ℹ️
🇬🇧
Search
Search for people relevant for "Mitochondrial disorder"
Mitochondrial disorder
Person
Class
Person
Publication
Programmes
Export current view
prof. MUDr. Jiří Zeman DrSc.
Academic staff at First Faculty of Medicine
5 classes
661 publications
Classes
class
Paediatrics for Students of Stomatology
+1
B00137 |
First Faculty of Medicine
class
Intesive Care in Paediatrics 1
B01566 |
First Faculty of Medicine
class
Intensive care in paediatrics 2
B01579 |
First Faculty of Medicine
class
Intensive care in paediatrics and neonatology
B02961 |
First Faculty of Medicine
Publications
publication
High-resolution melting analysis of 15 genes in 60 patients with cytochrome-c oxidase deficiency
2012 |
First Faculty of Medicine
publication
Elevated CSF-lactate is a reliable marker of mitochondrial disorders in children even after brief seizures
2011 |
First Faculty of Medicine, Faculty of Science
publication
Elevated CSF-lactate is a reliable marker of mitochondrial disorders in children even after brief seizures
2011 |
First Faculty of Medicine
publication
Myoclonic Epilepsy and Deafness in Siblings with the 7512T>C Mutation in the Mitochondrial Encoded tRNA(Ser(UCN)) Gene - Case Reports
2010 |
First Faculty of Medicine, Faculty of Science, Faculty of Physical Education and Sport, Faculty of Medicine in Hradec Králové
publication
Elevated lactate is a reliable marker pointing to mitochondrial disorders even in children after brief seizures.
2010 |
First Faculty of Medicine, Faculty of Science, Faculty of Physical Education and Sport
publication
Myoclonic Epilepsy and Deafness in Siblings with the 7512T > C Mutation in the Mitochondrial Encoded tRNA(Ser(UCN)) Gene - Case Reports
2010 |
First Faculty of Medicine
publication
Cytochrome C oxidase deficiency in childhood
2009 |
First Faculty of Medicine
publication
Hepatocellular carcinoma in an infant with tyrosinemia type 1
2023 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Inherited disorders of carbohydrate metabolism
2023 |
First Faculty of Medicine
publication
Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes
2023 |
First Faculty of Medicine
Load more publications (651)
Loading network view...