BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

231 related articles for article (PubMed ID: 29557549)

  • 1. [X-linked adrenoleukodystrophy with an atypical radiological pattern].
    Ulate-Campos A; Petanas-Argemi J; Rebollo-Polo M; Jou C; Sierra C; Armstrong J; Fons-Estupina MC
    Rev Neurol; 2018 Apr; 66(7):237-240. PubMed ID: 29557549
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Leukoencephalopathy With Predominant Infratentorial Involvement Caused by a Novel ABCD1 Mutation: Does the Spinocerebellar Variant of Adrenoleukodystrophy Exist?
    Benzoni C; Farina L; Pensato V; Marotta G; Kuqo A; Mauro E; Pareyson D; Salsano E
    Neurologist; 2019 Nov; 24(6):194-197. PubMed ID: 31688712
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [X-linked adrenoleukodystrophy: A case of acute childhood cerebral presentation].
    Posada Bustos S; Charry Lopez ML; Espinosa García E
    Andes Pediatr; 2021 Aug; 92(4):602-608. PubMed ID: 34652380
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

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

  • 7. 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]  

  • 8. Rare variability in adrenoleukodystrophy: a case report.
    Chen Y; Polara F; Pillai A
    J Med Case Rep; 2018 Jun; 12(1):182. PubMed ID: 29950168
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 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. Childhood cerebral X-linked adrenoleukodystrophy with atypical neuroimaging abnormalities and a novel mutation.
    Muranjan M; Karande S; Sankhe S; Eichler S
    J Postgrad Med; 2018; 64(1):59-63. PubMed ID: 29386416
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel temporal pattern of childhood cerebral X-linked adrenoleukodystrophy.
    Turco EC; Ormitti F; Andreolli A; Barsacchi M; Facini C; Pisani F
    Brain Dev; 2018 Mar; 40(3):238-241. PubMed ID: 29132975
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Progressive hemiparesis reveals X-linked adrenoleukodystrophy in a 3.5-year-old boy.
    Kosseifi CE; Seddiki K; Dumitriu D; Nassogne MC
    Acta Neurol Belg; 2021 Feb; 121(1):261-263. PubMed ID: 32107715
    [No Abstract]   [Full Text] [Related]  

  • 16. Profiling and Imaging of Phospholipids in Brains of Abcd1-Deficient Mice.
    Hama K; Fujiwara Y; Morita M; Yamazaki F; Nakashima Y; Takei S; Takashima S; Setou M; Shimozawa N; Imanaka T; Yokoyama K
    Lipids; 2018 Jan; 53(1):85-102. PubMed ID: 29469952
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Metformin-induced mitochondrial function and ABCD2 up-regulation in X-linked adrenoleukodystrophy involves AMP-activated protein kinase.
    Singh J; Olle B; Suhail H; Felicella MM; Giri S
    J Neurochem; 2016 Jul; 138(1):86-100. PubMed ID: 26849413
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Adrenoleukodystrophy siblings with a novel ABCD1 missense variant presenting with phenotypic differences: a case report and literature review.
    Shibata Y; Matsushima M; Matsukawa T; Ishiura H; Tsuji S; Yabe I
    J Hum Genet; 2021 May; 66(5):535-537. PubMed ID: 33127985
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.