Similar articles for PMID: 22396310

Year	Number of Results
2005	2
2006	3
2007	6
2008	3
2009	6
2010	13
2011	7
2012	10
2013	15
2014	10
2015	8
2016	7
2017	8
2018	7
2019	5
2020	6
2021	10
2022	13
2023	2
2024	0

1

Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy.

Böhm J, Biancalana V, Dechene ET, Bitoun M, Pierson CR, Schaefer E, Karasoy H, Dempsey MA, Klein F, Dondaine N, Kretz C, Haumesser N, Poirson C, Toussaint A, Greenleaf RS, Barger MA, Mahoney LJ, Kang PB, Zanoteli E, Vissing J, Witting N, Echaniz-Laguna A, Wallgren-Pettersson C, Dowling J, Merlini L, Oldfors A, Bomme Ousager L, Melki J, Krause A, Jern C, Oliveira AS, Petit F, Jacquette A, Chaussenot A, Mowat D, Leheup B, Cristofano M, Poza Aldea JJ, Michel F, Furby A, Llona JE, Van Coster R, Bertini E, Urtizberea JA, Drouin-Garraud V, Béroud C, Prudhon B, Bedford M, Mathews K, Erby LA, Smith SA, Roggenbuck J, Crowe CA, Brennan Spitale A, Johal SC, Amato AA, Demmer LA, Jonas J, Darras BT, Bird TD, Laurino M, Welt SI, Trotter C, Guicheney P, Das S, Mandel JL, Beggs AH, Laporte J. Böhm J, et al. Hum Mutat. 2012 Jun;33(6):949-59. doi: 10.1002/humu.22067. Epub 2012 Apr 4. Hum Mutat. 2012. PMID: 22396310 Free PMC article.

2

Different in vivo impacts of dynamin 2 mutations implicated in Charcot-Marie-Tooth neuropathy or centronuclear myopathy.

Massana Muñoz X, Buono S, Koebel P, Laporte J, Cowling BS. Massana Muñoz X, et al. Hum Mol Genet. 2019 Dec 15;28(24):4067-4077. doi: 10.1093/hmg/ddz249. Hum Mol Genet. 2019. PMID: 31628461

3

DNM2 mutations in Chinese Han patients with centronuclear myopathy.

Lin P, Liu X, Zhao D, Dai T, Wu H, Gong Y, Yan C. Lin P, et al. Neurol Sci. 2016 Jun;37(6):995-8. doi: 10.1007/s10072-016-2513-1. Epub 2016 Feb 23. Neurol Sci. 2016. PMID: 26908122

4

Sporadic centronuclear myopathy with muscle pseudohypertrophy, neutropenia, and necklace fibers due to a DNM2 mutation.

Liewluck T, Lovell TL, Bite AV, Engel AG. Liewluck T, et al. Neuromuscul Disord. 2010 Dec;20(12):801-4. doi: 10.1016/j.nmd.2010.07.273. Neuromuscul Disord. 2010. PMID: 20817456 Free PMC article.

5

Mild functional differences of dynamin 2 mutations associated to centronuclear myopathy and Charcot-Marie Tooth peripheral neuropathy.

Koutsopoulos OS, Koch C, Tosch V, Böhm J, North KN, Laporte J. Koutsopoulos OS, et al. PLoS One. 2011;6(11):e27498. doi: 10.1371/journal.pone.0027498. Epub 2011 Nov 11. PLoS One. 2011. PMID: 22096584 Free PMC article.

6

Phenotype variability and histopathological findings in centronuclear myopathy due to DNM2 mutations.

Hanisch F, Müller T, Dietz A, Bitoun M, Kress W, Weis J, Stoltenburg G, Zierz S. Hanisch F, et al. J Neurol. 2011 Jun;258(6):1085-90. doi: 10.1007/s00415-010-5889-5. Epub 2011 Jan 9. J Neurol. 2011. PMID: 21221624

7

Muscle-specific function of the centronuclear myopathy and Charcot-Marie-Tooth neuropathy-associated dynamin 2 is required for proper lipid metabolism, mitochondria, muscle fibers, neuromuscular junctions and peripheral nerves.

Tinelli E, Pereira JA, Suter U. Tinelli E, et al. Hum Mol Genet. 2013 Nov 1;22(21):4417-29. doi: 10.1093/hmg/ddt292. Epub 2013 Jun 27. Hum Mol Genet. 2013. PMID: 23813975

8

Clinicopathological features of centronuclear myopathy in Japanese populations harboring mutations in dynamin 2.

Mori-Yoshimura M, Okuma A, Oya Y, Fujimura-Kiyono C, Nakajima H, Matsuura K, Takemura A, Malicdan MC, Hayashi YK, Nonaka I, Murata M, Nishino I. Mori-Yoshimura M, et al. Clin Neurol Neurosurg. 2012 Jul;114(6):678-83. doi: 10.1016/j.clineuro.2011.10.040. Epub 2012 May 19. Clin Neurol Neurosurg. 2012. PMID: 22613877

9

Mutational and clinical spectrum of centronuclear myopathy in 9 cases and a literature review of Chinese patients.

Wang Q, Yu M, Xie Z, Liu J, Wang Q, Lv H, Zhang W, Yuan Y, Wang Z. Wang Q, et al. Neurol Sci. 2022 Apr;43(4):2803-2811. doi: 10.1007/s10072-021-05627-y. Epub 2021 Sep 30. Neurol Sci. 2022. PMID: 34595679 Review.

10

Subtle central and peripheral nervous system abnormalities in a family with centronuclear myopathy and a novel dynamin 2 gene mutation.

Echaniz-Laguna A, Nicot AS, Carré S, Franques J, Tranchant C, Dondaine N, Biancalana V, Mandel JL, Laporte J. Echaniz-Laguna A, et al. Neuromuscul Disord. 2007 Dec;17(11-12):955-9. doi: 10.1016/j.nmd.2007.06.467. Epub 2007 Sep 6. Neuromuscul Disord. 2007. PMID: 17825552

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