Results 81 to 90 of about 10,570 (239)
Ocular Neuromyotonia—A Rare but Reversible Cause of Intermittent Diplopia
Movement Disorders Clinical Practice, EarlyView.
Parthvi Ravat +4 more
wiley +1 more source
European Journal of Neurology, Volume 32, Issue 8, August 2025.We analysed the clinical, electrophysiological, and genetic features of 103 patients from 89 families with SH3TC2 gene mutations identified in 27 French University Hospitals causing Charcot–Marie‐Tooth type 4C (CMT4C) demyelinating peripheral neuropathy.
Pauline Jaubert +36 more
wiley +1 more source
Bilateral thalamic infarcts presenting oculomotor nerve palsy: case report [PDF]
, 2017 Bilateral thalamic infarctions are rare; oculomotor nerve palsy can be the result of direct or indirect damage to the oculomotor nerve. We report a case of oculomotor nerve palsy associated with changes in visual pattern and speech disturbances. There is
Jammula, Poornima +3 more
core +1 more source
Evaluation of strain values of critical anatomic regions for two different pterygomaxillary approaches in Le Fort I osteotomy : an experimental study [PDF]
, 2017 The purpose of this experimental study was to measure stresses both on the pterygoid plates and the skull base following two different pterygomaxillary approaches in Le Fort I osteotomy. The prepared skull models were randomly divided into 2 groups of 7.
Dolanmaz, Dogan +4 more
core +1 more source
The Two Faces of Pediatric SCA2
European Journal of Neurology, Volume 32, Issue 8, August 2025.We report 22 children with SCA2 and a review of the literature (20 patients). Two pediatric forms appear to be distinct (infantile and juvenile). Figure created with https://BioRender.com. ABSTRACT Introduction Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant neurological disease usually described in adults.
Nicolas Rive Le Gouard +36 more
wiley +1 more source
eNeurologicalSci, 2019 A 66 year-old woman presented with a pupil-sparing partial third cranial nerve palsy with aberrant regeneration. Imaging revealed a cystic lesion in the right cavernous sinus, demonstrating signal characteristics consistent with arachnoid cyst ...
Kelly A. Malloy +2 more
doaj
Are there predictive pupillometry markers in determining external ventricular device (EVD) weaning failure or success in subarachnoid hemorrhage patients? [PDF]
, 2018 Pupillometers objectively measure constriction (i.e., parasympathetic pathwy) and dilation (i.e., sympathetic pathway) velocities of the pupillary reflex.
Bezner, Tracy +4 more
core +1 more source
Protein Coaggregation in Caribbean Atypical Parkinsonism: The Contribution of Annonacin
Neuropathology and Applied Neurobiology, Volume 51, Issue 4, August 2025.Caribbean atypical Parkinsonism (CAP) is believed to be associated with the consumption of Annonaceae plant products containing the mitochondrial toxin, annonacin. The analysis of brain samples from CAP patients revealed a co‐pathology involving tau and α‐synuclein (αS) in the majority of cases.
Florencia González‐Lizárraga +13 more
wiley +1 more source
Radiology Case Reports, 2021 The oculomotor nerve palsy is a rare neurological deficit, it is associated with numerous underlying pathologies. Including stroke, neoplasms, trauma, post-surgical inflammation, and microvascular damage from chronic disease.
Nizar Almaghrabi, MBBS +2 more
doaj
Clinical factors underlying a single surgery or repetitive surgeries to treat superior oblique muscle palsy [PDF]
, 2015 The purpose of this study is to know clinical factors underlying either a single surgery or repetitive surgeries, required to treat superior oblique muscle palsy.
Aoba, Kana +3 more
core +1 more source