Evidence of enteric angiopathy and neuromuscular hypoxia in patients with mitochondrial neurogastrointestinal encephalomyopathy

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is a rare autosomal recessive disease caused by thymidine phosphorylase (TP) enzyme defect. As gastrointestinal changes do not revert in patients undergone TP replacement therapy, one can postulate that other unexplored mechanisms contrib...

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Publicado en:Am J Physiol Gastrointest Liver Physiol
Main Authors: Boschetti, Elisa, D’Angelo, Roberto, Tardio, Maria Lucia, Costa, Roberta, Giordano, Carla, Accarino, Anna, Malagelada, Carolina, Clavenzani, Paolo, Tugnoli, Vitaliano, Caio, Giacomo, Righi, Valeria, Garone, Caterina, D'Errico, Antonietta, Cenacchi, Giovanna, Dotti, Maria Teresa, Stanghellini, Vincenzo, Sternini, Catia, Pironi, Loris, Rinaldi, Rita, Carelli, Valerio, De Giorgio, Roberto
Formato: Artigo
Idioma:Inglês
Publicado: American Physiological Society 2021
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Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC8202202/
https://ncbi.nlm.nih.gov/pubmed/33655764
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpgi.00047.2021
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