Suchergebnisse - "Ciafaloni, Emma"

PubPharm (8)

1

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

2

Age at onset of first signs or symptoms predicts age at loss of ambulation in Duchenne and Becker Muscular Dystrophy : Data from the MD STARnet

enthalten in: Journal of pediatric rehabilitation medicine | 2016

von Ciafaloni, E. | Kumar, A. | Liu, K. | +9

3

Treatment options for Duchenne muscular dystrophy

enthalten in: Current treatment options in neurology | 2008

von Ciafaloni, E. | Moxley, R.

4

Treatment options for Duchenne muscular dystrophy

enthalten in: Current treatment options in neurology | 2008

von Ciafaloni, E. | Moxley, R.

5

Treatment options for Duchenne muscular dystrophy

enthalten in: Current treatment options in neurology | 2008

von Ciafaloni, E. | Moxley, R.

6

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

7

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

8

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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