Lunt PW - Search Results

1

Best practice guidelines on genetic diagnostics of Facioscapulohumeral muscular dystrophy: workshop 9th June 2010, LUMC, Leiden, The Netherlands.

Lemmers RJ, O'Shea S, Padberg GW, Lunt PW, van der Maarel SM. Lemmers RJ, et al. Among authors: lunt pw. Neuromuscul Disord. 2012 May;22(5):463-70. doi: 10.1016/j.nmd.2011.09.004. Epub 2011 Dec 16. Neuromuscul Disord. 2012. PMID: 22177830 Free article. No abstract available.

2

Diagnostic criteria for facioscapulohumeral muscular dystrophy.

Padberg GW, Lunt PW, Koch M, Fardeau M. Padberg GW, et al. Among authors: lunt pw. Neuromuscul Disord. 1991;1(4):231-4. doi: 10.1016/0960-8966(91)90094-9. Neuromuscul Disord. 1991. PMID: 1822799 No abstract available.

3

An exclusion map for facioscapulohumeral (Landouzy-Déjérine) disease.

Sarfarazi M, Upadhyaya M, Padberg G, Pericak-Vance M, Siddique T, Lucotte G, Lunt P. Sarfarazi M, et al. J Med Genet. 1989 Aug;26(8):481-4. doi: 10.1136/jmg.26.8.481. J Med Genet. 1989. PMID: 2769720 Free PMC article.

4

44th ENMC International Workshop: Facioscapulohumeral Muscular Dystrophy: Molecular Studies 19-21 July 1996, Naarden, The Netherlands.

Lunt PW. Lunt PW. Neuromuscul Disord. 1998 Apr;8(2):126-30. doi: 10.1016/s0960-8966(98)00012-1. Neuromuscul Disord. 1998. PMID: 9608567 No abstract available.

5

Report of the sixth International Workshop on Facioscapulohumeral Muscular Dystrophy: San Francisco, 11 November 1992; and current guidelines for clinical application of DNA rearrangements at locus D4S810. Muscular Dystrophy Group of America.

Lunt PW. Lunt PW. Neuromuscul Disord. 1994 Jan;4(1):83-6. doi: 10.1016/0960-8966(94)90052-3. Neuromuscul Disord. 1994. PMID: 8173356 No abstract available.

6

Siblings with recessive oculopharyngeal muscular dystrophy.

Hebbar S, Webberley MJ, Lunt P, Robinson DO. Hebbar S, et al. Neuromuscul Disord. 2007 Mar;17(3):254-7. doi: 10.1016/j.nmd.2006.11.009. Epub 2007 Feb 12. Neuromuscul Disord. 2007. PMID: 17296297

7

Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD).

Upadhyaya M, Maynard J, Osborn M, Jardine P, Harper PS, Lunt P. Upadhyaya M, et al. Muscle Nerve Suppl. 1995;(2):S45-9. Muscle Nerve Suppl. 1995. PMID: 23573586

8

A scapular onset muscular dystrophy without facial involvement: possible allelism with facioscapulohumeral muscular dystrophy.

Jardine PE, Upadhyaya M, Maynard J, Harper P, Lunt PW. Jardine PE, et al. Among authors: lunt pw. Neuromuscul Disord. 1994 Sep-Nov;4(5-6):477-82. doi: 10.1016/0960-8966(94)90087-6. Neuromuscul Disord. 1994. PMID: 7881292

9

Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy.

Lunt PW, Jardine PE, Koch M, Maynard J, Osborn M, Williams M, Harper PS, Upadhyaya M. Lunt PW, et al. Muscle Nerve Suppl. 1995;(2):S103-9. Muscle Nerve Suppl. 1995. PMID: 23573595

10

Design, set-up and utility of the UK facioscapulohumeral muscular dystrophy patient registry.

Evangelista T, Wood L, Fernandez-Torron R, Williams M, Smith D, Lunt P, Hudson J, Norwood F, Orrell R, Willis T, Hilton-Jones D, Rafferty K, Guglieri M, Lochmüller H. Evangelista T, et al. J Neurol. 2016 Jul;263(7):1401-8. doi: 10.1007/s00415-016-8132-1. Epub 2016 May 9. J Neurol. 2016. PMID: 27159994 Free PMC article.

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

87 results

Search Page

Filters