Results 11 to 20 of about 41,399 (306)

Unilateral ophthalmoplegia in anti-GQ1b antibody syndrome: case report and systematic literature review [PDF]

Frontiers in Immunology
IntroductionAnti-GQ1b antibody syndrome encompasses immune-mediated neuropathies targeting ganglioside GQ1b, classically presenting as Miller Fisher syndrome (MFS) with the triad of ophthalmoplegia, ataxia, and areflexia.
Juyuan Pan, Ningyu Zheng, Dan Yu, Huihua Jiang, Yuanlin Zhou   +4 more
doaj   +2 more sources

Miller-Fisher syndrome presenting with headache and ophthalmoparesis: a case report and literature review [PDF]

Frontiers in Medicine
Miller-Fisher syndrome (MFS) is a rare variant of Guillain-Barre syndrome, classically characterized by a triad of symptoms, including ataxia, areflexia, and ophthalmoplegia.
Jin Huang, Lingling Lin, Xuerong Huang, Xiaoxiao Yan   +3 more
doaj   +2 more sources

CHRONIC PROGRESSIVE OPHTHALMOPLEGIA EXTERNA, OR “INFANTILE NUCLEAR ATROPHY”(Moebius) [PDF]

British Journal of Ophthalmology, 1921
W. Mcmullen, M. Hine
semanticscholar   +2 more sources

Miller Fisher Variant of Guillain-Barré Syndrome Presenting With Dysphagia and Ophthalmoplegia. [PDF]

Cureus
Sharma R, Murdande S, Garcia-Corella J, Orogian A, Tran L.   +4 more
europepmc   +3 more sources

Clinical insights on Tolosa Hunt syndrome: a multidisciplinary approach on neurological-related symptomatology in maxillofacial region [PDF]

, 2018
Background Tolosa–Hunt syndrome (THS) related neurological symptoms are described in literature as “unilateral”, “recurrent”, “episodic”, “intense”, “severe”, “lancinating” or “stabbing” pain on the upper face and forehead and may be misdiagnosed ...
Ahmed Siddiqui, Ammar, Ali Khan, Zafar, Aziz Alanizy, Hamoud, Bollero, Patrizio, Cicconetti, Andrea, Falisi, Giovanni, Inchingolo, Francesco, Orefici, Alessandro, Syed, Jamaluddin   +8 more
core   +2 more sources

Seeing double: the low-carb diet [PDF]

, 2013
No abstract ...
Drummond, Russell S., Drummond, Suzannah, Lean, Michael E.J., McKenna, Louise A., Talwar, Dinesh   +4 more
core   +1 more source

The importance of social history in the work-up of painful ophthalmoplegia

Interdisciplinary Neurosurgery, 2014
Painful ophthalmoplegia is not one uncommon clinic phenomenon in both ophthalmological and neurological clinics, which can be caused by various pathological conditions and easily be misdiagnosed by some clinical practitioners.
Jun Mu, MD, PhD, Yong Li, MD, PhD, Zesong Yang, MD   +2 more
doaj   +1 more source

Chronic Progressive External Ophthalmoplegia Is Associated with a Novel Mutation in the Mitochondrial tRNA(Asn) Gene [PDF]

, 1994
Chronic progressive external ophthalmoplegia (CPEO) is caused by a decreased oxidative phosphorylation (OXPHOS) activity due to large-scale deletions of the mitochondrial genome in 50 % of the patients.
Kadenbach, B., Klopstock, Thomas, Lauber, J., Marsac, C., Reichmann, Heinz, Seibel, P.   +5 more
core   +1 more source

An autopsy study of a familial oculopharyngeal muscular dystrophy (OPMD) with distal spread and neurogenic involvement [PDF]

, 1981
An 81-year-old man from a family with a history of oculopharyngeal muscular dystrophy (OPMD) involving 6 members over 4 generations is described. The patient first noted drooping of his eyelids at the age of 65.
Aarli, Adams, Amyot, Barbeau, Bosch, Bray, Campanella, Cohen, Cox, Coërs, Croft, Direkze, Dutil, Fried, Fuchs, Goto, Graef von, Graf, Hartmann, Hayes, Julien, Kearns, Kiloh, Krause, Lakin, Lees, Lewis, Liversedge, Lundberg, Man, Maningand, Mater, Matsunaga, Murphy, Myrianthopoulos, Nicolaissen, Peterman, Radu, Rebeiz, Roberts, Satoyoshi, Saucier, Schmitt, Schmitt, Schotland, Schwarz, Szobar, Taylor, Victor, Zellweger   +49 more
core   +1 more source

Mitochondrial neurogastrointestinal encephalomyopathy: approaches to diagnosis and treatment [PDF]

, 2020
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is an ultra-rare disease caused by mutations in TYMP, the gene encoding for the enzyme thymidine phosphorylase.
Bax, BE
core   +1 more source