glycine has been researched along with Muscle Disorders in 31 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Sivelestat was given for the complication of ARDS." | 1.42 | Elevation of pivaloylcarnitine by sivelestat sodium in two children. ( Bo, R; Hasegawa, Y; Ishige, N; Kobayashi, H; Nakamura, M; Takahashi, T; Yamada, K; Yamaguchi, S, 2015) |
| "Treatment with creatine monohydrate (100-800 mg/kg/day) resulted in almost complete restoration of brain creatine levels and significant improvement of myopathy." | 1.42 | Arginine:glycine amidinotransferase (AGAT) deficiency: Clinical features and long term outcomes in 16 patients diagnosed worldwide. ( Apatean, D; Battini, R; DeBrosse, S; Dessoffy, K; Dowling, MD; Edvardson, S; Eichler, F; Johnston, K; Koeller, DM; Nouioua, S; Stockler-Ipsiroglu, S; Tazir, M; Verma, A; Wierenga, AM; Wierenga, KJ; Wong, LJ; Zhang, V, 2015) |
| "Brain MRI showed deep intracerebral hemorrhages of different age, diffuse leukoencephalopathy, multiple cerebral microbleeds and small aneurysms of the carotid siphon bilaterally." | 1.40 | COL4A2 mutation causing adult onset recurrent intracerebral hemorrhage and leukoencephalopathy. ( Audrezet, MP; Bereczki, D; Gunda, B; Hornyák, C; Kovács, T; Mine, M; Rudas, G; Tournier-Lasserve, E; Várallyay, G, 2014) |
| "Miyoshi distal myopathy (MM) and limb girdle muscular dystrophy type 2B (LGMD2B) were found to map to the same mutant gene encoding for dysferlin on chromosome 2p13." | 1.32 | Phenotypic features and genetic findings in 2 chinese families with Miyoshi distal myopathy. ( Chen, CM; Chen, ST; Lee-Chen, GJ; Lin, CY; Lin, TC; Ro, LS; Wu, YR, 2004) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 9 (29.03) | 18.7374 |
| 1990's | 1 (3.23) | 18.2507 |
| 2000's | 8 (25.81) | 29.6817 |
| 2010's | 9 (29.03) | 24.3611 |
| 2020's | 4 (12.90) | 2.80 |
| Authors | Studies |
|---|---|
| Jahn, P | 1 |
| Dobešová, D | 1 |
| Brumarová, R | 1 |
| Tóthová, K | 1 |
| Kopecká, A | 1 |
| Friedecký, D | 1 |
| Balestrino, M | 1 |
| Adriano, E | 1 |
| Neu, A | 1 |
| Hornig, S | 1 |
| Sasani, A | 1 |
| Isbrandt, D | 1 |
| Gerloff, C | 1 |
| Tsikas, D | 1 |
| Schwedhelm, E | 1 |
| Choe, CU | 1 |
| Bochnia, M | 2 |
| Ziemssen, E | 1 |
| Sander, J | 2 |
| Stief, B | 1 |
| Zeyner, A | 2 |
| Córdova-Noboa, HA | 2 |
| Oviedo-Rondón, EO | 2 |
| Sarsour, AH | 2 |
| Barnes, J | 2 |
| Sapcota, D | 1 |
| López, D | 1 |
| Gross, L | 1 |
| Rademacher-Heilshorn, M | 2 |
| Braun, U | 2 |
| Ferzola, P | 1 |
| Ziegler, J | 1 |
| Terhardt, M | 1 |
| Sander, S | 1 |
| Janzen, N | 1 |
| Cavalleri, JV | 1 |
| Zuraw, A | 1 |
| Wensch-Dorendorf, M | 1 |
| Butterfield, RJ | 1 |
| Foley, AR | 1 |
| Dastgir, J | 1 |
| Asman, S | 1 |
| Dunn, DM | 1 |
| Zou, Y | 1 |
| Hu, Y | 1 |
| Donkervoort, S | 1 |
| Flanigan, KM | 1 |
| Swoboda, KJ | 1 |
| Winder, TL | 1 |
| Weiss, RB | 1 |
| Bönnemann, CG | 1 |
| Gunda, B | 1 |
| Mine, M | 1 |
| Kovács, T | 1 |
| Hornyák, C | 1 |
| Bereczki, D | 1 |
| Várallyay, G | 1 |
| Rudas, G | 1 |
| Audrezet, MP | 1 |
| Tournier-Lasserve, E | 1 |
| Yamada, K | 1 |
| Kobayashi, H | 1 |
| Bo, R | 1 |
