leucine and Alexander Disease

leucine has been researched along with Alexander 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
Ichihashi, J; Kitada, M; Kusunoki, S; Mistui, Y; Nakagawa, M; Nishikawa, Y; Sasayama, H; Suzuki, H; Yoshida, T1
Adachi, M; Hayasaka, K; Kato, M; Sawaishi, Y; Shiihara, T1

Other Studies

2 other study(ies) available for leucine and Alexander Disease

ArticleYear
Late-onset Alexander disease with a V87L mutation in glial fibrillary acidic protein (GFAP) and calcifying lesions in the sub-cortex and cortex.
    Journal of neurology, 2012, Volume: 259, Issue:3

    Topics: Adult; Alexander Disease; Brain; Calcinosis; DNA Mutational Analysis; Female; Glial Fibrillary Acidic Protein; Humans; Leucine; Magnetic Resonance Imaging; Mutation; Valine

2012
Asymptomatic hereditary Alexander's disease caused by a novel mutation in GFAP.
    Journal of the neurological sciences, 2004, Oct-15, Volume: 225, Issue:1-2

    Topics: Alexander Disease; Brain; Child; DNA Mutational Analysis; Exons; Female; Glial Fibrillary Acidic Protein; Humans; Infant; Leucine; Magnetic Resonance Imaging; Male; Mutation; Proline; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger

2004