ℹ️
🇬🇧
Search
Search for publications relevant for "Gitelman Syndrome"
Gitelman Syndrome
Publication
Class
Person
Publication
Programmes
Export current view
publication
Mutation analysis in Bartter and Gitelman syndrome in Czech republic
Publication without faculty affiliation
publication
Bartter and Gitelman syndromes
2022 |
Second Faculty of Medicine
publication
Gitelman Syndrome as a Cause of Psychomotor Retardation in a Toddler
2013 |
First Faculty of Medicine, Faculty of Medicine in Hradec Králové
publication
Gitelman syndrome in pregnancy - a severe hypokalemia with favorable perinatal prognosis
2012 |
Faculty of Medicine in Pilsen
publication
Transient hyperphosphatasemia: a benign laboratory disorder in a boy with Gitelman syndrome
2016 |
Faculty of Medicine in Hradec Králové
publication
Genetic Analysis of Gitelman Syndrome Patients from the Czech Republic and Slovakia - Three Novel Mutations Found
2006 |
First Faculty of Medicine, Faculty of Science
publication
Gitelman's Syndrome: A Hereditary Disorder Characterized by Hypokalemia and Hypomagnesaemia
+1
2009 |
Publication without faculty affiliation
publication
Sudden cardiac arrest in a child with Gitelman syndrome: a case report and literature review
2023 |
Second Faculty of Medicine
publication
Mutation analysis in patients with gitelman's syndrome
2006 |
First Faculty of Medicine
publication
Gitelman syndrome: novel mutation and long-term follow-up
2012 |
First Faculty of Medicine
publication
Gitelman's syndrome as common cause of hypokalemia and hypomagnesemia
2016 |
First Faculty of Medicine
publication
DNA Analysis of Renal Electrolyte Transporter Genes Among Patients Suffering from Bartter and Gitelman Syndromes - Summary of Mutation Screening
2011 |
First Faculty of Medicine
publication
Homozygous missense mutation in SLC 12A3 gene caused Gitelmanś syndrome with chondrocalcinosis
Publication without faculty affiliation
publication
Mutation Screening for patients with Gitelman Syndrom in the Czech Republic. 2 novel mutations found
Publication without faculty affiliation
publication
Genetic analysis of SLC12A3 gene of patients with Gitelman syndrom in the Czech Republic
Publication without faculty affiliation
publication
Current views on the diagnosis and management of hypokalaemia in children
2016 |
Second Faculty of Medicine
publication
Bartter syndrome or renal tubular acidosis?
2003 |
First Faculty of Medicine