Suchergebnisse - (Person:"Wagner, Kathryn R")

PubPharm (152)

91

Clinical practice considerations in facioscapulohumeral muscular dystrophy Sydney, Australia, 21 September 2015

enthalten in: Neuromuscular disorders | 2016

von Tawil, R. | Mah, J. | Baker, S. | +2

92

In Vivo Selection Yields AAV-B1 Capsid for Central Nervous System and Muscle Gene Therapy

enthalten in: Molecular therapy | 2016

von Choudhury, S. | Fitzpatrick, Z. | Harris, A. | +15

93

Morpholino-mediated Knockdown of DUX4 Toward Facioscapulohumeral Muscular Dystrophy Therapeutics

enthalten in: Molecular therapy | 2016

von Chen, J. | King, O. | Zhang, Y. | +5

94

Myositis-specific autoantibodies are specific for myositis compared to genetic muscle disease

enthalten in: Neurology(R) neuroimmunology & neuroinflammation | 2015

von Mammen, A. | Casciola-Rosen, L. | Christopher-Stine, L. | +2

95

Whole-body magnetic resonance imaging evaluation of facioscapulohumeral muscular dystrophy

enthalten in: Muscle & nerve | 2015

von Leung, D. | Carrino, J. | Wagner, K. | +1

96

Genetic disruption of Smad7 impairs skeletal muscle growth and regeneration

enthalten in: The Journal of physiology | 2015

von Cohen, T. | Kollias, H. | Liu, N. | +2

97

Contemporary cardiac issues in Duchenne muscular dystrophy. Working Group of the National Heart, Lung, and Blood Institute in collaboration with Parent Project Muscular Dystrophy

enthalten in: Circulation | 2015

von McNally, E. | Kaltman, J. | Benson, D. | +20

ErratumIn: Circulation. 2015 Jun 23;131(25):e539 Groh, William J [added]. - PMID 26099961

98

The TREAT-NMD advisory committee for therapeutics (TACT) : an innovative de-risking model to foster orphan drug development

enthalten in: Orphanet journal of rare diseases | 2015

von Heslop, E. | Csimma, C. | Straub, V. | +85

99

The TREAT-NMD advisory committee for therapeutics (TACT): an innovative de-risking model to foster orphan drug development

enthalten in: Orphanet journal of rare diseases | 2015

von Heslop, E. | Csimma, C. | Straub, V. | +12

100

Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophy

enthalten in: Clinical epigenetics | 2015

von Jones, T. | King, O. | Himeda, C. | +8