isoleucine and Cerebellar Ataxia

isoleucine has been researched along with Cerebellar Ataxia 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	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Choi, JH; Choi, KD; Choi, SY; Jen, JC; Kim, HJ; Kim, HS; Kim, JS; Shin, JH	1
Cusimano, A; D'Adamo, MC; De Curtis, A; Imbrici, P; Pessia, M	1

Other Studies

2 other study(ies) available for isoleucine and Cerebellar Ataxia

Article	Year
Late-onset episodic ataxia associated with SLC1A3 mutation. Journal of human genetics, 2017, Volume: 62, Issue:3 Topics: Acetazolamide; Adult; Age of Onset; Amino Acid Sequence; Amino Acid Substitution; Anticonvulsants; Base Sequence; Cerebellar Ataxia; Excitatory Amino Acid Transporter 1; Female; Gene Expression; Heterozygote; Humans; Isoleucine; Male; Middle Aged; Models, Molecular; Mutation; Pedigree; Phenotype; Sequence Alignment; Valine	2017
Functional characterization of an episodic ataxia type-1 mutation occurring in the S1 segment of hKv1.1 channels. Pflugers Archiv : European journal of physiology, 2003, Volume: 446, Issue:3 Topics: Amino Acid Substitution; Animals; Asparagine; Biophysical Phenomena; Biophysics; Cerebellar Ataxia; Electric Conductivity; Humans; Ion Channel Gating; Isoleucine; Kinetics; Kv1.1 Potassium Channel; Mutation; Oocytes; Patch-Clamp Techniques; Potassium Channels; Potassium Channels, Voltage-Gated; Xenopus laevis	2003

Article

Year

Late-onset episodic ataxia associated with SLC1A3 mutation.

Journal of human genetics, 2017, Volume: 62, Issue:3

Topics: Acetazolamide; Adult; Age of Onset; Amino Acid Sequence; Amino Acid Substitution; Anticonvulsants; Base Sequence; Cerebellar Ataxia; Excitatory Amino Acid Transporter 1; Female; Gene Expression; Heterozygote; Humans; Isoleucine; Male; Middle Aged; Models, Molecular; Mutation; Pedigree; Phenotype; Sequence Alignment; Valine

2017

Functional characterization of an episodic ataxia type-1 mutation occurring in the S1 segment of hKv1.1 channels.

Pflugers Archiv : European journal of physiology, 2003, Volume: 446, Issue:3

Topics: Amino Acid Substitution; Animals; Asparagine; Biophysical Phenomena; Biophysics; Cerebellar Ataxia; Electric Conductivity; Humans; Ion Channel Gating; Isoleucine; Kinetics; Kv1.1 Potassium Channel; Mutation; Oocytes; Patch-Clamp Techniques; Potassium Channels; Potassium Channels, Voltage-Gated; Xenopus laevis

2003