| Takahashi, T | 1 |
| Hasegawa, Y | 1 |
| Nakamura, M | 1 |
| Ishige, N | 1 |
| Yamaguchi, S | 1 |
| Stockler-Ipsiroglu, S | 1 |
| Apatean, D | 1 |
| Battini, R | 1 |
| DeBrosse, S | 1 |
| Dessoffy, K | 1 |
| Edvardson, S | 1 |
| Eichler, F | 1 |
| Johnston, K | 1 |
| Koeller, DM | 1 |
| Nouioua, S | 1 |
| Tazir, M | 1 |
| Verma, A | 1 |
| Dowling, MD | 1 |
| Wierenga, KJ | 1 |
| Wierenga, AM | 1 |
| Zhang, V | 1 |
| Wong, LJ | 1 |
| Jeanne, M | 1 |
| Gould, DB | 1 |
| Nevzorov, I | 1 |
| Redwood, C | 1 |
| Levitsky, D | 1 |
| Briñas, L | 1 |
| Richard, P | 1 |
| Quijano-Roy, S | 1 |
| Gartioux, C | 1 |
| Ledeuil, C | 1 |
| Lacène, E | 1 |
| Makri, S | 1 |
| Ferreiro, A | 1 |
| Maugenre, S | 1 |
| Topaloglu, H | 1 |
| Haliloglu, G | 1 |
| Pénisson-Besnier, I | 1 |
| Jeannet, PY | 1 |
| Merlini, L | 1 |
| Navarro, C | 1 |
| Toutain, A | 1 |
| Chaigne, D | 1 |
| Desguerre, I | 1 |
| de Die-Smulders, C | 1 |
| Dunand, M | 1 |
| Echenne, B | 1 |
| Eymard, B | 1 |
| Kuntzer, T | 1 |
| Maincent, K | 1 |
| Mayer, M | 1 |
| Plessis, G | 1 |
| Rivier, F | 1 |
| Roelens, F | 1 |
| Stojkovic, T | 1 |
| Taratuto, AL | 1 |
| Lubieniecki, F | 1 |
| Monges, S | 1 |
| Tranchant, C | 1 |
| Viollet, L | 1 |
| Romero, NB | 1 |
| Estournet, B | 1 |
| Guicheney, P | 1 |
| Allamand, V | 1 |
| Gross, M | 1 |
| Rötzer, E | 1 |
| Kölle, P | 1 |
| Mortier, W | 1 |
| Reichmann, H | 1 |
| Goebel, HH | 1 |
| Lochmüller, H | 2 |
| Pongratz, D | 1 |
| Mahnke-Zizelman, DK | 1 |
| Sabina, RL | 1 |
| Dalakas, MC | 1 |
| Dagvadorj, A | 1 |
| Goudeau, B | 1 |
| Park, KY | 1 |
| Takeda, K | 1 |
| Simon-Casteras, M | 1 |
| Vasconcelos, O | 1 |
| Sambuughin, N | 1 |
| Shatunov, A | 1 |
| Nagle, JW | 1 |
| Sivakumar, K | 1 |
| Vicart, P | 1 |
| Goldfarb, LG | 1 |
| CUMINGS, JN | 1 |
| ALDES, JH | 1 |
| Schmidt, MR | 1 |
| Birkebaek, N | 1 |
| Gonzalez, I | 1 |
| Sunde, L | 1 |
| Ro, LS | 1 |
| Lee-Chen, GJ | 1 |
| Lin, TC | 1 |
| Wu, YR | 1 |
| Chen, CM | 1 |
| Lin, CY | 1 |
| Chen, ST | 1 |
| Stewart, HG | 1 |
| Mackenzie, IR | 1 |
| Eisen, A | 1 |
| Brännström, T | 1 |
| Marklund, SL | 1 |
| Andersen, PM | 1 |
| Horvath, R | 1 |
| Kley, RA | 1 |
| Vorgerd, M | 1 |
| Hamaguchi, C | 1 |
| Nozima, M | 1 |
| Nakata, T | 1 |
| Hatanaka, Y | 1 |
| Ueda, K | 1 |
| Afting, EG | 1 |
| Bernhardt, W | 1 |
| Janzen, RW | 1 |
| Röthig, HJ | 1 |
| Rabier, D | 1 |
| Diry, C | 1 |
| Rotig, A | 1 |
| Rustin, P | 1 |
| Heron, B | 1 |
| Bardet, J | 1 |
| Parvy, P | 1 |
| Ponsot, G | 1 |
| Marsac, C | 1 |
| Saudubray, JM | 1 |
| Munnich, A | 1 |
| Kamoun, P | 1 |
| Lamandé, SR | 1 |
| Mörgelin, M | 1 |
| Selan, C | 1 |
| Jöbsis, GJ | 1 |
| Baas, F | 1 |
| Bateman, JF | 1 |
| Turnbull, DM | 1 |
| Bartlett, K | 1 |
| Eyre, JA | 1 |
| Gardner-Medwin, D | 1 |
| Johnson, MA | 1 |
| Fisher, J | 1 |
| Watmough, NJ | 1 |
| Goto, I | 1 |
| Peters, HA | 1 |
| Reese, HH | 1 |
| Bachmann, C | 1 |
| Mihatsch, MJ | 1 |
| Baumgartner, RE | 1 |
| Brechbühler, T | 1 |
| Bühler, UK | 1 |
| Olafsson, A | 1 |
| Ohnacker, H | 1 |
| Wick, H | 1 |
| Hurwitz, LJ | 1 |
| Carson, NA | 1 |
| Allen, IV | 1 |
| Chopra, JS | 1 |
| Girlando, V | 1 |
