leucine and Autosomal Dominant Cerebellar Ataxia, Type II

leucine has been researched along with Autosomal Dominant Cerebellar Ataxia, Type II in 2 studies

Research

Studies (2)

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

Authors

Authors	Studies
Adrion, C; Bayer, O; Berger, I; Bösch, S; Claassen, J; Feil, K; Giordano, I; Hengel, H; Jacobi, H; Klockgether, T; Klopstock, T; Mansmann, U; Müller, HH; Nachbauer, W; Naumann, I; Schöls, L; Stendel, C; Strupp, M; Teufel, J; Uslar, E; van de Warrenburg, B	1
Michikawa, T; Mikoshiba, K; Nishizawa, M; Nozaki, H; Onodera, O; Yamazaki, H	1

Trials

1 trial(s) available for leucine and Autosomal Dominant Cerebellar Ataxia, Type II

Article	Year
Effects of acetyl-DL-leucine on cerebellar ataxia (ALCAT trial): study protocol for a multicenter, multinational, randomized, double-blind, placebo-controlled, crossover phase III trial. BMC neurology, 2017, Jan-10, Volume: 17, Issue:1 Topics: Adult; Cerebellar Ataxia; Cross-Over Studies; Double-Blind Method; Humans; Leucine; Psychiatric Status Rating Scales; Quality of Life; Spinocerebellar Ataxias	2017

Article

Year

Effects of acetyl-DL-leucine on cerebellar ataxia (ALCAT trial): study protocol for a multicenter, multinational, randomized, double-blind, placebo-controlled, crossover phase III trial.

BMC neurology, 2017, Jan-10, Volume: 17, Issue:1

Topics: Adult; Cerebellar Ataxia; Cross-Over Studies; Double-Blind Method; Humans; Leucine; Psychiatric Status Rating Scales; Quality of Life; Spinocerebellar Ataxias

2017

Other Studies

1 other study(ies) available for leucine and Autosomal Dominant Cerebellar Ataxia, Type II

Article	Year
Functional characterization of the P1059L mutation in the inositol 1,4,5-trisphosphate receptor type 1 identified in a Japanese SCA15 family. Biochemical and biophysical research communications, 2011, Jul-15, Volume: 410, Issue:4 Topics: Amino Acid Substitution; Asian People; Calcium; Cell Line; Humans; Inositol 1,4,5-Trisphosphate Receptors; Leucine; Pedigree; Proline; Protein Isoforms; Spinocerebellar Ataxias	2011

Article

Year

Functional characterization of the P1059L mutation in the inositol 1,4,5-trisphosphate receptor type 1 identified in a Japanese SCA15 family.

Biochemical and biophysical research communications, 2011, Jul-15, Volume: 410, Issue:4

Topics: Amino Acid Substitution; Asian People; Calcium; Cell Line; Humans; Inositol 1,4,5-Trisphosphate Receptors; Leucine; Pedigree; Proline; Protein Isoforms; Spinocerebellar Ataxias

2011