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 *

317 related articles for article (PubMed ID: 26081639)

  • 1. Ocular and neurodevelopmental features of Duchenne muscular dystrophy: a signature of dystrophin function in the central nervous system.
    Ricotti V; Jägle H; Theodorou M; Moore AT; Muntoni F; Thompson DA
    Eur J Hum Genet; 2016 Apr; 24(4):562-8. PubMed ID: 26081639
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Investigating the role of dystrophin isoform deficiency in motor function in Duchenne muscular dystrophy.
    Chesshyre M; Ridout D; Hashimoto Y; Ookubo Y; Torelli S; Maresh K; Ricotti V; Abbott L; Gupta VA; Main M; Ferrari G; Kowala A; Lin YY; Tedesco FS; Scoto M; Baranello G; Manzur A; Aoki Y; Muntoni F
    J Cachexia Sarcopenia Muscle; 2022 Apr; 13(2):1360-1372. PubMed ID: 35083887
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Effects of dystrophin isoforms on signal transduction through neural retina: genotype-phenotype analysis of duchenne muscular dystrophy mouse mutants.
    Pillers DA; Weleber RG; Green DG; Rash SM; Dally GY; Howard PL; Powers MR; Hood DC; Chapman VM; Ray PN; Woodward WR
    Mol Genet Metab; 1999 Feb; 66(2):100-10. PubMed ID: 10068512
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Altered visual processing in the mdx52 mouse model of Duchenne muscular dystrophy.
    Barboni MTS; Liber AMP; Joachimsthaler A; Saoudi A; Goyenvalle A; Rendon A; Roger JE; Ventura DF; Kremers J; Vaillend C
    Neurobiol Dis; 2021 May; 152():105288. PubMed ID: 33556541
    [TBL] [Abstract][Full Text] [Related]  

  • 5. ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy.
    Fitzgerald KM; Cibis GW; Gettel AH; Rinaldi R; Harris DJ; White RA
    J Med Genet; 1999 Apr; 36(4):316-22. PubMed ID: 10227401
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutations.
    Pillers DA; Fitzgerald KM; Duncan NM; Rash SM; White RA; Dwinnell SJ; Powell BR; Schnur RE; Ray PN; Cibis GW; Weleber RG
    Hum Genet; 1999; 105(1-2):2-9. PubMed ID: 10480348
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Central nervous system involvements in Duchenne/Becker muscular dystrophy].
    Kumagai T; Miura K; Ohki T; Matsumoto A; Miyazaki S; Nakamura M; Ochi N; Takahashi O
    No To Hattatsu; 2001 Nov; 33(6):480-6. PubMed ID: 11725514
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cognitive and Neurobehavioral Profile in Boys With Duchenne Muscular Dystrophy.
    Banihani R; Smile S; Yoon G; Dupuis A; Mosleh M; Snider A; McAdam L
    J Child Neurol; 2015 Oct; 30(11):1472-82. PubMed ID: 25660133
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy.
    Sigesmund DA; Weleber RG; Pillers DA; Westall CA; Panton CM; Powell BR; Héon E; Murphey WH; Musarella MA; Ray PN
    Ophthalmology; 1994 May; 101(5):856-65. PubMed ID: 8190471
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Asymmetrical Functional Deficits of ON and OFF Retinal Processing in the mdx3Cv Mouse Model of Duchenne Muscular Dystrophy.
    Tsai TI; Barboni MT; Nagy BV; Roux MJ; Rendon A; Ventura DF; Kremers J
    Invest Ophthalmol Vis Sci; 2016 Oct; 57(13):5788-5798. PubMed ID: 27792813
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Intelligence quotient-genotype association in dystrophinopathies: A systematic review and meta-analysis.
    Pascual-Morena C; Cavero-Redondo I; Sequí-Domínguez I; Rodríguez-Gutiérrez E; Visier-Alfonso ME; Martínez-Vizcaíno V
    Neuropathol Appl Neurobiol; 2023 Jun; 49(3):e12914. PubMed ID: 37312416
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Global prevalence of intellectual developmental disorder in dystrophinopathies: A systematic review and meta-analysis.
    Pascual-Morena C; Cavero-Redondo I; Álvarez-Bueno C; Jiménez-López E; Saz-Lara A; Martínez-García I; Martínez-Vizcaíno V
    Dev Med Child Neurol; 2023 Jun; 65(6):734-744. PubMed ID: 36440509
    [TBL] [Abstract][Full Text] [Related]  

  • 13. DMD and West syndrome.
    Cardas R; Iliescu C; Butoianu N; Seferian A; Gataullina S; Gargaun E; Nectoux J; Bienvenu T; Craiu D; Gidaro T; Servais L
    Neuromuscul Disord; 2017 Oct; 27(10):911-913. PubMed ID: 28802771
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The long dystrophin gene product Dp427 modulates retinal function and vascular morphology in response to age and retinal ischemia.
    Bucher F; Friedlander MSH; Aguilar E; Kurihara T; Krohne TU; Usui Y; Friedlander M
    Neurochem Int; 2019 Oct; 129():104489. PubMed ID: 31199961
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Attention deficit hyperactivity disorder and cognitive function in Duchenne muscular dystrophy: phenotype-genotype correlation.
    Pane M; Lombardo ME; Alfieri P; D'Amico A; Bianco F; Vasco G; Piccini G; Mallardi M; Romeo DM; Ricotti V; Ferlini A; Gualandi F; Vicari S; Bertini E; Berardinelli A; Mercuri E
    J Pediatr; 2012 Oct; 161(4):705-9.e1. PubMed ID: 22560791
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Startle responses in Duchenne muscular dystrophy: a novel biomarker of brain dystrophin deficiency.
    Maresh K; Papageorgiou A; Ridout D; Harrison NA; Mandy W; Skuse D; Muntoni F
    Brain; 2023 Jan; 146(1):252-265. PubMed ID: 35136951
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Slight alteration of the electroretinogram in mice lacking dystrophin dp71.
    Cia D; Simonutti M; Fort PE; Doly M; Rendon A
    Ophthalmic Res; 2014; 51(4):196-203. PubMed ID: 24662427
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dp71 and intellectual disability in Indonesian patients with Duchenne muscular dystrophy.
    Iskandar K; Triono A; Sunartini ; Dwianingsih EK; Indraswari BW; Kirana IR; Ivana G; Sutomo R; Patria SY; Herini ES; Gunadi
    PLoS One; 2022; 17(10):e0276640. PubMed ID: 36315559
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Third case of Duchenne muscular dystrophy and West syndrome: Expanding the spectrum of the DMD neuropsychiatric phenotype.
    Peña-Padilla C; Romero-Valenzuela I; Baldomero-López A; Sandoval-Talamantes AK; Castellanos-González A; Nagy PL; Kelly RR; Corona-Rivera JR
    Neuromuscul Disord; 2021 May; 31(5):462-465. PubMed ID: 33741226
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Reduced cerebral gray matter and altered white matter in boys with Duchenne muscular dystrophy.
    Doorenweerd N; Straathof CS; Dumas EM; Spitali P; Ginjaar IB; Wokke BH; Schrans DG; van den Bergen JC; van Zwet EW; Webb A; van Buchem MA; Verschuuren JJ; Hendriksen JG; Niks EH; Kan HE
    Ann Neurol; 2014 Sep; 76(3):403-11. PubMed ID: 25043804
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.