Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Anna Wuolikainen"'
Autor:
Arvin Behzadi, Fani Pujol-Calderón, Anton E. Tjust, Anna Wuolikainen, Kina Höglund, Karin Forsberg, Erik Portelius, Kaj Blennow, Henrik Zetterberg, Peter Munch Andersen
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract 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 e
Externí odkaz:
https://doaj.org/article/70da27f2754d45be8616d776ba5ad46a
Autor:
Anna Wuolikainen, Jure Acimovic, Anita Lövgren-Sandblom, Paolo Parini, Peter M Andersen, Ingemar Björkhem
Publikováno v:
PLoS ONE, Vol 9, Iss 11, p e113619 (2014)
High plasma levels of cholesterol have been suggested to be neuroprotective for the degenerative disease amyotrophic lateral sclerosis (ALS) and to be associated with increased survival time. The gene encoding cholesterol 27-hydroxylase, CYP27A1, was
Externí odkaz:
https://doaj.org/article/e6598c7ebb94454c83ee294f470972a6
Autor:
Mohsen Khademi, Ann M Dring, Jonathan D Gilthorpe, Anna Wuolikainen, Faiez Al Nimer, Robert A Harris, Magnus Andersson, Lou Brundin, Fredrik Piehl, Tomas Olsson, Anders Svenningsson
Publikováno v:
PLoS ONE, Vol 8, Iss 5, p e63172 (2013)
Inflammatory mediators have crucial roles in leukocyte recruitment and subsequent central nervous system (CNS) neuroinflammation. The extent of neuronal injury and axonal loss are associated with the degree of CNS inflammation and determine physical
Externí odkaz:
https://doaj.org/article/14b90a546e7f4ed99a4f715747416212
Publikováno v:
PLoS ONE, Vol 6, Iss 4, p e17947 (2011)
The changes in the cerebrospinal fluid (CSF) metabolome associated with the fatal neurodegenerative disease amyotrophic lateral sclerosis (ALS) are poorly understood and earlier smaller studies have shown conflicting results. The metabolomic methodol
Externí odkaz:
https://doaj.org/article/28b820081ad34356a1f827395947bee4
Autor:
Arvin Behzadi, Mads Nikolaj Olesen, Karin Forsberg, Fani Pujol-Calderón, Anton E. Tjust, Anna Wuolikainen, Jonna Skov Madsen, Ivan Brandslund, Kaj Blennow, Henrik Zetterberg, Nasrin Asgari, Peter Munch Andersen
Background Amyotrophic lateral sclerosis (ALS) is a heterogeneous neurodegenerative syndrome hallmarked by adult-onset degeneration of upper and lower motor neurons and their associated tracts. ALS may be difficult to differentiate from some other ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72b7485e273b49f776c8437c44c406d9
https://doi.org/10.21203/rs.3.rs-2126255/v1
https://doi.org/10.21203/rs.3.rs-2126255/v1
Autor:
Miles Trupp, Lars Forsgren, Anders Öhman, Anna Wuolikainen, Peter M. Andersen, Junfang Wu, Gunnar Wingsle, Shaochun Zhu, Thomas Moritz
Publikováno v:
Journal of Molecular Neuroscience
The neurodegenerative diseases amyotrophic lateral sclerosis (ALS) and Parkinson’s disease (PD) share some common molecular deficits including disruption of protein homeostasis leading to disease-specific protein aggregation. While insoluble protei
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:
Mads Nikolaj Olesen, Anna Christine Nilsson, Soeren Thue Lillevang, Ivan Brandslund, Karin Forsberg, Martin Wirenfeldt, Nasrin Asgari, Peter M. Andersen, Jonna Skov Madsen, Anna Wuolikainen
Publikováno v:
Neurology® Neuroimmunology & Neuroinflammation
Olesen, M N, Wuolikainen, A, Nilsson, A C, Wirenfeldt, M, Forsberg, K, Madsen, J S, Lillevang, S T, Brandslund, I, Andersen, P M & Asgari, N 2020, ' Inflammatory profiles relate to survival in subtypes of amyotrophic lateral sclerosis ', Neurology: Neuroimmunology & Neuroinflammation, vol. 7, no. 3, e697 . https://doi.org/10.1212/NXI.0000000000000697
