268 related articles for article (PubMed ID: 34652632)
1. 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]
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].
Aubourg P
Ann Endocrinol (Paris); 2007 Dec; 68(6):403-11. PubMed ID: 17532287
[TBL] [Abstract][Full Text] [Related]
4. Novel
Cho YK; Lee SY; Kim SW
Endocrinol Metab (Seoul); 2020 Mar; 35(1):188-191. PubMed ID: 32207279
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Management of adrenoleukodystrophy: From pre-clinical studies to the development of new therapies.
Ma CY; Li C; Zhou X; Zhang Z; Jiang H; Liu H; Chen HJ; Tse HF; Liao C; Lian Q
Biomed Pharmacother; 2021 Nov; 143():112214. PubMed ID: 34560537
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Spastic paraplegia as the predominant phenotype in a cohort of Chinese patients with adrenoleukodystrophy.
Luo WJ; Wei Q; Dong HL; Yan YT; Chen MJ; Li HF
Mol Genet Genomic Med; 2020 Jan; 8(1):e1065. PubMed ID: 31777199
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. X-linked adrenoleukodystrophy: pathogenesis and treatment.
Engelen M; Kemp S; Poll-The BT
Curr Neurol Neurosci Rep; 2014 Oct; 14(10):486. PubMed ID: 25115486
[TBL] [Abstract][Full Text] [Related]
12. X-linked adrenoleukodystrophy in women: a cross-sectional cohort study.
Engelen M; Barbier M; Dijkstra IM; Schür R; de Bie RM; Verhamme C; Dijkgraaf MG; Aubourg PA; Wanders RJ; van Geel BM; de Visser M; Poll-The BT; Kemp S
Brain; 2014 Mar; 137(Pt 3):693-706. PubMed ID: 24480483
[TBL] [Abstract][Full Text] [Related]
13. Dendrimer-N-acetyl-L-cysteine modulates monophagocytic response in adrenoleukodystrophy.
Turk BR; Nemeth CL; Marx JS; Tiffany C; Jones R; Theisen B; Kambhampati S; Ramireddy R; Singh S; Rosen M; Kaufman ML; Murray CF; Watkins PA; Kannan S; Kannan R; Fatemi A
Ann Neurol; 2018 Sep; 84(3):452-462. PubMed ID: 30069915
[TBL] [Abstract][Full Text] [Related]
14. A novel ABCD1 gene mutation causes adrenomyeloneuropathy presenting with spastic paraplegia: A case report.
Liu J; Wang X; Huang D; Qi Y; Xu L; Shao Y
Medicine (Baltimore); 2024 Apr; 103(16):e37874. PubMed ID: 38640304
[TBL] [Abstract][Full Text] [Related]
15. X-linked adrenoleukodystrophy diagnosed in three brothers.
Herman M; Jura M; Krakowska K; Barg E
Pediatr Endocrinol Diabetes Metab; 2019; 25(2):95-98. PubMed ID: 31343142
[TBL] [Abstract][Full Text] [Related]
16. Structure and Function of the
Mallack EJ; Gao K; Engelen M; Kemp S
Cells; 2022 Jan; 11(2):. PubMed ID: 35053399
[TBL] [Abstract][Full Text] [Related]
17. Adrenoleukodystrophy.
Cappa M; Bizzarri C; Vollono C; Petroni A; Banni S
Endocr Dev; 2011; 20():149-160. PubMed ID: 21164268
[TBL] [Abstract][Full Text] [Related]
18. A Distinct Clinical Phenotype in Two Siblings with X-linked Adrenoleukodystrophy.
Ozdemir Kutbay N; Ozbek MN; Sarer Yurekli B; Demirbilek H
Neuro Endocrinol Lett; 2019 Mar; 40(1):36-40. PubMed ID: 31184821
[TBL] [Abstract][Full Text] [Related]
19. Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders.
Corzo D; Gibson W; Johnson K; Mitchell G; LePage G; Cox GF; Casey R; Zeiss C; Tyson H; Cutting GR; Raymond GV; Smith KD; Watkins PA; Moser AB; Moser HW; Steinberg SJ
Am J Hum Genet; 2002 Jun; 70(6):1520-31. PubMed ID: 11992258
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
