Similar articles for PMID: 8411068

Year	Number of Results
1982	1
1983	1
1985	1
1988	5
1989	9
1990	10
1991	10
1992	21
1993	25
1994	16
1995	15
1996	8
1997	6
1998	8
1999	6
2000	2
2001	4
2002	1
2003	2
2004	2
2005	1
2006	1
2007	2
2008	3
2009	1
2010	2
2011	2
2012	2
2013	2
2014	5
2015	1
2016	4
2017	3
2018	2
2019	1
2020	2
2021	2
2023	1
2024	0

1

Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 2. Correlations within individual patients.

Nicholson LV, Johnson MA, Bushby KM, Gardner-Medwin D, Curtis A, Ginjaar IB, den Dunnen JT, Welch JL, Butler TJ, Bakker E, et al. Nicholson LV, et al. J Med Genet. 1993 Sep;30(9):737-44. doi: 10.1136/jmg.30.9.737. J Med Genet. 1993. PMID: 8411068 Free PMC article.

2

Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 3. Differential diagnosis and prognosis.

Nicholson LV, Johnson MA, Bushby KM, Gardner-Medwin D, Curtis A, Ginjaar IB, den Dunnen JT, Welch JL, Butler TJ, Bakker E, et al. Nicholson LV, et al. J Med Genet. 1993 Sep;30(9):745-51. doi: 10.1136/jmg.30.9.745. J Med Genet. 1993. PMID: 8411069 Free PMC article.

3

Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 1. Trends across the clinical groups.

Nicholson LV, Johnson MA, Bushby KM, Gardner-Medwin D, Curtis A, Ginjaar IB, den Dunnen JT, Welch JL, Butler TJ, Bakker E, et al. Nicholson LV, et al. J Med Genet. 1993 Sep;30(9):728-36. doi: 10.1136/jmg.30.9.728. J Med Genet. 1993. PMID: 8411067 Free PMC article.

4

Biochemical characterization of patients with in-frame or out-of-frame DMD deletions pertinent to exon 44 or 45 skipping.

Anthony K, Arechavala-Gomeza V, Ricotti V, Torelli S, Feng L, Janghra N, Tasca G, Guglieri M, Barresi R, Armaroli A, Ferlini A, Bushby K, Straub V, Ricci E, Sewry C, Morgan J, Muntoni F. Anthony K, et al. JAMA Neurol. 2014 Jan;71(1):32-40. doi: 10.1001/jamaneurol.2013.4908. JAMA Neurol. 2014. PMID: 24217213 Free article. Clinical Trial.

5

Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophy.

Winnard AV, Klein CJ, Coovert DD, Prior T, Papp A, Snyder P, Bulman DE, Ray PN, McAndrew P, King W, et al. Winnard AV, et al. Hum Mol Genet. 1993 Jun;2(6):737-44. doi: 10.1093/hmg/2.6.737. Hum Mol Genet. 1993. PMID: 8353493

6

Dystrophin expression in Duchenne patients with "in-frame" gene deletions.

Nicholson LV, Bushby KM, Johnson MA, Gardner-Medwin D, Ginjaar IB. Nicholson LV, et al. Neuropediatrics. 1993 Apr;24(2):93-7. doi: 10.1055/s-2008-1071521. Neuropediatrics. 1993. PMID: 8327067

7

Predicted and observed sizes of dystrophin in some patients with gene deletions that disrupt the open reading frame.

Nicholson LV, Bushby KM, Johnson MA, den Dunnen JT, Ginjaar IB, van Ommen GJ. Nicholson LV, et al. J Med Genet. 1992 Dec;29(12):892-6. doi: 10.1136/jmg.29.12.892. J Med Genet. 1992. PMID: 1479604 Free PMC article.

8

Deletions in the 5' region of dystrophin and resulting phenotypes.

Muntoni F, Gobbi P, Sewry C, Sherratt T, Taylor J, Sandhu SK, Abbs S, Roberts R, Hodgson SV, Bobrow M, et al. Muntoni F, et al. J Med Genet. 1994 Nov;31(11):843-7. doi: 10.1136/jmg.31.11.843. J Med Genet. 1994. PMID: 7853367 Free PMC article.

9

Deletions in the dystrophin gene: analysis of Duchenne and Becker muscular dystrophy patients in Quebec.

Simard LR, Gingras F, Delvoye N, Vanasse M, Melançon SB, Labuda D. Simard LR, et al. Hum Genet. 1992 Jun;89(4):419-24. doi: 10.1007/BF00194314. Hum Genet. 1992. PMID: 1618490

10

Analysis of a dystrophin gene deletion by amplification of mRNA isolated from DMD myotubes cultured in vitro.

Ehrenpreis J, Hillers M, Junkes B, Pfordt M, Schwinger E, Vosberg HP. Ehrenpreis J, et al. Genomics. 1991 Jul;10(3):551-7. doi: 10.1016/0888-7543(91)90435-h. Genomics. 1991. PMID: 1889805

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