2 reviews available for glycine and Muscle Disorders
| Article | Year |
|---|---|
Genotype-phenotype correlations in pathology caused by collagen type IV alpha 1 and 2 mutations.
Topics: Amino Acid Substitution; Animals; Basement Membrane; Cerebrovascular Disorders; Collagen Type IV; Ge | 2017 |
Stability of two beta-tropomyosin isoforms: effects of mutation Arg91Gly.
Topics: Animals; Arginine; Glycine; Humans; Muscular Diseases; Mutation; Protein Isoforms; Protein Stability | 2008 |
29 other studies available for glycine and Muscle Disorders
| Article | Year |
|---|---|
Dynamics of acylcarnitines, hypoglycin A, méthylènecyclopropylglycine and their metabolites in a Kladruber stallion with atypical myopathy.
Topics: Acyl-CoA Dehydrogenases; Animals; Carnitine; Creatine Kinase; Cyclopropanes; Fatty Acids; Glycine; H | 2022 |
Presence of guanidinoacetate may compensate creatine absence and account for less statin-induced muscle damage in GAMT-deficient compared to AGAT-deficient mice.
Topics: Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Animals; Creatine; Developmental Disabili | 2020 |
Creatine, guanidinoacetate and homoarginine in statin-induced myopathy.
Topics: Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Animals; Creatine; Developmental Disabili | 2020 |
Methylenecyclopropylglycine and hypoglycin A intoxication in three Pére David's Deers (Elaphurus davidianus) with atypical myopathy.
Topics: Acer; Animals; Cyclopropanes; Deer; Female; Gastrointestinal Contents; Glycine; Hypoglycins; Male; M | 2021 |
Effect of guanidinoacetic acid supplementation on live performance, meat quality, pectoral myopathies and blood parameters of male broilers fed corn-based diets with or without poultry by-products.
Topics: Animal Feed; Animal Nutritional Physiological Phenomena; Animals; Blood Chemical Analysis; Chickens; | 2018 |
Performance, meat quality, and pectoral myopathies of broilers fed either corn or sorghum based diets supplemented with guanidinoacetic acid.
Topics: Animal Feed; Animal Nutritional Physiological Phenomena; Animals; Chickens; Diet; Dietary Supplement | 2018 |
Detection of MCPG metabolites in horses with atypical myopathy.
Topics: Acer; Animals; Chromatography, High Pressure Liquid; Cyclopropanes; Female; Glycine; Horse Diseases; | 2019 |
Position of glycine substitutions in the triple helix of COL6A1, COL6A2, and COL6A3 is correlated with severity and mode of inheritance in collagen VI myopathies.
Topics: Adolescent; Adult; Amino Acid Substitution; Child; Child, Preschool; Collagen Type VI; Fibroblasts; | 2013 |
COL4A2 mutation causing adult onset recurrent intracerebral hemorrhage and leukoencephalopathy.
Topics: Adult; Cerebral Hemorrhage; Collagen Type IV; Genetic Testing; Glycine; Humans; Intracranial Aneurys | 2014 |
Elevation of pivaloylcarnitine by sivelestat sodium in two children.
Topics: Amino Acid Metabolism, Inborn Errors; Cardiomyopathies; Carnitine; Child, Preschool; Chromatography, | 2015 |
Arginine:glycine amidinotransferase (AGAT) deficiency: Clinical features and long term outcomes in 16 patients diagnosed worldwide.
