Results 21 to 30 of about 41,399 (306)
Flux control of cytochrome c oxidase in human skeletal muscle [PDF]
, 2000 In the present work, by titrating cytochrome c oxidase (COX) with the specific inhibitor KCN, the flux control coefficient and the metabolic reserve capacity of COX have been determined in human saponin-permeabilized muscle fibers. In the presence of the
Attardi, Giuseppe +5 more
core +1 more source
Ophthalmoplegia in Mitochondrial Disease
Yonsei medical journal, 2018 Purpose To evaluate the classification, diagnosis, and natural course of ophthalmoplegia associated with mitochondrial disease. Materials and Methods Among 372 patients with mitochondrial disease who visited our hospital between January 2006 and January ...
Sang Jun Lee +3 more
semanticscholar +1 more source
Alexandria Journal of Medicine, 2014 Introduction: Lesions in medial longitudinal fasciculus (MLF) produce internuclear ophthalmoplegia (INO) with characteristic horizontal gaze abnormality.
Yeshigeta Gelaw
doaj +1 more source
Progression of myopathology in Kearns-Sayre syndrome [PDF]
, 1992 We report on the progression of myopathology by comparing two biopsies from a patient with a Kearns-Sayre-Syndrome. The first biopsy was taken in 1979 and showed 10% ragged-red fibers.
B. Meurers +11 more
core +1 more source
Clinical and magnetic resonance imaging features of idiopathic oculomotor neuropathy in 14 dogs: Canine Idiopathic Oculomotor Neuropathy [PDF]
, 2017 Ophthalmoplegia/ophthalmoparesis (internal, external, or both) has been reported in dogs secondary to neoplasia affecting the oculomotor nerve and is usually given a poor prognosis.
Beltran, E +4 more
core +2 more sources
Clinical efficacy of the partial rectus muscle transportation procedure for paralytic strabismus [PDF]
International Journal of Ophthalmology, 2020 AIM: To analyze the clinical efficacy of the partial rectus muscle transportation (PRT) procedure for paralytic strabismus due to single rectus muscle palsy.
Yan-Qiong Tu +3 more
doaj +1 more source
Clinical and biochemical improvements in a patient with MNGIE following enzyme replacement. [PDF]
, 2013 Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is a rare autosomal recessive metabolic disorder caused by a deficiency of thymidine phosphorylase (TP, EC2.4.2.4) due to mutations in the nuclear gene TYMP.
Bain, MD +5 more
core +1 more source
Recurrent painful ophthalmoplegic neuropathy: a report of two new pediatric cases
The Turkish Journal of Pediatrics, 2022 Background. Recurrent painful ophthalmologic neuropathy (RPON), formerly known as ophthalmoplegic migraine, is characterized by repeated attacks of one or more ocular cranial nerve palsies with an ipsilateral headache.
Çağatay Günay +4 more
doaj +1 more source
Ophthalmoplegia due to Invasive Fungal Sinusitis: A Report of Three Cases
Türk Nöroloji Dergisi, 2017 Invasive fungal sinusitis is an infection of the paranasal sinuses that should be diagnosed early due to its high mortality and morbidity rates. Mucormycosis and aspergillus are the two most important agents of invasive fungal sinusitis. Although usually
Ayşe Yağmur Çolak +7 more
doaj +1 more source
BMC Neurology, 2023 Background Tolosa-Hunt syndrome (THS) is characterized by painful ophthalmoplegia caused by idiopathic granulomatous inflammation involving the cavernous sinus region. Patients respond well to steroid therapy.
Wei He +5 more
doaj +1 more source