138 related articles for article (PubMed ID: 18646563)
1. Patterns of dystrophin gene deletion in Egyptian Duchenne/Becker muscular dystrophy patients.
El Sherif RM; Fahmy NA; Nonaka I; Etribi MA
Acta Myol; 2007 Dec; 26(3):145-50. PubMed ID: 18646563
[TBL] [Abstract][Full Text] [Related]
2. Duchenne and Becker muscular dystrophy: a molecular and immunohistochemical approach.
Freund AA; Scola RH; Arndt RC; Lorenzoni PJ; Kay CK; Werneck LC
Arq Neuropsiquiatr; 2007 Mar; 65(1):73-6. PubMed ID: 17420831
[TBL] [Abstract][Full Text] [Related]
3. Deletion mutations in the dystrophin gene of Saudi patients with Duchenne and Becker muscular dystrophy.
Al-Jumah M; Majumdar R; Al-Rajeh S; Chaves-Carballo E; Salih MM; Awada A; Al-Shahwan S; Al-Uthaim S
Saudi Med J; 2002 Dec; 23(12):1478-82. PubMed ID: 12518196
[TBL] [Abstract][Full Text] [Related]
4. Comparative analysis of PCR-deletion detection and immunohistochemistry in Brazilian Duchenne and Becker muscular dystrophy patients.
Werneck LC; Scola RH; Maegawa GH; Werneck MC
Am J Med Genet; 2001 Oct; 103(2):115-20. PubMed ID: 11568916
[TBL] [Abstract][Full Text] [Related]
5. MLPA Analyses Reveal a Spectrum of Dystrophin Gene Deletions/Duplications in Pakistani Patients Suspected of Having Duchenne/Becker Muscular Dystrophy: A Retrospective Study.
Ansar Z; Nasir A; Moatter T; Khan S; Kirmani S; Ibrahim S; Imam K; Ather A; Samreen A; Hasan Z
Genet Test Mol Biomarkers; 2019 Jul; 23(7):468-472. PubMed ID: 31157985
[No Abstract] [Full Text] [Related]
6. Screening of dystrophin gene deletions in Egyptian patients with DMD/BMD muscular dystrophies.
Effat LK; El-Harouni AA; Amr KS; El-Minisi TI; Abdel Meguid N; El-Awady M
Dis Markers; 2000; 16(3-4):125-9. PubMed ID: 11381192
[TBL] [Abstract][Full Text] [Related]
7. Molecular deletion patterns in Duchenne and Becker muscular dystrophy patients from KwaZulu Natal.
Hallwirth Pillay KD; Bill PL; Madurai S; Mubaiwa L; Rapiti P
J Neurol Sci; 2007 Jan; 252(1):1-3. PubMed ID: 17141273
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. [Genetic analysis and prenatal diagnosis of Duchenne or Becker muscular dystrophy].
Zhao W; Jiang N; Li S; Li JS; Miao Y; Liang SY; Yu DY
Zhonghua Fu Chan Ke Za Zhi; 2019 Apr; 54(4):226-231. PubMed ID: 31006187
[No Abstract] [Full Text] [Related]
11. Duchenne muscular dystrophy: a clinical, histopathological and genetic study at a neurology tertiary care center in Southern India.
Swaminathan B; Shubha GN; Shubha D; Murthy AR; Kiran Kumar HB; Shylashree S; Gayathri N; Jamuna R; Jain S; Purushottam M; Nalini A
Neurol India; 2009; 57(6):734-8. PubMed ID: 20139501
[TBL] [Abstract][Full Text] [Related]
12. Distribution of dystrophin gene deletions in a Chinese population.
Li Y; Liu Z; OuYang S; Zhu Y; Wang L; Wu J
J Int Med Res; 2016 Feb; 44(1):99-108. PubMed ID: 26786758
[TBL] [Abstract][Full Text] [Related]
13. A comparative study of mPCR, MLPA, and muscle biopsy results in a cohort of children with Duchenne muscular dystrophy: a first study.
Manjunath M; Kiran P; Preethish-Kumar V; Nalini A; Singh RJ; Gayathri N
Neurol India; 2015; 63(1):58-62. PubMed ID: 25751470
[TBL] [Abstract][Full Text] [Related]
14. Analysis of dystrophin gene deletions by multiplex PCR in eastern India.
Basak J; Dasgupta UB; Banerjee TK; Senapati AK; Das SK; Mukherjee SC
Neurol India; 2006 Sep; 54(3):310-1. PubMed ID: 16936400
[TBL] [Abstract][Full Text] [Related]
15. Mutation spectrum of dystrophin gene in malaysian patients with Duchenne/Becker muscular dystrophy.
Rani AQ; Sasongko TH; Sulong S; Bunyan D; Salmi AR; Zilfalil BA; Matsuo M; Zabidi-Hussin ZA
J Neurogenet; 2013 Jun; 27(1-2):11-5. PubMed ID: 23438214
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Study of dystrophin gene non-deletion/duplication mutations causing Becker muscular dystrophy].
Cao JQ; Zhang C; Feng SW; Yang J; Li Z; Zhang M; Li SY; Sun XF; Wang YY; Zheng MY; Kong J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun; 28(3):308-12. PubMed ID: 21644230
[TBL] [Abstract][Full Text] [Related]
18. Absence of neuronal nitric oxide synthase (nNOS) as a pathological marker for the diagnosis of Becker muscular dystrophy with rod domain deletions.
Torelli S; Brown SC; Jimenez-Mallebrera C; Feng L; Muntoni F; Sewry CA
Neuropathol Appl Neurobiol; 2004 Oct; 30(5):540-5. PubMed ID: 15488030
[TBL] [Abstract][Full Text] [Related]
19. [Combining approach with multiplex PCR and MLPA to detect deletion and duplication in DMD patients, carriers, and prenatal diagnosis].
Li H; Ding J; Wang W; Chen Y; Lu W; Shao H; Wu BL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):318-22. PubMed ID: 19504448
[TBL] [Abstract][Full Text] [Related]
20. Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families - detection of carrier status in symptomatic and asymptomatic female relatives.
Pikó H; Vancsó V; Nagy B; Bán Z; Herczegfalvi A; Karcagi V
Neuromuscul Disord; 2009 Feb; 19(2):108-12. PubMed ID: 19084397
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
