Novel <i>SBF2</i> mutations and clinical spectrum of Charcot‐Marie‐Tooth neuropathy type 4B2Petra Laššuthová, Jan Senderek, Beate Schlotter‐Weigel et al.|Clinical Genetics|2018Cited by 12
Autosomal recessive hereditary spastic paraplegia type SPG35 due to a novel variant in the FA2H gene in a Czech patientAnna Uhrová Mészárosová, Pavel Seeman, Dana Šafka Brožková et al.|Journal of Clinical Neuroscience|2018Cited by 5
Hereditary spastic paraplegias: clinical and genetic aspectsAnna Uhrová Mészárosová, Pavel Seeman, Radim Mazanec|Neurologie pro praxi|2016Cited by 2
Spastic paraparesis as a clinical manifestation of severe X-linked adrenoleukodystrophyAnna Uhrová Mészárosová, Radim Mazanec, Filip Cihlář et al.|Neurologie pro praxi|2024Cited by 0