Suchergebnisse - "Mah, Jean K"

PubPharm (203)

11

Efficacy and Safety of Vamorolone vs Placebo and Prednisone Among Boys With Duchenne Muscular Dystrophy : A Randomized Clinical Trial

enthalten in: JAMA neurology | 2022

von Guglieri, M. | Clemens, P. | Perlman, S. | +43

12

Routine lung volume recruitment in boys with Duchenne muscular dystrophy : a randomised clinical trial

enthalten in: Thorax | 2022

von Katz, S. | Mah, J. | McMillan, H. | +16

CommentIn: Thorax. 2022 Aug;77(8):743-744. - PMID 35470244

13

Quantitative magnetic resonance imaging measures as biomarkers of disease progression in boys with Duchenne muscular dystrophy : a phase 2 trial of domagrozumab

enthalten in: Journal of neurology | 2022

von Sherlock, S. | Palmer, J. | Wagner, K. | +13

14

Progressive retinal changes in pediatric multiple sclerosis

enthalten in: Multiple sclerosis and related disorders | 2022

von Longoni, G. | Brown, R. | Oyefiade, A. | +17

15

Effect of Different Corticosteroid Dosing Regimens on Clinical Outcomes in Boys With Duchenne Muscular Dystrophy : A Randomized Clinical Trial

enthalten in: JAMA | 2022

von Guglieri, M. | Bushby, K. | McDermott, M. | +61

16

Quantitative magnetic resonance imaging measures as biomarkers of disease progression in boys with Duchenne muscular dystrophy: a phase 2 trial of domagrozumab

enthalten in: Journal of neurology | 2022

von Sherlock, S. | Palmer, J. | Wagner, K. | +13

17

Quantitative magnetic resonance imaging measures as biomarkers of disease progression in boys with Duchenne muscular dystrophy: a phase 2 trial of domagrozumab

enthalten in: Journal of neurology | 2022

von Sherlock, S. | Palmer, J. | Wagner, K. | +13

18

Quantitative magnetic resonance imaging measures as biomarkers of disease progression in boys with Duchenne muscular dystrophy: a phase 2 trial of domagrozumab

enthalten in: Journal of neurology | 2022

von Sherlock, S. | Palmer, J. | Wagner, K. | +13

19

Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity

enthalten in: American journal of human genetics | 2022

von Kurolap, A. | Kreuder, F. | Gonzaga-Jauregui, C. | +37

20

Clinical and Genetic Characteristics in Young, Glucocorticoid-Naive Boys With Duchenne Muscular Dystrophy

enthalten in: Neurology | 2022

von Schiava, M. | Amos, R. | VanRuiten, H. | +48