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amiloride and Acidosis, Renal Tubular Type IV

amiloride has been researched along with Acidosis, Renal Tubular Type IV in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Barbry, P; Bassilana, F; Champigny, G; Corvol, P; Dumont, C; Jeunemaitre, X; Lazdunski, M; Persu, A	1
Bonny, O; Chraibi, A; Gründer, S; Horisberger, JD; Jaeger, NF; Loffing, J; Rossier, BC	1

Other Studies

2 other study(ies) available for amiloride and Acidosis, Renal Tubular Type IV

Article	Year
Genotype-phenotype analysis of a newly discovered family with Liddle's syndrome. Journal of hypertension, 1997, Volume: 15, Issue:10 Topics: Adolescent; Adult; Amiloride; Amino Acid Sequence; Animals; Base Sequence; Blood Pressure; Diuretics; DNA Probes; DNA, Complementary; Female; Gene Expression; Genotype; Humans; Hypertension; Hypoaldosteronism; Hypokalemia; Male; Middle Aged; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutation; Pedigree; Phenotype; Renin; Sequence Deletion; Sodium Channels; Syndrome; Xenopus laevis	1997
Functional expression of a pseudohypoaldosteronism type I mutated epithelial Na+ channel lacking the pore-forming region of its alpha subunit. The Journal of clinical investigation, 1999, Volume: 104, Issue:7 Topics: Amiloride; Animals; Codon, Terminator; Epithelial Sodium Channels; Female; Genes, Recessive; Humans; Hypoaldosteronism; Macromolecular Substances; Mutagenesis, Site-Directed; Oocytes; Rats; Recombinant Proteins; Sequence Deletion; Sodium Channels; Xenopus laevis	1999

Article

Year

Genotype-phenotype analysis of a newly discovered family with Liddle's syndrome.

Journal of hypertension, 1997, Volume: 15, Issue:10

Topics: Adolescent; Adult; Amiloride; Amino Acid Sequence; Animals; Base Sequence; Blood Pressure; Diuretics; DNA Probes; DNA, Complementary; Female; Gene Expression; Genotype; Humans; Hypertension; Hypoaldosteronism; Hypokalemia; Male; Middle Aged; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutation; Pedigree; Phenotype; Renin; Sequence Deletion; Sodium Channels; Syndrome; Xenopus laevis

1997

Functional expression of a pseudohypoaldosteronism type I mutated epithelial Na+ channel lacking the pore-forming region of its alpha subunit.

The Journal of clinical investigation, 1999, Volume: 104, Issue:7

Topics: Amiloride; Animals; Codon, Terminator; Epithelial Sodium Channels; Female; Genes, Recessive; Humans; Hypoaldosteronism; Macromolecular Substances; Mutagenesis, Site-Directed; Oocytes; Rats; Recombinant Proteins; Sequence Deletion; Sodium Channels; Xenopus laevis

1999