Heatwole CR - Search Results

1

Quality-of-life in Charcot-Marie-Tooth disease: the patient's perspective.

Johnson NE, Heatwole CR, Dilek N, Sowden J, Kirk CA, Shereff D, Shy ME, Herrmann DN; Inherited Neuropathies Consortium. Johnson NE, et al. Among authors: heatwole cr. Neuromuscul Disord. 2014 Nov;24(11):1018-23. doi: 10.1016/j.nmd.2014.06.433. Epub 2014 Jun 27. Neuromuscul Disord. 2014. PMID: 25092060 Free PMC article.

2

The facioscapulohumeral muscular dystrophy - health index: Italian validation of a disease-specific measure of symptomatic burden.

Carraro E, Greco LC, Lizio A, Beretta M, Pozzi S, Casiraghi J, Becchiati S, Beshiri F, Frisoni MC, Iossa F, Heatwole C, Sansone V. Carraro E, et al. Disabil Rehabil. 2024 May;46(10):2130-2137. doi: 10.1080/09638288.2023.2212181. Epub 2023 May 17. Disabil Rehabil. 2024. PMID: 37194629

3

Facioscapulohumeral muscular dystrophy Health Index: Japanese translation and validation study.

Fujino H, Takahashi MP, Nakamura H, Heatwole CR, Takada H, Kuru S, Ogata K, Enomoto K, Hayashi Y, Imura O, Matsumura T. Fujino H, et al. Among authors: heatwole cr. Disabil Rehabil. 2024 Dec;46(25):6169-6178. doi: 10.1080/09638288.2024.2322035. Epub 2024 Mar 31. Disabil Rehabil. 2024. PMID: 38555736

4

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

5

Laboratory abnormalities in patients with myotonic dystrophy type 2.

Heatwole C, Johnson N, Goldberg B, Martens W, Moxley R 3rd. Heatwole C, et al. Arch Neurol. 2011 Sep;68(9):1180-4. doi: 10.1001/archneurol.2011.191. Arch Neurol. 2011. PMID: 21911698 Free PMC article.

6

Plasma exchange versus intravenous immunoglobulin for myasthenia gravis crisis: an acute hospital cost comparison study.

Heatwole C, Johnson N, Holloway R, Noyes K. Heatwole C, et al. J Clin Neuromuscul Dis. 2011 Dec;13(2):85-94. doi: 10.1097/CND.0b013e31822c34dd. J Clin Neuromuscul Dis. 2011. PMID: 22361692 Free PMC article.

7

Patient-reported impact of symptoms in myotonic dystrophy type 1 (PRISM-1).

Heatwole C, Bode R, Johnson N, Quinn C, Martens W, McDermott MP, Rothrock N, Thornton C, Vickrey B, Victorson D, Moxley R 3rd. Heatwole C, et al. Neurology. 2012 Jul 24;79(4):348-57. doi: 10.1212/WNL.0b013e318260cbe6. Epub 2012 Jul 11. Neurology. 2012. PMID: 22786587 Free PMC article.

8

Myotonic dystrophy: from bench to bedside.

Johnson NE, Heatwole CR. Johnson NE, et al. Among authors: heatwole cr. Semin Neurol. 2012 Jul;32(3):246-54. doi: 10.1055/s-0032-1329202. Epub 2012 Nov 1. Semin Neurol. 2012. PMID: 23117949 Review.

9

Patient-identified disease burden in facioscapulohumeral muscular dystrophy.

Johnson NE, Quinn C, Eastwood E, Tawil R, Heatwole CR. Johnson NE, et al. Among authors: heatwole cr. Muscle Nerve. 2012 Dec;46(6):951-3. doi: 10.1002/mus.23529. Muscle Nerve. 2012. PMID: 23225386 Free PMC article.

10

The impact of congenital and childhood myotonic dystrophy on quality of life: a qualitative study of associated symptoms.

Johnson NE, Luebbe E, Eastwood E, Chin N, Moxley RT 3rd, Heatwole CR. Johnson NE, et al. Among authors: heatwole cr. J Child Neurol. 2014 Jul;29(7):983-6. doi: 10.1177/0883073813484804. Epub 2013 Apr 22. J Child Neurol. 2014. PMID: 23611887

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