tryptophan and Encephalomyopathies, Mitochondrial

tryptophan has been researched along with Encephalomyopathies, Mitochondrial in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Karlsson, A; Larsson, NG; Lesko, N; Naess, K; Nennesmo, I; Solaroli, N; von Döbeln, U; Wibom, R	1

Other Studies

1 other study(ies) available for tryptophan and Encephalomyopathies, Mitochondrial

Article	Year
Two novel mutations in thymidine kinase-2 cause early onset fatal encephalomyopathy and severe mtDNA depletion. Neuromuscular disorders : NMD, 2010, Volume: 20, Issue:3 Topics: Adenosine Triphosphate; Arginine; Child; Child, Preschool; DNA Mutational Analysis; DNA, Mitochondrial; Female; Genetic Predisposition to Disease; Humans; Infant; Infant, Newborn; Male; Mitochondria; Mitochondria, Muscle; Mitochondrial Diseases; Mitochondrial Encephalomyopathies; Muscle, Skeletal; Mutagenesis, Site-Directed; Mutation; Thymidine Kinase; Tryptophan	2010

Article

Year

Two novel mutations in thymidine kinase-2 cause early onset fatal encephalomyopathy and severe mtDNA depletion.

Neuromuscular disorders : NMD, 2010, Volume: 20, Issue:3

Topics: Adenosine Triphosphate; Arginine; Child; Child, Preschool; DNA Mutational Analysis; DNA, Mitochondrial; Female; Genetic Predisposition to Disease; Humans; Infant; Infant, Newborn; Male; Mitochondria; Mitochondria, Muscle; Mitochondrial Diseases; Mitochondrial Encephalomyopathies; Muscle, Skeletal; Mutagenesis, Site-Directed; Mutation; Thymidine Kinase; Tryptophan

2010