glycine has been researched along with Muscular Dystrophy in 26 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Seven patients, aged 10-17 years, with Duchenne muscular dystrophy were treated orally with prednisolone (PSL) at a dose of 0." | 7.68 | Decrease in urinary excretion of 3-methylhistidine by patients with Duchenne muscular dystrophy during glucocorticoid treatment. ( Adachi, K; Inui, T; Kawai, H; Kimura, C; Nishida, Y; Saito, S, 1993) |
| "Seven patients, aged 10-17 years, with Duchenne muscular dystrophy were treated orally with prednisolone (PSL) at a dose of 0." | 3.68 | Decrease in urinary excretion of 3-methylhistidine by patients with Duchenne muscular dystrophy during glucocorticoid treatment. ( Adachi, K; Inui, T; Kawai, H; Kimura, C; Nishida, Y; Saito, S, 1993) |
| "Dropped head syndrome is characterized by severe weakness of neck extensor muscles with sparing of the flexors." | 1.33 | Two patients with 'Dropped head syndrome' due to mutations in LMNA or SEPN1 genes. ( Benedetti, S; Bertini, E; Bonne, G; D'Amico, A; Ferreiro, A; Guicheney, P; Haliloglu, G; Maugenre, S; Menditto, I; Richard, P; Talim, B; Topaloglu, H, 2005) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 19 (73.08) | 18.7374 |
| 1990's | 3 (11.54) | 18.2507 |
| 2000's | 4 (15.38) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Pace, RA | 1 |
| Peat, RA | 1 |
| Baker, NL | 1 |
| Zamurs, L | 1 |
| Mörgelin, M | 1 |
| Irving, M | 1 |
| Adams, NE | 1 |
| Bateman, JF | 1 |
| Mowat, D | 1 |
| Smith, NJ | 1 |
| Lamont, PJ | 1 |
| Moore, SA | 1 |
| Mathews, KD | 1 |
| North, KN | 1 |
| Lamandé, SR | 1 |
| NIELSEN, JM | 1 |
| Tagawa, K | 1 |
| Ogawa, M | 1 |
| Kawabe, K | 1 |
| Yamanaka, G | 1 |
| Matsumura, T | 1 |
| Goto, K | 1 |
| Nonaka, I | 1 |
| Nishino, I | 1 |
| Hayashi, YK | 1 |
| COLEMAN, DL | 2 |
| ASHWORTH, ME | 1 |
| MAGGI, V | 1 |
| MAGARO, M | 1 |
| GRECO, AV | 1 |
| SENSI, S | 1 |
| GAMBASSI, G | 1 |
| DIEHL, JF | 1 |
| RIDDELL, WM | 1 |
| REFSUM, S | 1 |
| ROCHE, M | 1 |
| BENEDICT, JD | 1 |
| YU, TF | 1 |
| BIEN, EJ | 1 |
| STETTEN, D | 1 |
| D'Amico, A | 1 |
| Haliloglu, G | 1 |
| Richard, P | 1 |
| Talim, B | 2 |
| Maugenre, S | 1 |
| Ferreiro, A | 1 |
| Guicheney, P | 2 |
| Menditto, I | 1 |
| Benedetti, S | 1 |
| Bertini, E | 2 |
| Bonne, G | 1 |
| Topaloglu, H | 2 |
| Giusti, B | 1 |
| Lucarini, L | 1 |
| Pietroni, V | 1 |
| Lucioli, S | 1 |
| Bandinelli, B | 1 |
| Sabatelli, P | 1 |
| Squarzoni, S | 1 |
| Petrini, S | 1 |
| Gartioux, C | 1 |
| Roelens, F | 1 |
| Merlini, L | 1 |
| Pepe, G | 1 |
| Berlinguet, L | 1 |
| Srivastava, U | 1 |
| Lester, JM | 1 |
| Silber, DI | 1 |
| Bradley, WG | 1 |
| Cohen, MH | 1 |
| Hirsch, RP | 1 |
| Brenner, JF | 1 |
| Kawai, H | 1 |
| Adachi, K | 1 |
| Nishida, Y | 1 |
| Inui, T | 1 |
| Kimura, C | 1 |
| Saito, S | 1 |
| Pan, TC | 1 |
| Zhang, RZ | 1 |
| Pericak-Vance, MA | 1 |
| Tandan, R | 1 |
| Fries, T | 1 |
| Stajich, JM | 1 |
| Viles, K | 1 |
| Vance, JM | 1 |
| Chu, ML | 1 |
| Speer, MC | 1 |
| Marklová, E | 1 |
| Haymond, MW | 1 |
| Strobel, KE | 1 |
| DeVivo, DC | 1 |
| Goto, I | 1 |
| Peters, HA | 1 |
| Reese, HH | 1 |
| Yoshino, Y | 1 |
| Mozai, T | 1 |
| Ionasescu, V | 1 |
| Zellweger, H | 1 |
| Conway, TW | 1 |
| Kibrick, AC | 1 |
| Milhorat, AT | 2 |
| Harvey, JC | 1 |
| Nakahara, M | 1 |
| Yamada, S | 1 |
| D'Agostino, AN | 1 |
| Ziter, FA | 1 |
| Bray, PF | 1 |
| Maskaleris, ML | 1 |
| Gross, S | 1 |
| Morgan, DF | 1 |
| Herrmann, H | 1 |
26 other studies available for glycine and Muscular Dystrophy
| Article | Year |
|---|---|
Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severity.
