Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 19

1.

Reader response: Pearls & Oy-sters: Pembrolizumab-induced myasthenia gravis.

Robbins NM, Mozaffar T, Mammen AL, Liewluck T, Guidon A, Lawson VH.

Neurology. 2019 Jul 23;93(4):183-184. doi: 10.1212/WNL.0000000000007845. No abstract available.

PMID:
31332091
2.

Patient hand and artistic depiction of chronic inflammatory demyelinating polyradiculoneuropathy.

Cichowski AJ, Lawson VH.

Neurology. 2019 Jul 2;93(1):35-36. doi: 10.1212/WNL.0000000000007731. No abstract available.

PMID:
31262986
3.

A charcot-marie-tooth type 1B kindred associated with hemifacial spasm and trigeminal neuralgia.

Caress JB, Lewis JA, Pinyan CW, Lawson VH.

Muscle Nerve. 2019 Jul;60(1):62-66. doi: 10.1002/mus.26478. Epub 2019 Apr 8.

PMID:
30920665
4.

Fibromyalgia syndrome and small fiber, early or mild sensory polyneuropathy.

Lawson VH, Grewal J, Hackshaw KV, Mongiovi PC, Stino AM.

Muscle Nerve. 2018 Nov;58(5):625-630. doi: 10.1002/mus.26131. Epub 2018 Apr 26.

5.

The management and treatment of children with Fabry disease: A United States-based perspective.

Hopkin RJ, Jefferies JL, Laney DA, Lawson VH, Mauer M, Taylor MR, Wilcox WR; Fabry Pediatric Expert Panel.

Mol Genet Metab. 2016 Feb;117(2):104-13. doi: 10.1016/j.ymgme.2015.10.007. Epub 2015 Oct 23. Review.

PMID:
26546059
6.

Neuromuscular junction disorders mimicking myopathy.

Mongiovi PC, Elsheikh B, Lawson VH, Kissel JT, Arnold WD.

Muscle Nerve. 2014 Nov;50(5):854-6. doi: 10.1002/mus.24300. Epub 2014 Sep 24.

7.

Multifocal motor neuropathy: a review of pathogenesis, diagnosis, and treatment.

Lawson VH, Arnold WD.

Neuropsychiatr Dis Treat. 2014 Apr 5;10:567-76. doi: 10.2147/NDT.S39592. eCollection 2014. Review.

8.

Bent spine syndrome as an early manifestation of myotonic dystrophy type 1.

Lawson VH, King WM, Arnold WD.

J Clin Neuromuscul Dis. 2013 Dec;15(2):58-62. doi: 10.1097/CND.0b013e3182a3012d.

PMID:
24263032
9.

Ethambutol toxicity exacerbating the phenotype of CMT2A2.

Fonkem E, Skordilis MA, Binkley EM, Raymer DS, Epstein A, Arnold WD, Kissel JT, Lawson VH.

Muscle Nerve. 2013 Jul;48(1):140-4. doi: 10.1002/mus.23766. Epub 2013 Jun 4.

PMID:
23733358
10.

Mutant small heat shock protein B3 causes motor neuropathy: utility of a candidate gene approach.

Kolb SJ, Snyder PJ, Poi EJ, Renard EA, Bartlett A, Gu S, Sutton S, Arnold WD, Freimer ML, Lawson VH, Kissel JT, Prior TW.

Neurology. 2010 Feb 9;74(6):502-6. doi: 10.1212/WNL.0b013e3181cef84a.

PMID:
20142617
11.

Diagnostic nerve ultrasound in Charcot-Marie-Tooth disease type 1B.

Cartwright MS, Brown ME, Eulitt P, Walker FO, Lawson VH, Caress JB.

Muscle Nerve. 2009 Jul;40(1):98-102. doi: 10.1002/mus.21292. Erratum in: Muscle Nerve. 2015 Jun;51(6):940.

PMID:
19533637
12.

Late-onset hereditary axonal neuropathies.

Bennett CL, Lawson VH, Brickell KL, Isaacs K, Seltzer W, Lipe HP, Weiss MD, Carter GT, Flanigan KM, Chance PF, Bird TD.

Neurology. 2008 Jul 1;71(1):14-20. doi: 10.1212/01.wnl.0000304048.94023.73. Epub 2008 May 21.

PMID:
18495953
13.

Mitochondrial fusion and function in Charcot-Marie-Tooth type 2A patient fibroblasts with mitofusin 2 mutations.

Amiott EA, Lott P, Soto J, Kang PB, McCaffery JM, DiMauro S, Abel ED, Flanigan KM, Lawson VH, Shaw JM.

Exp Neurol. 2008 May;211(1):115-27. doi: 10.1016/j.expneurol.2008.01.010. Epub 2008 Jan 26.

14.

Clinical and electrophysiologic features of CMT2A with mutations in the mitofusin 2 gene.

Lawson VH, Graham BV, Flanigan KM.

Neurology. 2005 Jul 26;65(2):197-204.

PMID:
16043786
15.

Comparison of conventional and decomposition-enhanced spike triggered averaging techniques.

Lawson VH, Bromberg MB, Stashuk D.

Clin Neurophysiol. 2004 Mar;115(3):564-8.

PMID:
15036051
16.

Assessment of axonal loss in Charcot-Marie-Tooth neuropathies.

Lawson VH, Gordon Smith A, Bromberg MB.

Exp Neurol. 2003 Dec;184(2):753-7.

PMID:
14769367
17.

Counting motor units in chronic motor neuropathies.

Bromberg MB, Swoboda KJ, Lawson VH.

Exp Neurol. 2003 Nov;184 Suppl 1:S53-7.

PMID:
14597327
19.

Supplemental Content

Loading ...
Support Center