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Syndrome CAN
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doc. MUDr. Hana Houšťková CSc.
Academic staff at First Faculty of Medicine
12 classes
61 publications
Classes
class
Paediatrics
+3
B00219 |
First Faculty of Medicine
class
Nursing in Paediatrics
B00256 |
First Faculty of Medicine
class
Nursing in Paediatrics 2 D
B00542 |
First Faculty of Medicine
class
Nursing in Paediatrics 1 D
B00545 |
First Faculty of Medicine
class
Pediatric Nursing
+1
B01799 |
First Faculty of Medicine
class
Pediatrics with a focus on nutrition
B02285 |
First Faculty of Medicine
class
Pediatrics
+1
B02471 |
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
Sudden infant death syndrome
+1
2008 |
First Faculty of Medicine
publication
Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome
2003 |
First Faculty of Medicine
publication
A Novel Missense Mutation 574C-T in SURF1 Gene - Biochemical and Molecular Studies in Seven Children with Leigh Disease
2002 |
First Faculty of Medicine
publication
Heterogeneous Manifestation of Heteroplasmic mtDNA Mutation 8993T-G in Two Families
2002 |
First Faculty of Medicine
publication
A Novel Missense Mutation 574C-T in SURF1 Gene - Biochemical and Molecular Studies in Seven Children with Leigh Disease
2002 |
Faculty of Physical Education and Sport
publication
Heterogeneous Manifestation of Heteroplasmic mtDNA Mutation 8993T-G in Two Families
2002 |
Faculty of Physical Education and Sport
publication
A Novel Mutation in SURF1 Causes Skipping of Exon 8 in a Patient with Cytochrome c Oxidase-Deficient Leigh Syndrome and Hypertrichosis
2001 |
First Faculty of Medicine
publication
The most frequent manifestation of mitochondrial DNA( mtDNA) mutation 8344 G Is MERRF.
1999 |
Faculty of Physical Education and Sport
publication
Renovascular hypertension and Mid-aortic syndrome in a 12-year-old girl: A case report
Publication without faculty affiliation
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