239 related articles for article (PubMed ID: 29136088)
1. ABCD1 dysfunction alters white matter microvascular perfusion.
Lauer A; Da X; Hansen MB; Boulouis G; Ou Y; Cai X; Liberato Celso Pedrotti A; Kalpathy-Cramer J; Caruso P; Hayden DL; Rost N; Mouridsen K; Eichler FS; Rosen B; Musolino PL
Brain; 2017 Dec; 140(12):3139-3152. PubMed ID: 29136088
[TBL] [Abstract][Full Text] [Related]
2. Brain endothelial dysfunction in cerebral adrenoleukodystrophy.
Musolino PL; Gong Y; Snyder JM; Jimenez S; Lok J; Lo EH; Moser AB; Grabowski EF; Frosch MP; Eichler FS
Brain; 2015 Nov; 138(Pt 11):3206-20. PubMed ID: 26377633
[TBL] [Abstract][Full Text] [Related]
3. X-linked adrenoleukodystrophy in a chimpanzee due to an ABCD1 mutation reported in multiple unrelated humans.
Curiel J; Steinberg SJ; Bright S; Snowden A; Moser AB; Eichler F; Dubbs HA; Hacia JG; Ely JJ; Bezner J; Gean A; Vanderver A
Mol Genet Metab; 2017 Nov; 122(3):130-133. PubMed ID: 28919002
[TBL] [Abstract][Full Text] [Related]
4. Metformin-induced mitochondrial function and ABCD2 up-regulation in X-linked adrenoleukodystrophy involves AMP-activated protein kinase.
Singh J; Olle B; Suhail H; Felicella MM; Giri S
J Neurochem; 2016 Jul; 138(1):86-100. PubMed ID: 26849413
[TBL] [Abstract][Full Text] [Related]
5. Hematopoietic stem-cell gene therapy is associated with restored white matter microvascular function in cerebral adrenoleukodystrophy.
Lauer A; Speroni SL; Choi M; Da X; Duncan C; McCarthy S; Krishnan V; Lusk CA; Rohde D; Hansen MB; Kalpathy-Cramer J; Loes DJ; Caruso PA; Williams DA; Mouridsen K; Emblem KE; Eichler FS; Musolino PL
Nat Commun; 2023 Apr; 14(1):1900. PubMed ID: 37019892
[TBL] [Abstract][Full Text] [Related]
6. Phenotypic variability in a Tunisian family with X-linked adrenoleukodystrophy caused by the p.Gln316Pro novel mutation.
Kallabi F; Ellouz E; Tabebi M; Ben Salah G; Kaabechi N; Keskes L; Triki C; Kamoun H
Clin Chim Acta; 2016 Jan; 453():141-6. PubMed ID: 26686776
[TBL] [Abstract][Full Text] [Related]
7. Molecular characterization of X-linked adrenoleukodystrophy in a Tunisian family: identification of a novel missense mutation in the ABCD1 gene.
Kallabi F; Hadj Salem I; Ben Salah G; Ben Turkia H; Ben Chehida A; Tebib N; Fakhfakh F; Kamoun H
Neurodegener Dis; 2013; 12(4):207-11. PubMed ID: 23651979
[TBL] [Abstract][Full Text] [Related]
8. [X-linked adrenoleukodystrophy].
Aubourg P
Ann Endocrinol (Paris); 2007 Dec; 68(6):403-11. PubMed ID: 17532287
[TBL] [Abstract][Full Text] [Related]
9. De novo ABCD1 gene mutation in an Indian patient with adrenoleukodystrophy.
Kumar N; Shukla P; Taneja KK; Kalra V; Bansal SK
Pediatr Neurol; 2008 Oct; 39(4):289-92. PubMed ID: 18805372
[TBL] [Abstract][Full Text] [Related]
10. Successful donor engraftment and repair of the blood-brain barrier in cerebral adrenoleukodystrophy.
Orchard PJ; Nascene DR; Miller WP; Gupta A; Kenney-Jung D; Lund TC
Blood; 2019 Mar; 133(12):1378-1381. PubMed ID: 30635285
[TBL] [Abstract][Full Text] [Related]
