glycerol has been researched along with Muscular Dystrophy in 10 studies
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| Excerpt | Relevance | Reference |
|---|---|---|
| "We describe an infant with adrenal insufficiency who was subsequently diagnosed with Duchenne muscular dystrophy (DMD) and hyperglycerolemia due to glycerol kinase deficiency." | 7.69 | Congenital adrenal hypoplasia, Duchenne muscular dystrophy, and glycerol kinase deficiency: importance of laboratory investigations in delineating a contiguous gene deletion syndrome. ( Clarke, LA; Cole, DE; Riddell, DC; Salisbury, S; Samson, KA; Seltzer, WK, 1994) |
| "In studies of the X chromosomes of two unrelated boys with adrenal hypoplasia, glycerol kinase deficiency, Duchenne muscular dystrophy, and mental retardation, conventional G banding did not reveal any numerical or structural abnormality, but direct DNA analysis with the X short-arm probes 754, C7, and OCT revealed a deletion in 1 of these patients." | 7.67 | Deletion on the X chromosome detected by direct DNA analysis in one of two unrelated boys with glycerol kinase deficiency, adrenal hypoplasia, and Duchenne muscular dystrophy. ( Davies, KE; Dillon, MJ; Dunger, DB; Lake, B; Pearson, P; Pembrey, M; Whitfield, A; Williams, D, 1986) |
| "We report an interstitial deletion in the short arm of the X chromosome in a 6-year-old boy with Duchenne muscular dystrophy, glycerol kinase deficiency, adrenal insufficiency, intermittent hypoglycemia, spasticity, psychomotor retardation, and growth delay." | 7.67 | Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletion. ( Bartley, JA; Davenport, S; Goldstein, D; Patil, S; Pickens, J, 1986) |
| "We describe an infant with adrenal insufficiency who was subsequently diagnosed with Duchenne muscular dystrophy (DMD) and hyperglycerolemia due to glycerol kinase deficiency." | 3.69 | Congenital adrenal hypoplasia, Duchenne muscular dystrophy, and glycerol kinase deficiency: importance of laboratory investigations in delineating a contiguous gene deletion syndrome. ( Clarke, LA; Cole, DE; Riddell, DC; Salisbury, S; Samson, KA; Seltzer, WK, 1994) |
| "In studies of the X chromosomes of two unrelated boys with adrenal hypoplasia, glycerol kinase deficiency, Duchenne muscular dystrophy, and mental retardation, conventional G banding did not reveal any numerical or structural abnormality, but direct DNA analysis with the X short-arm probes 754, C7, and OCT revealed a deletion in 1 of these patients." | 3.67 | Deletion on the X chromosome detected by direct DNA analysis in one of two unrelated boys with glycerol kinase deficiency, adrenal hypoplasia, and Duchenne muscular dystrophy. ( Davies, KE; Dillon, MJ; Dunger, DB; Lake, B; Pearson, P; Pembrey, M; Whitfield, A; Williams, D, 1986) |
| "We report an interstitial deletion in the short arm of the X chromosome in a 6-year-old boy with Duchenne muscular dystrophy, glycerol kinase deficiency, adrenal insufficiency, intermittent hypoglycemia, spasticity, psychomotor retardation, and growth delay." | 3.67 | Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletion. ( Bartley, JA; Davenport, S; Goldstein, D; Patil, S; Pickens, J, 1986) |
| "The incorporation of [3H] glycerol into lipids of fresh and cultured skeletal muscle obtained from patients with Duchenne muscular dystrophy (DMD), patients with myotonic dystrophy (My Dyst), controls, and aborted fetuses (10-12 weeks old) was studied." | 3.66 | Alterations in lipid incorporation in Duchenne muscular dystrophy. Studies of fresh and cultured muscle. ( Burmeister, L; Deprosse, C; Ionasescu, R; Ionasescu, V; Monaco, L; Sandra, A; Stern, LZ, 1981) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (50.00) | 18.7374 |
