Results 31 to 40 of about 39,959 (306)
Clinical and laboratory status in Parkinson’s disease patients with and without polyneuropathy [PDF]
Vojnosanitetski PregledBackground/Aim. The etiology of polyneuropathy (PNP) in patients with Parkinson’s disease (PD) is unclear, and there is a possible association between levodopa therapy, hyperhomocysteinemia, and PNP development due to methylation processes involving ...
Popović Sanela +4 more
doaj +1 more source
Allergic granulomatous angiitis [PDF]
Vojnosanitetski Pregled, 2004 Allergic granulomatous angiitis (AGA) - Churg-Strauss syndrome, is a rare autoimmune disease characterized by three distinct clinical phases prodromal, eosinophilic, and vasculitic, and most of respiratory symptoms and signs begin in the first two phases
Trifunović Gordana +4 more
doaj +1 more source
Disease networks identify specific conditions and pleiotropy influencing multimorbidity in the general population [PDF]
, 2018 Multimorbidity is an emerging topic in public health policy because of its increasing prevalence and socio-economic impact. However, the age- and gender-dependent trends of disease associations at fine resolution, and the underlying genetic factors ...
Amell, A. +3 more
core +2 more sources
DAMAGE OF NERVOUS SYSTEM IN TICK-BITE BORRELIOSIS (LYME DISEASE) IN СHILDREN IN THE KIROV REGION
Детские инфекции (Москва), 2017 During 1993—2016 there were treated 1255 children 9 months — 14 ages old with tick-bite infections in Kirov Infectious Clinical Hospital and 1214 children from them with the verified diagnosis of Lyme disease. Damage of nervous system was detected in 98 (
T. V. Egorova +2 more
doaj +1 more source
Syndrome of Inappropriate Secretion of Antidiuretic Hormone Preceding Guillain-Barré Syndrome [PDF]
Journal of Clinical and Diagnostic Research, 2017 Guillain–Barré Syndrome (GBS) is an inflammatory polyradiculoneuropathy which is known to produce syndrome of inappropriate Secretion of Antidiuretic Hormone (SIADH). However, the hyponatremia is usually seen after the onset of weakness. Here, we report
JOE JAMES, JAMES JOSE
doaj +1 more source
Case series of pyridoxine-induced neuropathy [PDF]
Journal of Medicine and Life ScienceExcess of pyridoxine, in contrast to other nutrients, may result in neuropathy. Case reports are sparse, and little is known about the clinical and electrophysiological findings.
Jihee Ko, Sa-Yoon Kang
doaj +1 more source
Giant axonal neuropathy: A differential diagnosis of consideration
The Turkish Journal of Pediatrics, 2019 Giant axonal neuropathy (GAN) is a rare neurodegenerative disorder affecting both the central and peripheral nervous systems progressively. The recessive mutations of the GAN gene are responsible for the disease.
Pınar Edem +4 more
doaj +1 more source
Diagnostics, 2023 Various primarily non-autoimmune neurological disorders occur synchronously with autoantibodies against tissues in the nervous system. We aimed to assess serum and cerebrospinal fluid (CSF) autoantibodies in children with neurologic disorders.
Karol Lubarski +5 more
doaj +1 more source
Postgraduate Medical Journal, 1975 Summary Two cases of polyneuropathy occurring after rubella infections are described, together with the nerve biopsy and serological findings.
openaire +2 more sources
Familial amyloidosis with polyneuropathy type 1 caused by transthyretin mutation Val50Met (Val30Met): 4 cases in a non-endemic area [PDF]
, 2018 Introduction: Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) typically arises as an autonomic neuropathy primarily affecting small fibres and it occurs in adult patients in their second or third decades of life. It progresses rapidly and
Andrés, N. +2 more
core +3 more sources