Results 21 to 30 of about 13,407 (248)

Chronic Progressive External Ophthalmoplegia [PDF]

British Journal of Ophthalmology, 1953
C. Orgen
openaire   +4 more sources

Primary histiocytic sarcoma in the brain with renal metastasis causing internal ophthalmoparesis and external ophthalmoplegia in a Maine Coon cat. [PDF]

JFMS Open Rep, 2021
Monteiro S, Hughes K, Genain MA, Alves L.   +3 more
europepmc   +2 more sources

Progressive external ophthalmoplegia

Russian neurological journal, 2020
E. V. Iakovenko, E. Yu. Fedotova, S. N. Illarioshkin   +2 more
openaire   +3 more sources

Progressive External Ophthalmoplegia [PDF]

British Journal of Ophthalmology, 1956
F. McAuley
openaire   +3 more sources

Whole-Exome Sequencing Identifies a Novel POLG Frameshift Variant in an Adult Patient Presenting with Progressive External Ophthalmoplegia and Mitochondrial DNA Depletion. [PDF]

Case Rep Genet, 2021
Kurtz J, Fernandes JA, Mansukhani M, Copeland WC, Naini AB.   +4 more
europepmc   +3 more sources

Clinical, neuroelectrophysiological and muscular pathological analysis of chronic progressive external ophthalmoplegia. [PDF]

Exp Ther Med, 2020
Lv H, Qu Q, Liu H, Qian Q, Zheng X, Zhang Y.   +5 more
europepmc   +3 more sources

Progressive external ophthalmoplegia – A case report

Indian Journal of Pathology and Microbiology, 2023
Progressive external ophthalmoplegia is a slowly progressive hereditary mitochondrial myopathy. Most mitochondrial disorders overlap clinically, enzymatically, and genetically.
Ashmeet Kaur, Kusum Mathur, Anita Harsh, Kapil Thakar   +3 more
doaj   +1 more source

Opening One's Eyes to Mosaicism in Progressive External Ophthalmoplegia. [PDF]

Neurol Genet, 2017
Sommerville EW, Jones RL, Hardy SA, Blakely EL, Pyle A, Schaefer AM, Chinnery PF, Turnbull DM, Gorman GS, Taylor RW.   +9 more
europepmc   +3 more sources

Mitochondrial mutations in 12S rRNA and 16S rRNA presenting as chronic progressive external ophthalmoplegia (CPEO) plus: A case report. [PDF]

Medicine (Baltimore), 2017
Lv ZY, Xu XM, Cao XF, Wang Q, Sun DF, Tian WJ, Yang Y, Wang YZ, Hao YL.   +8 more
europepmc   +2 more sources

Changing faces of mitochondrial disease: autosomal recessive POLG disease mimicking myasthenia gravis and progressive supranuclear palsy

BMJ Neurology Open, 2022
Background Mitochondrial disorders are known to cause diverse neurological phenotypes which cause a diagnostic challenge to most neurologists. Pathogenic polymerase gamma (POLG) variants have been described as a cause of chronic progressive external ...
Naomi Warren, Andrew M Schaefer, Robert W Taylor, Emma L Blakely, Sila Hopton, Menatalla Elwan, Kate Craig, Gavin Falkous   +7 more
doaj   +1 more source