Results 191 to 200 of about 3,165 (200)

Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy

Neuromuscular Disorders, 2002
Kati Donner, Miina Ollikainen, Maaret Ridanpaa   +2 more
exaly  

Review of Cardiac Disease in Nemaline Myopathy

Pediatric Neurology, 2015
exaly  

[Nemaline myopathy].

Der Pathologe, 1992
K, Oemus, H J, Holzhausen, D, Stiller
openaire   +1 more source

Fetal Akinesia Sequence Caused by Nemaline Myopathy

Neuropediatrics, 1997
Martin Lammens, N Goemans
exaly  

Nemaline myopathy and non-fatal hypertrophic cardiomyopathy caused by a novel ACTA1 E239K mutation

Journal of the Neurological Sciences, 2011
Sunyoung Kim, Hyang-Sook Kim, Dae-Seong Kim   +2 more
exaly  

Nemaline Myopathy

2008
openaire   +1 more source

[Myopathy, nemaline].

Ryoikibetsu shokogun shirizu, 2001
A, Yamamoto, I, Nishino
openaire   +1 more source

Anaesthesia for cardiac surgery in children with nemaline myopathy

Anaesthesia, 1992
exaly  

Nemaline myopathy.

Acta medica Iugoslavica, 1980
D, Voncina, A, Dekleva, I, Tivadar
openaire   +1 more source

Nemaline Myopathies

2012
openaire   +1 more source