Dilek N - Search Results

1

Prospective study of muscle cramps in Charcot-Marie-tooth disease.

Johnson NE, Sowden J, Dilek N, Eichinger K, Burns J, Mcdermott MP, Shy ME, Herrmann DN. Johnson NE, et al. Among authors: dilek n. Muscle Nerve. 2015 Apr;51(4):485-8. doi: 10.1002/mus.24333. Epub 2015 Feb 11. Muscle Nerve. 2015. PMID: 25042364 Free PMC article. Clinical Trial.

2

Quantitative analysis of the "warm-up" phenomenon in myotonic dystrophy type 1.

Logigian EL, Blood CL, Dilek N, Martens WB, Moxley RT 4th, Wiegner AW, Thornton CA, Moxley RT 3rd. Logigian EL, et al. Among authors: dilek n. Muscle Nerve. 2005 Jul;32(1):35-42. doi: 10.1002/mus.20339. Muscle Nerve. 2005. PMID: 15880468 Clinical Trial.

3

Severity, type, and distribution of myotonic discharges are different in type 1 and type 2 myotonic dystrophy.

Logigian EL, Ciafaloni E, Quinn LC, Dilek N, Pandya S, Moxley RT 3rd, Thornton CA. Logigian EL, et al. Among authors: dilek n. Muscle Nerve. 2007 Apr;35(4):479-85. doi: 10.1002/mus.20722. Muscle Nerve. 2007. PMID: 17230537 Clinical Trial.

4

Computerized hand grip myometry reliably measures myotonia and muscle strength in myotonic dystrophy (DM1).

Moxley RT 3rd, Logigian EL, Martens WB, Annis CL, Pandya S, Moxley RT 4th, Barbieri CA, Dilek N, Wiegner AW, Thornton CA. Moxley RT 3rd, et al. Among authors: dilek n. Muscle Nerve. 2007 Sep;36(3):320-8. doi: 10.1002/mus.20822. Muscle Nerve. 2007. PMID: 17587223

5

Less is more, or almost as much: a 15-item quality-of-life instrument for myasthenia gravis.

Burns TM, Conaway MR, Cutter GR, Sanders DB; Muscle Study Group. Burns TM, et al. Muscle Nerve. 2008 Aug;38(2):957-63. doi: 10.1002/mus.21053. Muscle Nerve. 2008. PMID: 18642357

6

Disease-specific measure of quality of life for myasthenia gravis.

Mullins LL, Carpentier MY, Paul RH, Sanders DB; Muscle Study Group. Mullins LL, et al. Muscle Nerve. 2008 Aug;38(2):947-56. doi: 10.1002/mus.21016. Muscle Nerve. 2008. PMID: 18697209

7

Evoked myotonia can be "dialed-up" by increasing stimulus train length in myotonic dystrophy type 1.

Logigian EL, Twydell P, Dilek N, Martens WB, Quinn C, Wiegner AW, Heatwole CR, Thornton CA, Moxley RT 3rd. Logigian EL, et al. Among authors: dilek n. Muscle Nerve. 2010 Feb;41(2):191-6. doi: 10.1002/mus.21481. Muscle Nerve. 2010. PMID: 19750543 Free PMC article.

8

Mexiletine is an effective antimyotonia treatment in myotonic dystrophy type 1.

Logigian EL, Martens WB, Moxley RT 4th, McDermott MP, Dilek N, Wiegner AW, Pearson AT, Barbieri CA, Annis CL, Thornton CA, Moxley RT 3rd. Logigian EL, et al. Among authors: dilek n. Neurology. 2010 May 4;74(18):1441-8. doi: 10.1212/WNL.0b013e3181dc1a3a. Neurology. 2010. PMID: 20439846 Free PMC article. Clinical Trial.

9

High-dosage ascorbic acid treatment in Charcot-Marie-Tooth disease type 1A: results of a randomized, double-masked, controlled trial.

Lewis RA, McDermott MP, Herrmann DN, Hoke A, Clawson LL, Siskind C, Feely SM, Miller LJ, Barohn RJ, Smith P, Luebbe E, Wu X, Shy ME; Muscle Study Group. Lewis RA, et al. JAMA Neurol. 2013 Aug;70(8):981-7. doi: 10.1001/jamaneurol.2013.3178. JAMA Neurol. 2013. PMID: 23797954 Free PMC article. Clinical Trial.

10

Visualization of the diaphragm muscle with ultrasound improves diagnostic accuracy of phrenic nerve conduction studies.

Johnson NE, Utz M, Patrick E, Rheinwald N, Downs M, Dilek N, Dogra V, Logigian EL. Johnson NE, et al. Among authors: dilek n. Muscle Nerve. 2014 May;49(5):669-75. doi: 10.1002/mus.24059. Epub 2014 Apr 8. Muscle Nerve. 2014. PMID: 24037990

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