Barbara Ryniewicz
Warsaw, MZ 02097, Poland
Last Updated: 09/26/2026
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Found 11 publications
Spinal muscular atrophy with an overlapping syndrome - "double trouble" or a potentially better outcome?
Journal: Neurologia i neurochirurgia polska
Published: April 27, 2020
Treatment outcome in juvenile-onset myasthenia gravis.
Journal: Muscle & nerve
Published: January 18, 2018
The Frequency of c.550delA Mutation of the CANP3 Gene in the Polish LGMD2A Population.
Journal: Genetic testing and molecular biomarkers
Published: October 21, 2015
Are electrophysiological criteria useful in distinguishing childhood demyelinating neuropathies?
Journal: Journal of the peripheral nervous system : JPNS
Published: September 04, 2015
Motor unit loss estimation by the multipoint incremental MUNE method in children with spinal muscular atrophy--a preliminary study.
Journal: Neuromuscular disorders : NMD
Published: September 23, 2014
Antititin antibody in early- and late-onset myasthenia gravis.
Journal: Acta neurologica Scandinavica
Published: May 20, 2014
Early-onset facioscapulohumeral muscular dystrophy type 1 with some atypical features.
Journal: Journal of child neurology
Published: April 11, 2014
Novel point mutations in survival motor neuron 1 gene expand the spectrum of phenotypes observed in spinal muscular atrophy patients.
Journal: Neuromuscular disorders : NMD
Published: January 09, 2014
Muscle pathology in 31 patients with calpain 3 gene mutations..
Journal: Neurologia i neurochirurgia polska
Published: July 04, 2013
Showing 1-11 of 11
Last Updated: 09/26/2026