236 related articles for article (PubMed ID: 22914231)
1. Adrenoleukodystrophy: a forgotten diagnosis in children with primary Addison's disease.
Nascimento M; Rodrigues N; Espada F; Fonseca M
BMJ Case Rep; 2012 Aug; 2012():. PubMed ID: 22914231
[TBL] [Abstract][Full Text] [Related]
2. A 29-year-old patient with adrenoleukodystrophy presenting with Addison's disease.
Tanaka H; Amano N; Tanaka K; Katsuki T; Adachi T; Shimozawa N; Kawai T
Endocr J; 2020 Jun; 67(6):655-658. PubMed ID: 32101828
[TBL] [Abstract][Full Text] [Related]
3. X-linked adrenoleukodystrophy and primary adrenal insufficiency.
Cappa M; Todisco T; Bizzarri C
Front Endocrinol (Lausanne); 2023; 14():1309053. PubMed ID: 38034003
[TBL] [Abstract][Full Text] [Related]
4. [Primary adrenal insufficiency as the form of onset of adrenoleukodystrophy in a 4-year-old boy].
Tornero Patricio S; de la Vega JA; Nehme Alvarez D; Gentil González FJ; Lluch Fernández MD; González Hachero J
Endocrinol Nutr; 2009 Jan; 56(1):40-2. PubMed ID: 19627707
[TBL] [Abstract][Full Text] [Related]
5. Novel
Cho YK; Lee SY; Kim SW
Endocrinol Metab (Seoul); 2020 Mar; 35(1):188-191. PubMed ID: 32207279
[TBL] [Abstract][Full Text] [Related]
6. X-linked adrenoleukodystrophy is a frequent cause of idiopathic Addison's disease in young adult male patients.
Laureti S; Casucci G; Santeusanio F; Angeletti G; Aubourg P; Brunetti P
J Clin Endocrinol Metab; 1996 Feb; 81(2):470-4. PubMed ID: 8636252
[TBL] [Abstract][Full Text] [Related]
7. The clinical spectrum of X-linked adrenoleukodystrophy: from Addison's-only in men to middle-age neurologic manifestations in women.
Fadiga L; Melo M; Saraiva J; Paiva I
Hormones (Athens); 2022 Mar; 21(1):33-40. PubMed ID: 34652632
[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. Adult cerebral adrenoleukodystrophy and Addison's disease in a female carrier.
Chen X; Chen Z; Huang D; Liu X; Gui Q; Yu S
Gene; 2014 Jul; 544(2):248-51. PubMed ID: 24768737
[TBL] [Abstract][Full Text] [Related]
10. Two Single Nucleotide Deletions in the
Dohr KA; Tokic S; Gastager-Ehgartner M; Stojakovic T; Dumic M; Plecko B; Dumic KK
Int J Mol Sci; 2023 Mar; 24(6):. PubMed ID: 36983033
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Diagnosis, treatment and genetic analysis of a case of skin hyperpigmentation as the only manifestation with X-linked adrenoleukodystrophy.
Yu JY; Chen T; Wang ZH; Zheng J; Zeng TS
Yi Chuan; 2022 Oct; 44(10):983-989. PubMed ID: 36384734
[TBL] [Abstract][Full Text] [Related]
13. [Adrenoleukodystrophy: molecular pathogenesis and development of therapeutic agents].
Morita M
Yakugaku Zasshi; 2007 Jul; 127(7):1059-64. PubMed ID: 17603264
[TBL] [Abstract][Full Text] [Related]
14. Clinical profile of adrenoleukodysrophy.
Acharya SV; Gopal RA; Bandgar TR; Joshi SR; Menon PS; Shah NS
Indian J Pediatr; 2009 Oct; 76(10):1045-7. PubMed ID: 19907937
[TBL] [Abstract][Full Text] [Related]
15. Caffeic acid phenethyl ester induces adrenoleukodystrophy (Abcd2) gene in human X-ALD fibroblasts and inhibits the proinflammatory response in Abcd1/2 silenced mouse primary astrocytes.
Singh J; Khan M; Singh I
Biochim Biophys Acta; 2013 Apr; 1831(4):747-58. PubMed ID: 23318275
[TBL] [Abstract][Full Text] [Related]
16. X-linked adrenoleukodystrophy in a 6-year-old boy initially presenting with psychiatric symptoms.
İncecik F; Hergüner MÖ; Mert G; Önenli-Mungan N; Ceylaner S; Kör D; Altunbaşak Ş
Turk J Pediatr; 2014; 56(6):651-3. PubMed ID: 26388597
[TBL] [Abstract][Full Text] [Related]
17. Adrenoleukodystrophy in the Differential Diagnosis of Boys Presenting with Primary Adrenal Insufficiency without Adrenal Antibodies.
Ryalls MR; Gan HW; Davison JE
J Clin Res Pediatr Endocrinol; 2021 Jun; 13(2):212-217. PubMed ID: 32394691
[TBL] [Abstract][Full Text] [Related]
18. HDAC inhibitor SAHA normalizes the levels of VLCFAs in human skin fibroblasts from X-ALD patients and downregulates the expression of proinflammatory cytokines in Abcd1/2-silenced mouse astrocytes.
Singh J; Khan M; Singh I
J Lipid Res; 2011 Nov; 52(11):2056-69. PubMed ID: 21891797
[TBL] [Abstract][Full Text] [Related]
19. Adrenomyeloneuropathy: a rare cause of Addison's disease?
Hochstenbag MM; Peters FP; Anten HW; Moers AM
Neth J Med; 1996 Aug; 49(2):77-81. PubMed ID: 8824109
[TBL] [Abstract][Full Text] [Related]
20. A report on state-wide implementation of newborn screening for X-linked Adrenoleukodystrophy.
Wiens K; Berry SA; Choi H; Gaviglio A; Gupta A; Hietala A; Kenney-Jung D; Lund T; Miller W; Pierpont EI; Raymond G; Winslow H; Zierhut HA; Orchard PJ
Am J Med Genet A; 2019 Jul; 179(7):1205-1213. PubMed ID: 31074578
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
