Results 211 to 220 of about 41,399 (306)

Thymidine kinase 2 mutations in autosomal recessive progressive external ophthalmoplegia with multiple mitochondrial DNA deletions.

open access: yesHuman Molecular Genetics, 2012
H. Tyynismaa   +10 more
semanticscholar   +1 more source

A Patient with Vexas Syndrome Presenting with Complete Ophthalmoplegia. [PDF]

open access: yesEur J Case Rep Intern Med
Krzowski J   +3 more
europepmc   +1 more source

A Scoping Review of POLG-Related Cerebellar Ataxia: Insights and Clinical Perspectives. [PDF]

open access: yesTremor Other Hyperkinet Mov (N Y)
Kalampokini S   +5 more
europepmc   +1 more source

Multisystem Disorder in Late-Onset Chronic Progressive External Ophthalmoplegia

open access: yesCanadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 2011

semanticscholar   +1 more source

A Case of Miller-Fisher Overlap Syndrome With Positive Anti-GM4 Antibody and Atypical Symptoms. [PDF]

open access: yesImmun Inflamm Dis
Tang M   +9 more
europepmc   +1 more source

Congenital external ophthalmoplegia.

open access: yesJournal of the All-India Ophthalmological Society, 1966
Sen D, Thomas A
openaire   +2 more sources

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