatal outcome.Deoxynucleoside stress exacerbates the phenotype of a mouse model of mitochondrial neurogastrointestinal encephalopathy.Mitochondrial neuro-gastrointestinal encephalomyopathy presenting with recurrent bowel perforations and intra-abdominal abscesses.Mitochondrial Neurogastrointestinal Encephalomyopathy Caused by Thymidine Phosphorylase Enzyme Deficiency: From Pathogenesis to Emerging Therapeutic Options.Enteric neuropathies: Yesterday, Today and Tomorrow.Chronic intestinal pseudo-obstruction in children and adults: diagnosis and therapeutic options.A Novel Mutation in Nucleoporin 35 Causes Murine Degenerative Colonic Smooth Muscle Myopathy.MtDNA-maintenance defects: syndromes and genes.Association of Romo1 gene genetic polymorphisms with risk of gastric cancer in northwestern Chinese population.Emergency surgery in chronic intestinal pseudo-obstruction due to mitochondrial neurogastrointestinal encephalomyopathy: case reports.Fatal congenital myopathy and gastrointestinal pseudo-obstruction due to POLG1 mutations.Visceral smooth muscle α-actin deficiency associated with chronic intestinal pseudo-obstruction in a Bengal cat (Felis catus x Prionailurus bengalensis).Impact of age-related mitochondrial dysfunction and exercise on intestinal microbiota composition.Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)-like phenotype: an expanded clinical spectrum of POLG1 mutations.Mitochondrial Depletion Syndromes in Children and AdultsTransplantation, gene therapy and intestinal pathology in MNGIE patients and mice
P2860
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P2860
Gastrointestinal dysmotility in mitochondrial neurogastrointestinal encephalomyopathy is caused by mitochondrial DNA depletion
description
2008 nî lūn-bûn
@nan
2008 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Gastrointestinal dysmotility i ...... by mitochondrial DNA depletion
@ast
Gastrointestinal dysmotility i ...... by mitochondrial DNA depletion
@en
type
label
Gastrointestinal dysmotility i ...... by mitochondrial DNA depletion
@ast
Gastrointestinal dysmotility i ...... by mitochondrial DNA depletion
@en
prefLabel
Gastrointestinal dysmotility i ...... by mitochondrial DNA depletion
@ast
Gastrointestinal dysmotility i ...... by mitochondrial DNA depletion
@en
P2093
P2860
P50
P1476
Gastrointestinal dysmotility i ...... by mitochondrial DNA depletion
@en
P2093
Andrea Tancredi
Claudia Travaglini
Giulia d'Amati
Mariangela Sebastiani
Marzio Bellan
Michio Hirano
P2860
P304
P356
10.2353/AJPATH.2008.080252
P407
P577
2008-09-11T00:00:00Z