Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Elke Ydens"'
Autor:
Elke Ydens, Guillaume Lornet, Veerle Smits, Sofie Goethals, Vincent Timmerman, Sophie Janssens
Publikováno v:
Neurobiology of Disease, Vol 55, Iss , Pp 95-103 (2013)
Peripheral neuropathies are associated with a variety of clinical symptoms ranging from motor and sensory symptoms to autonomic dysfunction. The primary disease causes for peripheral nerve disorders are also very heterogeneous, including genetic caus
Externí odkaz:
https://doaj.org/article/6c2eaf00bff44ac0be1d73e2a43a0c35
Autor:
Donovan Low, Lukas Amann, Elke Ydens, Vincent Timmerman, Ralf Stumm, Martin Guilliams, Thomas Blank, Florent Ginhoux, Takahiro Masuda, Liesbet Martens, Omar Mossad, Dorine Sichien, Sofie De Prijck, Sophie Janssens, Charlotte L. Scott, Yvan Saeys, Bob Asselbergh, Marco Prinz
Publikováno v:
NATURE NEUROSCIENCE
Nature Neuroscience
Nature neuroscience
Nat Neurosci
Nature Neuroscience
Nature neuroscience
Nat Neurosci
The authors identify two subsets of peripheral nerve macrophages residing in the endoneurium and the epineurium and displaying a distinct transcriptome and response to injury. These cells lack the main microglia identity and have a distinct origin. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b1e208048b968baa86be95d924ad74e
https://biblio.ugent.be/publication/8660957/file/8660958
https://biblio.ugent.be/publication/8660957/file/8660958
In traumatic spinal cord injury (SCI) patients, the assessment of the exact degree of lesion severity and neurological prognosis has proven to be extremely challenging. The current tools for predicting functional outcome in SCI patients such as clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e28858c08be828641c7948af43b2f9c
http://hdl.handle.net/1942/23294
http://hdl.handle.net/1942/23294
Autor:
Magdalena Zimoń, Vincent Timmerman, Bob Asselbergh, Teodora Chamova, Ivailo Tournev, Thomas Geuens, Tinne Ooms, Albena Jordanova, Els De Vriendt, Elke Ydens, Vicky De Winter, Leonardo Almeida-Souza, Ivan Litvinenko, K. Peeters, Joy Irobi
Publikováno v:
The American journal of human genetics
The most common form of spinal muscular atrophy (SMA) is a recessive disorder caused by deleterious SMN1 mutations in 5q13, whereas the genetic etiologies of non-5q SMA are very heterogeneous and largely remain to be elucidated. In a Bulgarian family
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d419d4ce0e28de43c761efc6a6ad103
https://doi.org/10.1016/j.ajhg.2013.04.013
https://doi.org/10.1016/j.ajhg.2013.04.013
Autor:
Vicky De Winter, Guillaume Lornet, Elke Ydens, Vincent Timmerman, Dieter Demon, Mohamed Lamkanfi, Sophie Janssens
Publikováno v:
JOURNAL OF NEUROINFLAMMATION
Journal of Neuroinflammation
Journal of neuroinflammation
Journal of Neuroinflammation
Journal of neuroinflammation
Background: NOD-like receptors (Nlrs) are key regulators of immune responses during infection and autoimmunity. A subset of Nlrs assembles inflammasomes, molecular platforms that are activated in response to endogenous danger and microbial ligands an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8389b914151ca2d8ce387cd2823c8d9
https://doi.org/10.1186/s12974-015-0367-8
https://doi.org/10.1186/s12974-015-0367-8
Autor:
Guillaume Lornet, Elke Ydens, Vincent Timmerman, Sofie Goethals, Veerle Smits, Sophie Janssens
Publikováno v:
Neurobiology of disease
Neurobiology of Disease, Vol 55, Iss, Pp 95-103 (2013)
Neurobiology of Disease, Vol 55, Iss, Pp 95-103 (2013)
Peripheral neuropathies are associated with a variety of clinical symptoms ranging from motor and sensory symptoms to autonomic dysfunction. The primary disease causes for peripheral nerve disorders are also very heterogeneous, including genetic caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7fce4bd523bb714294d713da09dcefe
https://hdl.handle.net/10067/1089790151162165141
https://hdl.handle.net/10067/1089790151162165141
Autor:
Leonardo Almeida-Souza, Vincent Timmerman, Jo A. Van Ginderachter, Sophie Janssens, Bob Asselbergh, Elke Ydens, Anje Cauwels, Guillaume Lornet, Lieve Peeraer, Sofie Goethals
Publikováno v:
Journal of Neuroinflammation
Journal of Neuroinflammation, Vol 9, Iss 1, p 176 (2012)
Journal of neuroinflammation
Vrije Universiteit Brussel
JOURNAL OF NEUROINFLAMMATION
Journal of Neuroinflammation, Vol 9, Iss 1, p 176 (2012)
Journal of neuroinflammation
Vrije Universiteit Brussel
JOURNAL OF NEUROINFLAMMATION
Background The activation of the immune system in neurodegeneration has detrimental as well as beneficial effects. Which aspects of this immune response aggravate the neurodegenerative breakdown and which stimulate regeneration remains an open questi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daff3a03a5b70673fb7760e3aeb53c9d
https://pubmed.ncbi.nlm.nih.gov/22818207
https://pubmed.ncbi.nlm.nih.gov/22818207
Autor:
Mariana Gospodinova, Vanyo Mitev, C. Tzekov, P. De Jonghe, Teodora Chamova, Stoyan Bichev, Hanns Lochmüller, Chantal Ceuterick-de Groote, K. Storm, E. Reyniers, Vincent Timmerman, Elke Ydens, G. Hadjidekov, V. Mihaylova, Leonardo Almeida-Souza, Albena Jordanova, E. De Vriendt, A Suls, Jonathan Baets, I. Tournev, P.F.M. van der Ven, J. J. Martin, K. Peeters, Velina Guergueltcheva, Dieter O. Fürst
Publikováno v:
Neurology
Objective: In this study, we investigated the detailed clinical findings and underlying genetic defect in 3 presumably related Bulgarian families displaying dominantly transmitted adult onset distal myopathy with upper limb predominance. Methods: We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cc09a5eab8334dc040c48894e873e02
https://hdl.handle.net/10067/927420151162165141
https://hdl.handle.net/10067/927420151162165141
Publikováno v:
Glia
Toll-like receptors comprise a family of evolutionary conserved pattern recognition receptors that act as a first defense line in the innate immune system. Upon stimulation with microbial ligands, they orchestrate the induction of a host defense resp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89bb82e57a350317511902a9f0c48974
https://pubmed.ncbi.nlm.nih.gov/20578041
https://pubmed.ncbi.nlm.nih.gov/20578041
Autor:
Leonardo Almeida-Souza, Tinne Ooms, Joy Irobi, Magdalena Zimoń, Bob Asselbergh, E. De Vriendt, I. Tournev, V. De Winter, Elke Ydens, Thomas Geuens, Vincent Timmerman, Teodora Chamova, Ivan Litvinenko, Albena Jordanova, K. Peeters
Publikováno v:
Neuromuscular Disorders. 24:888
Spinal muscular atrophy (SMA) refers to a group of genetic disorders characterized by degeneration of anterior horn cells of the spinal cord. Initially, the disease was considered purely as an autosomal recessive condition caused by deleterious SMN1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db0046bca5918b65a79c9cea5e736a51
https://doi.org/10.1016/j.nmd.2014.06.313
https://doi.org/10.1016/j.nmd.2014.06.313