creatine has been researched along with Glycogen Storage Disease in 5 studies
Glycogen Storage Disease: A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Glycogen storage disease was suspected in a 10-month-old boy." | 7.68 | In vivo 13C-NMR evaluation of glycogen content in a patient with glycogen storage disease. ( Jehenson, P; Labrune, P; Odièvre, M; Syrota, A, 1992) |
| "Glycogen storage disease was suspected in a 10-month-old boy." | 3.68 | In vivo 13C-NMR evaluation of glycogen content in a patient with glycogen storage disease. ( Jehenson, P; Labrune, P; Odièvre, M; Syrota, A, 1992) |
| "Besides myotonic dystrophy some generalized myotonias exist, until now mostly diagnosed as "Thomsen's disease." | 1.25 | Genetic approaches to the nosology of muscular disease: myotonias and similar diseases. ( Becker, PE, 1971) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (60.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Vorgerd, M | 1 |
| O'Sullivan, WJ | 1 |
| Labrune, P | 1 |
| Jehenson, P | 1 |
| Syrota, A | 1 |
| Odièvre, M | 1 |
| Prader, A | 1 |
| Zachmann, M | 1 |
| Poley, JR | 1 |
| Illig, R | 1 |
| Becker, PE | 1 |
1 review available for creatine and Glycogen Storage Disease
| Article | Year |
|---|---|
Therapeutic options in other metabolic myopathies.
Topics: Animals; Carnitine O-Palmitoyltransferase; Creatine; Exercise Therapy; Glycogen Storage Disease; Gly | 2008 |
4 other studies available for creatine and Glycogen Storage Disease
| Article | Year |
|---|---|
Nuclear magnetic resonance: this new diagnostic tool has direct clinical application.
Topics: Adenosine Triphosphate; Animals; Creatine; Dogs; Glycogen Storage Disease; Glycogen Storage Disease | 1981 |
In vivo 13C-NMR evaluation of glycogen content in a patient with glycogen storage disease.
Topics: Creatine; Glycogen; Glycogen Storage Disease; Glycogen Storage Disease Type V; Humans; Infant; Liver | 1992 |
The metabolic effect of a small uniform dose of human growth hormone in hypopituitary dwarfs and in control children. I. Nitrogen, alpha-amino-N, creatine-creatinine and calcium excretion and serum urea-N, alpha-amino-N, inorganic phosphorus and alkaline
Topics: Adolescent; Adult; Alkaline Phosphatase; Amino Acids; Blood Urea Nitrogen; Bone Marrow Diseases; Bra | 1968 |
Genetic approaches to the nosology of muscular disease: myotonias and similar diseases.
Topics: Adult; Cold Temperature; Creatine; Diagnosis, Differential; Facial Muscles; Female; Genes, Dominant; | 1971 |