arginine has been researched along with Mitochondrial Diseases in 22 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 5 (22.73) | 29.6817 |
| 2010's | 13 (59.09) | 24.3611 |
| 2020's | 4 (18.18) | 2.80 |
| Authors | Studies |
|---|---|
| Amit, I; Buchrieser, C; Cama, A; Croft, CA; Dardalhon, V; Di Santo, JP; Doisne, JM; Escoll, P; Guillemot, V; Marie, S; Musumeci, O; Petrosemoli, N; Surace, L; Taylor, N; Thaller, A; Topazio, D | 1 |
| Blain, AP; Errington, L; Gorman, GS; McFarland, R; Ng, YS; Stefanetti, RJ | 1 |
| Demczko, MM; Ganetzky, RD; He, M; Hong, X; Master, SR; Wongkittichote, P | 1 |
| Fukuda, M; Nagao, Y | 1 |
| Barros, CDS; Higa, EMS; Livramento, JB; Moraes, CT; Mouro, MG; Tengan, CH | 1 |
| Almannai, M; El-Hattab, AW; Scaglia, F; Zarante, AM | 1 |
| Goto, K; Ishikawa, T; Nakamura, K; Shimasaki, R; Umehara, F | 1 |
| Falk, MJ; Ganetzky, RD | 1 |
| Alberti, JM; Baloh, RH; Biris, N; Dorn, GW; Franco, A; Gavathiotis, E; Janetka, JW; Kitsis, RN; Knight, WC; Krezel, AM; Mochly-Rosen, D; Rocha, AG; Rumsey, JM; Townsend, RR; Zacharioudakis, E | 1 |
| Cintoni, M; Mele, MC; Pizzoferrato, M; Rinninella, E; Servidei, S | 1 |
| Ben-Sira, L; Blumkin, L; Edvardson, S; Henneke, M; Lerman-Sagie, T; Leshinsky-Silver, E; Lev, D; Nishri, D | 1 |
| Bordoni, A; Bresolin, N; Comi, GP; Corti, S; Crugnola, V; Del Bo, R; Donadoni, C; Fortunato, F; Lucchini, V; Moggio, M; Papadimitriou, D; Ronchi, D; Salani, S; Santoro, D | 1 |
| Kerr, DS | 2 |
| Karlsson, A; Larsson, NG; Lesko, N; Naess, K; Nennesmo, I; Solaroli, N; von Döbeln, U; Wibom, R | 1 |
| Bindoff, LA; Engelsen, BE; Ersland, L; Moen, G; Mørk, SJ; Neckelmann, G; Tzoulis, C; Viscomi, C; Zeviani, M | 1 |
| Finnilä, S; Hassinen, I; Hinttala, R; Kärppä, M; Komulainen, T; Majamaa, K; Pajunen, L; Rantala, H; Tuominen, H; Uusimaa, J | 1 |
| Kakimoto, N; Katayama, K; Koga, Y; Matsuishi, T; Nishioka, J; Povalko, N | 1 |
| Goto, Y; Momoi, M | 1 |
| Blakely, EL; Fisher, N; Jackson, MJ; Meunier, B; Mitchell, AL; Nijtmans, LG; Schaefer, AM; Taylor, RW; Turnbull, DM | 1 |
| Hara, T; Kanazawa, N; Kira, R; Sakai, Y; Sanefuji, M; Takemoto, M; Torisu, H; Tsujino, S | 1 |
| Ohashi, T; Ohno, K | 1 |
7 review(s) available for arginine and Mitochondrial Diseases
| Article | Year |
|---|---|
l-Arginine in Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes: A Systematic Review.
Topics: Acidosis, Lactic; Anticonvulsants; Arginine; Humans; Mitochondrial Diseases; Mitochondrial Encephalomyopathies; Retrospective Studies; Stroke | 2022 |
Therapies for mitochondrial diseases and current clinical trials.
