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Items: 23

1.

Tempering our metrics: Findings new ways to refine tried and true instruments.

Lawson VH, Baets J.

Neurology. 2020 Feb 10. pii: 10.1212/WNL.0000000000009028. doi: 10.1212/WNL.0000000000009028. [Epub ahead of print] No abstract available.

PMID:
32041725
2.

Green shoots but deep roots: New antibodies in small fiber neuropathy.

Tiwana HK, Lawson VH.

Muscle Nerve. 2020 Jan 30. doi: 10.1002/mus.26818. [Epub ahead of print] No abstract available.

PMID:
31998971
3.

Clinical and Statistical Considerations when Assessing Oxygen Levels in Tumors: Illustrative Results from Clinical EPR Oximetry Studies.

Flood AB, Schaner PE, Vaupel P, Williams BB, Gallez B, Chen EY, Ali A, Liu T, Lawson VH, Schreiber W, Swartz HM.

Adv Exp Med Biol. 2020;1232:155-168. doi: 10.1007/978-3-030-34461-0_20. Review.

PMID:
31893406
4.

Distribution of serum creatine kinase levels in amyotrophic lateral sclerosis.

Prior DE, Stommel E, Lawson VH, Kandel J, Robbins NM.

Muscle Nerve. 2020 Mar;61(3):E16-E18. doi: 10.1002/mus.26776. Epub 2019 Dec 23. No abstract available.

PMID:
31811651
5.

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
6.

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
7.

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
8.

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.

9.

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
10.

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.

11.

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.

12.

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
13.

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
14.

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
15.

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
16.

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
17.

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.

18.

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
19.

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
20.

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
21.

Counting motor units in chronic motor neuropathies.

Bromberg MB, Swoboda KJ, Lawson VH.

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

PMID:
14597327
23.

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