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- HyperCKemia – aetiology, clinical significance and differential diagnosis
Doc. MUDr. Peter Špalek, PhD.
(5/2018, Interdisciplinary consilium )
- Congenital myopathy associated with RYR1 gene mutation (case report)
MUDr. Patrícia Balážová, MUDr. Karin Viestová, MUDr. Miriam Kolníková, PhD.
(3/2021, Case reports ) - Congenital myopathies
MUDr. Josef Kraus, CSc. , assoc. prof. Jiří Vajsar MD, MSc, FRCPC, doc. MUDr. Josef Zámečník, Ph.D.
(4/2012, Main topic ) - Congenital muscular dystrophies
MUDr. Josef Kraus, CSc. , assoc. prof. Jiří Vajsar MD, MSc, FRCPC
(4/2012, Main topic ) - Congenital muscular dystrophies
MUDr. Ondřej Havlín, MUDr. Zdeňka Bálintová, MUDr. Lenka Juříková, doc. MUDr. Hana Ošlejšková, Ph.D.
(1/2022, Main topic )
- Floppy baby with skin abnormality – a case report of 6 years old boy with diagnosis of congenital muscular dystrophy type Ullrich
MUDr. Jana Haberlová, Ph.D., MUDr. Zuzana Libá, Ph.D., MUDr. Martin Kynčl, prof. MUDr. Pavel Seeman, Ph.D.
(5/2016, Original articles & Case reports )