BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 36925939)

  • 1. 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]  

  • 2. 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]  

  • 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. 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]  

  • 5. [X-linked adrenoleukodystrophy].
    Aubourg P
    Ann Endocrinol (Paris); 2007 Dec; 68(6):403-11. PubMed ID: 17532287
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. A novel
    Zhang Y; Zhang G; Chen W; Pu Z; Song L; Tang X; Liu Z
    Genes Dis; 2021 Sep; 8(5):709-714. PubMed ID: 34291142
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chinese patients with adrenoleukodystrophy and Zellweger spectrum disorder presenting with hereditary spastic paraplegia.
    Chen YJ; Wang MW; Dong EL; Lin XH; Wang N; Zhang ZQ; Lin X; Chen WJ
    Parkinsonism Relat Disord; 2019 Aug; 65():256-260. PubMed ID: 31227335
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. X-linked adrenoleukodystrophy caused by a novel mutation presenting with various phenotypes in a Taiwanese family.
    Chien CY; Chang KH; Chen CM
    Clin Chim Acta; 2021 Mar; 514():100-106. PubMed ID: 33359056
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Defining diagnostic cutoffs in neurological patients for serum very long chain fatty acids (VLCFA) in genetically confirmed X-Adrenoleukodystrophy.
    Rattay TW; Rautenberg M; Söhn AS; Hengel H; Traschütz A; Röben B; Hayer SN; Schüle R; Wiethoff S; Zeltner L; Haack TB; Cegan A; Schöls L; Schleicher E; Peter A
    Sci Rep; 2020 Sep; 10(1):15093. PubMed ID: 32934269
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. A Novel Variant in
    Chen Y; Zhang J; Wang J; Wang K
    Front Neurol; 2018; 9():271. PubMed ID: 29740390
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A man with progressive spastic paraparesis].
    Sanaker PS; Lindland S; Rekeland F; Bindoff LA
    Tidsskr Nor Laegeforen; 2007 Nov; 127(23):3085-7. PubMed ID: 18098376
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of Two Novel Mutations of
    Dong B; Lv W; Xu L; Zhao Y; Sun X; Wang Z; Cheng B; Fu Z; Wang Y
    Int J Endocrinol; 2022; 2022():5479781. PubMed ID: 35479665
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.