creatine and Fragile X Syndrome
creatine has been researched along with Fragile X Syndrome in 2 studies
Fragile X Syndrome: A condition characterized genotypically by mutation of the distal end of the long arm of the X chromosome (at gene loci FRAXA or FRAXE) and phenotypically by cognitive impairment, hyperactivity, SEIZURES, language delay, and enlargement of the ears, head, and testes. INTELLECTUAL DISABILITY occurs in nearly all males and roughly 50% of females with the full mutation of FRAXA. (From Menkes, Textbook of Child Neurology, 5th ed, p226)
Research
Studies (2)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors
Authors | Studies |
---|---|
Utine, GE | 1 |
Akpınar, B | 1 |
Arslan, U | 1 |
Kiper, PÖ | 1 |
Volkan-Salancı, B | 1 |
Alanay, Y | 1 |
Aktaş, D | 1 |
Haliloğlu, G | 1 |
Oğuz, KK | 1 |
Boduroğlu, K | 1 |
Alikaşifoğlu, M | 1 |
Kesler, SR | 1 |
Lightbody, AA | 1 |
Reiss, AL | 1 |
Trials
1 trial available for creatine and Fragile X Syndrome
Article | Year |
---|---|
Cholinergic dysfunction in fragile X syndrome and potential intervention: a preliminary 1H MRS study.
Topics: Adolescent; Adult; Case-Control Studies; Choline; Cholinesterase Inhibitors; Cognition; Creatine; Do | 2009 |
Other Studies
1 other study available for creatine and Fragile X Syndrome
Article | Year |
---|---|
Neurochemical evaluation of brain function with 1H magnetic resonance spectroscopy in patients with fragile X syndrome.
Topics: Aspartic Acid; Brain; Case-Control Studies; Child; Child, Preschool; Choline; Creatine; Fragile X Sy | 2014 |