Results 121 to 130 of about 221,497 (291)

Risk of Non‐Arteritic Anterior Ischemic Optic Neuropathy in Idiopathic Intracranial Hypertension Patients Treated with GLP‐1 Receptor Agonists

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Introduction Glucagon‐like peptide‐1 receptor agonists (GLP‐1 RAs) have demonstrated significant weight‐reducing effects and may offer benefits in idiopathic intracranial hypertension (IIH); however, recent concerns about the risk of non‐arteritic anterior ischemic optic neuropathy (NAION) have emerged.
Faisal A. Al‐Harbi, Mohanad A. Alkuwaiti, Yazeed B. Alaql, Ahmed K. Alsaif, Ahmed A. Alessa, Meshari Ayed Alharbi, Mohammed Alfalah, Saud A. Alnaaim, Sajjad M. AlHaddad, Ahmed Y. Azzam   +9 more
wiley   +1 more source

Anti‐CD19 CAR T Cells in Autoimmune Encephalitis: Inflammation Controlled, Neurodegeneration Unchecked?

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Just recently, successful chimeric antigen receptor (CAR) T cell therapy was reported in the first patient with refractory, anti‐diacylglycerol lipase alpha (DAGLA) antibody‐mediated autoimmune encephalitis, achieving partial clinical remission.
Dimitrios Mougiakakos, Marwa Al‐Dubai, Denise Walther, Dominic Borie, Jan D. Lünemann, Marc Pawlitzki, Sven G. Meuth, Solveig Henneicke, Stefan Vielhaber, Stefanie Schreiber   +9 more
wiley   +1 more source

Cerebellar form of multiple system atrophy: A case report

Multiple system atrophy is a form of synucleinopathy with an unknown etiology that causes progressive neurodegeneration. It may affect the cerebellum, autonomic nerves, and pyramidal and extrapyramidal systems.
Houda Alloussi, MD, Ahmad Bourazza, MD, Mohamed Hamid, MD, Sara Slimani, MD   +3 more
core   +1 more source

Clinical and imaging characteristics of dementia in multiple system atrophy

, 2019
Amyloid; Cortical thickness; Dementia; Multiple system atrophy (MSA); Pittsburgh Compound B ...
윤지영
core   +1 more source

Association Between Motor Pathway Damage and Motor Deficit in Upper and Lower Limb in People With MS

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Corticospinal tract damage is common in people with MS, but the degree of clinical symptoms varies. We hypothesize that corticospinal tract lesions are more extensive and severe in people with MS with motor impairments in both upper and lower limbs.
Mathilde Liffran, Malo Gaubert, Alice Dufey, Elise Bannier, Audrey Rico, Jean‐Christophe Ferré, Raphaël Chouteau, Laure Michel, Emmanuelle Le Page, Virginie Callot, Bertrand Audoin, Sarah Demortière, Benoît Combès, Anne Kerbrat   +13 more
wiley   +1 more source

Editorial: Autonomic dysfunction in multiple system atrophy

Frontiers in Neurology, 2022
Tatsuya Yamamoto, Tatsuya Yamamoto, Maria Teresa Pellecchia, Ryuji Sakakibara   +3 more
doaj   +1 more source

Recurrent Hypothermia and Autonomic Dysfunction Secondary to Shapiro Syndrome

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT A 44‐year‐old man presented with recurrent hypothermia, diaphoresis and hypertension. Extensive investigation for infectious, inflammatory, metabolic and endocrine aetiologies was negative. MR scan of the brain demonstrated no lesions but revealed callosal dysgenesis, consistent with Shapiro syndrome.
Naveen Kumar, Jeremy Johnson, Susanne Watkins, Eoin Mulroy   +3 more
wiley   +1 more source

Uric acid as a potential disease modifier in patients with multiple system atrophy

, 2011
BACKGROUND: Recent studies have suggested that mitochondrial dysfunction and oxidative stress play a key role in the pathogenesis of multiple system atrophy.
이지은, 이필휴, 손영호
core   +1 more source

MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives The study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first‐time pediatric ON in the post‐MOG‐IgG era. Methods This was a single‐center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first‐time ON between 2018–2024, with follow‐up data collected through 2025.
Chaitanya Aduru, Akansha Chandrasekar, Kyla Blasingame, Jonathan Rosen, Jesse M. Levine, Karla Salazar, Madhuri Chilakapati, Rod Foroozan, Victoria Hardwick, Jonathan M. Yarimi, Nikita Shukla, Timothy E. Lotze, Kristen S. Fisher, Alexander J. Sandweiss   +13 more
wiley   +1 more source

Intronic FGF14 GAA repeat expansions impact progression and survival in multiple system atrophy.

Partial phenotypic overlap has been suggested between multiple system atrophy and spinocerebellar ataxia 27B, the autosomal dominant ataxia caused by an intronic GAA•TTC repeat expansion in FGF14. In this study, we investigated the frequency of FGF14 GAA•
Vijiaratnam, Nirosen, Pastinen, Tomi, Meissner, Wassilios G., Cras, Patrick, Hadjivassiliou, Marios, Murphy, David, Leigh, P. Nigel, Chelban, Viorica, Cheung, Warren A., Dicaire, Marie-Jos\ue9e, Brais, Bernard, Beichert, Lukas, Crosiers, David, Self, Eleanor, Danzi, Matt C., Ashton, Catherine, Foltynie, Tom, Goh, Yen Yee, Rowe, James B., Corvol, Jean-Christophe, Jaunmuktane, Zane, Pellerin, David, Bonnet, C\ue9line, De Vil, Bart, Lee, Cameron, Lee, Hamin, Trinh, Joanne, Archibald, Neil, Seilhean, Danielle, Girges, Christine, Renaud, Mathilde, Synofzik, Matthis, Mohammad, Rahema, Scardamaglia, Annarita, Farrer, Matthew J., Gveric, Djordje O., La\u3b2, Joshua, Iruzubieta, Pablo, Gustavsson, Emil K., Morris, Huw R., Roth, Virginie, Warner, Tom, Zuchner, Stephan, Follett, Jordan, Wandzel, Marion, Rittman, Timothy, Brown, Lauren, Houlden, Henry, Sambin, Sara, Ostrozovicova, Miriama, Sieben, Anne, Lehericy, Stephane, Curless, Toby   +52 more
core   +3 more sources