- Charcot-Marie-Tooth type X : A novel mutation in the Cx32 gene with central conduction slowing2001 | 2. lékařská fakulta
- MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 22006 | 2. lékařská fakulta
- Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 22018 | 2. lékařská fakulta
- Czech family confirms the link between FBLN5 and Charcot-Marie-Tooth type 1 neuropathy2013 | 2. lékařská fakulta
- L239F founder mutation in GDAP1 is associated with a mild Charcot-Marie-Tooth type 4C4 (CMT4C4) phenotype2010 | 2. lékařská fakulta
- Charcot-Marie-Tooth disease type 1A (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP): Reliable detection of the CMT1A duplication and HNPP deletion using 8 microsatellite markers in 2 multiplex PCRs2000 | 2. lékařská fakulta
- Pes cavus2015 | Lékařská fakulta v Plzni
- Utility of Charcot-Marie-Tooth Neuropathy Score in Children With Type 1A Disease2010 | 2. lékařská fakulta
- PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth disease2018 | 2. lékařská fakulta