Weihl CC - Search Results

1

Optimizing hand-function patient outcome measures for inclusion body myositis.

Lin AY, Siener CS, Faino AV, Seiffert M, Weihl CC, Wang LH. Lin AY, et al. Among authors: weihl cc. Neuromuscul Disord. 2020 Oct;30(10):807-814. doi: 10.1016/j.nmd.2020.08.358. Epub 2020 Aug 19. Neuromuscul Disord. 2020. PMID: 32928647 Free PMC article.

2

Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia.

Weihl CC, Pestronk A, Kimonis VE. Weihl CC, et al. Neuromuscul Disord. 2009 May;19(5):308-15. doi: 10.1016/j.nmd.2009.01.009. Epub 2009 Apr 19. Neuromuscul Disord. 2009. PMID: 19380227 Free PMC article. Review.

3

Sporadic inclusion body myositis: possible pathogenesis inferred from biomarkers.

Weihl CC, Pestronk A. Weihl CC, et al. Curr Opin Neurol. 2010 Oct;23(5):482-8. doi: 10.1097/WCO.0b013e32833d3897. Curr Opin Neurol. 2010. PMID: 20664349 Free PMC article. Review.

4

Novel GNE mutations in two phenotypically distinct HIBM2 patients.

Weihl CC, Miller SE, Zaidman CM, Pestronk A, Baloh RH, Al-Lozi M. Weihl CC, et al. Neuromuscul Disord. 2011 Feb;21(2):102-5. doi: 10.1016/j.nmd.2010.11.002. Epub 2010 Dec 4. Neuromuscul Disord. 2011. PMID: 21131200 Free PMC article.

5

Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis.

Weihl CC, Baloh RH, Lee Y, Chou TF, Pittman SK, Lopate G, Allred P, Jockel-Balsarotti J, Pestronk A, Harms MB. Weihl CC, et al. Neuromuscul Disord. 2015 Apr;25(4):289-96. doi: 10.1016/j.nmd.2014.12.009. Epub 2015 Jan 6. Neuromuscul Disord. 2015. PMID: 25617006 Free PMC article.

6

Sporadic inclusion body myositis - a myodegenerative disease or an inflammatory myopathy.

Weihl CC, Mammen AL. Weihl CC, et al. Neuropathol Appl Neurobiol. 2017 Feb;43(1):82-91. doi: 10.1111/nan.12384. Neuropathol Appl Neurobiol. 2017. PMID: 28111778 Review.

7

Homozygous recessive MYH2 mutation mimicking dominant MYH2 associated myopathy.

Findlay AR, Harms MB, Pestronk A, Weihl CC. Findlay AR, et al. Among authors: weihl cc. Neuromuscul Disord. 2018 Aug;28(8):675-679. doi: 10.1016/j.nmd.2018.05.006. Epub 2018 May 21. Neuromuscul Disord. 2018. PMID: 29934118 Free PMC article.

8

A cross-sectional study of hand function in inclusion body myositis: Implications for functional rating scale.

Lin AY, Clapp M, Karanja E, Dooley K, Weihl CC, Wang LH. Lin AY, et al. Among authors: weihl cc. Neuromuscul Disord. 2020 Mar;30(3):200-206. doi: 10.1016/j.nmd.2019.12.002. Epub 2019 Dec 17. Neuromuscul Disord. 2020. PMID: 32057637 Free PMC article.

9

Phenotypic diversity in an international Cure VCP Disease registry.

Ikenaga C, Findlay AR, Seiffert M, Peck A, Peck N, Johnson NE, Statland JM, Weihl CC. Ikenaga C, et al. Among authors: weihl cc. Orphanet J Rare Dis. 2020 Sep 29;15(1):267. doi: 10.1186/s13023-020-01551-0. Orphanet J Rare Dis. 2020. PMID: 32993728 Free PMC article.

10

Clinical utility of anti-cytosolic 5'-nucleotidase 1A antibody in idiopathic inflammatory myopathies.

Ikenaga C, Findlay AR, Goyal NA, Robinson S, Cauchi J, Hussain Y, Wang LH, Kershen JC, Beson BA, Wallendorf M, Bucelli RC, Mozaffar T, Pestronk A, Weihl CC. Ikenaga C, et al. Among authors: weihl cc. Ann Clin Transl Neurol. 2021 Mar;8(3):571-578. doi: 10.1002/acn3.51294. Epub 2021 Feb 8. Ann Clin Transl Neurol. 2021. PMID: 33556224 Free PMC article.

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