Results 201 to 210 of about 18,796 (241)

Dysautonomia in the Ehlers–Danlos syndromes and hypermobility spectrum disorders—With a focus on the postural tachycardia syndrome

American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 2021
Dysautonomia (autonomic dysfunction) occurs in the Ehlers–Danlos syndromes (EDS) and hypermobility spectrum disorders (HSD). Symptoms include palpitations, dizziness, presyncope, and syncope, especially when standing upright.
C. Mathias, A. Owens, V. Iodice, A. Hakim   +3 more
semanticscholar   +1 more source

Cardiovascular dysautonomia and cognitive impairment in Parkinson's disease (Review)

Medicine International
Cognitive impairment is a prevalent non-motor symptom of Parkinson's disease (PD), which can result in significant disability and distress for patients and caregivers. There is a marked variation in the timing, characteristics and rate at which cognitive
I. Khalil, R. Sayad, A. Kedwany, Hager Hamdy Sayed, A. Caprara, J. Rissardo   +5 more
semanticscholar   +1 more source

Assessing Full Stomach Prevalence with Ultrasound Following Preoperative Fasting in Diabetic Patients with Dysautonomia: A Comparative Observational Study

Anesthesia and Analgesia
BACKGROUND: Traditionally, diabetics have been considered patients with a high risk of aspiration due to having delayed gastric emptying; However, the evidence concerning residual gastric volume (GV) in fasting diabetic patients is inconsistent.
J. A. Sastre, Teresa López, Roberto Julián, Domingo Bustos, Raquel Sanchís-Dux, Yaiza Molero-Diez, Álvaro Sánchez-Tabernero, F. A. Ruiz-Simón, M. Sanchez-Hernandez, M. Gómez-Ríos   +9 more
semanticscholar   +1 more source

TS‐HDS and FGFR3 antibodies in small fiber neuropathy and Dysautonomia

Muscle and Nerve, 2021
The specificity of trisulfated heparin disaccharide/fibroblast growth factor receptor 3 (TS‐HDS/FGFR3) antibodies in the diagnosis of autoimmune small fiber neuropathy (SFN) is unclear.
J. A. Trevino, P. Novak
semanticscholar   +1 more source

Postganglionic cholinergic dysautonomia

Annals of Neurology, 1977
AbstractA 9‐year‐old boy presented with symptoms and signs of marked postganglionic cholinergic autonomic dysfunction manifested by bilateral internal ophthalmoplegia, impaired secretion of tears and saliva, lack of gastrointestinal motility, atony of the bladder, generalized absence of sweating, and hypertension.
S I, Harik, M H, Ghandour, F S, Farah, A K, Afifi   +3 more
openaire   +2 more sources

Sympathetic Cardioneuropathy in Dysautonomias

New England Journal of Medicine, 1997
The classification of dysautonomias has been confusing, and the pathophysiology obscure. We examined sympathetic innervation of the heart in patients with acquired, idiopathic dysautonomias using thoracic positron-emission tomography and assessments of the entry rate of the sympathetic neurotransmitter norepinephrine into the cardiac venous drainage ...
D S, Goldstein, C, Holmes, R O, Cannon, G, Eisenhofer, I J, Kopin   +4 more
openaire   +3 more sources

Intelligence in Dysautonomia

Pediatrics, 1979
The study of 53 patients with dysautonomia by Welton et al (Pediatrics 63:708, 1979) is the most extensive survey of mental ability in this condition yet published. The conclusion is drawn "that the same proportion of the dysautonomic population scored within the average range of intelligence as if found in the general population." The ...
openaire   +2 more sources

Dysautonomia associated with immune checkpoint inhibitors

Journal of Neurology, 2023
Toshiki Tezuka, S. Okuzumi, Chiho Nakashima, T. Ide, S. Imai, Satoru Mitsuboshi, Y. Kuwahara, T. Takizawa, Morinobu Seki, N. Minematsu, N. Aragane, J. Nakahara, Satoko Hori, S. Nakane, Shigeaki Suzuki   +14 more
semanticscholar   +1 more source

Dysautonomia, Hypermobility Spectrum Disorders and Mast Cell Activation Syndrome as Migraine Comorbidities

Current Neurology and Neuroscience Reports, 2023
S. Blitshteyn
semanticscholar   +1 more source

Dysautonomias in amyloidosis

Nervenheilkunde, 2013
SummarySystemic amyloidosis is a life-threatening and frequently unrecognized cause of dysautonomia. Autonomic neuropathy is a common manifestation of AL amyloidosis (caused by deposition of an immunoglobulin free light chain produced by an underlying plasma cell clone) and of autosomal dominant hereditary ATTR amyloidosis (caused by a transthyretin ...
openaire   +2 more sources