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.
147 related articles for article (PubMed ID: 37385106)
1. Clinical study on cognitive impairment in Duchenne muscular dystrophy. Zhang XF; Luo YY; Jiang L; Hong SQ Neuromuscul Disord; 2023 Jul; 33(7):596-604. PubMed ID: 37385106 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. Intellectual ability in the duchenne muscular dystrophy and dystrophin gene mutation location. Milic Rasic V; Vojinovic D; Pesovic J; Mijalkovic G; Lukic V; Mladenovic J; Kosac A; Novakovic I; Maksimovic N; Romac S; Todorovic S; Savic Pavicevic D Balkan J Med Genet; 2014 Dec; 17(2):25-35. PubMed ID: 25937795 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. Neuropsychological impairments and the impact of dystrophin mutations on general cognitive functioning of patients with Duchenne muscular dystrophy. Wingeier K; Giger E; Strozzi S; Kreis R; Joncourt F; Conrad B; Gallati S; Steinlin M J Clin Neurosci; 2011 Jan; 18(1):90-5. PubMed ID: 21109441 [TBL] [Abstract][Full Text] [Related]
10. Computational cognitive modeling and validation of Dp140 induced alteration of working memory in Duchenne Muscular Dystrophy. Tyagi R; Aggarwal P; Mohanty M; Dutt V; Anand A Sci Rep; 2020 Jul; 10(1):11989. PubMed ID: 32686699 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. In Vivo Evaluation of White Matter Abnormalities in Children with Duchenne Muscular Dystrophy Using DTI. Preethish-Kumar V; Shah A; Kumar M; Ingalhalikar M; Polavarapu K; Afsar M; Rajeswaran J; Vengalil S; Nashi S; Thomas PT; Sadasivan A; Warrier M; Nalini A; Saini J AJNR Am J Neuroradiol; 2020 Jul; 41(7):1271-1278. PubMed ID: 32616576 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Are Dp71 and Dp140 brain dystrophin isoforms related to cognitive impairment in Duchenne muscular dystrophy? Moizard MP; Billard C; Toutain A; Berret F; Marmin N; Moraine C Am J Med Genet; 1998 Oct; 80(1):32-41. PubMed ID: 9800909 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Assessing mental health in boys with Duchenne muscular dystrophy: Emotional, behavioural and neurodevelopmental profile in an Italian clinical sample. Colombo P; Nobile M; Tesei A; Civati F; Gandossini S; Mani E; Molteni M; Bresolin N; D'Angelo G Eur J Paediatr Neurol; 2017 Jul; 21(4):639-647. PubMed ID: 28392227 [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]