threonine and Aldosteronism with Hyperplasia of the Adrenal Cortex

threonine has been researched along with Aldosteronism with Hyperplasia of the Adrenal Cortex in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bilbao, JR; Castaño, L; Pérez de Nanclares, G; Rodríguez-Soriano, J; Vallo, A1

Other Studies

1 other study(ies) available for threonine and Aldosteronism with Hyperplasia of the Adrenal Cortex

ArticleYear
A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain.
    Pediatric nephrology (Berlin, Germany), 2005, Volume: 20, Issue:7

    Topics: Adolescent; Alanine; Amino Acid Substitution; Anion Transport Proteins; Bartter Syndrome; Base Sequence; Child; Child, Preschool; Chloride Channels; DNA Mutational Analysis; Founder Effect; Genotype; Homozygote; Humans; Infant; Membrane Proteins; Mutation, Missense; Phenotype; Point Mutation; Spain; Threonine

2005