410 related articles for article (PubMed ID: 29966135)
1. Novel ABCD1 Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum.
Qiu Y; Xin L; Wang Y; Yu Y; Zou K; Zhou Q; Chen Y; Chen S; Zhu M; Hong D
Neurodegener Dis; 2018; 18(2-3):156-164. PubMed ID: 29966135
[TBL] [Abstract][Full Text] [Related]
2. A novel ABCD1 gene mutation causes adrenomyeloneuropathy in a Chinese family.
Wang C; Liu H; Han B; Zhu H; Liu J
Brain Behav; 2019 Oct; 9(10):e01416. PubMed ID: 31557422
[TBL] [Abstract][Full Text] [Related]
3. Investigating ABCD1 mutations in a Taiwanese cohort with hereditary spastic paraplegia phenotype.
Hsu SL; Chen YH; Chou CT; Chou YT; Tsai YS; Hsiao CT; Liao YC; Lee YC
Parkinsonism Relat Disord; 2021 Nov; 92():7-12. PubMed ID: 34649108
[TBL] [Abstract][Full Text] [Related]
4. ABCD1 translation-initiator mutation demonstrates genotype-phenotype correlation for AMN.
O'Neill GN; Aoki M; Brown RH
Neurology; 2001 Dec; 57(11):1956-62. PubMed ID: 11739809
[TBL] [Abstract][Full Text] [Related]
5. Clinical, neuroimaging, biochemical, and genetic features in six Chinese patients with Adrenomyeloneuropathy.
Li J; Wang H; He Z; Wang X; Tang J; Huang D
BMC Neurol; 2019 Sep; 19(1):227. PubMed ID: 31526374
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. A novel ABCD1 mutation detected by next generation sequencing in presumed hereditary spastic paraplegia: A 30-year diagnostic delay caused by misleading biochemical findings.
Koutsis G; Lynch DS; Tucci A; Houlden H; Karadima G; Panas M
J Neurol Sci; 2015 Aug; 355(1-2):199-201. PubMed ID: 26049658
[TBL] [Abstract][Full Text] [Related]
8. Adrenomyeloneuropathy with Later Development of Cerebral Form Caused by a Hemizygous Splice-site Variant in ABCD1.
Takegami N; Matsukawa T; Hamada M; Tanifuji S; Tamura T; Yamaguchi-Takegami N; Ishiura H; Mitsui J; Sakuishi K; Tsuji S; Toda T
Intern Med; 2024 Apr; 63(7):999-1004. PubMed ID: 37558478
[TBL] [Abstract][Full Text] [Related]
9. Eight novel mutations in the ABCD1 gene and clinical characteristics of 25 Chinese patients with X-linked adrenoleukodystrophy.
Chu SS; Ye J; Zhang HW; Han LS; Qiu WJ; Gao XL; Gu XF
World J Pediatr; 2015 Nov; 11(4):366-73. PubMed ID: 26454440
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. A Large Family with p.Arg554His Mutation in
Campopiano R; Femiano C; Chiaravalloti MA; Ferese R; Centonze D; Buttari F; Zampatti S; Fanelli M; Amatori S; D'Alessio C; Giardina E; Fornai F; Biagioni F; Storto M; Gambardella S
Genes (Basel); 2021 May; 12(5):. PubMed ID: 34069712
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Novel mutations in the ABCD1 gene caused adrenomyeloneuropathy in the Chinese population.
He R; Zhang J; Huang T; Cai G; Zou Z; Ye Q
Front Neurol; 2023; 14():1126729. PubMed ID: 36925939
[TBL] [Abstract][Full Text] [Related]
14. Clinical and genetic aspects in twelve Korean patients with adrenomyeloneuropathy.
Park HJ; Shin HY; Kang HC; Choi BO; Suh BC; Kim HJ; Choi YC; Lee PH; Kim SM
Yonsei Med J; 2014 May; 55(3):676-82. PubMed ID: 24719134
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Late onset neurological phenotype of the X-ALD gene inactivation in mice: a mouse model for adrenomyeloneuropathy.
Pujol A; Hindelang C; Callizot N; Bartsch U; Schachner M; Mandel JL
Hum Mol Genet; 2002 Mar; 11(5):499-505. PubMed ID: 11875044
[TBL] [Abstract][Full Text] [Related]
17. Adrenomyeloneuropathy due to mutation in the ABCD1 gene as underlying factor in spastic paraparesis.
Ylikallio E; Rahikkala E; Keski-Filppula R; Auranen M; Tyynismaa H
Duodecim; 2017; 133(7):683-7. PubMed ID: 29243459
[TBL] [Abstract][Full Text] [Related]
18. [X-linked adrenoleukodystrophy].
Aubourg P
Ann Endocrinol (Paris); 2007 Dec; 68(6):403-11. PubMed ID: 17532287
[TBL] [Abstract][Full Text] [Related]
19. Adrenomyeloneuropathy: report of a new mutation in a French Canadian female.
Dionne A; Brunet D; McCampbell A; Dupré N
Can J Neurol Sci; 2005 May; 32(2):261-3. PubMed ID: 16018167
[TBL] [Abstract][Full Text] [Related]
20. Exome sequencing released a case of X-linked adrenoleukodystrophy mimicking recessive hereditary spastic paraplegia.
Zhan ZX; Liao XX; Du J; Luo YY; Hu ZT; Wang JL; Yan XX; Zhang JG; Dai MZ; Zhang P; Xia K; Tang BS; Shen L
Eur J Med Genet; 2013 Jul; 56(7):375-8. PubMed ID: 23664929
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