Topics: Amino Acid Sequence; Cells, Cultured; Collagen Diseases; Collagen Type VI; Connective Tissue; Diseas | 2008 |
Glycine in childhood muscular dystrophy.
Topics: Glycine; Humans; Muscular Dystrophies | 1947 |
Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patients.
Topics: Age of Onset; Alanine; Blotting, Western; Calpain; Cysteine; Cytoskeletal Proteins; DNA Mutational A | 2003 |
Effects of dietary creatine and glycine on transamidinase activity in dystrophic mice.
Topics: Amidinotransferases; Animals; Creatine; Creatinine; Diet; Glycine; Kidney; Mice; Muscular Dystrophie | 1961 |
Incorporation of glycine-I-C14 into nucleic acids and proteins of mice with hereditary muscular dystrophy.
Topics: Animals; Biochemical Phenomena; Glycine; Mice; Muscles; Muscular Dystrophies; Nucleic Acids; Protein | 1959 |
[Research on hereditary myodystrophic mice. II. Protein].
Topics: Glycine; Muscular Dystrophies; Proteins | 1959 |
Incorporation of labeled glycine into erythrocyte glutathione of rabbits; effect of nutritional muscular dystrophy.
Topics: Animals; Erythrocytes; Glutathione; Glycine; Metabolic Diseases; Muscular Dystrophies; Rabbits; Vita | 1963 |
[RECENT TREATMENT OF MUSCULAR DYSTOPHY].
Topics: Amino Acids; Fabaceae; Glycine; Humans; Muscles; Muscular Dystrophies; Pyridoxine; Vitamin E | 1964 |
Origin of urinary creatine in progressive muscular dystrophy.
Topics: Creatine; Glycine; Humans; Muscular Dystrophies | 1952 |
Two patients with 'Dropped head syndrome' due to mutations in LMNA or SEPN1 genes.
Topics: Arginine; Child; DNA Mutational Analysis; Female; Glycine; Humans; Infant; Lamin Type A; Lamins; Mal | 2005 |
Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy.
Topics: Adolescent; Blotting, Northern; Blotting, Western; Child; Child, Preschool; Collagen Type VI; Connec | 2005 |
Effect of various amino acids on the incorporation of 14C-L-leucine in the tissue proteins of normal and dystrophic mice.
Topics: Amino Acids; Animals; Antineoplastic Agents; Aspartic Acid; Brain; Carbon Isotopes; Cycloparaffins; | 1967 |
Discrimination and consistency of five myosin ATPase stains in human normal and Duchenne dystrophic muscle.
Topics: Adenosine Triphosphatases; Adult; Ca(2+) Mg(2+)-ATPase; Calcium-Transporting ATPases; Child, Prescho | 1982 |
Decrease in urinary excretion of 3-methylhistidine by patients with Duchenne muscular dystrophy during glucocorticoid treatment.
Topics: Adolescent; Child; Creatine Kinase; Glycine; Humans; Male; Methylhistidines; Muscles; Muscular Dystr | 1993 |
Missense mutation in a von Willebrand factor type A domain of the alpha 3(VI) collagen gene (COL6A3) in a family with Bethlem myopathy.
Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Chromosomes, Human, Pair 2; Collagen; Contrac | 1998 |
Where does indolylacrylic acid come from?
Topics: Aging; Burns; Diet; Glycine; Humans; Indoles; Muscular Dystrophies; Skin Diseases; Tryptophan; Urina | 1999 |
Muscle wasting and carbohydrate homeostasis in Duchenne muscular dystrophy.
Topics: Adolescent; Alanine; Carbohydrate Metabolism; Child; Child, Preschool; Fasting; Glucose; Glucose Tol | 1978 |
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 |
[Aminoaciduria in patients with progressive muscular dystrophy].
Topics: Adolescent; Adult; Amino Acids; Child; Glycine; Humans; Male; Muscular Dystrophies; Taurine | 1972 |
Ribosomal protein synthesis in Duchenne muscular dystrophy.
Topics: Amino Acids; Carbon Isotopes; Cell Fractionation; Centrifugation, Density Gradient; Chemical Precipi | 1971 |
Glycylprolylhydroxyproline: methods for its quantitative determination in urine and blood serum.
Topics: Adult; Carbon Isotopes; Chemical Phenomena; Chemistry; Chromatography, Ion Exchange; Chromatography, | 1970 |
Reduced renal arginine-glycine transamidinase activity in myotonic goats and in patients with myotonic muscular dystrophy.
Topics: Acetates; Adult; Aged; Animals; Arginine; Autopsy; Biopsy; Creatine; Disease Models, Animal; Glycine | 1969 |
Studies on progressive muscular dystrophy. IV. Effects of original amino acids mixture on progressive muscular dystrophy.
Topics: Adenosine Triphosphate; Adolescent; Adult; Amino Acids; Arginine; Asparagine; Aspartic Acid; Blood P | 1967 |
Hereditary myopathy with abnormal muscle mitochondria.
Topics: Adolescent; Child; Female; Glycine; Growth Disorders; Humans; Mitochondria, Muscle; Muscular Dystrop | 1967 |
Urinary amino acid and peptide excretion patterns in patients with muscular dystrophy (Duchenne). A preliminary study with the autoanalyzer.
Topics: Adolescent; Alanine; Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Autoanalysis; Child; Child | 1969 |
Comparison of muscle tissue from normal and dystrophic chick at different stages of development.
Topics: Animals; DNA; Glycine; In Vitro Techniques; Muscle Proteins; Muscles; Muscular Dystrophies; Poultry | 1965 |