creatine has been researched along with Decreased Muscle Tone in 4 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "We report the first X-linked creatine-deficiency syndrome caused by a defective creatine transporter." | 7.71 | X-linked creatine-transporter gene (SLC6A8) defect: a new creatine-deficiency syndrome. ( Ball, WS; Cecil, KM; Degrauw, TJ; Jakobs, C; Salomons, GS; van Dooren, SJ; Verhoeven, NM, 2001) |
| "We report the first X-linked creatine-deficiency syndrome caused by a defective creatine transporter." | 3.71 | X-linked creatine-transporter gene (SLC6A8) defect: a new creatine-deficiency syndrome. ( Ball, WS; Cecil, KM; Degrauw, TJ; Jakobs, C; Salomons, GS; van Dooren, SJ; Verhoeven, NM, 2001) |
| "The sister showed additional muscular hypotonia and more pronounced dysmorphic features compared to her brother." | 1.62 | Locus heterogeneity in two siblings presenting with developmental delay, intellectual disability and autism spectrum disorder. ( Boy, N; Brugger, M; Brunet, T; Orec, LE; Schwaibold, EMC; Wagner, M, 2021) |
| " The progressive reduction of corticosteroid dosage led rapidly to a distinct improvement, but not to a remission, of symptoms." | 1.28 | Steroid myopathy: clinical and immunohistochemical study of a case. ( Camporeale, FS; Carandente, M; Cioffi, M; Gentile, A; Marolda, M; Orsini, AV; Palma, V, 1991) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (25.00) | 2.80 |
| Authors | Studies |
|---|---|
| Brugger, M | 1 |
| Brunet, T | 1 |
| Wagner, M | 1 |
| Orec, LE | 1 |
| Schwaibold, EMC | 1 |
| Boy, N | 1 |
| Salomons, GS | 1 |
| van Dooren, SJ | 1 |
| Verhoeven, NM | 1 |
| Cecil, KM | 1 |
| Ball, WS | 1 |
| Degrauw, TJ | 1 |
| Jakobs, C | 1 |
| Marolda, M | 1 |
| Palma, V | 1 |
| Camporeale, FS | 1 |
| Carandente, M | 1 |
| Cioffi, M | 1 |
| Orsini, AV | 1 |
| Gentile, A | 1 |
4 other studies available for creatine and Decreased Muscle Tone
| Article | Year |
|---|---|
Locus heterogeneity in two siblings presenting with developmental delay, intellectual disability and autism spectrum disorder.
Topics: Autism Spectrum Disorder; Brain Diseases, Metabolic, Inborn; Child; Chromosomes, Human, Pair 16; Com | 2021 |
X-linked creatine-transporter gene (SLC6A8) defect: a new creatine-deficiency syndrome.
Topics: Amino Acid Sequence; Base Sequence; Carrier Proteins; Child; Chromosome Mapping; Codon, Nonsense; Cr | 2001 |
[Limits and possibilities of additional diagnostic studies in specialized laboratories].
Topics: Biopsy; Creatine; Electromyography; Glucose Tolerance Test; Humans; Immobilization; Muscle Hypotonia | 1978 |
Steroid myopathy: clinical and immunohistochemical study of a case.
Topics: Adult; Creatine; Electromyography; Female; Foot Diseases; Humans; Muscle Hypotonia; Muscular Atrophy | 1991 |