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Ataluren in patients with nonsense mutation Duchenne muscular dystrophy (ACT DMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial
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F. Muntoni,
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R. Spiegel,
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E. Mercuri,
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Lausanne Canton de Vaud,
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8 |
2017 |
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Human and rodent bronchial epithelial cells express functional nicotinic acetylcholine receptors.
9 auth.
A. Maus,
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7 |
1998 |
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Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures.
46 auth.
S. Petrovski,
S. Küry,
Candace T. Myers,
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T. Besnard,
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6 |
2016 |
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Prevention of experimental myasthenia gravis by nasal administration of synthetic acetylcholine receptor T epitope sequences.
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6 |
1997 |
6 🦁
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Motor and cognitive assessment of infants and young boys with Duchenne Muscular Dystrophy: results from the Muscular Dystrophy Association DMD Clinical Research Network
32 auth.
A. Connolly,
J. Florence,
M. Cradock,
E. Malkus,
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J. Miller,
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L. Viollet-Callendret,
K. Flanigan,
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J. Mendell,
C. McDonald,
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J. M. Farber,
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6 |
2013 |
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Absence of IFN-γ or IL-12 Has Different Effects on Experimental Myasthenia Gravis in C57BL/6 Mice1
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N. Ostlie,
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6 |
2000 |
6 🦁
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Outcome reliability in non‐Ambulatory Boys/Men with duchenne muscular dystrophy
22 auth.
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5 |
2015 |
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TANGO2: expanding the clinical phenotype and spectrum of pathogenic variants
33 auth.
J. N. Dines,
J. N. Dines,
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5 |
2018 |
5 🐜
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Myasthenia in SCID mice grafted with myasthenic patient lymphocytes
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5 |
1999 |
5 🐬
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Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy
44 auth.
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5 |
2017 |
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