creatine has been researched along with Adrenoleukodystrophy in 11 studies
Adrenoleukodystrophy: An X-linked recessive disorder characterized by the accumulation of saturated very long chain fatty acids in the LYSOSOMES of ADRENAL CORTEX and the white matter of CENTRAL NERVOUS SYSTEM. This disease occurs almost exclusively in the males. Clinical features include the childhood onset of ATAXIA; NEUROBEHAVIORAL MANIFESTATIONS; HYPERPIGMENTATION; ADRENAL INSUFFICIENCY; SEIZURES; MUSCLE SPASTICITY; and DEMENTIA. The slowly progressive adult form is called adrenomyeloneuropathy. The defective gene ABCD1 is located at Xq28, and encodes the adrenoleukodystrophy protein (ATP-BINDING CASSETTE TRANSPORTERS).
| Excerpt | Relevance | Reference |
|---|---|---|
| "The BCAP31 gene is located between SLC6A8, associated with X-linked creatine transporter deficiency, and ABCD1, associated with X-linked adrenoleukodystrophy." | 3.81 | Genotype-phenotype correlation of contiguous gene deletions of SLC6A8, BCAP31 and ABCD1. ( Anselm, I; Errami, A; Howidi, M; Mancini, GM; Osaka, H; Phalin-Roque, J; Salomons, GS; Steinberg, SJ; van de Kamp, JM; van Dooren, SJ; Winter, S, 2015) |
| "X-linked cerebral adrenoleukodystrophy is an aggressive, rapidly progressive disorder resulting in considerable morbidity and, left untreated, mortality." | 1.34 | Magnetic resonance spectroscopy changes following haemopoietic stem cell transplantation in children with cerebral adrenoleukodystrophy. ( Connolly, DJ; Griffiths, PD; Sharrard, MJ; Warren, DJ; Wilkinson, ID, 2007) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (27.27) | 18.2507 |
| 2000's | 6 (54.55) | 29.6817 |
| 2010's | 1 (9.09) | 24.3611 |
| 2020's | 1 (9.09) | 2.80 |
| Authors | Studies |
|---|---|
| van de Stadt, SIW | 1 |
| Schrantee, A | 1 |
| Huffnagel, IC | 1 |
| van Ballegoij, WJC | 1 |
| Caan, MWA | 1 |
| Pouwels, PJW | 1 |
| Engelen, M | 1 |
| van de Kamp, JM | 1 |
| Errami, A | 1 |
| Howidi, M | 1 |
| Anselm, I | 1 |
| Winter, S | 1 |
| Phalin-Roque, J | 1 |
| Osaka, H | 1 |
| van Dooren, SJ | 1 |
| Mancini, GM | 1 |
| Steinberg, SJ | 1 |
| Salomons, GS | 1 |
| Ratai, E | 1 |
| Kok, T | 1 |
| Wiggins, C | 1 |
| Wiggins, G | 1 |
| Grant, E | 1 |
| Gagoski, B | 1 |
| O'Neill, G | 1 |
| Adalsteinsson, E | 1 |
| Eichler, F | 1 |
| Eichler, FS | 1 |
| Itoh, R | 1 |
| Barker, PB | 4 |
| Mori, S | 1 |
| Garrett, ES | 1 |
| van Zijl, PC | 2 |
| Moser, HW | 3 |
| Raymond, GV | 2 |
| Melhem, ER | 1 |
| Dubey, P | 1 |
| Fatemi, A | 1 |
| Degaonkar, M | 1 |
| Troeger, M | 1 |
| Zackowski, K | 1 |
| Bastian, A | 1 |
| Smith, SA | 1 |
| Pomper, MG | 1 |
| Oz, G | 1 |
| Tkác, I | 1 |
| Charnas, LR | 1 |
| Choi, IY | 1 |
| Bjoraker, KJ | 1 |
| Shapiro, EG | 1 |
| Gruetter, R | 1 |
| Warren, DJ | 1 |
| Connolly, DJ | 1 |
| Wilkinson, ID | 1 |
| Sharrard, MJ | 1 |
| Griffiths, PD | 1 |
| Bizzi, A | 1 |
| Castelli, G | 1 |
| Bugiani, M | 1 |
| Herskovits, EH | 1 |
| Danesi, U | 1 |
| Erbetta, A | 1 |
| Moroni, I | 1 |
| Farina, L | 1 |
| Uziel, G | 1 |
| Kruse, B | 1 |
| Duyn, JH | 1 |
| Moonen, CT | 1 |
| Tzika, AA | 1 |
| Ball, WS | 1 |
| Vigneron, DB | 1 |
| Dunn, RS | 1 |
| Nelson, SJ | 1 |
| Kirks, DR | 1 |
| Confort-Gouny, S | 1 |
| Vion-Dury, J | 1 |
| Chabrol, B | 1 |
| Nicoli, F | 1 |
| Cozzone, PJ | 1 |
11 other studies available for creatine and Adrenoleukodystrophy
| Article | Year |
|---|---|
Magnetic resonance spectroscopy as marker for neurodegeneration in X-linked adrenoleukodystrophy.
