Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Vahid M. Harandi"'
Autor:
Vahid M. Harandi, Bernardo Moreira Soares Oliveira, Valérie Allamand, Ariana Friberg, Cibely C. Fontes-Oliveira, Madeleine Durbeej
Publikováno v:
Antioxidants, Vol 9, Iss 3, p 244 (2020)
Congenital muscular dystrophy with laminin α2 chain-deficiency (LAMA2-CMD) is a severe neuromuscular disorder without a cure. Using transcriptome and proteome profiling as well as functional assays, we previously demonstrated significant metabolic i
Externí odkaz:
https://doaj.org/article/90a1ec39ad814e69b3fac1dbb915b07e
Autor:
Vahid M Harandi, Susanne Lindquist, Shrikant Shantilal Kolan, Thomas Brännström, Jing-Xia Liu
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e109833 (2014)
Amyotrophic lateral sclerosis (ALS) is currently an incurable fatal motor neuron syndrome characterized by progressive weakness, muscle wasting and death ensuing 3-5 years after diagnosis. Neurotrophic factors (NTFs) are known to be important in both
Externí odkaz:
https://doaj.org/article/b1cea193b18c4a03b403d46d16591a99
Autor:
Håkan Alfredson, Bruno Domokos, Christoph Spang, Florian Maria Alfen, Christoph Raschka, Witold Golonka, Vahid M. Harandi
Publikováno v:
Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 10, Iss 2430, p 2430 (2021)
Volume 10
Issue 11
Journal of Clinical Medicine, Vol 10, Iss 2430, p 2430 (2021)
Volume 10
Issue 11
(1) Background: Reconditioning of the paraspinal lumbar extensor muscles by isolated lumbar extension resistance exercises (ILEX) has shown good clinical results for patients with chronic unspecific low back pain. However, the clinical value and safe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a843da2d6d49fe324471a999d2564e3
https://pubmed.ncbi.nlm.nih.gov/34070780
https://pubmed.ncbi.nlm.nih.gov/34070780
Publikováno v:
Matrix Biology. 70:36-49
Muscular dystrophies, including laminin α2 chain-deficient muscular dystrophy (LAMA2-CMD), are associated with immense personal, social and economic burdens. Thus, effective treatments are urgently needed. LAMA2-CMD is either a severe, early-onset c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f569b7f912da3e7bec462b23ef9cb705
https://doi.org/10.1016/j.matbio.2018.02.024
https://doi.org/10.1016/j.matbio.2018.02.024
Autor:
Zandra Körner, Madeleine Durbeej, Bernardo Moreira Soares Oliveira, Cibely C. Fontes-Oliveira, Vahid M. Harandi
Publikováno v:
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-15 (2018)
Scientific Reports, Vol 8, Iss 1, Pp 1-15 (2018)
Congenital muscular dystrophy with laminin α2 chain-deficiency (LAMA2-CMD) is a severe muscle disorder with complex underlying pathogenesis. We have previously employed profiling techniques to elucidate molecular patterns and demonstrated significan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07ca2b21ab82da0cca7786c50eef8492
http://europepmc.org/articles/PMC6214987
http://europepmc.org/articles/PMC6214987
Autor:
Ariana Friberg, Madeleine Durbeej, Kinga I. Gawlik, Vahid M. Harandi, B. Moreira Soares Oliveira
Publikováno v:
Neuromuscular Disorders. 29:S163-S164
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37fb2f568e13a1d9a2d98e73cf19a7bd
https://doi.org/10.1016/j.nmd.2019.06.445
https://doi.org/10.1016/j.nmd.2019.06.445
Purpose: To investigate the impact of amyotrophic lateral sclerosis (ALS) on the extraocular muscles (EOMs) by examining the distribution of neurotrophic factors (NTFs) and their receptors in EOMs and limb muscles from ALS transgenic mice. Methods: M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d93240bf9e79624e4ab75e45b265417
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-129395
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-129395
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e109833 (2014)
PLoS ONE
PLoS ONE
Amyotrophic lateral sclerosis (ALS) is currently an incurable fatal motor neuron syndrome characterized by progressive weakness, muscle wasting and death ensuing 3–5 years after diagnosis. Neurotrophic factors (NTFs) are known to be important in bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3d7e04bd3ee7672540120c3c147016d
https://doi.org/10.1371/journal.pone.0109833
https://doi.org/10.1371/journal.pone.0109833
Publikováno v:
Investigative Opthalmology & Visual Science. 55:5482
The extraocular muscles (EOM) and their motor neurons are spared in amyotrophic lateral sclerosis (ALS). In limb muscle, axon retraction from the neuromuscular junctions occurs early in the disease. Wnts, a conserved family of secreted signaling mole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42ae688d4b43de5afd2dbac77ddd43a3
https://doi.org/10.1167/iovs.14-14886
https://doi.org/10.1167/iovs.14-14886
Publikováno v:
British Journal of Sports Medicine. 48:A63.1-A63
Introduction Recent studies have highlighted the plantaris tendon and its possible involvement in midportion Achilles tendinopathy. In several patients an enlarged/thickened plantaris tendon has been found to lay in close relationship to the Achilles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14f1b11d6381d806aaf30a7896f2127c
https://doi.org/10.1136/bjsports-2014-094114.96
https://doi.org/10.1136/bjsports-2014-094114.96