These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

259 related articles for article (PubMed ID: 31665121)

  • 1. Novel ABCD1 gene mutations in Iranian pedigrees with X-linked adrenoleukodystrophy.
    Emamalizadeh B; Daneshmandpour Y; Tafakhori A; Ranji-Burachaloo S; Shafiee S; Ghods E; Darvish H
    J Pediatr Endocrinol Metab; 2019 Nov; 32(11):1207-1215. PubMed ID: 31665121
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Novel
    Cho YK; Lee SY; Kim SW
    Endocrinol Metab (Seoul); 2020 Mar; 35(1):188-191. PubMed ID: 32207279
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Eight novel ABCD1 gene mutations and three polymorphisms in patients with X-linked adrenoleukodystrophy: The first polymorphism causing an amino acid exchange.
    Dvoráková L; Storkánová G; Unterrainer G; Hujová J; Kmoch S; Zeman J; Hrebícek M; Berger J
    Hum Mutat; 2001; 18(1):52-60. PubMed ID: 11438993
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [X-linked adrenoleukodystrophy ABCD1 gene mutation analysis in China].
    Pan H; Xiong H; Zhang YH; Wu Y; Bao XH; Jiang YW; Wu XR
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):1-4. PubMed ID: 14767898
    [TBL] [Abstract][Full Text] [Related]  

  • 8. ABCD1 gene mutations in Chinese patients with X-linked adrenoleukodystrophy.
    Pan H; Xiong H; Wu Y; Zhang YH; Bao XH; Jiang YW; Wu XR
    Pediatr Neurol; 2005 Aug; 33(2):114-20. PubMed ID: 16087056
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel mutation in the ABCD1 gene of a Korean boy diagnosed with X-linked adrenoleukodystrophy.
    Park JA; Jun KR; Han SH; Kim GH; Yoo HW; Hur YJ
    Gene; 2012 Apr; 498(1):131-3. PubMed ID: 22326269
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. [Preliminary analysis of mutations in X-linked adrenoleukodystrophy gene(ABCD1) in Chinese patients].
    Xiong H; Pan H; Zhang YH; Wu XR
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Oct; 20(5):400-3. PubMed ID: 14556192
    [TBL] [Abstract][Full Text] [Related]  

  • 13. X-linked adrenoleukodystrophy: molecular and functional analysis of the ABCD1 gene in Argentinean patients.
    Amorosi CA; Myskóva H; Monti MR; Argaraña CE; Morita M; Kemp S; Dodelson de Kremer R; Dvoráková L; Oller de Ramírez AM
    PLoS One; 2012; 7(12):e52635. PubMed ID: 23300730
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Mutational analyses on X-linked adrenoleukodystrophy reveal a novel cryptic splicing and three missense mutations in the ABCD1 gene.
    Hung KL; Wang JS; Keng WT; Chen HJ; Liang JS; Ngu LH; Lu JF
    Pediatr Neurol; 2013 Sep; 49(3):185-90. PubMed ID: 23835273
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Adult onset cerebral form of X-linked adrenoleukodystrophy with dementia of frontal lobe type with new L160P mutation in ABCD1 gene.
    Sutovský S; Petrovic R; Chandoga J; Turcáni P
    J Neurol Sci; 2007 Dec; 263(1-2):149-53. PubMed ID: 17662307
    [TBL] [Abstract][Full Text] [Related]  

  • 17. ABCD1 mutations and phenotype distribution in Chinese patients with X-linked adrenoleukodystrophy.
    Niu YF; Ni W; Wu ZY
    Gene; 2013 Jun; 522(1):117-20. PubMed ID: 23566833
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. A novel mutation in the ABCD1 gene of a Chinese patient with X-linked adrenoleukodystrophy: Case report.
    Wang J; Zhu Q; Liu H
    Medicine (Baltimore); 2018 May; 97(21):e10837. PubMed ID: 29794777
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.