Suchergebnisse - "Ciafaloni, Emma"

PubPharm (175)

11

Newborn Screening for Spinal Muscular Atrophy in New York State : Clinical Outcomes From the First 3 Years

enthalten in: Neurology | 2022

von Lee, B. | Deng, S. | Chiriboga, C. | +16

12

Time to diagnosis of Duchenne muscular dystrophy remains unchanged : Findings from the Muscular Dystrophy Surveillance, Tracking, and Research Network, 2000-2015

enthalten in: Muscle & nerve | 2022

von Thomas, S. | Conway, K. | Fapo, O. | +9

CommentIn: Muscle Nerve. 2022 Aug;66(2):116-117. - PMID 35560237

13

Selected clinical and demographic factors and all-cause mortality among individuals with Duchenne muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking, and Research Network

enthalten in: Neuromuscular disorders : NMD | 2022

von Paramsothy, P. | Wang, Y. | Cai, B. | +8

14

The 4-Copy Conundrum in the Treatment of Infants with Spinal Muscular Atrophy

enthalten in: Annals of neurology | 2022

von Deng, S. | Lee, B. | Ciafaloni, E. | +1

CommentOn: Ann Neurol. 2022 Mar;91(3):305-316. - PMID 34981567

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

Differentiation of Pediatric-Onset Duchenne and Becker Muscular Dystrophy Subphenotypes Using Data from the Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet)

enthalten in: Journal of neuromuscular diseases | 2022

von Andrews, J. | Lamb, M. | Conway, K. | +6

17

Phase 2 Trial of Rituximab in Acetylcholine Receptor Antibody-Positive Generalized Myasthenia Gravis : The BeatMG Study

enthalten in: Neurology | 2022

von Nowak, R. | Coffey, C. | Goldstein, J. | +27

18

Parent Perceptions in Choosing Treatment for Infants With Spinal Muscular Atrophy Diagnosed Through Newborn Screening

enthalten in: Journal of child neurology | 2022

von Deng, S. | Lee, B. | Ciafaloni, E.

19

The 4‐Copy Conundrum in the Treatment of Infants with Spinal Muscular Atrophy

enthalten in: Annals of Neurology | 2022

von Deng, S. | Lee, B. | Ciafaloni, E. | +1

20

Time to diagnosis of Duchenne muscular dystrophy remains unchanged : Findings from the Muscular Dystrophy Surveillance, Tracking, and Research Network, 2000‐2015

enthalten in: Muscle & Nerve | 2022

von Thomas, S. | Conway, K. | Fapo, O. | +8