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Review
Endocrinology & Metabolism
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Position paper on diagnosis, prognosis, and treatment by theMNGIEInternational Network
Michio Hirano et al.
Summary: MNGIE is a rare autosomal recessive disease caused by TYMP mutations, leading to gastrointestinal and neurological symptoms. Diagnosis is challenging and treatment options are limited, with a need for standardized monitoring methods.
JOURNAL OF INHERITED METABOLIC DISEASE (2021)
Article
Biochemistry & Molecular Biology
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE):: Biochemical features and therapeutic approaches
M. C. Lara et al.
BIOSCIENCE REPORTS (2007)
Article
Radiology, Nuclear Medicine & Medical Imaging
MRI of five patients with mitochondrial neurogastrointestinal encephalomyopathy
WS Millar et al.
AMERICAN JOURNAL OF ROENTGENOLOGY (2004)
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