Similar articles for PMID: 12082049

Year	Number of Results
1995	1
1996	2
1998	3
1999	5
2000	4
2001	12
2002	14
2003	21
2004	16
2005	4
2006	2
2007	4
2008	3
2009	3
2010	1
2011	2
2012	2
2014	1
2015	1
2016	1
2019	1
2020	2
2021	1
2023	2
2024	0

1

Familial isolated hyperCKaemia associated with a new mutation in the caveolin-3 (CAV-3) gene.

Merlini L, Carbone I, Capanni C, Sabatelli P, Tortorelli S, Sotgia F, Lisanti MP, Bruno C, Minetti C. Merlini L, et al. J Neurol Neurosurg Psychiatry. 2002 Jul;73(1):65-7. doi: 10.1136/jnnp.73.1.65. J Neurol Neurosurg Psychiatry. 2002. PMID: 12082049 Free PMC article.

2

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

3

Dysferlin in a hyperCKaemic patient with caveolin 3 mutation and in C2C12 cells after p38 MAP kinase inhibition.

Capanni C, Sabatelli P, Mattioli E, Ognibene A, Columbaro M, Lattanzi G, Merlini L, Minetti C, Maraldi NM, Squarzoni S. Capanni C, et al. Exp Mol Med. 2003 Dec 31;35(6):538-44. doi: 10.1038/emm.2003.70. Exp Mol Med. 2003. PMID: 14749532

4

Mutation in the caveolin-3 gene causes a peculiar form of distal myopathy.

Tateyama M, Aoki M, Nishino I, Hayashi YK, Sekiguchi S, Shiga Y, Takahashi T, Onodera Y, Haginoya K, Kobayashi K, Iinuma K, Nonaka I, Arahata K, Itoyama Y. Tateyama M, et al. Neurology. 2002 Jan 22;58(2):323-5. doi: 10.1212/wnl.58.2.323. Neurology. 2002. PMID: 11805270

5

Limb-girdle muscular dystrophy in a 71-year-old woman with an R27Q mutation in the CAV3 gene.

Figarella-Branger D, Pouget J, Bernard R, Krahn M, Fernandez C, Lévy N, Pellissier JF. Figarella-Branger D, et al. Neurology. 2003 Aug 26;61(4):562-4. doi: 10.1212/01.wnl.0000076486.57572.5c. Neurology. 2003. PMID: 12939441 Review.

6

Phenotypic behavior of caveolin-3 R26Q, a mutant associated with hyperCKemia, distal myopathy, and rippling muscle disease.

Sotgia F, Woodman SE, Bonuccelli G, Capozza F, Minetti C, Scherer PE, Lisanti MP. Sotgia F, et al. Am J Physiol Cell Physiol. 2003 Nov;285(5):C1150-60. doi: 10.1152/ajpcell.00166.2003. Epub 2003 Jul 2. Am J Physiol Cell Physiol. 2003. PMID: 12839838 Free article.

7

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

8

Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemia.

Carbone I, Bruno C, Sotgia F, Bado M, Broda P, Masetti E, Panella A, Zara F, Bricarelli FD, Cordone G, Lisanti MP, Minetti C. Carbone I, et al. Neurology. 2000 Mar 28;54(6):1373-6. doi: 10.1212/wnl.54.6.1373. Neurology. 2000. PMID: 10746614

9

Immunohistochemical study of caveolin-3 in idiopathic hyperCKaemia.

Capasso M, Lupo S, Di Muzio A, Uncini A, Servidei S. Capasso M, et al. J Neurol Neurosurg Psychiatry. 2003 Apr;74(4):547-8. doi: 10.1136/jnnp.74.4.547-a. J Neurol Neurosurg Psychiatry. 2003. PMID: 12640091 Free PMC article. No abstract available.

10

Two novel CAV3 gene mutations in Japanese families.

Sugie K, Murayama K, Noguchi S, Murakami N, Mochizuki M, Hayashi YK, Nonaka I, Nishino I. Sugie K, et al. Neuromuscul Disord. 2004 Dec;14(12):810-4. doi: 10.1016/j.nmd.2004.08.008. Neuromuscul Disord. 2004. PMID: 15564037

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