11. Intra familial phenotypical variations in adrenoleukodystrophy.
Gosalakkal J; Balky AP
Neurol India; 2010; 58(1):109-11. PubMed ID: 20228476
[TBL] [Abstract][Full Text] [Related]
12. Lentiviral hematopoietic cell gene therapy for X-linked adrenoleukodystrophy.
Cartier N; Hacein-Bey-Abina S; Bartholomae CC; Bougnères P; Schmidt M; Kalle CV; Fischer A; Cavazzana-Calvo M; Aubourg P
Methods Enzymol; 2012; 507():187-98. PubMed ID: 22365775
[TBL] [Abstract][Full Text] [Related]
13. Adult-onset cerebello-brainstem dominant form of X-linked adrenoleukodystrophy presenting as multiple system atrophy: case report and literature review.
Ogaki K; Koga S; Aoki N; Lin W; Suzuki K; Ross OA; Dickson DW
Neuropathology; 2016 Feb; 36(1):64-76. PubMed ID: 26227820
[TBL] [Abstract][Full Text] [Related]
14. Childhood Cerebral Adrenoleukodystrophy: MR Perfusion Measurements and Their Use in Predicting Clinical Outcome after Hematopoietic Stem Cell Transplantation.
McKinney AM; Benson JC; Nascene DR; Eisengart J; Salmela MB; Loes DJ; Zhang L; Patel K; Raymond GV; Miller WP
AJNR Am J Neuroradiol; 2016 Sep; 37(9):1713-20. PubMed ID: 27079370
[TBL] [Abstract][Full Text] [Related]
15. [X-linked adrenoleukodystrophy with an atypical radiological pattern].
Ulate-Campos A; Petanas-Argemi J; Rebollo-Polo M; Jou C; Sierra C; Armstrong J; Fons-Estupina MC
Rev Neurol; 2018 Apr; 66(7):237-240. PubMed ID: 29557549
[TBL] [Abstract][Full Text] [Related]
16. Novel ABCD1 variant causes phenotype of adrenomyeloneuropathy with cerebral involvement in Ukrainian siblings: first adult hematopoietic stem cell transplantation for ALD in Ukraine: a case report.
Shchubelka K; Herasymenko O; Budzyn A; Lysytsia O; Rusyn A; Oleksyk O; Tynta S; Oleksyk T
J Med Case Rep; 2024 Jan; 18(1):25. PubMed ID: 38245786
[TBL] [Abstract][Full Text] [Related]
17. Splicing defects in ABCD1 gene leading to both exon skipping and partial intron retention in X-linked adrenoleukodystrophy Tunisian patient.
Kallabi F; Hadj Salem I; Ben Chehida A; Ben Salah G; Ben Turkia H; Tebib N; Keskes L; Kamoun H
Neurosci Res; 2015 Aug; 97():7-12. PubMed ID: 25835712
[TBL] [Abstract][Full Text] [Related]
18. Hematopoietic Stem-Cell Gene Therapy for Cerebral Adrenoleukodystrophy.
Eichler F; Duncan C; Musolino PL; Orchard PJ; De Oliveira S; Thrasher AJ; Armant M; Dansereau C; Lund TC; Miller WP; Raymond GV; Sankar R; Shah AJ; Sevin C; Gaspar HB; Gissen P; Amartino H; Bratkovic D; Smith NJC; Paker AM; Shamir E; O'Meara T; Davidson D; Aubourg P; Williams DA
N Engl J Med; 2017 Oct; 377(17):1630-1638. PubMed ID: 28976817
[TBL] [Abstract][Full Text] [Related]
19. Hypoperfusion predicts lesion progression in cerebral X-linked adrenoleukodystrophy.
Musolino PL; Rapalino O; Caruso P; Caviness VS; Eichler FS
Brain; 2012 Sep; 135(Pt 9):2676-83. PubMed ID: 22961546
[TBL] [Abstract][Full Text] [Related]
20. ABCD1 deletion-induced mitochondrial dysfunction is corrected by SAHA: implication for adrenoleukodystrophy.
Baarine M; Beeson C; Singh A; Singh I
J Neurochem; 2015 May; 133(3):380-96. PubMed ID: 25393703
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
