Results 81 to 90 of about 95,248 (189)

Progressive respiratory depression and bulbar palsy: question

, 2016
Progressive respiratory depression and bulbar palsy ...
HK Kok (14446083), A O'Hare (13627480), J Thornton (9247274), C Logan (13379202), Hamed Asadi (13059153), F Kavanagh (13655752), P Brennan (7696562), S Looby (13601470)   +7 more
core  

Misdiagnosis: Hypoglossal palsy mimicking bulbar onset amyotrophic lateral sclerosis

eNeurologicalSci, 2019
Bulbar onset amyotrophic lateral sclerosis (bALS) is a currently incurable neurodegenerative condition characterized by insidious progression of bulbar muscle paresis; namely dyspnea, dysarthria, and dysphagia. The diagnosis of bALS requires exclusion of
Eric D. Goldstein, Benjamin H. Eidelman
doaj   +1 more source

Thermoregulatory and plasma neurobiomarker responses to heat tolerance assessment in exertional heat illness and matched controls

Experimental Physiology, EarlyView.
Abstract Exercise in the heat and elevated tissue temperature are associated with neuronal stress and changes in blood–brain barrier (BBB) function. More severe thermal insult may manifest as exertional heat illness (EHI) and complication by central nervous system (CNS) dysfunction may persist post‐EHI.
Tom W. Palin, Jo Corbett, Lisa J. Hill, David R. Woods, Alex A. M. Gould, Barney Wainwright, James A. Roberts, Chloe N. Thomas, Daniel Snape, Carol House, Omar Tayari, Richard J. Elsworthy, James L. Mitchell, Andrew J. Roberts, John P. O'Hara, Michael J. Stacey   +15 more
wiley   +1 more source

A case of bulbar palsy associated with Sjoegren syndrome.

Nihon Naika Gakkai Zasshi, 1988
61才,男性,構語障害,舌の軽度萎縮,線維性〓縮を認めたが,四肢の脱力,筋萎縮はなし.血沈1時間52mm, CRP(+), ANF80倍(sp). IgG 2040mg/dl.免疫複合体1.21μg/ml.筋電図上,舌筋で神経原性変化を認めた. Sjogren症候群の合併が認められ,ステロイドパルス治療で,血液検査値は改善,症状もやや改善した.最近,筋萎縮性側索硬化症における免疫異常などが注目されており,興味ある症例と考えられる.
YAMASHITA, Kazuya, KOBAYASHI, Shotai, YAMAGUCHI, Shuhei, OKADA, Kazunori, ARIMOTO, Satao, FUJIHARA, Shigeyoshi, SHIMODE, Kouichi, IMAOKA, Kaoru, TSUNEMATSU, Tokugoro   +8 more
openaire   +3 more sources

Innovative Therapeutic Endoscopy of the Upper Gastrointestinal Tract: Review of the Japan Gastroenterological Endoscopy Society Core Sessions

DEN Open, Volume 7, Issue 1, April 2027.
ABSTRACT The Japanese Gastroenterological Endoscopy Society (JGES) established four core sessions on endoscopic treatment for upper gastrointestinal diseases under the theme ‘Innovative Therapeutic Endoscopy’ between 2023 and 2024. This review summarizes these sessions and compiles them as a conference report. At the 105th JGES Core Session, 14 studies
Mikitaka Iguchi, Tomoki Michida, Yasuhiko Abe, Hisashi Doyama, Noriya Uedo, Hajime Isomoto, Masayuki Ohta, Junko Fujisaki   +7 more
wiley   +1 more source

A longitudinal study of motor, oculomotor and cognitive function in progressive supranuclear palsy

, 2013
ObjectiveWe studied the annual change in measures of motor, oculomotor and cognitive function in progressive supranuclear palsy. This had twin objectives, to assess the potential for clinical parameters to monitor disease progression in clinical trials ...
Boyd C P Ghosh, Roger H. S. Carpenter, Roger H S Carpenter, James B. Rowe, Carpenter, Roger H.S., Rowe, James B., James B Rowe, Ghosh, Boyd C.P., Boyd C. P. Ghosh, Ghosh Boyd C. P., Rowe James B., Carpenter Roger H. S.   +11 more
core   +1 more source

A Case of Miller−Fisher Overlap Syndrome With Positive Anti‐GM4 Antibody and Atypical Symptoms

Immunity, Inflammation and Disease
Background Miller−Fisher syndrome (MFS) is a recognized clinical variant of Guillain−Barré syndrome (GBS), characterized by the classic triad of ophthalmoplegia, ataxia, and areflexia.
Miao Tang, Runhong Tang, Jian Xu, Zhenyu Yang, Bo Zhang, Yinhua Yan, Jiahui Xie, Qiong Long, Zhi Li, Ewen Tu   +9 more
doaj   +1 more source

Guillain‐Barré Syndrome in Late Pregnancy Following Respiratory Syncytial Virus Infection: A Diagnostic Dilemma

Clinical Case Reports, Volume 14, Issue 11, November 2026.
ABSTRACT The diagnosis of Guillain–Barré syndrome (GBS) relies on evolving clinical features, supported by cerebrospinal fluid (CSF), laboratory investigations, and electrodiagnostic studies. Early investigations may be nondiagnostic and should not delay treatment when progressive neurological deterioration raises clinical suspicion of GBS.
Rhiana Pereira‐Lindley, Mesharck Gariba, Darshan Lal   +2 more
wiley   +1 more source

Isolated bulbar palsy with anti-GM3 and GT1b antibodies

, 2013
Isolated acute bulbar palsy has been described as one of the more rare variants of Guillain-Barre? syndrome. IgG anti-ganglioside antibodies are associated with axonal subtypes of Guillain-Barre? syndrome as well as Fisher syndrome.
Siti Ayuni Binti Zakyudin
core  

A CADASIL Case Presenting with Progressive Bulbar Palsy Caused by Acute Simultaneous Multiple Subcortical Infarcts

Bezmiâlem Science, 2019
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an adult-onset inherited small vessel disease of the brain caused by NOTCH3 mutations.
Elif GÖKÇAL, Mehmet KOLUKISA, Nihat MUSTAFAYEV, Talip ASİL   +3 more
doaj   +1 more source