Similar articles for PMID: 18930476

Year	Number of Results
1998	1
2000	1
2002	1
2003	2
2004	6
2005	10
2006	19
2007	24
2008	27
2009	24
2010	7
2011	6
2012	5
2013	4
2014	3
2015	2
2016	4
2017	2
2018	5
2019	1
2020	1
2021	1
2024	0

1

Phenotypic variability in a Spanish family with a Caveolin-3 mutation.

González-Pérez P, Gallano P, González-Quereda L, Rivas-Infante E, Teijeira S, Navarro C, Bautista-Lorite J. González-Pérez P, et al. J Neurol Sci. 2009 Jan 15;276(1-2):95-8. doi: 10.1016/j.jns.2008.09.009. Epub 2008 Oct 19. J Neurol Sci. 2009. PMID: 18930476

2

Consequences of a novel caveolin-3 mutation in a large German family.

Fischer D, Schroers A, Blümcke I, Urbach H, Zerres K, Mortier W, Vorgerd M, Schröder R. Fischer D, et al. Ann Neurol. 2003 Feb;53(2):233-41. doi: 10.1002/ana.10442. Ann Neurol. 2003. PMID: 12557291

3

Early-onset toe walking in rippling muscle disease due to a new caveolin-3 gene mutation.

Madrid RE, Kubisch C, Hays AP. Madrid RE, et al. Neurology. 2005 Oct 25;65(8):1301-3. doi: 10.1212/01.wnl.0000180963.85963.73. Neurology. 2005. PMID: 16247063

4

Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350P.

Walter MC, Reilich P, Huebner A, Fischer D, Schröder R, Vorgerd M, Kress W, Born C, Schoser BG, Krause KH, Klutzny U, Bulst S, Frey JR, Lochmüller H. Walter MC, et al. Brain. 2007 Jun;130(Pt 6):1485-96. doi: 10.1093/brain/awm039. Epub 2007 Apr 17. Brain. 2007. PMID: 17439987

5

New phenotype and pathology features in MYH7-related distal myopathy.

Tasca G, Ricci E, Penttilä S, Monforte M, Giglio V, Ottaviani P, Camastra G, Silvestri G, Udd B. Tasca G, et al. Neuromuscul Disord. 2012 Jul;22(7):640-7. doi: 10.1016/j.nmd.2012.03.003. Epub 2012 Apr 20. Neuromuscul Disord. 2012. PMID: 22521714

6

Novel DYSF mutations in Thai patients with distal myopathy.

Liewluck T, Pongpakdee S, Witoonpanich R, Sangruchi T, Pho-Iam T, Limwongse C, Thongnoppakhun W, Boonyapisit K, Sopassathit V, Phudhichareonrat S, Suthiponpaisan U, Raksadawan N, Goto K, Hayashi YK, Nishino I. Liewluck T, et al. Clin Neurol Neurosurg. 2009 Sep;111(7):613-8. doi: 10.1016/j.clineuro.2009.05.001. Epub 2009 Jun 2. Clin Neurol Neurosurg. 2009. PMID: 19493611

7

A novel missense mutation in the caveolin-3 gene in rippling muscle disease.

Lorenzoni PJ, Scola RH, Vieira N, Vainzof M, Carsten AL, Werneck LC. Lorenzoni PJ, et al. Muscle Nerve. 2007 Aug;36(2):258-60. doi: 10.1002/mus.20781. Muscle Nerve. 2007. PMID: 17405141

8

A novel mutation in the caveolin-3 gene causing familial isolated hyperCKaemia.

Alias L, Gallano P, Moreno D, Pujol R, Martínez-Matos JA, Baiget M, Ferrer I, Olivé M. Alias L, et al. Neuromuscul Disord. 2004 May;14(5):321-4. doi: 10.1016/j.nmd.2004.01.006. Neuromuscul Disord. 2004. PMID: 15099591

9

Myotilinopathy in a family with late onset myopathy.

Pénisson-Besnier I, Talvinen K, Dumez C, Vihola A, Dubas F, Fardeau M, Hackman P, Carpen O, Udd B. Pénisson-Besnier I, et al. Neuromuscul Disord. 2006 Jul;16(7):427-31. doi: 10.1016/j.nmd.2006.04.009. Epub 2006 Jun 21. Neuromuscul Disord. 2006. PMID: 16793270

10

Rippling muscle disease: variable phenotype in a family with five afflicted members.

Jacobi C, Ruscheweyh R, Vorgerd M, Weber MA, Storch-Hagenlocher B, Meinck HM. Jacobi C, et al. Muscle Nerve. 2010 Jan;41(1):128-32. doi: 10.1002/mus.21446. Muscle Nerve. 2010. PMID: 19697367

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