Compounds > threonine

threonine and Dystonic Disorders

threonine has been researched along with Dystonic Disorders in 5 studies

Research

Studies (5)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	5 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Amouri, R; Driss, A; Hentati, F; Kefi, M; Murayama, K; Nishino, I	1
Funayama, M; Hasegawa, K; Ichinose, H; Obata, F; Ohta, E; Toyoshima, I	1
Funayama, M; Hasegawa, K; Ichinose, H; Maeda, K; Matsuo, M; Obata, F; Ohta, E; Shimazu, H; Tomoko, N; Toyoshima, I; Urano, F; Yokoyama, H; Yoshino, S; Yukihiko, K	1
Gollamudi, S; Jeon, BS; Kim, JY; Lee, JY; Ozelius, LJ	1
Chung, SJ; Ko, TS; Yoo, HW; Yum, MS	1

Other Studies

5 other study(ies) available for threonine and Dystonic Disorders

Article	Year
Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy. Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:5 Topics: Adult; DNA Mutational Analysis; Dystonic Disorders; Extremities; Family Health; Female; Histidine; Humans; Leucine; Male; Methionine; Middle Aged; Multienzyme Complexes; Muscle, Skeletal; Mutation; Myositis, Inclusion Body; Staining and Labeling; Threonine; Tunisia	2005
A new mutation (Thr106Ile) of the GTP cyclohydrolase 1 gene associated with DYT5 dystonia (Segawa disease). Movement disorders : official journal of the Movement Disorder Society, 2005, Volume: 20, Issue:8 Topics: Adult; Child; DNA Mutational Analysis; Dystonic Disorders; Exons; Female; GTP Cyclohydrolase; Humans; Isoleucine; Mutation; Threonine	2005
Novel mutations in the guanosine triphosphate cyclohydrolase 1 gene associated with DYT5 dystonia. Archives of neurology, 2006, Volume: 63, Issue:11 Topics: Adolescent; Adult; Animals; Biopterins; Child; Child, Preschool; DNA Mutational Analysis; Dystonic Disorders; Exons; Female; GTP Cyclohydrolase; Humans; Isoleucine; Japan; Male; Microsatellite Repeats; Mutation; Neopterin; Threonine	2006
ATP1A3 mutation in the first asian case of rapid-onset dystonia-parkinsonism. Movement disorders : official journal of the Movement Disorder Society, 2007, Sep-15, Volume: 22, Issue:12 Topics: Adult; Dystonic Disorders; Humans; Korea; Male; Methionine; Mutation; Parkinsonian Disorders; Sodium-Potassium-Exchanging ATPase; Threonine	2007
Autosomal-dominant guanosine triphosphate cyclohydrolase I deficiency with novel mutations. Pediatric neurology, 2008, Volume: 38, Issue:5 Topics: Child; DNA Mutational Analysis; Dystonic Disorders; Female; GTP Cyclohydrolase; Humans; Isoleucine; Korea; Male; Mutation; Threonine	2008