Publikace
- Paradoxes of neurogenetic programme: Charcoot Marie Tooth Diseases (CMT) - Hereditary motor sensory neuropathy (HMSN)2003 | 2. lékařská fakulta
- Charcot-Marie-Tooth type X : A novel mutation in the Cx32 gene with central conduction slowing2001 | 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
- Charcot-Marie-Tooth - gonosomáln ě dominantní typ (CMTX1) - první nálezy mutací v genu pro connexin 32 v České republice2000 | 2. lékařská fakulta
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