tryptophan and Chronic Progressive External Ophthalmoplegia

tryptophan 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	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bamberg, C; Baron, M; Deschauer, M; Klockgether, T; Kornblum, C; Kunz, WS; Paus, S; Zsurka, G	1
Ceuterick, C; De Jonghe, P; Dehaene, I; Dermaut, B; Löfgren, A; Martin, JJ; Moonen, M; Tack, P; Van Broeckhoven, C; Van Goethem, G; Van Zandijcke, M; Ververken, D; Wibail, A	1

Other Studies

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

Article	Year
Apraxia of lid opening mimicking ptosis in compound heterozygosity for A467T and W748S POLG1 mutations. Movement disorders : official journal of the Movement Disorder Society, 2008, Jul-15, Volume: 23, Issue:9 Topics: Adult; Apraxias; Blepharoptosis; DNA Mutational Analysis; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Female; Heterozygote; Humans; Mutation; Ophthalmoplegia, Chronic Progressive External; Serine; Siblings; Tryptophan	2008
Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia. Neuromuscular disorders : NMD, 2003, Volume: 13, Issue:2 Topics: Adolescent; Adult; Aged; Arginine; Ataxia; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Electron Transport Complex IV; Female; Genes, Recessive; Heterozygote; Humans; Magnetic Resonance Imaging; Male; Microscopy, Electron; Middle Aged; Molecular Sequence Data; Muscle, Skeletal; Mutation, Missense; Ophthalmoplegia, Chronic Progressive External; Pedigree; Succinate Dehydrogenase; Tryptophan	2003

Article

Year

Apraxia of lid opening mimicking ptosis in compound heterozygosity for A467T and W748S POLG1 mutations.

Movement disorders : official journal of the Movement Disorder Society, 2008, Jul-15, Volume: 23, Issue:9

Topics: Adult; Apraxias; Blepharoptosis; DNA Mutational Analysis; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Female; Heterozygote; Humans; Mutation; Ophthalmoplegia, Chronic Progressive External; Serine; Siblings; Tryptophan

2008

Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia.

Neuromuscular disorders : NMD, 2003, Volume: 13, Issue:2

Topics: Adolescent; Adult; Aged; Arginine; Ataxia; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Electron Transport Complex IV; Female; Genes, Recessive; Heterozygote; Humans; Magnetic Resonance Imaging; Male; Microscopy, Electron; Middle Aged; Molecular Sequence Data; Muscle, Skeletal; Mutation, Missense; Ophthalmoplegia, Chronic Progressive External; Pedigree; Succinate Dehydrogenase; Tryptophan

2003