Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Payam Soltanzadeh"'
Autor:
Shomik Ati, BS, Dinesh Chhetri, MD, Martina Wiedau, MD, Payam Soltanzadeh, MD, Yvette Bordelon, MD, PhD, Robert K. Chin, MD, PhD, Ricky R. Savjani, MD, PhD
Publikováno v:
Advances in Radiation Oncology, Vol 8, Iss 1, Pp 101116- (2023)
Externí odkaz:
https://doaj.org/article/fbfd685d9d5b4240b34df786940d948e
Autor:
Asma Ben Ammar, Payam Soltanzadeh, Stéphanie Bauché, Pascale Richard, Evelyne Goillot, Ruth Herbst, Karen Gaudon, Caroline Huzé, Laurent Schaeffer, Yuji Yamanashi, Osamu Higuchi, Antoine Taly, Jeanine Koenig, Jean-Paul Leroy, Fayçal Hentati, Hossein Najmabadi, Kimia Kahrizi, Manouchehr Ilkhani, Michel Fardeau, Bruno Eymard, Daniel Hantaï
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e53826 (2013)
Congenital myasthenic syndromes (CMSs) are a heterogeneous group of genetic disorders affecting neuromuscular transmission. The agrin/muscle-specific kinase (MuSK) pathway is critical for proper development and maintenance of the neuromuscular juncti
Externí odkaz:
https://doaj.org/article/e68477a48eb441748de3168741d93310
Autor:
Asma Ben Ammar, Payam Soltanzadeh, Stéphanie Bauché, Pascale Richard, Evelyne Goillot, Ruth Herbst, Karen Gaudon, Caroline Huzé, Laurent Schaeffer, Yuji Yamanashi, Osamu Higuchi, Antoine Taly, Jeanine Koenig, Jean-Paul Leroy, Fayçal Hentati, Hossein Najmabadi, Kimia Kahrizi, Manouchehr Ilkhani, Michel Fardeau, Bruno Eymard, Daniel Hantaï
Publikováno v:
PLoS ONE, Vol 8, Iss 9 (2013)
Externí odkaz:
https://doaj.org/article/fe5ec470c1604ae592a6404a4f5d845e
Autor:
Andrew L Mammen, Anthony A Amato, Mazen M Dimachkie, Hector Chinoy, Yessar Hussain, James B Lilleker, Iago Pinal-Fernandez, Yves Allenbach, Babak Boroojerdi, Mark Vanderkelen, Eumorphia Maria Delicha, Harold Koendgen, Ramin Farzaneh-Far, Petra W Duda, Camil Sayegh, Olivier Benveniste, Anthony A. Amato, Suur Biliciler, Mazen M. Dimachkie, Christyn Edmundson, Miriam Freimer, Anthony Geraci, Pedro Machado, Andrew L. Mammen, Tahseen Mozaffar, Payam Soltanzadeh, Niraja Suresh, Anneke van der Kooi, Matthew Appleby, Richard J Barohn, Nicolas Champtiaux, Christopher Doughty, Jerrica Farias, Constantine Farmakidis, Ali A. Habib, Chafic Karam, James Lilleker, Samantha Lorusso, Mamatha Pasnoor, Giorgia Querin, Joost Raaphorst, George Ransley, Sami Saba, Kazim Sheikh, Andrew Snedden, Jeffrey Statland, Tuan Vu
Publikováno v:
The Lancet Rheumatology, 5(2), e67-e76. Lancet Publishing Group
Background: Immune-mediated necrotising myopathy is an autoimmune myopathy characterised by proximal muscle weakness, high creatine kinase concentrations, and autoantibodies recognising 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) or the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::226dfb286f8e7e3dd1c850014b828f66
https://doi.org/10.1016/s2665-9913(23)00003-6
https://doi.org/10.1016/s2665-9913(23)00003-6
Autor:
Nicholas Johnson, John Day, Johanna Hamel, Charles Thornton, S Subramony, Payam Soltanzadeh, Jeffrey Statland, William Arnold, Matthew Wicklund, Kelly Ditrapani, Carrie Heusner, Chao-Yin Chen, Bradley McEvoy, Yiming Zhu, Li-Jung Tai, Elizabeth Ackermann
Publikováno v:
Thursday, April 27.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8916fd2cb0933c368b50cb0371a030e8
https://doi.org/10.1212/wnl.0000000000202529
https://doi.org/10.1212/wnl.0000000000202529
Autor:
Frank Diaz, Payam Soltanzadeh, Shaweta Khosa, Negar Khanlou, Robert Freundlich, Shri K. Mishra
Publikováno v:
Muscle & Nerve. 67
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1e30eacc6f7da371547c6ee77301da8
https://doi.org/10.1002/mus.27806
https://doi.org/10.1002/mus.27806
Autor:
Masoumeh Pourhadi, Ameneh Mehri-Ghahfarrokhi, Sayedeh Azimeh Hosseini, Payam Soltanzadeh, Morteza Hashemzadeh Chaleshtori, Zahra Pourteymourfard-Tabrizi, Abbas Doosti, Mohammad-Saeid Jami, Fatemeh Ghanavatinejad, Karim Mahnam
Publikováno v:
Cell Biology International. 44:671-683
Charcot-Marie-Tooth (CMT) diseases are a heterogeneous group of genetic peripheral neuropathies caused by mutations in a variety of genes, which are involved in the development and maintenance of peripheral nerves. Myelin protein zero (MPZ) is expres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b92ba378c36d0868089f95ec1f557438
https://doi.org/10.1002/cbin.11268
https://doi.org/10.1002/cbin.11268
Autor:
Payam Soltanzadeh
Publikováno v:
Electrodiagnostic Medicine ISBN: 9783030749965
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a91d7d6f173842fcde148c6de355a96
https://doi.org/10.1007/978-3-030-74997-2_12
https://doi.org/10.1007/978-3-030-74997-2_12
Autor:
Fabiola Mavillard, Aurelio Hernández-Lain, Emilia Servián-Morilla, Joshua S. Clayton, J. Esteban Perez, Leigh B. Waddell, Nigel G. Laing, Sandra T. Cooper, P. Rodrigo, Katrina Reardon, Macarena Cabrera-Serrano, Montse Olivé, Frances J. Evesson, Payam Soltanzadeh, Cristina Domínguez-González, N. Ermolova, A. Arteche‐López, M. Spencer, A. Corbett, Laura Gonzalez-Mera, C. Navas, Gianina Ravenscroft, E. Rivas-Infante, C. Paradas‐Lopez, A. Sanchez
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
[Aims] Recessive variants in CAPN3 gene are the cause of the commonest form of autosomal recessive limb girdle muscle dystrophy. However, two distinct in-frame deletions in CAPN3 (NM_000070.3:c.643_663del21 and c.598_621del15) and more recently, Gly4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16687d4e6e551c8df8f28621eec86ecd
https://pubmed.ncbi.nlm.nih.gov/32896923
https://pubmed.ncbi.nlm.nih.gov/32896923
Autor:
Payam Soltanzadeh
Publikováno v:
Genes. 13:367
Myotonic dystrophies (DM) are the most common muscular dystrophies in adults, which can affect other non-skeletal muscle organs such as the heart, brain and gastrointestinal system. There are two genetically distinct types of myotonic dystrophy: myot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c697d6a8aa36f8e4ffa658a8b29f92bc
https://doi.org/10.3390/genes13020367
https://doi.org/10.3390/genes13020367