Suchergebnisse - "Ciafaloni, Emma"

PubPharm (5)

1

Association of genetic mutations and loss of ambulation in childhood-onset dystrophinopathy

enthalten in: Muscle & nerve | 2021

von Haber, G. | Conway, K. | Paramsothy, P. | +19

2

Open-Label Evaluation of Eteplirsen in Patients with Duchenne Muscular Dystrophy Amenable to Exon 51 Skipping : PROMOVI Trial

enthalten in: Journal of neuromuscular diseases | 2021

von McDonald, C. | Shieh, P. | Abdel-Hamid, H. | +12

3

Diagnostic and clinical characteristics of early-manifesting females with Duchenne or Becker muscular dystrophy

enthalten in: American journal of medical genetics. Part A | 2014

von Imbornoni, L. | Price, E. | Andrews, J. | +3

4

Mutation analysis in a population-based cohort of boys with Duchenne or Becker muscular dystrophy

enthalten in: Journal of child neurology | 2009

von Cunniff, C. | Andrews, J. | Meaney, F. | +10

5

An intragenic deletion/inversion event in the DMD gene determines a novel exon creation and results in a BMD phenotype

enthalten in: Human genetics | 2004

von Cagliani, R. | Sironi, M. | Ciafaloni, E. | +6

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