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

PubPharm (156)

101

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

102

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

103

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

104

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

105

Mammalian Mss51 is a skeletal muscle-specific gene modulating cellular metabolism

enthalten in: Journal of neuromuscular diseases | 2015

von Moyer, A. | Wagner, K.

106

Results of a two-year pilot study of clinical outcome measures in collagen VI- and laminin alpha2-related congenital muscular dystrophies

enthalten in: Neuromuscular disorders : NMD | 2015

von Meilleur, K. | Jain, M. | Hynan, L. | +30

107

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

108

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

109

Results of a two-year pilot study of clinical outcome measures in collagen VI- and laminin alpha2-related congenital muscular dystrophies

enthalten in: Neuromuscular disorders | 2015

von Meilleur, K. | Jain, M. | Hynan, L. | +30

110

Whole‐body magnetic resonance imaging evaluation of facioscapulohumeral muscular dystrophy

enthalten in: Muscle & nerve | 2015

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