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 *

366 related articles for article (PubMed ID: 28974727)

  • 1. Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy.
    Doorenweerd N; Mahfouz A; van Putten M; Kaliyaperumal R; T' Hoen PAC; Hendriksen JGM; Aartsma-Rus AM; Verschuuren JJGM; Niks EH; Reinders MJT; Kan HE; Lelieveldt BPF
    Sci Rep; 2017 Oct; 7(1):12575. PubMed ID: 28974727
    [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. 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]  

  • 4. 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]  

  • 5. Combining genetics, neuropsychology and neuroimaging to improve understanding of brain involvement in Duchenne muscular dystrophy - a narrative review.
    Doorenweerd N
    Neuromuscul Disord; 2020 Jun; 30(6):437-442. PubMed ID: 32522501
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Brain metabolite composition in relation to cognitive function and dystrophin mutations in boys with Duchenne muscular dystrophy.
    Kreis R; Wingeier K; Vermathen P; Giger E; Joncourt F; Zwygart K; Kaufmann F; Boesch C; Steinlin M
    NMR Biomed; 2011 Apr; 24(3):253-62. PubMed ID: 21404337
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations.
    Ricotti V; Mandy WP; Scoto M; Pane M; Deconinck N; Messina S; Mercuri E; Skuse DH; Muntoni F
    Dev Med Child Neurol; 2016 Jan; 58(1):77-84. PubMed ID: 26365034
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Dystrophin gene mutation location and the risk of cognitive impairment in Duchenne muscular dystrophy.
    Taylor PJ; Betts GA; Maroulis S; Gilissen C; Pedersen RL; Mowat DR; Johnston HM; Buckley MF
    PLoS One; 2010 Jan; 5(1):e8803. PubMed ID: 20098710
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Disrupted structural connectome and neurocognitive functions in Duchenne muscular dystrophy: classifying and subtyping based on Dp140 dystrophin isoform.
    Preethish-Kumar V; Shah A; Polavarapu K; Kumar M; Safai A; Vengalil S; Nashi S; Deepha S; Govindaraj P; Afsar M; Rajeswaran J; Nalini A; Saini J; Ingalhalikar M
    J Neurol; 2022 Apr; 269(4):2113-2125. PubMed ID: 34505932
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophy.
    Felisari G; Martinelli Boneschi F; Bardoni A; Sironi M; Comi GP; Robotti M; Turconi AC; Lai M; Corrao G; Bresolin N
    Neurology; 2000 Aug; 55(4):559-64. PubMed ID: 10953192
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy.
    Giliberto F; Ferreiro V; Dalamon V; Szijan I
    Neurol Res; 2004 Jan; 26(1):83-7. PubMed ID: 14977063
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Validation of DE50-MD dogs as a model for the brain phenotype of Duchenne muscular dystrophy.
    Crawford AH; Hildyard JCW; Rushing SAM; Wells DJ; Diez-Leon M; Piercy RJ
    Dis Model Mech; 2022 Mar; 15(3):. PubMed ID: 35019137
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Loss of Dp140 regulatory sequences is associated with cognitive impairment in dystrophinopathies.
    Bardoni A; Felisari G; Sironi M; Comi G; Lai M; Robotti M; Bresolin N
    Neuromuscul Disord; 2000 Mar; 10(3):194-9. PubMed ID: 10734267
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neurocognitive profiles in Duchenne muscular dystrophy and gene mutation site.
    D'Angelo MG; Lorusso ML; Civati F; Comi GP; Magri F; Del Bo R; Guglieri M; Molteni M; Turconi AC; Bresolin N
    Pediatr Neurol; 2011 Nov; 45(5):292-9. PubMed ID: 22000308
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Transcriptional activation of the non-muscle, full-length dystrophin isoforms in Duchenne muscular dystrophy skeletal muscle.
    Sironi M; Bardoni A; Felisari G; Cagliani R; Robotti M; Comi GP; Moggio M; Bresolin N
    J Neurol Sci; 2001 May; 186(1-2):51-7. PubMed ID: 11412872
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Learning, memory and blood-brain barrier pathology in Duchenne muscular dystrophy mice lacking Dp427, or Dp427 and Dp140.
    Verhaeg M; Adamzek K; van de Vijver D; Putker K; Engelbeen S; Wijnbergen D; Overzier M; Suidgeest E; van der Weerd L; Aartsma-Rus A; van Putten M
    Genes Brain Behav; 2024 Jun; 23(3):e12895. PubMed ID: 38837620
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.