Martens W - Search Results

1

A longitudinal study of disease progression in facioscapulohumeral muscular dystrophy (FSHD).

Varma A, Todinca MS, Eichinger K, Heininger S, Dilek N, Martens W, Tawil R, Statland J, Kissel JT, McDermott MP, Heatwole C. Varma A, et al. Among authors: martens w. Muscle Nerve. 2024 Mar;69(3):362-367. doi: 10.1002/mus.28031. Epub 2024 Jan 8. Muscle Nerve. 2024. PMID: 38189531

2

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: martens wb. Muscle Nerve. 2007 Sep;36(3):320-8. doi: 10.1002/mus.20822. Muscle Nerve. 2007. PMID: 17587223

3

An expanded version of the Hammersmith Functional Motor Scale for SMA II and III patients.

O'Hagen JM, Glanzman AM, McDermott MP, Ryan PA, Flickinger J, Quigley J, Riley S, Sanborn E, Irvine C, Martens WB, Annis C, Tawil R, Oskoui M, Darras BT, Finkel RS, De Vivo DC. O'Hagen JM, et al. Neuromuscul Disord. 2007 Oct;17(9-10):693-7. doi: 10.1016/j.nmd.2007.05.009. Epub 2007 Jul 19. Neuromuscul Disord. 2007. PMID: 17658255

4

Inclusion body myositis functional rating scale: a reliable and valid measure of disease severity.

Jackson CE, Barohn RJ, Gronseth G, Pandya S, Herbelin L; Muscle Study Group. Jackson CE, et al. Muscle Nerve. 2008 Apr;37(4):473-6. doi: 10.1002/mus.20958. Muscle Nerve. 2008. PMID: 18236463 Clinical Trial.

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: martens wb. Muscle Nerve. 2010 Feb;41(2):191-6. doi: 10.1002/mus.21481. Muscle Nerve. 2010. PMID: 19750543 Free PMC article.

8

What determines quality of life in inclusion body myositis?

Sadjadi R, Rose MR; Muscle Study Group. Sadjadi R, et al. J Neurol Neurosurg Psychiatry. 2010 Oct;81(10):1164-6. doi: 10.1136/jnnp.2009.183863. Epub 2010 Jul 2. J Neurol Neurosurg Psychiatry. 2010. PMID: 20601666

9

Open-label trial of recombinant human insulin-like growth factor 1/recombinant human insulin-like growth factor binding protein 3 in myotonic dystrophy type 1.

Heatwole CR, Eichinger KJ, Friedman DI, Hilbert JE, Jackson CE, Logigian EL, Martens WB, McDermott MP, Pandya SK, Quinn C, Smirnow AM, Thornton CA, Moxley RT 3rd. Heatwole CR, et al. Arch Neurol. 2011 Jan;68(1):37-44. doi: 10.1001/archneurol.2010.227. Epub 2010 Sep 13. Arch Neurol. 2011. PMID: 20837825 Free PMC article. Clinical Trial.

10

Association of plastin 3 expression with disease severity in spinal muscular atrophy only in postpubertal females.

Stratigopoulos G, Lanzano P, Deng L, Guo J, Kaufmann P, Darras B, Finkel R, Tawil R, McDermott MP, Martens W, Devivo DC, Chung WK. Stratigopoulos G, et al. Among authors: martens w. Arch Neurol. 2010 Oct;67(10):1252-6. doi: 10.1001/archneurol.2010.239. Arch Neurol. 2010. PMID: 20937953

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