Nicholson LV - Search Results

1

Muscle X-inactivation patterns and dystrophin expression in Duchenne muscular dystrophy carriers.

Matthews PM, Benjamin D, Van Bakel I, Squier MV, Nicholson LV, Sewry C, Barnes PR, Hopkin J, Brown R, Hilton-Jones D, et al. Matthews PM, et al. Among authors: nicholson lv. Neuromuscul Disord. 1995 May;5(3):209-20. doi: 10.1016/0960-8966(94)00057-g. Neuromuscul Disord. 1995. PMID: 7633186

2

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. Among authors: nicholson lv. Neuromuscul Disord. 1993 Jan;3(1):57-64. doi: 10.1016/0960-8966(93)90042-i. Neuromuscul Disord. 1993. PMID: 8329890

3

The "rescue" of dystrophin synthesis in boys with Duchenne muscular dystrophy.

Nicholson LV. Nicholson LV. Neuromuscul Disord. 1993 Sep-Nov;3(5-6):525-31. doi: 10.1016/0960-8966(93)90109-w. Neuromuscul Disord. 1993. PMID: 8186705

4

Sarcolemmal distribution of abnormal dystrophin in Xp21 carriers.

Vainzof M, Nicholson LV, Bulman DE, Tsanaclis AM, Passos-Bueno MR, Pavanello RC, Zatz M. Vainzof M, et al. Among authors: nicholson lv. Neuromuscul Disord. 1993 Mar;3(2):135-40. doi: 10.1016/0960-8966(93)90005-5. Neuromuscul Disord. 1993. PMID: 7689380

5

Investigation of a female manifesting Becker muscular dystrophy.

Glass IA, Nicholson LV, Watkiss E, Johnson MA, Roberts RG, Abbs S, Brittain-Jones S, Boddie HG. Glass IA, et al. Among authors: nicholson lv. J Med Genet. 1992 Aug;29(8):578-82. doi: 10.1136/jmg.29.8.578. J Med Genet. 1992. PMID: 1518025 Free PMC article.

6

Very mild muscular dystrophy associated with the deletion of 46% of dystrophin.

England SB, Nicholson LV, Johnson MA, Forrest SM, Love DR, Zubrzycka-Gaarn EE, Bulman DE, Harris JB, Davies KE. England SB, et al. Among authors: nicholson lv. Nature. 1990 Jan 11;343(6254):180-2. doi: 10.1038/343180a0. Nature. 1990. PMID: 2404210

7

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. Among authors: nicholson lv. J Neurol. 1993 Feb;240(2):105-12. doi: 10.1007/BF00858726. J Neurol. 1993. PMID: 8437017

8

Identification of a mutation in the promoter region of the dystrophin gene in a patient with atypical Becker muscular dystrophy.

Bushby KM, Cleghorn NJ, Curtis A, Haggerty ID, Nicholson LV, Johnson MA, Harris JB, Bhattacharya SS. Bushby KM, et al. Among authors: nicholson lv. Hum Genet. 1991 Dec;88(2):195-9. doi: 10.1007/BF00206071. Hum Genet. 1991. PMID: 1757094

9

Dystrophin analysis in the diagnosis of muscular dystrophy.

Norman AM, Hughes HE, Gardner-Medwin D, Nicholson LV. Norman AM, et al. Among authors: nicholson lv. Arch Dis Child. 1989 Oct;64(10):1501-3. doi: 10.1136/adc.64.10.1501. Arch Dis Child. 1989. PMID: 2684033 Free PMC article.

10

Dystrophin and dystrophin-related protein (utrophin) distribution in normal and dystrophin-deficient skeletal muscles.

Pons F, Nicholson LV, Robert A, Voit T, Leger JJ. Pons F, et al. Among authors: nicholson lv. Neuromuscul Disord. 1993 Sep-Nov;3(5-6):507-14. doi: 10.1016/0960-8966(93)90106-t. Neuromuscul Disord. 1993. PMID: 8186702

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

74 results

Search Page

Filters