ℹ️
🇬🇧
Search
Search for people relevant for "new ages"
new ages
Person
Class
Person
Publication
Programmes
prof. MUDr. Tomáš Honzík Ph.D.
Academic staff at First Faculty of Medicine
12 classes
251 publications
Classes
class
Paediatrics - Summer Practice
+1
B03304 |
First Faculty of Medicine
class
Paediatrics
B00141 |
First Faculty of Medicine
class
Propaedeutics in Paediatrics - Summer Practice
B00609 |
First Faculty of Medicine
class
Propaedeutics in Paediatrics
+2
B00610 |
First Faculty of Medicine
class
Paediatrics Practice before State Examination
B01057 |
First Faculty of Medicine
class
Pediatric Nursing 1
B03453 |
First Faculty of Medicine
class
Paediatric Nursing 2
B03468 |
First Faculty of Medicine
class
Paediatrics SE
B80141 |
First Faculty of Medicine
class
Curriculum of Paediatrics before State Examination
B81057 |
First Faculty of Medicine
Load more classes (2)
Publications
publication
Different laboratory and muscle biopsy findings in a family with an m.8851T > C mutation in the mitochondrial MTATP6 gene
2013 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Importance of early diagnostics of inherited metabolic disorders in neonatal age
2013 |
First Faculty of Medicine
publication
Novel Mutations in the TAZ Gene in Patients with Barth Syndrome
2013 |
First Faculty of Medicine
publication
Congenital Myasthenia as a Cause of Respiratory Failure in two Infants and a Toddler - Case Reports
2012 |
First Faculty of Medicine
publication
Novel Mutations in the Tyrosine Hydroxylase Gene in the First Czech Patient with Tyrosine Hydroxylase Deficiency
2012 |
First Faculty of Medicine
publication
Clinical picture of S-adenosylhomocysteine hydrolase deficiency resembles phosphomannomutase 2 deficiency
2012 |
First Faculty of Medicine
publication
Clinical symptoms and laboratory data in 75 children with neonatal manifestation of mitochondrial disease: Proposed diagnostics algorithms
2010 |
First Faculty of Medicine
publication
A new case of ALG8 deficiency (CDG Ih)
2009 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Hepatocellular carcinoma in an infant with tyrosinemia type 1
2023 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Case report: A rare variant m.4135T>C in the MT-ND1 gene leads to Leber hereditary optic neuropathy and altered respiratory chain supercomplexes
+1
2023 |
Faculty of Science, First Faculty of Medicine
Load more publications (241)
Loading network view...