Gardner-Medwin D - Search Results

1

Dystrophin in skeletal muscle. II. Immunoreactivity in patients with Xp21 muscular dystrophy.

Nicholson LV, Davison K, Johnson MA, Slater CR, Young C, Bhattacharya S, Gardner-Medwin D, Harris JB. Nicholson LV, et al. J Neurol Sci. 1989 Dec;94(1-3):137-46. doi: 10.1016/0022-510x(89)90224-4. J Neurol Sci. 1989. PMID: 2693618

2

Heterogeneity of dystrophin expression in patients with Duchenne and Becker muscular dystrophy.

Nicholson LV, Johnson MA, Gardner-Medwin D, Bhattacharya S, Harris JB. Nicholson LV, et al. Acta Neuropathol. 1990;80(3):239-50. doi: 10.1007/BF00294640. Acta Neuropathol. 1990. PMID: 2205076

3

Functional significance of dystrophin positive fibres in Duchenne muscular dystrophy.

Nicholson LV, Johnson MA, Bushby KM, Gardner-Medwin D. Nicholson LV, et al. Arch Dis Child. 1993 May;68(5):632-6. doi: 10.1136/adc.68.5.632. Arch Dis Child. 1993. PMID: 8323331 Free PMC article.

4

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

5

Variability in clinical, genetic and protein abnormalities in manifesting carriers of Duchenne and Becker muscular dystrophy.

Bushby KM, Goodship JA, Nicholson LV, Johnson MA, Haggerty ID, Gardner-Medwin D. Bushby KM, et al. Neuromuscul Disord. 1993 Jan;3(1):57-64. doi: 10.1016/0960-8966(93)90042-i. Neuromuscul Disord. 1993. PMID: 8329890

6

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.

7

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.

8

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.

9

The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II. Correlation of phenotype with genetic and protein abnormalities.

Bushby KM, Gardner-Medwin D, Nicholson LV, Johnson MA, Haggerty ID, Cleghorn NJ, Harris JB, Bhattacharya SS. Bushby KM, et al. J Neurol. 1993 Feb;240(2):105-12. doi: 10.1007/BF00858726. J Neurol. 1993. PMID: 8437017

10

Population frequencies of three DNA alleles linked to the Duchenne muscular dystrophy gene.

Papiha SS, Roberts DF, Clarke A, Burn J, Gardner-Medwin D, Bhattacharya SS. Papiha SS, et al. J Med Genet. 1989 Jun;26(6):390-2. doi: 10.1136/jmg.26.6.390. J Med Genet. 1989. PMID: 2567785 Free PMC article.

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