Similar articles for PMID: 25864073

Year	Number of Results
1990	1
1992	2
1993	1
2001	1
2002	1
2004	2
2005	4
2006	5
2007	7
2008	2
2009	3
2010	10
2011	8
2012	8
2013	7
2014	7
2015	11
2016	6
2017	10
2018	13
2019	16
2020	5
2021	14
2022	13
2023	5
2024	0

1

Clinical and genetic features of anoctaminopathy in Saudi Arabia.

Bohlega S, Monies DM, Abulaban AA, Murad HN, Alhindi HN, Meyer BF. Bohlega S, et al. Neurosciences (Riyadh). 2015 Apr;20(2):173-7. doi: 10.17712/nsj.2015.2.20140547. Neurosciences (Riyadh). 2015. PMID: 25864073 Free PMC article.

2

Novel ANO5 homozygous microdeletion causing myalgia and unprovoked rhabdomyolysis in an Arabic man.

Lahoria R, Winder TL, Lui J, Al-Owain MA, Milone M. Lahoria R, et al. Muscle Nerve. 2014 Oct;50(4):610-3. doi: 10.1002/mus.24302. Epub 2014 Aug 30. Muscle Nerve. 2014. PMID: 24889862

3

A Japanese male with a novel ANO5 mutation with minimal muscle weakness and muscle pain till his late fifties.

Kadoya M, Ogata K, Suzuki M, Honma Y, Momma K, Yatabe K, Tamura T, Kaida K, Miyata N, Nishino I, Nonaka I, Kawai M. Kadoya M, et al. Neuromuscul Disord. 2017 May;27(5):477-480. doi: 10.1016/j.nmd.2017.01.012. Epub 2017 Jan 18. Neuromuscul Disord. 2017. PMID: 28214267

4

ANO5 mutations in the Dutch limb girdle muscular dystrophy population.

van der Kooi AJ, Ten Dam L, Frankhuizen WS, Straathof CS, van Doorn PA, de Visser M, Ginjaar IB. van der Kooi AJ, et al. Neuromuscul Disord. 2013 Jun;23(6):456-60. doi: 10.1016/j.nmd.2013.03.012. Epub 2013 Apr 19. Neuromuscul Disord. 2013. PMID: 23607914

5

Eight new mutations and the expanding phenotype variability in muscular dystrophy caused by ANO5.

Penttilä S, Palmio J, Suominen T, Raheem O, Evilä A, Muelas Gomez N, Tasca G, Waddell LB, Clarke NF, Barboi A, Hackman P, Udd B. Penttilä S, et al. Neurology. 2012 Mar 20;78(12):897-903. doi: 10.1212/WNL.0b013e31824c4682. Epub 2012 Mar 7. Neurology. 2012. PMID: 22402862

6

Clinical spectrum and gene mutations in a Chinese cohort with anoctaminopathy.

Cai S, Gao M, Xi J, Liu Z, Yue D, Wu H, Bi H, Li J, Liang Z, Zhao C, Udd B, Luo S, Lu J. Cai S, et al. Neuromuscul Disord. 2019 Aug;29(8):628-633. doi: 10.1016/j.nmd.2019.06.005. Epub 2019 Jun 12. Neuromuscul Disord. 2019. PMID: 31350120

7

Decreased Aerobic Capacity in ANO5-Muscular Dystrophy.

Ylikallio E, Auranen M, Mahjneh I, Lamminen A, Kousi M, Träskelin AL, Muurinen T, Löfberg M, Salmi T, Paetau A, Lehesjoki AE, Piirilä P, Kiuru-Enari S. Ylikallio E, et al. J Neuromuscul Dis. 2016 Nov 29;3(4):475-485. doi: 10.3233/JND-160186. J Neuromuscul Dis. 2016. PMID: 27911336

8

A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophy.

Hicks D, Sarkozy A, Muelas N, Köehler K, Huebner A, Hudson G, Chinnery PF, Barresi R, Eagle M, Polvikoski T, Bailey G, Miller J, Radunovic A, Hughes PJ, Roberts R, Krause S, Walter MC, Laval SH, Straub V, Lochmüller H, Bushby K. Hicks D, et al. Brain. 2011 Jan;134(Pt 1):171-182. doi: 10.1093/brain/awq294. Brain. 2011. PMID: 21186264 Free PMC article.

9

Use of Whole-Exome Sequencing for Diagnosis of Limb-Girdle Muscular Dystrophy: Outcomes and Lessons Learned.

Ghaoui R, Cooper ST, Lek M, Jones K, Corbett A, Reddel SW, Needham M, Liang C, Waddell LB, Nicholson G, O'Grady G, Kaur S, Ong R, Davis M, Sue CM, Laing NG, North KN, MacArthur DG, Clarke NF. Ghaoui R, et al. JAMA Neurol. 2015 Dec;72(12):1424-32. doi: 10.1001/jamaneurol.2015.2274. JAMA Neurol. 2015. PMID: 26436962

10

Novel ANO5 mutations causing hyper-CK-emia, limb girdle muscular weakness and Miyoshi type of muscular dystrophy.

Schessl J, Kress W, Schoser B. Schessl J, et al. Muscle Nerve. 2012 May;45(5):740-2. doi: 10.1002/mus.23281. Muscle Nerve. 2012. PMID: 22499103

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