Results 201 to 210 of about 41,399 (306)

RYR1 mutations as a cause of ophthalmoplegia, facial weakness, and malignant hyperthermia.

open access: yesJAMA ophthalmology, 2013
S. Shaaban   +7 more
semanticscholar   +1 more source

Volumetric brain analysis and associated retinal thinning in autosomal dominant optic atrophy patients. [PDF]

open access: yesNeuroimage Rep
Pajareeyapong P   +7 more
europepmc   +1 more source

Das Kearns-Sayre-Syndrom. [PDF]

open access: yes, 1980
Dobiasch, H., Krause, Klaus-Henning
core  

Neurobrucellosis in an 11-year-old child: A rare case report of brain microabscesses from an endemic region. [PDF]

open access: yesJ Int Med Res
Alghamdi AO   +7 more
europepmc   +1 more source

CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA: A CASE SERIES [PDF]

open access: bronze
GAGANDEEP SINGH DIGRA   +3 more
openalex   +1 more source

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