Zobrazeno 21 - 30
of 237
pro vyhledávání: '"Tahseen Mozaffar"'
Autor:
Mari Perez-Rosendahl, Tahseen Mozaffar
Publikováno v:
Current opinion in neurology. 35(5)
To discuss recent developments in our understanding of epidemiology, diagnostics, biomarkers, pathology, pathogenesis, outcome measures, and therapeutics in inclusion body myositis (IBM).Recent epidemiology data confirms a relatively higher prevalenc
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
Autor:
Vera Bril, Andrzej Szczudlik, Antanas Vaitkus, Csilla Rozsa, Anna Kostera-Pruszczyk, Petr Hon, Josef Bednarik, Michaela Tyblova, Wolfgang Köhler, Toomas Toomsoo, Richard J. Nowak, Tahseen Mozaffar, Miriam L. Freimer, Michael W. Nicolle, Tim Magnus, Michael T. Pulley, Michael Rivner, Mazen M. Dimachkie, B. Jane Distad, Robert M. Pascuzzi, Donna Babiar, Jiang Lin, Montse Querolt Coll, Rhonda Griffin, Elsa Mondou
Publikováno v:
Neurology, vol 100, iss 7
Background and ObjectivesMyasthenia gravis (MG) is an autoimmune disease characterized by dysfunction at the neuromuscular junction. Treatment frequently includes corticosteroids (CSs) and IV immunoglobulin (IVIG). This study was conducted to determi
Publikováno v:
Journal of Clinical Neuromuscular Disease. 24:55-58
Facial onset sensory and motor neuronopathy syndrome (FOSMN) is a rare motor neuron disorder characterized by facial sensory and motor aberrations that progress to the upper limbs. We present a case of FOSMN-like syndrome that has characteristics of
Publikováno v:
Current treatment options in neurology, vol 24, iss 11
Purpose of ReviewThis review summarizes the clinical presentation and provides an update on the current strategies for diagnosis of Pompe disease. We will review the available treatment options. We examine newly approved treatments as well as upcomin
Autor:
Nicholas Johnson, Kameron Bates, Han Xie, Lindsay Alfano, John Vissing, Tahseen Mozaffar, Katherine Mathews, Linda Lowes, Matthew Wicklund, Conrad Weihl, Doris Leung, Peter Kang, Carla Zingariello, Urvi Desai, Erin DeSpain, Mary St. Romain, Jeffrey Statland
Publikováno v:
Monday, April 24.
Autor:
Dennis Huang, Tahseen Mozaffar
Publikováno v:
Monday, April 24.
Publikováno v:
Monday, April 24.
Autor:
Tahseen Mozaffar, Benedikt Schoser, Priya Kishnani, Drago Bratkovic, Paula R. Clemens, Ozlem Goker-Alpan, Xue Ming, Mark Roberts, Kumaraswamy Sivakumar, Ans Van Der Ploeg, Mitchell Goldman, Jacquelyn Wright, Fred Holdbrook, Vipul Jain, Sheela Sitaraman, Yasmine Wasfi, Barry Byrne
Publikováno v:
Thursday, April 27.
Autor:
Michael Pulley, Samir Macwan, Richard Nowak, Tahseen Mozaffar, Ema Rodrigues, Houari Korideck, Brian Werneburg, Pushpa Narayanaswami
Publikováno v:
Sunday, April 23.