threonine and Leigh Disease

threonine has been researched along with Leigh Disease in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Baracca, A; Carelli, V; Lenaz, G; Sgarbi, G; Solaini, G; Valentino, LM	1
Bertini, E; De Meirleir, L; Dionisi-Vici, C; Fariello, G; Rimoldi, M; Seneca, S; Zeviani, M	1

Other Studies

2 other study(ies) available for threonine and Leigh Disease

Article	Year
Inefficient coupling between proton transport and ATP synthesis may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the T8993G mutation in mtDNA. The Biochemical journal, 2006, May-01, Volume: 395, Issue:3 Topics: Adenosine Triphosphate; Cell Membrane Permeability; Cells, Cultured; Digitonin; DNA, Mitochondrial; Female; Humans; Ion Transport; Leigh Disease; Male; Mutation; Pedigree; Protons; Retinitis Pigmentosa; Substrate Specificity; Syndrome; Threonine	2006
Fulminant Leigh syndrome and sudden unexpected death in a family with the T9176C mutation of the mitochondrial ATPase 6 gene. Journal of inherited metabolic disease, 1998, Volume: 21, Issue:1 Topics: Adenosine Triphosphatases; Cysteine; DNA, Mitochondrial; Humans; Infant; Leigh Disease; Male; Mitochondria; Pedigree; Point Mutation; Radiography; Sudden Infant Death; Threonine; Tomography Scanners, X-Ray Computed	1998

Article

Year

Inefficient coupling between proton transport and ATP synthesis may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the T8993G mutation in mtDNA.

The Biochemical journal, 2006, May-01, Volume: 395, Issue:3

Topics: Adenosine Triphosphate; Cell Membrane Permeability; Cells, Cultured; Digitonin; DNA, Mitochondrial; Female; Humans; Ion Transport; Leigh Disease; Male; Mutation; Pedigree; Protons; Retinitis Pigmentosa; Substrate Specificity; Syndrome; Threonine

2006

Fulminant Leigh syndrome and sudden unexpected death in a family with the T9176C mutation of the mitochondrial ATPase 6 gene.

Journal of inherited metabolic disease, 1998, Volume: 21, Issue:1

Topics: Adenosine Triphosphatases; Cysteine; DNA, Mitochondrial; Humans; Infant; Leigh Disease; Male; Mitochondria; Pedigree; Point Mutation; Radiography; Sudden Infant Death; Threonine; Tomography Scanners, X-Ray Computed

1998