Suchergebnisse - "Wagner, Kathryn R"

PubPharm (6)

1

Novel FHL1 Mutation Associated With Hypertrophic Cardiomyopathy, Sudden Cardiac Death, and Myopathy

enthalten in: JACC. Case reports | 2020

von Binder, M. | Brown, E. | Aversano, T. | +3

CommentIn: JACC Case Rep. 2020 Mar 18;2(3):361-364. - PMID 34319296

2

Facioscapulohumeral Muscular Dystrophies

enthalten in: Continuum (Minneapolis, Minn.) | 2019

von Wagner, K.

3

'Double trouble' : diagnostic challenges in Duchenne muscular dystrophy in patients with an additional hereditary skeletal dysplasia

enthalten in: Neuromuscular disorders : NMD | 2013

von Donkervoort, S. | Schindler, A. | Tesi-Rocha, C. | +8

4

Etiology of limb girdle muscular dystrophy 1D/1E determined by laser capture microdissection proteomics

enthalten in: Annals of neurology | 2012

von Greenberg, S. | Salajegheh, M. | Judge, D. | +5

5

Hydroxychloroquine causes severe vacuolar myopathy in a patient with chronic graft-versus-host disease

enthalten in: American journal of hematology | 2005

von Bolaños-Meade, J. | Zhou, L. | Hoke, A. | +3

6

Myostatin mutation associated with gross muscle hypertrophy in a child

enthalten in: The New England journal of medicine | 2004

von Schuelke, M. | Wagner, K. | Stolz, L. | +6

CommentIn: N Engl J Med. 2004 Jun 24;350(26):2642-4. - PMID 15215479

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