Zobrazeno 1 - 10
of 43
pro vyhledávání: '"hereditary polyneuropathy"'
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-9 (2024)
Abstract Background Charcot–Marie–Tooth disease is a spectrum of inherited disorders characterized by both motor and sensory manifestations, which include prominent distal muscle weakness, foot deformities (pes cavus and hammer toes), and sensory
Externí odkaz:
https://doaj.org/article/a33b7b57e8154d93a792d00b39ae99f2
Akademický článek
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Autor:
Britt Stævnsbo Pedersen, Louise Sloth Kodal, Anna Bundgaard Kaalund, Sonja Holm-Yildiz, Mette Merete Pedersen, Tina Dysgaard
Publikováno v:
Frontiers in Physiology, Vol 14 (2023)
Introduction: Polyneuropathy (PNP) is a chronic progressive disease that over time can lead to damage of sensory, motor and/or autonomic peripheral nerves. Symptoms vary from predominantly sensory to severe sensorimotor affection both proximally and
Externí odkaz:
https://doaj.org/article/83678a4e65e5407db2a35912e507db0e
Autor:
Olga A. Klochkova, Alexey L. Kurenkov, Natalya V. Zhurkova, Kirill V. Savostyanov, Ilya S. Zhanin, Ayaz M. Mamedyarov, Ilona M. Tardova
Publikováno v:
Вопросы современной педиатрии, Vol 16, Iss 4, Pp 326-333 (2017)
Autosomal recessive peripheral neuropathy with neuromyotonia (ARAN-NM) is a relatively newly described disease associated with mutations in the HINT1 gene. It accounts for a significant part of the poorly differentiated forms of axonal polyneuropathi
Externí odkaz:
https://doaj.org/article/1e08c8c623fc4af59ecbada229c00dea
Autor:
Dominique Endres, Simon J. Maier, Christiane Ziegler, Kathrin Nickel, Anne N. Riering, Benjamin Berger, Johann Lambeck, Miriam Fritz, Birgitta Gläser, Friedrich Stock, Michael Dacko, Thomas Lange, Irina Mader, Katharina Domschke, Ludger Tebartz van Elst
Publikováno v:
Frontiers in Psychiatry, Vol 10 (2019)
Background: Schizophrenic disorders are common and debilitating due to their symptoms, which can include delusions, hallucinations, and other negative symptoms. Organic forms can result from various cerebral disorders. In this paper, we discuss a pot
Externí odkaz:
https://doaj.org/article/d9bf7022727a420e9ee92af52d603cc4
Autor:
Trubelja, Tamara
Polineuropatija je bolest koja zahvaća više skupina živaca uz veoma širok spektar simptoma što navodi na potrebu za vrlo pažljivom dijagnostikom same bolesti. Oštećenja koja izaziva ta bolest zahvaćaju motorna, senzorna i autonomna živčana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3702::4ab8cd0bd31a832280735991ddc6b7eb
https://repozitorij.unin.hr/islandora/object/unin:5847
https://repozitorij.unin.hr/islandora/object/unin:5847
Publikováno v:
Brain Sciences, Vol 10, Iss 12, p 952 (2020)
Hereditary amyloid transthyretin (ATTRv) amyloidosis with polyneuropathy is a progressive disease that is transmitted as an autosomal dominant trait and characterized by multiple organ failure, including axonal sensory-motor neuropathy, cardiac invol
Externí odkaz:
https://doaj.org/article/eb1ecf720024411b8765ac80c6a8b566
Publikováno v:
Brain Sciences
Brain Sciences, Vol 10, Iss 952, p 952 (2020)
Brain Sciences, Vol 10, Iss 952, p 952 (2020)
Hereditary amyloid transthyretin (ATTRv) amyloidosis with polyneuropathy is a progressive disease that is transmitted as an autosomal dominant trait and characterized by multiple organ failure, including axonal sensory-motor neuropathy, cardiac invol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9c580d9ace19b5c242ed4499eee7824
http://europepmc.org/articles/PMC7763612
http://europepmc.org/articles/PMC7763612
Publikováno v:
Volume: 8, Issue: 1 68-74
Akdeniz Tıp Dergisi
Akdeniz Tıp Dergisi
Objective:To assess the clinical and electrophysiological features of patients with a pre-diagnosis of hereditary polyneuropathy.Methods:The files of 75 patients with a pre-diagnosis of hereditary polyneuropathy who were followed up in adult and pedi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::a6df23da95b00bae77cb2951583d507e
https://dergipark.org.tr/tr/pub/akd/issue/66264/1037759
https://dergipark.org.tr/tr/pub/akd/issue/66264/1037759
Akademický článek
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