155 related articles for article (PubMed ID: 37312416)
1. 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]
2. 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]
3. 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]
4. Dystrophin Genotype and Risk of Neuropsychiatric Disorders in Dystrophinopathies: A Systematic Review and Meta-Analysis.
Pascual-Morena C; Cavero-Redondo I; Martínez-Vizcaíno V; Sequí-Domínguez I; Fernández-Bravo-Rodrigo J; Jiménez-López E
J Neuromuscul Dis; 2023; 10(2):159-172. PubMed ID: 36565132
[TBL] [Abstract][Full Text] [Related]
5. Epileptic disorders in Becker and Duchenne muscular dystrophies: a systematic review and meta-analysis.
Pascual-Morena C; Martínez-Vizcaíno V; Saz-Lara A; López-Gil JF; Fernández-Bravo-Rodrigo J; Cavero-Redondo I
J Neurol; 2022 Jul; 269(7):3461-3469. PubMed ID: 35229191
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. Association between loss of dp140 and cognitive impairment in duchenne and becker dystrophies.
Chamova T; Guergueltcheva V; Raycheva M; Todorov T; Genova J; Bichev S; Bojinova V; Mitev V; Tournev I; Todorova A
Balkan J Med Genet; 2013 Jun; 16(1):21-30. PubMed ID: 24265581
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. 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]
12. 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]
13. Patients with Duchenne muscular dystrophy are significantly shorter than those with Becker muscular dystrophy, with the higher incidence of short stature in Dp71 mutated subgroup.
Matsumoto M; Awano H; Lee T; Takeshima Y; Matsuo M; Iijima K
Neuromuscul Disord; 2017 Nov; 27(11):1023-1028. PubMed ID: 28734761
[TBL] [Abstract][Full Text] [Related]
14. Longitudinal follow-up of verbal span and processing speed in Duchenne muscular dystrophy.
Hellebrekers DMJ; Doorenweerd N; Sweere DJJ; van Kuijk SMJ; Aartsma-Rus AM; Klinkenberg S; Vles JSH; Hendriksen JGM
Eur J Paediatr Neurol; 2020 Mar; 25():120-126. PubMed ID: 31964551
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. The expression of the distal dystrophin isoforms Dp140 and Dp71 in the human epileptic hippocampus in relation to cognitive functioning.
Hoogland G; Hendriksen RGF; Slegers RJ; Hendriks MPH; Schijns OEMG; Aalbers MW; Vles JSH
Hippocampus; 2019 Feb; 29(2):102-110. PubMed ID: 30069964
[TBL] [Abstract][Full Text] [Related]
17. Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression.
Daoud F; Angeard N; Demerre B; Martie I; Benyaou R; Leturcq F; Cossée M; Deburgrave N; Saillour Y; Tuffery S; Urtizberea A; Toutain A; Echenne B; Frischman M; Mayer M; Desguerre I; Estournet B; Réveillère C; Penisson-Besnier ; Cuisset JM; Kaplan JC; Héron D; Rivier F; Chelly J
Hum Mol Genet; 2009 Oct; 18(20):3779-94. PubMed ID: 19602481
[TBL] [Abstract][Full Text] [Related]
18. 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]
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. Altered presynaptic ultrastructure in excitatory hippocampal synapses of mice lacking dystrophins Dp427 or Dp71.
Miranda R; Nudel U; Laroche S; Vaillend C
Neurobiol Dis; 2011 Jul; 43(1):134-41. PubMed ID: 21397023
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
