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- 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 ) - Pompeho nemoc
doc. MUDr. Martin Magner, Ph.D., MUDr. Jitka Jirečková
(3/2018, Review articles )
- 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 )
- Neurodegeneration and lysosomal storage disorders
MUDr. Katarína Juríčková, PhD., MUDr. Anna Hlavatá, PhD., MPH
(1/2024, Main topic )