creatine has been researched along with Autosomal Chromosome Disorders in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (14.29) | 18.7374 |
| 1990's | 2 (28.57) | 18.2507 |
| 2000's | 2 (28.57) | 29.6817 |
| 2010's | 2 (28.57) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Calhoun, AR | 1 |
| Raymond, GV | 1 |
| Tada, H | 1 |
| Takanashi, J | 1 |
| Lion-François, L | 1 |
| Cheillan, D | 1 |
| Pitelet, G | 1 |
| Acquaviva-Bourdain, C | 1 |
| Bussy, G | 1 |
| Cotton, F | 1 |
| Guibaud, L | 1 |
| Gérard, D | 1 |
| Rivier, C | 1 |
| Vianey-Saban, C | 1 |
| Jakobs, C | 1 |
| Salomons, GS | 1 |
| des Portes, V | 1 |
| Hanefeld, F | 1 |
| Holzbach, U | 1 |
| Kruse, B | 1 |
| Wilichowski, E | 1 |
| Christen, HJ | 1 |
| Frahm, J | 1 |
| Mano, T | 1 |
| Ono, J | 1 |
| Kaminaga, T | 1 |
| Imai, K | 1 |
| Sakurai, K | 1 |
| Harada, K | 1 |
| Nagai, T | 1 |
| Rizzo, WB | 1 |
| Okada, S | 1 |
| Gabis, L | 1 |
| Parton, P | 1 |
| Roche, P | 1 |
| Lenn, N | 1 |
| Tudorica, A | 1 |
| Huang, W | 1 |
| Bethlem, J | 1 |
| van Wijngaarden, GK | 1 |
| de Jong, J | 1 |
7 other studies available for creatine and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
Distal Xq28 microdeletions: clarification of the spectrum of contiguous gene deletions involving ABCD1, BCAP31, and SLC6A8 with a new case and review of the literature.
Topics: Abnormalities, Multiple; ATP Binding Cassette Transporter, Subfamily D, Member 1; ATP-Binding Casset | 2014 |
MR spectroscopy in 18q(-) syndrome suggesting other than hypomyelination.
Topics: Aspartic Acid; Brain; Child, Preschool; Choline; Chromosome Deletion; Chromosome Disorders; Chromoso | 2014 |
High frequency of creatine deficiency syndromes in patients with unexplained mental retardation.
Topics: Adolescent; Amidinotransferases; Brain; Brain Diseases, Metabolic, Inborn; Child; Child, Preschool; | 2006 |
Diffuse white matter disease in three children: an encephalopathy with unique features on magnetic resonance imaging and proton magnetic resonance spectroscopy.
Topics: Aspartic Acid; Blood Glucose; Brain; Brain Diseases, Metabolic; Child; Child, Preschool; Choline; Ch | 1993 |
Proton MR spectroscopy of Sjögren-Larsson's syndrome.
Topics: Aldehyde Oxidoreductases; Aspartic Acid; Brain; Brain Diseases, Metabolic, Inborn; Child; Child, Pre | 1999 |
In vivo 1H magnetic resonance spectroscopic measurement of brain glycine levels in nonketotic hyperglycinemia.
Topics: Aspartic Acid; Brain; Brain Diseases, Metabolic; Choline; Chromosome Aberrations; Chromosome Disorde | 2001 |
The incidence of lobulated fibres in the facioscapulo-humeral type of muscular dystrophy and the limb-girdle syndrome.
Topics: Alanine Transaminase; Aspartate Aminotransferases; Calcium; Chromosome Aberrations; Chromosome Disor | 1973 |