Медицинский совет, 2017 In summary, this review provides complex presentation of the most contemporary concepts of pathogenesis, clinical presentation and therapy of diabetic polyneuropathies.
M. M. Tanashyan +2 more
doaj +1 more source
Advances in the diagnosis, immunopathogenesis and therapies of IgM-anti-MAG antibody-mediated neuropathies. [PDF]
, 2018 Polyneuropathy with immunoglobulin M (IgM) monoclonal gammopathy is the most common paraproteinemic neuropathy, comprising a clinicopathologically and immunologically distinct entity.
Dalakas, Marinos
core +2 more sources
Health-related quality of life in hereditary transthyretin amyloidosis polyneuropathy: a prospective, observational study [PDF]
, 2020 Background Hereditary Transthyretin Amyloidosis Polyneuropathy is a rare life-threatening neurologic disease that imposes considerable mortality and it is associated with progressive related disabilities.
Coelho, Teresa +5 more
core +2 more sources
Polüneuropaatiad ja nende diagnoosimise tänapäevased kriteeriumid [PDF]
, 2002 Polüneuropaatiad on suhteliselt suure levimusega haigusterühm, mille diagnoosimine ei ole alati lihtne. Lisaks kliiniliste avalduste tundmisele on paljudel juhtudel vältimatu elektrofüsioloogiliste uurimismeetodite rakendamine.
Asser, Toomas +3 more
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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
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Нервно-мышечные болезни, 2021 Dysimmune polyneuropathies are the etiologically heterogeneous group of diseases with autoimmune damage to the peripheral nervous system. The rarity of these diseases doesn’t exclude the possibility of their development or exacerbation in patients ...
A. E. Khrulev +7 more
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Broadening the Clinical Spectrum of Axonal Hereditary Neuropathies: A Comparative Case Study on DNAJB2- and HINT1-Related Disease. [PDF]
J Peripher Nerv SystABSTRACT Background and Aims Differentiating hereditary axonal polyneuropathies caused by distinct gene variants remains a clinical challenge. This comparative case study of DNAJB2‐ and HINT1‐related neuropathies aimed to broaden the phenotypic spectrum associated with these genes and to explore non‐motor symptoms and quality of life (QoL) in affected ...
Bjelica B +8 more
europepmc +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
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Clinical case of atypical course of Crohn’s disease
Patologìâ, 2023 Crohn’s disease (CD) is a chronic recurrent inflammatory bowel disease with a wide variety of clinical manifestations – from classical gastrointestinal phenotypes to predominance of extraintestinal symptoms.
L. V. Zhuravlyova +5 more
doaj +1 more source
Clinical and electrophysiological features of peripheral neuropathy in older patients with lung carcinoma [PDF]
Vojnosanitetski Pregled, 2020 Background/Aim. Peripheral nervous system affection in people with lung cancer is commonly associated with paraneoplastic neuropathy. However, clinical studies evaluating the frequency, clinical, and electrophysiological characteristics of peripheral ...
Tomanović-Vujadinović Sanja +9 more
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