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- Pompe disease – clinical case report
MUDr. Ing. Ivana Patáková, CSc.
(6/2014, Case reports ) - Pompe disease – pathogenesis, clinical features, diagnosis and enzyme replacement therapy
doc. MUDr. Peter Špalek, PhD.
(1/2009, Review articles ) - Treatable lysosomal storage disorders with movement disorder manifestations
MUDr. Alexandra Lacková, Doc. MUDr. Matej Škorvánek, PhD.
(2/2022, Main topic ) - Glycogen storage disease type II (GSD II, Pompe disease). Current diagnostic and therapeutic options. Clinical case report
MUDr. Věra Malinová
(5/2010, Review articles ) - Pokroky v léčbě dědičných metabolických poruch s neurologickou symptomatologií
doc. MUDr. Martin Magner, Ph.D., MUDr. Hana Kolářová, doc. MUDr. Tomáš Honzík, Ph.D.
(2/2018, Main topic ) - Pompe disease – case report of the juvenile form
MUDr. Katarína Okáľová, PhD., Mgr. Slavomíra Mattošová, doc. MUDr. Ján Chandoga CSc., MUDr. Viera Holecová
(1/2015, Case reports ) - Pompeho nemoc
doc. MUDr. Martin Magner, Ph.D., MUDr. Jitka Jirečková
(3/2018, Review articles ) - Pompe‘s disease in the Czech Republic – blood-screening project in risk patients using a „dried blood spot“
doc. MUDr. Hana Ošlejšková Ph.D., MUDr. Štefania Rusnáková, MUDr. Stanislav Voháňka, CSc. MBA, MUDr. Eva Slouková
(2/2009, Review articles ) - The late-onset form of Pompe disease
MUDr. Radka Mišurová, MUDr. Věra Malinová
(4/2021, Case reports )
- Lysosomal storage diseases: current diagnostic and therapeutic options
MUDr. Věra Malinová, doc. MUDr. Tomáš Honzík, Ph.D.
(3/2013, Review articles ) - Lysosomal storage diseases: current diagnostic and therapeutic options (continued)
MUDr. Věra Malinová, doc. MUDr. Tomáš Honzík, Ph.D.
(4/2013, Review articles ) - Pompe disease
MUDr. Eva Slouková, doc. MUDr. Hana Ošlejšková, Ph.D., MUDr. Stanislav Voháňka, CSc., MBA, MUDr. RNDr. Pavel Ješina, Ph.D.
(5/2009, Review articles )
- Neurodegeneration and lysosomal storage disorders
MUDr. Katarína Juríčková, PhD., MUDr. Anna Hlavatá, PhD., MPH
(1/2024, Main topic )