leucine and Fabry Disease

leucine has been researched along with Fabry Disease in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Imai, H; Kitagawa, W; Komatsuda, A; Miura, N; Nishikawa, K; Suzuki, K; Suzuki, S; Watanabe, D1
Fervenza, FC; Lager, D; Lai, LW; Leung, N; Lien, YH; Rosenthal, D; Shang, S1

Reviews

1 review(s) available for leucine and Fabry Disease

ArticleYear
Progressive renal failure despite long-term biweekly enzyme replacement therapy in a patient with Fabry disease secondary to a new α-galactosidase mutation of Leu311Arg (L311R).
    Clinical and experimental nephrology, 2011, Volume: 15, Issue:6

    Topics: Adult; alpha-Galactosidase; Arginine; Biopsy; Disease Progression; DNA Mutational Analysis; Drug Administration Schedule; Enzyme Replacement Therapy; Fabry Disease; Glomerular Filtration Rate; Humans; Isoenzymes; Kidney; Leucine; Male; Mutation; Recombinant Proteins; Renal Insufficiency; Time Factors; Treatment Outcome

2011

Other Studies

1 other study(ies) available for leucine and Fabry Disease

ArticleYear
A novel alpha-galactosidase a mutant (M42L) identified in a renal variant of Fabry disease.
    American journal of kidney diseases : the official journal of the National Kidney Foundation, 2004, Volume: 44, Issue:5

    Topics: Aged; alpha-Galactosidase; Amino Acid Substitution; Fabry Disease; Genetic Variation; Humans; Leucine; Male; Methionine; Mutation, Missense

2004