Olesen, M N, Wuolikainen, A, Nilsson, A C, Wirenfeldt, M, Forsberg, K, Madsen, J S, Lillevang, S T, Brandslund, I, Andersen, P M & Asgari, N 2020, ' Inflammatory profiles relate to survival in subtypes of amyotrophic lateral sclerosis ', Neurology: Neuroimmunology & Neuroinflammation, vol. 7, no. 3, e697 . https://doi.org/10.1212/NXI.0000000000000697
ObjectiveTo investigate inflammatory cytokines in patients with motor neuron disease (MND) evaluating the putative contribution of amyotrophic lateral sclerosis (ALS)-causing gene variants.MethodsThis study is a retrospective case series with prospec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd8ea817049b61cf9fd61c80847e3e07
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-173325
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-173325
Autor:
Thomas Brännström, Annemarie Hübers, Peter Baumann, Nasrin Asgari, Mitsuya Morita, Albert C. Ludolph, Joanne Wuu, Peter M. Andersen, Thomas Meyer, Anna Wuolikainen, Ilkka Tarvainen, Mamede de Carvalho, Dale J. Lange, Christian Burkhardt, Frida Nordin, Carsten Bisgård, Michael Benatar, Trygve Holmøy, Jochen H. Weishaupt, Angelica Nordin, Markus Weber, Ole-Bjørn Tysnes, Kathi Schweikert, Susana Pinto, Karin Forsberg, Torsten Grehl, Chizuru Akimoto, Christoph Neuwirth, Helena Alstermark
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Nordin, A, Akimoto, C, Wuolikainen, A, Alstermark, H, Forsberg, K, Baumann, P, Pinto, S, de Carvalho, M, Hübers, A, Nordin, F, Ludolph, A C, Weishaupt, J H, Meyer, T, Grehl, T, Schweikert, K, Weber, M, Burkhardt, C, Neuwirth, C, Holmøy, T, Morita, M, Tysnes, O B, Benatar, M, Wuu, J, Lange, D J, Bisgård, C, Asgari, N, Tarvainen, I, Brännström, T & Andersen, P M 2017, ' Sequence variations in C9orf72 downstream of the hexanucleotide repeat region and its effect on repeat-primed PCR interpretation : a large multinational screening study ', Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, vol. 18, no. 3-4, pp. 256-264 . https://doi.org/10.1080/21678421.2016.1262423
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Nordin, A, Akimoto, C, Wuolikainen, A, Alstermark, H, Forsberg, K, Baumann, P, Pinto, S, de Carvalho, M, Hübers, A, Nordin, F, Ludolph, A C, Weishaupt, J H, Meyer, T, Grehl, T, Schweikert, K, Weber, M, Burkhardt, C, Neuwirth, C, Holmøy, T, Morita, M, Tysnes, O B, Benatar, M, Wuu, J, Lange, D J, Bisgård, C, Asgari, N, Tarvainen, I, Brännström, T & Andersen, P M 2017, ' Sequence variations in C9orf72 downstream of the hexanucleotide repeat region and its effect on repeat-primed PCR interpretation : a large multinational screening study ', Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, vol. 18, no. 3-4, pp. 256-264 . https://doi.org/10.1080/21678421.2016.1262423
Copyright © 2016 World Federation of Neurology on behalf of the Research Group on Motor Neuron Diseases
A large GGGGCC-repeat expansion mutation (HREM) in C9orf72 is the most common known cause of ALS and FTD in European populations. Sequence v
A large GGGGCC-repeat expansion mutation (HREM) in C9orf72 is the most common known cause of ALS and FTD in European populations. Sequence v
Autor:
Rayomand Press, Caroline Ingre, Anna Birve, Peter M Andersen, Anna Wuolikainen, Stefan L. Marklund
Publikováno v:
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 17:452-457
Mutations in the superoxide dismutase (SOD1) gene have been linked to amyotrophic lateral sclerosis (ALS). A 50 base pair (bp) deletion of SOD1 has been suggested to reduce transcription and to be associated with later disease onset in ALS. This stud