Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Neurofilamentos"'
Publikováno v:
Neurología (English Edition), Vol 38, Iss 9, Pp 663-670 (2023)
Introduction: In most cases, multiple sclerosis (MS) initially presents as clinically isolated syndrome (CIS). Differentiating CIS from other acute or subacute neurological diseases and estimating the risk of progression to clinically definite MS is
Externí odkaz:
https://doaj.org/article/91b4fdeccf3f484e8ee89bdaf001fa4b
Autor:
Thomas Williams, Carmen Tur, Arman Eshaghi, Anisha Doshi, Dennis Chan, Sophie Binks, Henny Wellington, Amanda Heslegrave, Henrik Zetterberg, Jeremy Chataway
Publikováno v:
Scientia
Magnetic resonance imaging; Neurofilament light; Secondary progressive multiple sclerosis Imatge per ressonància magnètica; Llum del neurofilament; Esclerosi múltiple secundària progressiva Imagen por resonancia magnética; Luz de neurofilamento;
Autor:
Bar-Or, Amit, Montalban, Xavier, Hu, Xixi, Kropshofer, Harald, Kukkaro, Petra, Coello, Neva, Ludwig, Inga, Willi, Roman, Zalesak, Martin, Ramanathan, Krishnan, Kieseier, Bernd C., Häring, Dieter A., Bagger, Morten, Fox, Edward, Universitat Autònoma de Barcelona
Publikováno v:
Scientia
Biomarker; Ofatumumab; Relapsing multiple sclerosis Biomarcador; Ofatumumab; Esclerosis múltiple recurrente Biomarcador; Ofatumumab; Esclerosi múltiple recurrent Introduction Several studies have described prognostic value of serum neurofilament li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80586cc727bc203517709ef89bedb5cb
https://ddd.uab.cat/record/275799
https://ddd.uab.cat/record/275799
Autor:
Rodolfo A, Kölliker Frers, Matilde, Otero-Losada, Tamara, Kobiec, Lucas D, Udovin, María Laura, Aon Bertolino, María I, Herrera, Francisco, Capani
Publikováno v:
Front. Immunol. 2022, 13:912005
Repositorio Institucional (UCA)
Pontificia Universidad Católica Argentina
instacron:UCA
Repositorio Institucional (UCA)
Pontificia Universidad Católica Argentina
instacron:UCA
Fil: Kölliker Frers, Rodolfo. Universidad Abierta Interamericana. Centro de Altos Estudios en Ciencias Humanas y de la Salud; Argentina Fil: Kölliker Frers, Rodolfo. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Otero
Publikováno v:
Brain
Scientia
Scientia
Multiple sclerosis is a highly heterogeneous disease, and the detection of neuroaxonal damage as well as its quantification is a critical step for patients. Blood-based serum neurofilament light chain (sNfL) is currently under close investigation as
Autor:
Antoni Parcerisas, Eliandre de Oliveira, Marc Hernaiz-Llorens, Fausto Ulloa, Eduardo Soriano, Miquel Bosch, Maria Antonia Odena, Lluís Pujadas, Alba Ortega-Gascó
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 7404, p 7404 (2021)
International Journal of Molecular Sciences
Volume 22
Issue 14
International Journal of Molecular Sciences
Volume 22
Issue 14
Neuronal cell adhesion molecule 2 (NCAM2) is a membrane protein with an important role in the morphological development of neurons. In the cortex and the hippocampus, NCAM2 is essential for proper neuronal differentiation, dendritic and axonal outgro
Autor:
Martín Aguilar, Lorena
Publikováno v:
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
TDX (Tesis Doctorals en Xarxa)
TDR. Tesis Doctorales en Red
instname
Universitat Autònoma de Barcelona
TDX (Tesis Doctorals en Xarxa)
TDR. Tesis Doctorales en Red
instname
El dany axonal és el substrat patològic de la discapacitat permanent en molts trastorns neurològics, entre els quals es troben les neuropaties autoimmunes. Actualment no hi ha biomarcadors predictors de resposta terapèutica o de pronòstic a llar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::09403bfb3df33ad5ab3d05a41c048ec1
https://ddd.uab.cat/record/251465
https://ddd.uab.cat/record/251465
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::885481bebe25c8e8b94800c089db7a68
Serum Neurofilament Levels and PML Risk in Patients With Multiple Sclerosis Treated With Natalizumab
Autor:
Fissolo, Nicolás, Pignolet, Beatrice, Rio, Jordi, Vermersch, Patrick, Ruet, Aurélie, deSèze, Jerome, Labauge, Pierre, Vukusic, Sandra, Papeix, Caroline, Martinez-Almoyna, Laurent, Tourbah, Ayman, Clavelou, Pierre, Moreau, Thibault, Pelletier, Jean, Lebrun-Frenay, Christine, Bourre, Bertrand, Defer, Gilles, Montalban, Xavier, Brassat, David, Comabella, Manuel, Universitat Autònoma de Barcelona
Publikováno v:
Neurology Neuroimmunology & Neuroinflammation
Neurology Neuroimmunology & Neuroinflammation, American Academy of neurology, 2021, 8 (4), pp.e1003. ⟨10.1212/NXI.0000000000001003⟩
Neurology Neuroimmunology & Neuroinflammation, 2021, 8 (4), pp.e1003. ⟨10.1212/NXI.0000000000001003⟩
Scientia
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Neurology® Neuroimmunology & Neuroinflammation
article-version (Version of Record) 3
Neurology Neuroimmunology & Neuroinflammation, American Academy of neurology, 2021, 8 (4), pp.e1003. ⟨10.1212/NXI.0000000000001003⟩
Neurology Neuroimmunology & Neuroinflammation, 2021, 8 (4), pp.e1003. ⟨10.1212/NXI.0000000000001003⟩
Scientia
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Neurology® Neuroimmunology & Neuroinflammation
article-version (Version of Record) 3
ObjectivesThe study aimed to assess the potential for serum neurofilament light chain (NFL) levels to predict the risk of progressive multifocal leukoencephalopathy (PML) in natalizumab (NTZ)-treated patients with multiple sclerosis (MS) and to discr
Autor:
Martínez Tamés, Míriam
Publikováno v:
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Universidad de Cantabria (UC)
En este estudio, hemos re‐evaluado dos familias de Charcot‐Marie‐Tooth intermedia con herencia autosómica dominante (DI‐CMT). La primera familia está asociada a la mutación E396K del gen NEFL, y la segunda a la mutación N98S de este gen.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::da6ecfe6ab407de0b454023301cd2795
http://hdl.handle.net/10902/11688
http://hdl.handle.net/10902/11688