Zobrazeno 1 - 10
of 136
pro vyhledávání: '"Yoram, Nevo"'
Autor:
Lana Meshnik, Dan Bar-Yaacov, Dana Kasztan, Tali Neiger, Tal Cohen, Mor Kishner, Itay Valenci, Sara Dadon, Christopher J. Klein, Jeffery M. Vance, Yoram Nevo, Stephan Züchner, Ofer Ovadia, Dan Mishmar, Anat Ben-Zvi
Publikováno v:
BMC Biology, Vol 20, Iss 1, Pp 1-17 (2022)
Abstract Background Mitochondrial DNA (mtDNA) is present at high copy numbers in animal cells, and though characterized by a single haplotype in each individual due to maternal germline inheritance, deleterious mutations and intact mtDNA molecules fr
Externí odkaz:
https://doaj.org/article/b201b8a14eb44511992dfb57115e956e
Autor:
Itay Tokatly Latzer, Liora Sagi, Revital Lavi, Sharon Aharoni, Jacob Bistritzer, Iris Noyman, Mira Ginsburg, Angela Lev-Or, Sharona Katzenellenbogen, Yoram Nevo, Aviva Fattal-Valevski
Publikováno v:
Pediatric Neurology. 144:60-68
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15a42c08f87ba988376095e74c52b1fb
https://doi.org/10.1016/j.pediatrneurol.2023.04.007
https://doi.org/10.1016/j.pediatrneurol.2023.04.007
Autor:
Edward C Smith, Laurie S Conklin, Eric P Hoffman, Paula R Clemens, Jean K Mah, Richard S Finkel, Michela Guglieri, Mar Tulinius, Yoram Nevo, Monique M Ryan, Richard Webster, Diana Castro, Nancy L Kuntz, Laurie Kerchner, Lauren P Morgenroth, Adrienne Arrieta, Maya Shimony, Mark Jaros, Phil Shale, Heather Gordish-Dressman, Laura Hagerty, Utkarsh J Dang, Jesse M Damsker, Benjamin D Schwartz, Laurel J Mengle-Gaw, Craig M McDonald, CINRG VBP15 and DNHS Investigators
Publikováno v:
PLoS Medicine, Vol 17, Iss 9, p e1003222 (2020)
BackgroundTreatment with corticosteroids is recommended for Duchenne muscular dystrophy (DMD) patients to slow the progression of weakness. However, chronic corticosteroid treatment causes significant morbidities. Vamorolone is a first-in-class anti-
Externí odkaz:
https://doaj.org/article/b45ccb68e7754878b721301c83d6bdc1
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 13 (2020)
Muscle stem cells (MuSCs), known as satellite cells (SCs) have an incredible ability to regenerate, which enables the maintenance and growth of muscle tissue. In response to damaging stimuli, SCs are activated, proliferate, differentiate, and fuse to
Externí odkaz:
https://doaj.org/article/bb9a1391407444eea828d6819812701d
Autor:
Dekel Avital, Shlomi Peretz, Eliauh Perlow, Osnat Konen, Edna Inbar, Yarden Bulkowstein, Elhanan Nahum, Sharon Aharoni, Lital Cohen Vig, Yoram Nevo, Eitan Auriel, Rachel Straussberg
Publikováno v:
European Journal of Paediatric Neurology. 40:40-43
Pediatric stroke is considered an infrequent complication of COVID-19. Focal cerebral arteriopathy (FCA) is one of the most common causes of arterial ischemic stroke in a previously healthy child. The present report describes a toddler with FCA most
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2263ac6a53619de65b7f12bd30583358
https://doi.org/10.1016/j.ejpn.2022.07.007
https://doi.org/10.1016/j.ejpn.2022.07.007
Publikováno v:
Pharmaceutics, Vol 13, Iss 2, p 185 (2021)
We previously reported the development of a novel formulation of an ultra-long-acting local anesthetic based on bupivacaine encapsulated in large multivesicular liposomes (Bupisomes) embedded in hydrogel. This formulation (Bupigel) prolonged bupivaca
Externí odkaz:
https://doaj.org/article/d7dcb06054fe4e68844feaeb8306ccc4
Autor:
Hagit Levine, Itai Goldfarb, Julia Katz, Moriah Carmeli, Tzippy Shochat, Huda Mussaffi, Sharon Aharoni, Dario Prais, Yoram Nevo
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992).
In Duchenne muscular dystrophy (DMD), lung disease contributes significantly to morbidity and mortality. This study aimed to assess the usefulness of various pulmonary function tests in evaluating DMD severity.This retrospective study analysed lung f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75b033ae67ed37ce69f688bd5822810e
https://pubmed.ncbi.nlm.nih.gov/36596294
https://pubmed.ncbi.nlm.nih.gov/36596294
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 12, p 4511 (2020)
Duchenne muscular dystrophy (DMD) is a severe muscle wasting disease typically caused by protein-truncating mutations that preclude synthesis of a functional dystrophin. Exonic deletions are the most common type of DMD lesion, however, whole exon dup
Externí odkaz:
https://doaj.org/article/d8aa94d9c05d4327902ca365603ed2a6
Autor:
Tehila Mizrachi, Livnat Brill, Malcolm Rabie, Yoram Nevo, Yakov Fellig, Mayan Zur, Dimitrios Karussis, Oded Abramsky, Talma Brenner, Adi Vaknin-Dembinsky
Publikováno v:
Journal of Immunology Research, Vol 2018 (2018)
Neuromyelitis optica (NMO) and myasthenia gravis (MG) are autoimmune diseases mediated by autoantibodies against either aquaporin 4 (AQP4) or acetylcholine receptor (AChR), respectively. Recently, we and others have reported an increased prevalence o
Externí odkaz:
https://doaj.org/article/403e8ae6eaa84e13b8a97379aea65d94
Autor:
John W. Day, Mar Tulinius, Alan Pestronk, Tina Duong, Tulio E. Bertorini, Alberto Dubrovsky, Nanette C. Joyce, Anne M. Connolly, Hanna Kolski, Lauren P. Morgenroth, Hoda Abdel-Hamid, Ksenija Gorni, Craig M. McDonald, Erik K Henricson, Erik Landfeldt, Yoram Nevo, Jose Carlo, Sherilyn W. Driscoll, Laura McAdam, S. Chidambaranathan, Paula R. Clemens, Avital Cnaan, Jean Teasley, W. Douglas Biggar, Joel Iff, Andrew J. Kornberg, Nancy L. Kuntz, E. Henricson, Jean K. Mah, Carolina Tesi-Rocha, Robert T. Leshner, Mathula Thangarajh, Richard D. Webster, V. Vishwanathan, Monique M. Ryan, John B. Bodensteiner, Timothy Lotze, Richard T. Abresch, Peter I. Karachunski
Publikováno v:
Value Health
OBJECTIVES: The objective of this study was to examine the psychometric properties of the Pediatric Quality of Life Inventory 4.0 Generic Core Scales (PedsQL 4.0 GCS) in Duchenne muscular dystrophy (DMD), a rare, severely debilitating, and ultimately
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dd36dd2d6151eb55eab84c122ed70a8
https://doi.org/10.1016/j.jval.2021.05.016
https://doi.org/10.1016/j.jval.2021.05.016