L. Baránková

Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosis

Emilie Mikešová, Kathrin Hühne, Radim Mazanec et al. · Neuromuscular Disorders · 2005 · 27 citations

Cmt Type 1, Genetics, Pathology +4

GDAP1 mutations in Czech families with early-onset CMT

L. Baránková, Emílie Vyhnálková, Stephan Züchner et al. · Neuromuscular Disorders · 2007 · 19 citations

Mendelian Disorder, Genetic Disorder, Genetics +4

A 71‐nucleotide deletion in the periaxin gene in a Romani patient with early‐onset slowly progressive demyelinating CMT

L. Baránková, Dana Šišková, Kathrin Hühne et al. · European Journal of Neurology · 2008 · 18 citations

L239F founder mutation in GDAP1 is associated with a mild Charcot–Marie–Tooth type 4C4 (CMT4C4) phenotype

Dagmara Kabzińska, Halina Strugalska-Cynowska, Anna Kostera‐Pruszczyk et al. · Neurogenetics · 2010 · 18 citations

Mendelian Disorder, Genetic Disorder, Genetics +6

Phenotypic Variability in a Large Czech Family with a Dynamin 2–Associated Charcot-Marie-Tooth Neuropathy

Jana Haberlová, Radim Mazanec, Petr Ridzoň et al. · Journal of Neurogenetics · 2011 · 12 citations