Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Anton Tjust"'
Autor:
Kina Höglund, Peter M. Andersen, Arvin Behzadi, Anton Tjust, Henrik Zetterberg, Anna Wuolikainen, Kaj Blennow, Karin Forsberg, Fani Pujol-Calderón, Erik Portelius
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Delayed diagnosis and misdiagnosis are frequent in people with amyotrophic lateral sclerosis (ALS), the most common form of motor neuron disease (MND). Neurofilament light chain (NFL) and phosphorylated neurofilament heavy chain (pNFH) are elevated i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64e5160bb8a5602110f3eef02a3dfea0
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-189808
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-189808
Autor:
Rhonda L. Taylor, Yalda Nilipour, Nigel G. Laing, Shahriar Nafissi, V. Varasteh, K. Kiiski, Mark R. Davis, Montse Olivé, Anton Tjust, H. Hossein Nejad Nedai, Homa Tajsharghi, Mahdi Zangi, Seyed Hassan Tonekaboni, F. Pedrosa Domellof, L. Sagath, Gianina Ravenscroft
Publikováno v:
European Journal of Neurology. 25:841-847
Background: Nemaline myopathy has been associated with mutations in twelve genes to date. However, for some patients diagnosed with nemaline myopathy, definitive mutations are not identified in the known genes, suggesting there are other genes involv
PURPOSE. To analyze the proportion and cross-sectional area of myofibers containing myosin heavy chain slow-twitch (MyHCI) and myosin heavy chain slow tonic (MyHCsto) in extraocular muscles of autopsied amyotrophic lateral sclerosis (ALS) patients wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99cb7aa0b16bf789f5fe0f9420cc07de
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-140482
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-140482
Publikováno v:
Investigative ophthalmologyvisual science. 56(10)
We quantified and investigated the distribution of Pax7-positive cells/satellite cells (SCs) in the human extraocular muscles (EOMs).An immunofluorescence multiple-marker method simultaneously combining two SC markers (Pax7, NCAM), detection of the b
Publikováno v:
Frontiers in bioscience (Scholar edition). 4(4)
Amyotrophic lateral sclerosis (ALS) is a progressive, lethal neurodegenerative disorder characterised by selective loss of motor neurons with accompanying muscle paralysis and respiratory failure. Despite progressive paralysis in trunk and extremity