Mitochondrial neurogastrointestinal encephalopathy: a case report
The Egyptian Journal of Radiology and Nuclear MedicineBackground Mitochondrial neurogastrointestinal encephalopathy (MNGIE) is an autosomal recessive disease associated with alterations in mitochondrial DNA (mtDNA). The typical age of onset of MNGIE is between the first and second decade of life.
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Porous polyethylene in reconstructive head and neck surgery [PDF]
, 1985 Berghaus, Alexander
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Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance [PDF]
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Novel and recurrent nuclear gene variations in a cohort of Chinese progressive external ophthalmoplegia patients with multiple mtDNA deletions. [PDF]
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A Case of Chronic Progresive External Ophthalmoplegia (CPEO)
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Association between external ophthalmoplegia with diplopia due to brain injury and FIM motor items: a case-control study. [PDF]
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HEREDITARY EXTERNAL OPHTHALMOPLEGIA [PDF]
The Journal of Nervous and Mental Disease, 1908 T H Weisenburg, Wm M. Sweet
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Atheromatosis of the Scalp: A Novel Feature of Chronic Progressive External Ophthalmoplegia Plus Due to a Single Mitochondrial DNA Deletion. [PDF]
Cureus, 2021 Finsterer J.
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Clinical, Histological, and Genetic Features of 25 Patients with Autosomal Dominant Progressive External Ophthalmoplegia (ad-PEO)/PEO-Plus Due to TWNK Mutations. [PDF]
J Clin Med, 2021 Bermejo-Guerrero L +12 more
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