Topics: Animals; Antioxidants; Arginine; Cardiolipins; Catechin; Clinical Trials as Topic; Electron Transport; Genetic Therapy; Humans; Liver Transplantation; Mice; Mitochondria; Mitochondrial Diseases; Nitric Oxide; Oxidative Phosphorylation; Triterpenes | 2017 |
Treatment of mitochondrial electron transport chain disorders: a review of clinical trials over the past decade.
Topics: Arginine; Clinical Trials as Topic; Dichloroacetic Acid; Humans; Mitochondrial Diseases; Randomized Controlled Trials as Topic; Treatment Outcome; Ubiquinone | 2010 |
MELAS and L-arginine therapy: pathophysiology of stroke-like episodes.
Topics: Arginine; Brain; Endothelium; Glucose; Homeostasis; Humans; Magnetic Resonance Imaging; MELAS Syndrome; Mitochondria; Mitochondrial Diseases; Models, Biological; Muscles; Oxygen; Stroke; Tomography, Emission-Computed, Single-Photon | 2010 |
Review of clinical trials for mitochondrial disorders: 1997-2012.
Topics: Antioxidants; Arginine; Clinical Trials as Topic; Creatine; Exercise Therapy; Humans; Mitochondrial Diseases; Ubiquinone | 2013 |
[Treatment for mitochondrial diseases].
Topics: Antioxidants; Arginine; Child; Dichloroacetic Acid; DNA, Mitochondrial; Humans; Mitochondrial Diseases; Mutation; Ubiquinone; Vitamins | 2004 |
[Diagnosis and treatment of hereditary neurological disorders during childhood].
Topics: alpha-Galactosidase; Arginine; Child; Coenzymes; Glucosylceramidase; Heredodegenerative Disorders, Nervous System; Humans; Isoenzymes; Lysosomal Storage Diseases; Mitochondrial Diseases; Molecular Diagnostic Techniques; Myotonic Dystrophy; Peripheral Nervous System Diseases; Peroxisomal Disorders; Trinucleotide Repeats; Ubiquinone; Vitamin E | 2007 |
15 other study(ies) available for arginine and Mitochondrial Diseases
| Article | Year |
|---|---|
Dichotomous metabolic networks govern human ILC2 proliferation and function.
Topics: Amino Acids, Branched-Chain; Arginine; Case-Control Studies; Cell Proliferation; Cells, Cultured; Cytokines; Energy Metabolism; Humans; Immunity, Innate; Interleukin-33; Lymphocyte Activation; Mitochondria; Mitochondrial Diseases; Phenotype; Th2 Cells | 2021 |
Low Plasma Citrulline Guiding the Diagnosis of a Mitochondrial Disorder.
Topics: Arginine; Citrulline; Humans; Mitochondrial Diseases | 2023 |
Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report.
Topics: Arginine; Aspartic Acid; Biomarkers; Deafness; Diabetes Mellitus, Type 2; DNA, Mitochondrial; Growth Differentiation Factor 15; Humans; Male; MELAS Syndrome; Middle Aged; Mitochondrial Diseases; Mutation | 2019 |
L-Arginine Reduces Nitro-Oxidative Stress in Cultured Cells with Mitochondrial Deficiency.
Topics: Arginine; Cell Line; DNA, Mitochondrial; Humans; Mitochondria; Mitochondrial Diseases; Mutation; Nitric Oxide; Oxidative Stress | 2021 |
[A case of mitochondrial disease with multiple mitochondrial DNA deletions suspected amyotrophic lateral sclerosis-frontotemporal dementia].
Topics: Aged; Amyotrophic Lateral Sclerosis; Arginine; Diagnosis, Differential; DNA, Mitochondrial; Fatal Outcome; Female; Frontotemporal Dementia; Gene Deletion; Humans; Mitochondria, Muscle; Mitochondrial Diseases; Muscle, Skeletal | 2018 |
8-year retrospective analysis of intravenous arginine therapy for acute metabolic strokes in pediatric mitochondrial disease.
