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Publications by Naoya Morisada
Differential Diagnosis of Bartter Syndrome, Gitelman Syndrome, and Pseudo–Bartter/Gitelman Syndrome Based on Clinical Characteristics
Genetics in Medicine
Medicine
Genetics
Breakpoint Analysis of the Recurrent Constitutional T(8;22)(q24.13;q11.21) Translocation
Molecular Cytogenetics
Biochemistry
Molecular Medicine
Genetics
Molecular Biology
Related publications
Unusual Suspects of Secondary Diabetes and Growth Retardation: Bartter and Gitelman Syndrome
Medical Science and Discovery
Persistent Severe Hypokalemia: Gitelman Syndrome and Differential Diagnosis
Journal of Kidney
Gitelman Syndrome
Hypertension
Internal Medicine
Gitelman Syndrome
Classic Bartter Syndrome
The Challenges of Diagnosis and Management of Gitelman Syndrome
Clinical Endocrinology
Endocrinology
Metabolism
Diabetes
Bartter Syndrome in Homozygous Twins
Problemy Endokrinologii
Endocrinology
Metabolism
Diabetes
Bartter- And Gitelman-Like Syndromes: Salt-Losing Tubulopathies With Loop or DCT Defects
Pediatric Nephrology
Child Health
Pediatrics
Perinatology
Nephrology
A Rare Cause of Rhabdomyolysis: Gitelman Syndrome
International Journal of Case Reports and Images