| 1990's | 1 (10.00) | 18.2507 |
| 2000's | 1 (10.00) | 29.6817 |
| 2010's | 3 (30.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Imae, R | 1 |
| Manya, H | 1 |
| Tsumoto, H | 1 |
| Osumi, K | 1 |
| Tanaka, T | 1 |
| Mizuno, M | 1 |
| Kanagawa, M | 1 |
| Kobayashi, K | 1 |
| Toda, T | 1 |
| Endo, T | 1 |
| Demonbreun, AR | 1 |
| Rossi, AE | 1 |
| Alvarez, MG | 1 |
| Swanson, KE | 1 |
| Deveaux, HK | 1 |
| Earley, JU | 1 |
| Hadhazy, M | 1 |
| Vohra, R | 1 |
| Walter, GA | 1 |
| Pytel, P | 1 |
| McNally, EM | 1 |
| Pisani, DF | 1 |
| Bottema, CD | 1 |
| Butori, C | 1 |
| Dani, C | 1 |
| Dechesne, CA | 1 |
| Ellis, DA | 1 |
| Ionasescu, V | 1 |
| Monaco, L | 1 |
| Sandra, A | 1 |
| Ionasescu, R | 1 |
| Burmeister, L | 1 |
| Deprosse, C | 1 |
| Stern, LZ | 1 |
| Cole, DE | 1 |
| Clarke, LA | 1 |
| Riddell, DC | 1 |
| Samson, KA | 1 |
| Seltzer, WK | 1 |
| Salisbury, S | 1 |
| Sjarif, DR | 1 |
| Ploos van Amstel, JK | 1 |
| Duran, M | 1 |
| Beemer, FA | 1 |
| Poll-The, BT | 1 |
| Dunger, DB | 1 |
| Davies, KE | 1 |
| Pembrey, M | 1 |
| Lake, B | 1 |
| Pearson, P | 1 |
| Williams, D | 1 |
| Whitfield, A | 1 |
| Dillon, MJ | 1 |
| Bartley, JA | 1 |
| Patil, S | 1 |
| Davenport, S | 1 |
| Goldstein, D | 1 |
| Pickens, J | 1 |
| Aronson, JF | 1 |
2 reviews available for glycerol and Muscular Dystrophy
| Article | Year |
|---|---|
Intermediary metabolism of muscle in Duchenne muscular dystrophy.
Topics: Fructose; Glucose; Glucosephosphates; Glycerol; Glycogen; Humans; Lactates; Muscles; Muscular Dystro | 1980 |
Isolated and contiguous glycerol kinase gene disorders: a review.
Topics: Adrenal Insufficiency; Amino Acid Sequence; Carbohydrate Metabolism, Inborn Errors; Genetic Linkage; | 2000 |
8 other studies available for glycerol and Muscular Dystrophy
| Article | Year |
|---|---|
CDP-glycerol inhibits the synthesis of the functional
Topics: Dystroglycans; Glycerol; Glycosylation; Humans; Kinetics; Membrane Proteins; Muscular Dystrophies; P | 2018 |
Dysferlin and myoferlin regulate transverse tubule formation and glycerol sensitivity.
Topics: Animals; Disease Models, Animal; Dysferlin; Female; Glycerol; Immunoblotting; Male; Membrane Protein | 2014 |
Mouse model of skeletal muscle adiposity: a glycerol treatment approach.
Topics: Adipocytes; Adiposity; Animals; Disease Models, Animal; Female; Glycerol; Male; Mice; Mice, Mutant S | 2010 |
Alterations in lipid incorporation in Duchenne muscular dystrophy. Studies of fresh and cultured muscle.
Topics: Adolescent; Adult; Child; Child, Preschool; Culture Techniques; Female; Glycerol; Humans; Lipid Meta | 1981 |
Congenital adrenal hypoplasia, Duchenne muscular dystrophy, and glycerol kinase deficiency: importance of laboratory investigations in delineating a contiguous gene deletion syndrome.
Topics: Adrenal Insufficiency; Blotting, Southern; Chromosome Mapping; Gene Deletion; Glycerol; Glycerol Kin | 1994 |
Deletion on the X chromosome detected by direct DNA analysis in one of two unrelated boys with glycerol kinase deficiency, adrenal hypoplasia, and Duchenne muscular dystrophy.
Topics: Adrenal Insufficiency; Child; Child, Preschool; Chromosome Banding; Chromosome Deletion; DNA; Glycer | 1986 |
Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletion.
Topics: Adrenal Insufficiency; Child; Chromosome Banding; Chromosome Deletion; Chromosome Mapping; Female; G | 1986 |
Proposed mechanism for the turnover of myosin and its relation to muscular dystrophy.
Topics: Animals; Anura; Back; Glycerol; In Vitro Techniques; Leg; Mice; Muscular Dystrophies; Rabbits; Tempe | 1966 |