nad has been researched along with Acquired Metabolic Diseases, Brain in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (40.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 2 (40.00) | 24.3611 |
2020's | 1 (20.00) | 2.80 |
Authors | Studies |
---|---|
Bommireddipalli, S; Bournazos, AM; Christodoulou, J; Cooper, ST; Garza, D; Gooley, S; Gunanayagam, K; Jones, DL; Linster, CL; Lunke, S; McLean, CA; Naidoo, P; Patraskaki, M; Rajasekaran, M; Sebire, D; Semcesen, LN; Sikora, T; Stroud, DA; Van Bergen, NJ; Wallis, M; Walvekar, AS; Warmoes, MO | 1 |
Fu, X; Gao, H; Gao, J; Liang, Y; Lou, L; Luo, X; Ning, Q; Tian, F | 1 |
Amaral, AU; de Souza, DO; Goodman, SI; Leipnitz, G; Rodrigues, MD; Seminotti, B; Wajner, M; Woontner, M | 1 |
Becker, L; De Meirleir, L; Glerum, M; Robinson, BH; Sherwood, G | 1 |
Siemes, H | 1 |
5 other study(ies) available for nad and Acquired Metabolic Diseases, Brain
Article | Year |
---|---|
Severe NAD(P)HX Dehydratase (NAXD) Neurometabolic Syndrome May Present in Adulthood after Mild Head Trauma.
Topics: Adult; Brain Concussion; Brain Diseases, Metabolic; Child; Child, Preschool; Humans; Hydro-Lyases; Mitochondria; NAD; Neurodegenerative Diseases; Proteomics | 2023 |
Mechanistic effects of amino acids and glucose in a novel glutaric aciduria type 1 cell model.
Topics: Adenosine Triphosphate; Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Animals, Newborn; Apoptosis; Apoptosis Regulatory Proteins; Brain Diseases, Metabolic; Cell Culture Techniques; Cell Survival; Cells, Cultured; Citric Acid Cycle; Corpus Striatum; Flow Cytometry; Gene Expression; Glucose; Glutaryl-CoA Dehydrogenase; NAD; Neurons; Rats | 2014 |
Experimental evidence that overexpression of NR2B glutamate receptor subunit is associated with brain vacuolation in adult glutaryl-CoA dehydrogenase deficient mice: A potential role for glutamatergic-induced excitotoxicity in GA I neuropathology.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain Diseases, Metabolic; Brain Injuries; Catalase; Disease Models, Animal; Excitatory Amino Acid Transporter 2; Fluoresceins; Gene Expression Regulation; Glucosephosphate Dehydrogenase; Glutaryl-CoA Dehydrogenase; Glutathione; Glutathione Peroxidase; Glutathione Reductase; Malondialdehyde; Mice; Mice, Transgenic; NAD; Receptors, N-Methyl-D-Aspartate; Sulfhydryl Compounds; Superoxide Dismutase | 2015 |
Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase: clues to pathogenesis of Leigh disease.
Topics: Brain Diseases, Metabolic; Child; Child, Preschool; Citric Acid Cycle; Cytochrome-c Oxidase Deficiency; Female; Fibroblasts; Humans; Infant; Infant, Newborn; Lactates; Leigh Disease; Male; Mitochondria; NAD; NAD(P)H Dehydrogenase (Quinone); Pyruvates; Quinone Reductases | 1987 |
[Mitochondrial myopathies and encephalomyopathies. Neuromuscular and central nervous system diseases caused by defects in mitochondrial oxidative metabolism].
Topics: Brain; Brain Diseases, Metabolic; Carnitine O-Acetyltransferase; Child; Citric Acid Cycle; Cytochromes; Energy Metabolism; Enzymes; Humans; Lactates; Lactic Acid; Mitochondria, Muscle; Muscles; NAD; Neuromuscular Diseases; Pyruvate Dehydrogenase Complex Deficiency Disease; Pyruvates; Pyruvic Acid; Succinates; Succinic Acid | 1985 |