Topics: Adrenoleukodystrophy; Adult; Aspartic Acid; Biomarkers; Brain; Choline; Creatine; Female; Humans; Ma | 2021 |
Genotype-phenotype correlation of contiguous gene deletions of SLC6A8, BCAP31 and ABCD1.
Topics: Adrenoleukodystrophy; Adult; ATP Binding Cassette Transporter, Subfamily D, Member 1; ATP-Binding Ca | 2015 |
Seven-Tesla proton magnetic resonance spectroscopic imaging in adult X-linked adrenoleukodystrophy.
Topics: Adrenoleukodystrophy; Adult; Aged; Brain; Choline; Creatine; Disability Evaluation; Fatty Acids; Fem | 2008 |
Proton MR spectroscopic and diffusion tensor brain MR imaging in X-linked adrenoleukodystrophy: initial experience.
Topics: Adolescent; Adrenoleukodystrophy; Adult; Aspartic Acid; Brain; Brain Chemistry; Brain Diseases; Chil | 2002 |
Spectroscopic evidence of cerebral axonopathy in patients with "pure" adrenomyeloneuropathy.
Topics: Adrenoleukodystrophy; Adult; Aspartic Acid; Axons; Biomarkers; Brain; Brain Chemistry; Choline; Crea | 2005 |
Assessment of adrenoleukodystrophy lesions by high field MRS in non-sedated pediatric patients.
Topics: Adolescent; Adrenoleukodystrophy; Aspartic Acid; Brain Chemistry; Child; Child, Preschool; Creatine; | 2005 |
Magnetic resonance spectroscopy changes following haemopoietic stem cell transplantation in children with cerebral adrenoleukodystrophy.
Topics: Adrenoleukodystrophy; Aspartic Acid; Child; Child, Preschool; Choline; Creatine; Female; Hematopoiet | 2007 |
Classification of childhood white matter disorders using proton MR spectroscopic imaging.
Topics: Adrenoleukodystrophy; Adult; Alexander Disease; Aspartic Acid; Brain; Child; Child, Preschool; Choli | 2008 |
Multislice proton magnetic resonance spectroscopic imaging in X-linked adrenoleukodystrophy.
Topics: Adolescent; Adrenoleukodystrophy; Adult; Aged; Aspartic Acid; Brain Diseases; Child; Child, Preschoo | 1994 |
Childhood adrenoleukodystrophy: assessment with proton MR spectroscopy.
Topics: Adolescent; Adrenoleukodystrophy; Aspartic Acid; Child; Child, Preschool; Choline; Creatine; gamma-A | 1993 |
Localised proton magnetic resonance spectroscopy in X-linked adrenoleukodystrophy.
Topics: Adolescent; Adrenoleukodystrophy; Adult; Aspartic Acid; Brain; Child; Creatine; Demyelinating Diseas | 1995 |