Topics: Adolescent; Adult; Arginine; Brain; Child; Child, Preschool; Citrulline; DNA, Mitochondrial; Female; Humans; Infant; Infusions, Intravenous; Magnetic Resonance Imaging; Male; Mitochondria; Mitochondrial Diseases; Nitric Oxide; Prospective Studies; Retrospective Studies; Stroke; Treatment Outcome; Young Adult | 2018 |
MFN2 agonists reverse mitochondrial defects in preclinical models of Charcot-Marie-Tooth disease type 2A.
Topics: Amino Acid Substitution; Animals; Arginine; Axons; Charcot-Marie-Tooth Disease; Disease Models, Animal; Drug Design; Glutamine; GTP Phosphohydrolases; Humans; Methionine; Mice; Mice, Inbred C57BL; Mitochondria; Mitochondrial Diseases; Mitochondrial Proteins; Oligopeptides; Phosphorylation; Protein Kinases; Sciatic Nerve; Small Molecule Libraries; Threonine | 2018 |
Nutritional support in mitochondrial diseases: the state of the art.
Topics: Arginine; Deglutition Disorders; Diet, High-Fat; Energy Metabolism; Humans; Mitochondria; Mitochondrial Diseases; Nutritional Support; Thioctic Acid; Ubiquinone | 2018 |
Diagnosis by whole exome sequencing of atypical infantile onset Alexander disease masquerading as a mitochondrial disorder.
Topics: Alexander Disease; Arginine; Child, Preschool; Exome; Female; Frontal Lobe; Glial Fibrillary Acidic Protein; High-Throughput Nucleotide Sequencing; Humans; Magnetic Resonance Imaging; Mitochondrial Diseases; Mutation; Tryptophan; White Matter | 2014 |
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction.
Topics: Adult; Amyotrophic Lateral Sclerosis; Arginine; Cytochromes c; DNA Mutational Analysis; Family Health; Genetic Linkage; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Mitochondria, Muscle; Mitochondrial Diseases; Mutation; Superoxide Dismutase; Superoxide Dismutase-1 | 2009 |
Two novel mutations in thymidine kinase-2 cause early onset fatal encephalomyopathy and severe mtDNA depletion.
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 |
Localized cerebral energy failure in DNA polymerase gamma-associated encephalopathy syndromes.
Topics: Arginine; Brain; Brain Diseases; Cerebellum; Cysteine; Diffuse Cerebral Sclerosis of Schilder; Diffusion Magnetic Resonance Imaging; Disease Progression; DNA Polymerase gamma; DNA-Directed DNA Polymerase; DNA, Mitochondrial; Electroencephalography; Energy Metabolism; Epilepsy; Glycine; Humans; Magnetic Resonance Angiography; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Mitochondrial Diseases; Mutation; Neocortex; Sensitivity and Specificity; Spinocerebellar Ataxias; Stroke; Syndrome; Thalamus; Tomography, X-Ray Computed | 2010 |
POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype.
Topics: Aged, 80 and over; Arginine; Brain; Deglutition Disorders; Diabetes Mellitus, Type 2; Disease Progression; DNA Polymerase gamma; DNA-Directed DNA Polymerase; DNA, Mitochondrial; Histidine; Humans; Male; Mitochondrial Diseases; Mutation; Ophthalmoplegia; Phenotype | 2010 |
A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast.
Topics: Adult; Amino Acid Sequence; Animals; Arginine; Base Sequence; Biopsy; Cytochromes b; DNA, Mitochondrial; Female; Guanidine; Humans; Mitochondrial Diseases; Models, Molecular; Molecular Sequence Data; Muscles; Mutation; Protein Structure, Quaternary; Protein Subunits; Saccharomyces cerevisiae | 2005 |
A novel R275X mutation of the SLC25A15 gene in a Japanese patient with the HHH syndrome.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acid Transport Systems, Basic; Arginine; DNA Mutational Analysis; Female; Humans; Hyperammonemia; Japan; Male; Mitochondrial Diseases; Mitochondrial Membrane Transport Proteins; Mutation; Proteins | 2006 |