Results 1 to 10 of about 8,863 (108)
Oculomotor Nerve Palsy After Influenza Vaccine in Inflammatory Bowel Disease [PDF]
Influenza and pneumococcal vaccines are recommended in inflammatory bowel disease patients. Several neurologic complications have been reported after influenza vaccines, such as Guillain-Barre syndrome, chronic inflammatory demyelinating polyneuropathy, and acute disseminated encephalomyelitis; however, rarely, oculomotor palsy will occur.
Essrani, Rajesh +4 more
openaire +2 more sources
We present pathology of the peripheral nerves of a patient with Adult-onset Charcot-Marie-Tooth disease 4F caused by periaxin gene mutation p.D651N. The patient was a 72-year-old woman. She had hoarseness and underwent continuous positive airway pressure therapy at night due to sleep apnea. The patient died abruptly.
Kengo Maeda +8 more
openaire +3 more sources
Protein S deficiency manifesting simultaneously as central retinal artery occlusion, oculomotor nerve palsy, and systemic arterial occlusive diseases [PDF]
Protein S deficiency manifesting simultaneously as central retinal artery occlusion, oculomotor nerve palsy, and systemic arterial occlusive ...
B K Loh, S Y Lee, K Y Goh
openaire +1 more source
A case of oculomotor nerve paresis associated with paranasal sinusitis disease.
症例は64歳の男性。両眼性複視を主訴に2000年3月9日に来院した。眼位は第一眼位で右眼20ΔXT、外斜偏位は左方視で増加した。眼球運動検査ではむき眼位、ひき眼位でともに右眼内直筋の著明な遅動が認められた。他に右眼眼瞼下垂と輻輳不全が見られた。瞳孔反応は正常であった。右眼動眼神経不全麻痺の状態を呈していた。症例には蓄膿の手術歴があったので、精査目的で耳鼻咽喉科に紹介した。CTとMRI検査の結果、右上顎洞に膿貯留と思われるmassが認められ、右術後性上顎洞嚢胞と診断された。2000年3月15日穿刺排膿術を受けた。1週間後、両眼性複視は消失し眼球運動も正常となった。症例は副鼻腔疾患が原因で動眼神経不全麻痺を呈したものと思われた。両眼性複視を主訴とする症例に対しては、関連臨床科 ...
Takasaki, Hiroko +2 more
openaire +2 more sources
This review presents recent progress in vision‐augmented wearable interfaces that combine artificial vision, soft wearable sensors, and exoskeletal robots. Inspired by biological visual systems, these technologies enable multimodal perception and intelligent human–machine interaction.
Jihun Lee +4 more
wiley +1 more source
Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet +10 more
wiley +1 more source
ABSTRACT Arthrogryposis Multiplex Congenita (AMC) encompasses several hundred conditions with diverse genetic, pathophysiological, and clinical origins. The overarching EXPLAIN study explores underlying causes and implications of AMC and represents the largest clinical cohort of adults with AMC reported to date.
My Vuong Hermansen +5 more
wiley +1 more source
Precision therapies for genetic epilepsies in 2025: Promises and pitfalls
Abstract By targeting the underlying etiology, precision therapies offer an exciting paradigm shift to improve the stagnant outcomes of drug‐resistant epilepsies, including developmental and epileptic encephalopathies. Unlike conventional antiseizure medications (ASMs) which only treat the symptoms (seizures) but have no effect on the underlying ...
Shuyu Wang +3 more
wiley +1 more source
Abstract Purpose To investigate the diagnostic performance of ultrasound, 2‐deoxy‐2‐[18F]fluoro‐D‐glucose positron emission tomography/computed tomography (2‐[18F]FDG PET/CT) and temporal artery biopsy (TAB) in giant cell arteritis (GCA). Methods This was a prospective single‐centre diagnostic accuracy study (ClinicalTrials.gov NCT05248906).
Michael S. Hansen +10 more
wiley +1 more source
Abstract Purpose Physiological pulsations driven by cardiac, respiratory, and vasomotor activity are essential for solute transport within perivascular and perineural cerebrospinal fluid (CSF) pathways that support brain and eye clearance systems. Previous studies have shown that parasympathetic blockade significantly reduces ocular pulsation power and
Ebrahimi Seyed‐Mohsen +9 more
wiley +1 more source