Topics: Adolescent; Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Crea | 2015 |
Early onset collagen VI myopathies: Genetic and clinical correlations.
Topics: Adolescent; Adult; Cells, Cultured; Child; Child, Preschool; Collagen Type VII; Europe; Female; Fibr | 2010 |
A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian population.
Topics: Alleles; AMP Deaminase; Blotting, Western; DNA Probes; DNA, Complementary; Electromyography; Genotyp | 2002 |
Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutations.
Topics: Alanine; Animals; Carcinoma; Cell Line; Cysteine; Desmin; DNA Mutational Analysis; Female; Fluoresce | 2003 |
Creatine and guanidoacetic acid metabolism in muscle disease.
Topics: Acetates; Blood; Creatine; Disease; Glycine; Muscles; Muscular Diseases; Urine | 1953 |
Glycocyamine betaine as an adjunct in the treatment of neuromuscular disease patients.
Topics: Amidines; Betaine; Choline; Disease; Glycine; Humans; Muscles; Muscular Diseases; Neuromuscular Dise | 1957 |
Barth syndrome without 3-methylglutaconic aciduria.
Topics: Arginine; Cardiomyopathies; Chromosomes, Human, X; Fatal Outcome; Glutarates; Glycine; Humans; Infan | 2004 |
Phenotypic features and genetic findings in 2 chinese families with Miyoshi distal myopathy.
Topics: Adolescent; Adult; Asian People; Distal Myopathies; DNA Mutational Analysis; Dysferlin; Exons; Famil | 2004 |
Clinicopathological phenotype of ALS with a novel G72C SOD1 gene mutation mimicking a myopathy.
Topics: Aged; Amyotrophic Lateral Sclerosis; Blotting, Western; Creatine; Cysteine; DNA Mutational Analysis; | 2006 |
Parkinson syndrome, neuropathy, and myopathy caused by the mutation A8344G (MERRF) in tRNALys.
Topics: Aged; Alanine; Amino Acid Substitution; Glycine; Humans; Male; MERRF Syndrome; Muscle, Skeletal; Mus | 2007 |
Enzymatic studies on the mechanism of creatinuria in rats with experimental thyrotoxic myopathy and dystrophic mice.
Topics: Amidinotransferases; Animals; Creatine; Enzyme Activation; Glycine; Kidney; Male; Mice; Mice, Inbred | 1981 |
Quantitative importance of non-skeletal-muscle N tau-methylhistidine and creatine in human urine.
Topics: Creatine; Creatinine; Glycine; Histidine; Humans; Male; Methylhistidines; Middle Aged; Muscles; Musc | 1981 |
Persistent hypocitrullinaemia as a marker for mtDNA NARP T 8993 G mutation?
Topics: Abnormalities, Multiple; Ataxia; Biomarkers; Child, Preschool; Citrulline; DNA, Mitochondrial; Femal | 1998 |
Kinked collagen VI tetramers and reduced microfibril formation as a result of Bethlem myopathy and introduced triple helical glycine mutations.
Topics: Biopolymers; Cells, Cultured; Collagen; Glycine; Heterozygote; Humans; Microscopy, Electron; Muscula | 2002 |
Lipid storage myopathy due to glutaric aciduria type II: treatment of a potentially fatal myopathy.
Topics: Carnitine; Female; Glutarates; Glutaryl-CoA Dehydrogenase; Glycine; Humans; Infant; Lipid Metabolism | 1988 |
Pyruvic and lactic acid metabolism in muscular dystrophy, neuropathies and other neuromuscular disorders.
Topics: Adolescent; Adult; Child; Child, Preschool; Edetic Acid; Female; Glycine; Humans; Lactates; Male; Mi | 1967 |
[Non-ketotic hyperglycinemia: peracute course in neonatal period].
Topics: Acute Disease; Amino Acids; Biopsy; Brain; Cerebellum; Fatty Liver; Glycine; Hiccup; Humans; Infant, | 1971 |
Congenital ophthalmoplegia, floppy baby syndrome, myopathy, and aminoaciduria. Report of a family.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Biopsy; Child; Chromatography, Paper; Chrom | 1969 |
[New etio-pathogenetic, clinical and therapeutic trend in idiopathic scoliosis].
Topics: Adolescent; Amino Acids; Child; Child, Preschool; Creatine Kinase; Female; Fructose-Bisphosphate Ald | 1970 |