Results 111 to 116 of about 1,216 (116)

Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy

Neuromuscular Disorders, 1999
Nigel G Laing, Kathryn North, S D Wilton
exaly  

Feeding and speech difficulties in typical congenital Nemaline Myopathy

International Journal of Speech-Language Pathology, 2006
Adnan Y Manzur
exaly  

‘An artefact gone awry’: Identification of the first case of nemaline myopathy by Dr R.D.K. Reye

Neuromuscular Disorders, 2000
Kathryn North, A Kan
exaly  

Nemaline Cardiomyopathy in a Young Adult: An Ultraimmunohistochemical Study and Review of the Literature

Ultrastructural Pathology, 2000
Hanns Lochmüller, Josef Müller-Höcker
exaly  

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

Journal of the Neurological Sciences, 2011
Dae-Seong Kim
exaly  

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

Neuromuscular Disorders, 2002
Kati Donner, Marianne de Visser, Katarina Pelin   +2 more
exaly