threonine and Chronic Progressive External Ophthalmoplegia

threonine has been researched along with Chronic Progressive External Ophthalmoplegia 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
Abicht, A; Bindoff, LA; Chinnery, PF; Czermin, B; de Coo, IF; De Vries, M; Dimauro, S; Gorman, GG; Hirano, M; Holinski-Feder, E; Horvath, R; Hudson, G; Jardel, C; Keiling, BC; Klopstock, T; Lochmüller, H; Lombès, A; Neeve, VC; Saft, C; Samuels, DC; Smeets, H; Smeitink, J; Smits, BW; Taylor, RW; Turnbull, DM; van den Bosch, B; Van Goethem, G	1
Blakely, EL; Deschauer, M; He, L; Kiefer, R; Taylor, RW; Turnbull, DM; Zierz, S	1

Other Studies

2 other study(ies) available for threonine and Chronic Progressive External Ophthalmoplegia

Article	Year
What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr? Brain : a journal of neurology, 2012, Volume: 135, Issue:Pt 12 Topics: Adolescent; Adult; Age of Onset; Alanine; Child; Cohort Studies; Diffuse Cerebral Sclerosis of Schilder; DNA Mutational Analysis; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Europe; Family Health; Female; Genetic Predisposition to Disease; Homozygote; Humans; Male; Middle Aged; Mitochondrial Diseases; Muscle, Skeletal; Mutation; Ophthalmoplegia, Chronic Progressive External; Statistics as Topic; Statistics, Nonparametric; Threonine; Young Adult	2012
A novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia. Neuromuscular disorders : NMD, 2003, Volume: 13, Issue:7-8 Topics: Adult; Aged; Base Sequence; Blotting, Southern; DNA Helicases; DNA Mutational Analysis; DNA Primase; DNA-Binding Proteins; Family Health; Female; Heterozygote; Humans; Lysine; Male; Middle Aged; Mitochondrial Proteins; Molecular Biology; Muscles; Mutation; Ophthalmoplegia, Chronic Progressive External; Pedigree; Polymorphism, Restriction Fragment Length; Reverse Transcriptase Polymerase Chain Reaction; Sequence Alignment; Threonine; Viral Proteins	2003

Article

Year

What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr?

Brain : a journal of neurology, 2012, Volume: 135, Issue:Pt 12

Topics: Adolescent; Adult; Age of Onset; Alanine; Child; Cohort Studies; Diffuse Cerebral Sclerosis of Schilder; DNA Mutational Analysis; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Europe; Family Health; Female; Genetic Predisposition to Disease; Homozygote; Humans; Male; Middle Aged; Mitochondrial Diseases; Muscle, Skeletal; Mutation; Ophthalmoplegia, Chronic Progressive External; Statistics as Topic; Statistics, Nonparametric; Threonine; Young Adult

2012

A novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia.

Neuromuscular disorders : NMD, 2003, Volume: 13, Issue:7-8

Topics: Adult; Aged; Base Sequence; Blotting, Southern; DNA Helicases; DNA Mutational Analysis; DNA Primase; DNA-Binding Proteins; Family Health; Female; Heterozygote; Humans; Lysine; Male; Middle Aged; Mitochondrial Proteins; Molecular Biology; Muscles; Mutation; Ophthalmoplegia, Chronic Progressive External; Pedigree; Polymorphism, Restriction Fragment Length; Reverse Transcriptase Polymerase Chain Reaction; Sequence Alignment; Threonine; Viral Proteins

2003