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prof. MUDr. Tomáš Honzík Ph.D.
Academic staff at First Faculty of Medicine
12 classes
251 publications
Classes
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
Paediatrics - Summer Practice
+1
B03304 |
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
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Publications
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
Mucopolysaccharidosis I – clinical manifestations in 24 children from the Czech Republic and Slovakia
2011 |
First Faculty of Medicine
publication
Sco2 Protein Deficiency-Based Mitochondrial Encephalomyopathy with the SMA-like Picture of Neurogenic Muscle Atrophy - Case Reports
2010 |
First Faculty of Medicine
publication
Clinical presentation and metabolic consequences in 40 breastfed infants with nutritional vitamin B-12 deficiency - What have we learned?
2010 |
First Faculty of Medicine
publication
Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation
2010 |
First Faculty of Medicine
publication
Effect of a novel intronic FBN1 mutation on splicing revealed by splicing minigene assay
Publication without faculty affiliation
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
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