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Items: 1 to 20 of 194

1.

Response to Comment on Crews et al. Role and Determinants of Adherence to Off-loading in Diabetic Foot Ulcer Healing: A Prospective Investigation. Diabetes Care 2016;39:1371-1377.

Crews RT, Shen BJ, Campbell L, Lamont PJ, Hardman M, Boulton AJ, Peyrot M, Kirsner RS, Vileikyte L.

Diabetes Care. 2016 Dec;39(12):e222-e223. No abstract available.

PMID:
27879362
2.

New era in genetics of early-onset muscle disease: Breakthroughs and challenges.

Ravenscroft G, Davis MR, Lamont P, Forrest A, Laing NG.

Semin Cell Dev Biol. 2016 Aug 9. pii: S1084-9521(16)30241-5. doi: 10.1016/j.semcdb.2016.08.002. [Epub ahead of print] Review.

PMID:
27519468
3.

CAV3 mutations causing exercise intolerance, myalgia and rhabdomyolysis: Expanding the phenotypic spectrum of caveolinopathies.

Scalco RS, Gardiner AR, Pitceathly RD, Hilton-Jones D, Schapira AH, Turner C, Parton M, Desikan M, Barresi R, Marsh J, Manzur AY, Childs AM, Feng L, Murphy E, Lamont PJ, Ravenscroft G, Wallefeld W, Davis MR, Laing NG, Holton JL, Fialho D, Bushby K, Hanna MG, Phadke R, Jungbluth H, Houlden H, Quinlivan R.

Neuromuscul Disord. 2016 Aug;26(8):504-10. doi: 10.1016/j.nmd.2016.05.006. Epub 2016 May 11.

PMID:
27312022
4.

Role and Determinants of Adherence to Off-loading in Diabetic Foot Ulcer Healing: A Prospective Investigation.

Crews RT, Shen BJ, Campbell L, Lamont PJ, Boulton AJ, Peyrot M, Kirsner RS, Vileikyte L.

Diabetes Care. 2016 Aug;39(8):1371-7. doi: 10.2337/dc15-2373. Epub 2016 Jun 6.

PMID:
27271185
5.

A mutation in MT-TW causes a tRNA processing defect and reduced mitochondrial function in a family with Leigh syndrome.

Duff RM, Shearwood AM, Ermer J, Rossetti G, Gooding R, Richman TR, Balasubramaniam S, Thorburn DR, Rackham O, Lamont PJ, Filipovska A.

Mitochondrion. 2015 Nov;25:113-9. doi: 10.1016/j.mito.2015.10.008. Epub 2015 Oct 30.

PMID:
26524491
6.

Problems with the mapping of magic tricks.

Lamont P.

Front Psychol. 2015 Jun 23;6:855. doi: 10.3389/fpsyg.2015.00855. eCollection 2015 Jun 23. No abstract available.

7.
8.

Laing Distal Myopathy.

Lamont P, Laing NG.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2006 Oct 17 [updated 2015 Mar 12].

9.

Clinical utility gene card for: Nemaline myopathy - update 2015.

Nowak KJ, Davis MR, Wallgren-Pettersson C, Lamont PJ, Laing NG.

Eur J Hum Genet. 2015 Nov;23(11). doi: 10.1038/ejhg.2015.12. Epub 2015 Feb 25. No abstract available.

10.

Expanding the phenotype of GMPPB mutations.

Cabrera-Serrano M, Ghaoui R, Ravenscroft G, Johnsen RD, Davis MR, Corbett A, Reddel S, Sue CM, Liang C, Waddell LB, Kaur S, Lek M, North KN, MacArthur DG, Lamont PJ, Clarke NF, Laing NG.

Brain. 2015 Apr;138(Pt 4):836-44. doi: 10.1093/brain/awv013. Epub 2015 Feb 12.

PMID:
25681410
11.

Adult onset distal and proximal myopathy with complete ophthalmoplegia associated with a novel de novo p.(Leu1877Pro) mutation in MYH2.

Cabrera-Serrano M, Fabian VA, Boutilier J, Wise C, Faiz F, Lamont PJ, Laing NG.

Clin Genet. 2015 Dec;88(6):573-8. doi: 10.1111/cge.12552. Epub 2015 Jan 20.

PMID:
25529940
12.

Novel CHKB mutation expands the megaconial muscular dystrophy phenotype.

Cabrera-Serrano M, Junckerstorff RC, Atkinson V, Sivadorai P, Allcock RJ, Lamont P, Laing NG.

Muscle Nerve. 2015 Jan;51(1):140-3. doi: 10.1002/mus.24446. Epub 2014 Nov 22.

PMID:
25187204
13.

Novel mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7) distal myopathy.

Lamont PJ, Wallefeld W, Hilton-Jones D, Udd B, Argov Z, Barboi AC, Bonneman C, Boycott KM, Bushby K, Connolly AM, Davies N, Beggs AH, Cox GF, Dastgir J, DeChene ET, Gooding R, Jungbluth H, Muelas N, Palmio J, Penttilä S, Schmedding E, Suominen T, Straub V, Staples C, Van den Bergh PY, Vilchez JJ, Wagner KR, Wheeler PG, Wraige E, Laing NG.

Hum Mutat. 2014 Jul;35(7):868-79. doi: 10.1002/humu.22553. Epub 2014 May 21.

14.

Endovascular or open repair strategy for ruptured abdominal aortic aneurysm: 30 day outcomes from IMPROVE randomised trial.

IMPROVE Trial Investigators., Powell JT, Sweeting MJ, Thompson MM, Ashleigh R, Bell R, Gomes M, Greenhalgh RM, Grieve R, Heatley F, Hinchliffe RJ, Thompson SG, Ulug P.

BMJ. 2014 Jan 13;348:f7661. doi: 10.1136/bmj.f7661.

15.

Change blindness in a dynamic scene due to endogenous override of exogenous attentional cues.

Smith TJ, Lamont P, Henderson JM.

Perception. 2013;42(8):884-6.

PMID:
24303751
16.

NKX2-1 mutations in brain-lung-thyroid syndrome: a case series of four patients.

Shetty VB, Kiraly-Borri C, Lamont P, Bikker H, Choong CS.

J Pediatr Endocrinol Metab. 2014 Mar;27(3-4):373-8. doi: 10.1515/jpem-2013-0109.

PMID:
24129101
17.

Update on the diabetic foot 2012: the 14th biennial Malvern Diabetic Foot Conference, May 9-11, 2012.

Lamont P, Franklyn K, Rayman G, Boulton AJ.

Int J Low Extrem Wounds. 2013 Mar;12(1):71-5. doi: 10.1177/1534734613476519. Epub 2013 Feb 26. Review.

PMID:
23446363
18.

Simulator training on pulsatile vascular models significantly improves surgical skills and the quality of carotid patch plasty.

Duschek N, Assadian A, Lamont PM, Klemm K, Schmidli J, Mendel H, Eckstein HH.

J Vasc Surg. 2013 Apr;57(4):1148-54. doi: 10.1016/j.jvs.2012.08.109. Epub 2013 Jan 9.

19.

Remodelling of vascular (surgical) services in the UK.

Earnshaw JJ, Mitchell DC, Wyatt MG, Lamont PM, Naylor AR.

Eur J Vasc Endovasc Surg. 2012 Nov;44(5):465-7. doi: 10.1016/j.ejvs.2012.09.004. Epub 2012 Sep 21.

20.

The penny drops: change blindness at fixation.

Smith TJ, Lamont P, Henderson JM.

Perception. 2012;41(4):489-92.

PMID:
22896921

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