241 related articles for article (PubMed ID: 28216480)
21. Frameshift deletion mechanisms in Egyptian Duchenne and Becker muscular dystrophy families.
Elhawary NA; Shawky RM; Hashem N
Mol Cells; 2004 Oct; 18(2):141-9. PubMed ID: 15528988
[TBL] [Abstract][Full Text] [Related]
22. [Duchenne muscular dystrophy: Case of atypical presentation and early diagnosis].
Cabezudo García P; Moreno Medinilla E; Calvo Medina R; Mora Ramírez MD; Martínez Antón J
Arch Argent Pediatr; 2015 Jun; 113(3):e149-52. PubMed ID: 25996334
[TBL] [Abstract][Full Text] [Related]
23. Co-occurrence of mutations in both dystrophin- and androgen-receptor genes is a novel cause of female Duchenne muscular dystrophy.
Katayama Y; Tran VK; Hoan NT; Zhang Z; Goji K; Yagi M; Takeshima Y; Saiki K; Nhan NT; Matsuo M
Hum Genet; 2006 Jun; 119(5):516-9. PubMed ID: 16528518
[TBL] [Abstract][Full Text] [Related]
24. Intragenic deletions in the dystrophin gene in 211 Pakistani Duchenne muscular dystrophy patients.
Hassan MJ; Mahmood S; Ali G; Bibi N; Waheed I; Rafiq MA; Ansar M; Ahmad W
Pediatr Int; 2008 Apr; 50(2):162-6. PubMed ID: 18353051
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Molecular characterization of an X(p21.2;q28) chromosomal inversion in a Duchenne muscular dystrophy patient with mental retardation reveals a novel long non-coding gene on Xq28.
Tran TH; Zhang Z; Yagi M; Lee T; Awano H; Nishida A; Okinaga T; Takeshima Y; Matsuo M
J Hum Genet; 2013 Jan; 58(1):33-9. PubMed ID: 23223008
[TBL] [Abstract][Full Text] [Related]
27. Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy--double trouble as an explanation for an atypical phenotype.
Rudnik-Schöneborn S; Weis J; Kress W; Häusler M; Zerres K
Neuromuscul Disord; 2008 Nov; 18(11):881-5. PubMed ID: 18684626
[TBL] [Abstract][Full Text] [Related]
28. A new model mouse for Duchenne muscular dystrophy produced by 2.4 Mb deletion of dystrophin gene using Cre-loxP recombination system.
Kudoh H; Ikeda H; Kakitani M; Ueda A; Hayasaka M; Tomizuka K; Hanaoka K
Biochem Biophys Res Commun; 2005 Mar; 328(2):507-16. PubMed ID: 15694376
[TBL] [Abstract][Full Text] [Related]
29. [Genotype-phenotype discordance in a Duchenne muscular dystrophy patient due to a novel mutation: insights into the shock absorber function of dystrophin].
López-Hernández LB; van Heusden D; Soriano-Ursúa MA; Figuera-Villanueva L; Vázquez-Cárdenas NA; Canto P; Gómez-Díaz B; Coral-Vázquez RM
Rev Neurol; 2011 Jun; 52(12):720-4. PubMed ID: 21594857
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Symptomatic female carriers of Duchenne muscular dystrophy (DMD): genetic and clinical characterization.
Giliberto F; Radic CP; Luce L; Ferreiro V; de Brasi C; Szijan I
J Neurol Sci; 2014 Jan; 336(1-2):36-41. PubMed ID: 24135430
[TBL] [Abstract][Full Text] [Related]
32. A rare co-occurrence of duchenne muscular dystrophy, congenital adrenal hypoplasia and glycerol kinase deficiency due to Xp21 contiguous gene deletion syndrome: case report.
Rathnasiri A; Senarathne U; Arunath V; Hoole T; Kumarasiri I; Muthukumarana O; Jasinge E; Mettananda S
BMC Endocr Disord; 2021 Oct; 21(1):214. PubMed ID: 34689766
[TBL] [Abstract][Full Text] [Related]
33. Genetic diagnosis of Duchenne and Becker muscular dystrophy using next-generation sequencing technology: comprehensive mutational search in a single platform.
Lim BC; Lee S; Shin JY; Kim JI; Hwang H; Kim KJ; Hwang YS; Seo JS; Chae JH
J Med Genet; 2011 Nov; 48(11):731-6. PubMed ID: 21969337
[TBL] [Abstract][Full Text] [Related]
34. Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization.
del Gaudio D; Yang Y; Boggs BA; Schmitt ES; Lee JA; Sahoo T; Pham HT; Wiszniewska J; Chinault AC; Beaudet AL; Eng CM
Hum Mutat; 2008 Sep; 29(9):1100-7. PubMed ID: 18752307
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Duchenne muscular dystrophy in a 46 XY female.
Wulfsberg EA; Skoglund RR
Clin Pediatr (Phila); 1986 May; 25(5):276-8. PubMed ID: 3698449
[TBL] [Abstract][Full Text] [Related]
37. Diagnostic and clinical characteristics of early-manifesting females with Duchenne or Becker muscular dystrophy.
Imbornoni L; Price ET; Andrews J; Meaney FJ; Ciafaloni E; Cunniff C
Am J Med Genet A; 2014 Nov; 164A(11):2769-74. PubMed ID: 25125379
[TBL] [Abstract][Full Text] [Related]
38. Muscular dystrophy in the Japanese Spitz: an inversion disrupts the DMD and RPGR genes.
Atencia-Fernandez S; Shiel RE; Mooney CT; Nolan CM
Anim Genet; 2015 Apr; 46(2):175-84. PubMed ID: 25644216
[TBL] [Abstract][Full Text] [Related]
39. Molecular diagnosis of Duchenne muscular dystrophy.
Nallamilli BR; Ankala A; Hegde M
Curr Protoc Hum Genet; 2014 Oct; 83():9.25.1-29. PubMed ID: 25271841
[TBL] [Abstract][Full Text] [Related]
40.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]