Results 91 to 100 of about 16,532 (175)

MSA Mimic? Rare Occurrence of Anti-Hu Autonomic Failure and Thymoma in a Patient with Parkinsonism: Case Report and Literature Review

Frontiers in Neuroscience, 2018
Thymoma is a tumor originating from thymic gland, frequently manifesting with paraneoplastic neurological disorders. Its association with paraneoplastic dysautonomia is relatively uncommon.
Vito A. G. Ricigliano, Barbara Fossati, Lorenzo Saraceno, Michele Cavalli, Elena Bazzigaluppi, Giovanni Meola, Giovanni Meola   +6 more
doaj   +1 more source

Dysautonomia and its underlying mechanisms in the hypermobility type of Ehlers-Danlos syndrome

, 2014
Objectives: Many non-musculoskeletal complaints in EDS-HT may be related to dysautonomia. This study therefore aims to investigate whether dysautonomia is present and to explore the underlying mechanisms. Methods: A total of 39 females with EDS-HT and 35
De Wandele, Inge, Malfait, Fransiska, Leybaert, Luc, Van de Borne, Philippe, De Paepe, Anne, Calders, Patrick, Rombaut, Lies, De Backer, Tine   +7 more
core   +1 more source

Clinical Neuro-Ophthalmic Findings in Familial Dysautonomia

, 2011
Familial dysautonomia (FD) or Riley Day Syndrome is a recessive hereditary sensory and autonomic neuropathy caused by mutations in the IKBKAP gene.
Carlos Mendoza-Santiesteban; Thomas R. Hedges III; Felicia Axerold; Horacio Kaufmann; Floyd Warren
core  

Dysautonomia after traumatic brain injury: a forgotten syndrome?

, 1999
Objectives—To better establish the clinical features, natural history, clinical management, and rehabilitation implications of dysautonomia after traumatic brain injury, and to highlight difficulties with previous nomenclature.
Kim Felmingham (14736400), Nicholls, JL (15543785), Gurka, JA (15543788), Crooks, J (15543782), Wade, LD (15543791), Baguley, IJ (15543686)   +5 more
core  

Cardiac-locked bursts of muscle sympathetic nerve activity are absent in familial dysautonomia

, 2013
Familial dysautonomia (Riley–Day syndrome) is an hereditary sensory and autonomic neuropathy (HSAN type III), expressed at birth, that is associated with reduced pain and temperature sensibilities and absent baroreflexes, causing orthostatic hypotension ...
Norcliffe-Kaufmann, Lucy, Kaufmann, Horacio, Axelrod, Felicia B., Macefield, Vaughan G. (R11708)   +3 more
core   +1 more source

Early‐Onset Wild‐Type Transthyretin Amyloidosis Polyneuropathy

Muscle &Nerve, Volume 74, Issue 5, Page 1471-1475, November 2026.
Chafic Karam, Kaylee Baker, Sami Khella, Brian Drachman, Pranav Chandrashekar, MacLean Nasrallah, Shunsuke Koga, Janice Pieretti   +7 more
wiley   +1 more source

Outbreak of dysautonomia (Key-Gaskell syndrome) in a closed colony of pet cats

, 2003
Six of eight pet cats in a closed colony developed overt signs of dysautonomia over a period of seven days; two of them died and one was euthanased. Dysautonomia was confirmed histopathologically in two of these cats, and in the others the diagnosis was ...
Nart, P., Reid, S.W.J., D. J. Mellor, F. Nunn, Mellor, D.J., T. A. Cave, C. Knottenbelt, Cave, T.A., P. Nart, Knottenbelt, C., Nunn, F., S. W. J. Reid   +11 more
core   +1 more source

Complex Dysautonomia in a Patient With Cerebral Cavernous Malformations Due to a KRIT1 Pleiotropic Gene Mutation

Dysautonomia is a disruption of the body's autonomic processes. Symptoms vary among patients, depending on the underlying disease pathways. Given that symptoms can affect all organ functions, dysautonomia often significantly impacts quality of life ...
Koek, Ger, Jacobi, Linda; id_orcid, Ariëns, Maxime, van Genugten, Jessie, Janssen, Roel   +4 more
core   +1 more source

Hyperventilation during rest and exercise in orthostatic intolerance and Spiky-Leaky Syndrome

Frontiers in Neurology
BackgroundOrthostatic intolerance, with or without postural orthostatic tachycardia syndrome (POTS), is collectively referred to as orthostatic intolerance dysautonomia syndromes (OIDS).
Amir Hashemizad, Jerriel Dela Cruz, Aditya Narayan, Andrew J. Maxwell   +3 more
doaj   +1 more source

Case report: Treatable immune-mediated severe orthostatic hypotension in SARS-CoV-2 infection

Frontiers in Neuroscience
We report a patient with autonomic dysfunction following acute SARS-CoV-2 infection, presenting progressively worsening severe orthostatic hypotension to the point where she could no longer sit or stand. The patient experienced a delay in diagnosis after
Kenji Theiler, Maroussia Bronchain, Eric Grouzmann, Serge Duflon, Lorenz Hirt, Renaud Du Pasquier, Gérard Waeber, Grégoire Wuerzner, Karin Diserens, Julien F. Bally   +9 more
doaj   +1 more source