Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Lower motor neuron signs"'
Publikováno v:
Interdisciplinary Neurosurgery, Vol 23, Iss , Pp 100910- (2021)
Cryptococcus meningoencephalitis is increasing in human immunodeficiency virus (HIV)-negative patients, especially in Asian population. In patients who respond well to anti-cryptococcal therapy, some later developed muscle atrophy and weakness. The p
Externí odkaz:
https://doaj.org/article/55b78a3027ac4bbd95235bf8a6508406
Publikováno v:
Interdisciplinary Neurosurgery, Vol 23, Iss, Pp 100910-(2021)
Cryptococcus meningoencephalitis is increasing in human immunodeficiency virus (HIV)-negative patients, especially in Asian population. In patients who respond well to anti-cryptococcal therapy, some later developed muscle atrophy and weakness. The p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3318d31a3ee31b15f7471f8048bca450
http://www.sciencedirect.com/science/article/pii/S2214751920304710
http://www.sciencedirect.com/science/article/pii/S2214751920304710
Publikováno v:
Clinical neurology and neurosurgery. 202
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8637a0a6c606eb0b6c65b4eb4c9ee1b6
https://pubmed.ncbi.nlm.nih.gov/33540173
https://pubmed.ncbi.nlm.nih.gov/33540173
Autor:
Pedro Gonzalez-Alegre, David S. Goldstein, Tanya Bardakjian, Diana Nguyen, Debra Ehrlich, Alice B. Schindler, Derek P. Narendra, Risa Isonaka, Angela Kokkinis, Tsao-Wei Liang
Publikováno v:
Neurology. 94(21)
We welcome the additional confirmed DJ1/PARK7 case and another probable case reported by Namnah et al. in their comment on our article.1 They further substantiate the occurrence of early cataracts in DJ1/PARK7 present in 5/35 (14.3%) cases. The case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b7cbe49869658952cb0bba0a9d9d989
https://pubmed.ncbi.nlm.nih.gov/32451337
https://pubmed.ncbi.nlm.nih.gov/32451337
Autor:
Mary Kay Floeter, Rachel F Smallwood Shoukry, Mike Clark, Caleb J Huang, Laura E. Danielian, Devin Bageac
Publikováno v:
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 19:562-569
OBJECTIVE: The clinical diagnosis of primary lateral sclerosis can only be made after upper motor neuron symptoms have progressed for several years without developing lower motor neuron signs. The goal of the study was to identify neuroimaging change
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2d04190872505a951695130620be955
https://doi.org/10.1080/21678421.2018.1517180
https://doi.org/10.1080/21678421.2018.1517180
Publikováno v:
Clinical Neurology and Neurosurgery. 181:73-75
Objectives Upper and lower motor neuron signs are required for the diagnosis of amyotrophic lateral sclerosis. The detection of upper motor neuron signs is key for the diagnosis, as quite a few patients with amyotrophic lateral sclerosis lack upper m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f01e1584b383d5549aeb4d1ba3d73b2
https://doi.org/10.1016/j.clineuro.2019.04.015
https://doi.org/10.1016/j.clineuro.2019.04.015
Publikováno v:
Frontiers in Neurology, Vol 9 (2019)
The clinical diagnosis of amyotrophic lateral sclerosis (ALS) relies on determination of progressive dysfunction of both cortical as well as spinal and bulbar motor neurons. However, the variable mix of upper and lower motor neuron signs result in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5710afd3bcda2c6ab2520755cd0153ba
https://doi.org/10.3389/fneur.2018.01141
https://doi.org/10.3389/fneur.2018.01141
Akademický článek
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Publikováno v:
Irish Veterinary Journal, Vol 65, Iss 1, p 19 (2012)
Abstract A seven-year old Australian Shepherd, suffering from idiopathic epilepsy under treatment with phenobarbitone and potassium bromide, was presented with generalised lower motor neuron signs. Electrophysiology and muscle-nerve biopsies revealed
Externí odkaz:
https://doaj.org/article/10492ee4e0774de4b97c29ee899a05f1
Publikováno v:
Journal of clinical neuromuscular disease. 20(1)
Amyotrophic lateral sclerosis is a neurodegenerative disorder, which is characterized by progressive upper and lower motor neuron signs and symptoms, resulting in progressive muscle weakness. There are very rare reports of magnetic resonance imaging
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8dac12cbc2986a1d67a0695ea7f4903
https://pubmed.ncbi.nlm.nih.gov/30124559
https://pubmed.ncbi.nlm.nih.gov/30124559