threonine and Autosomal Dominant Hereditary Spastic Paraplegia

threonine has been researched along with Autosomal Dominant Hereditary Spastic Paraplegia in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (33.33)	18.2507
2000's	2 (66.67)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Blair, M; Fenichel, GM; Haines, JL; Hedera, P	1
Dam, M; Eiberg, H; Grønbech-Jensen, M; Hasholt, L; Johnsen, B; Koefoed, P; Krabbe, K; Krarup, C; Law, I; Nielsen, JE; Nørremølle, A; Paulson, OB; Rehfeld, JF; Scheuer, KH; Søndergård, H; Sørensen, SA	1
Growdon, JH; Nader, TM; Schoenfeld, J; Wurtman, RJ	1

Trials

1 trial(s) available for threonine and Autosomal Dominant Hereditary Spastic Paraplegia

Article	Year
L-threonine in the treatment of spasticity. Clinical neuropharmacology, 1991, Volume: 14, Issue:5 Topics: Adult; Aged; Double-Blind Method; Female; Humans; Male; Middle Aged; Spastic Paraplegia, Hereditary; Threonine	1991

Other Studies

2 other study(ies) available for threonine and Autosomal Dominant Hereditary Spastic Paraplegia

Article	Year
Novel mutation in the SPG3A gene in an African American family with an early onset of hereditary spastic paraplegia. Archives of neurology, 2004, Volume: 61, Issue:10 Topics: Adolescent; Adult; Black or African American; Child; Child, Preschool; Chromosomes, Human, Pair 14; DNA Mutational Analysis; Family Health; Female; Genotype; GTP Phosphohydrolases; GTP-Binding Proteins; Humans; Isoleucine; Male; Membrane Proteins; Middle Aged; Mutation; Pedigree; Spastic Paraplegia, Hereditary; Threonine	2004
Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation. European journal of neurology, 2004, Volume: 11, Issue:12 Topics: Adenosine Triphosphatases; Adult; Brain Mapping; Case-Control Studies; Cerebellar Ataxia; Cognition; Cysteine; DNA Mutational Analysis; Electroencephalography; Electromyography; Evoked Potentials; Family Health; Female; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Neural Conduction; Neuropsychological Tests; Phenotype; Positron-Emission Tomography; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Spastic Paraplegia, Hereditary; Spastin; Threonine	2004

Article

Year

Novel mutation in the SPG3A gene in an African American family with an early onset of hereditary spastic paraplegia.

Archives of neurology, 2004, Volume: 61, Issue:10

Topics: Adolescent; Adult; Black or African American; Child; Child, Preschool; Chromosomes, Human, Pair 14; DNA Mutational Analysis; Family Health; Female; Genotype; GTP Phosphohydrolases; GTP-Binding Proteins; Humans; Isoleucine; Male; Membrane Proteins; Middle Aged; Mutation; Pedigree; Spastic Paraplegia, Hereditary; Threonine

2004

Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.

European journal of neurology, 2004, Volume: 11, Issue:12

Topics: Adenosine Triphosphatases; Adult; Brain Mapping; Case-Control Studies; Cerebellar Ataxia; Cognition; Cysteine; DNA Mutational Analysis; Electroencephalography; Electromyography; Evoked Potentials; Family Health; Female; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Neural Conduction; Neuropsychological Tests; Phenotype; Positron-Emission Tomography; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Spastic Paraplegia, Hereditary; Spastin; Threonine

2004