Similar articles for PMID: 27519903

Year	Number of Results
1993	1
1997	1
1998	1
2003	1
2004	5
2005	6
2006	5
2007	6
2008	5
2009	9
2010	9
2011	15
2012	12
2013	14
2014	14
2015	15
2016	20
2017	15
2018	14
2019	18
2020	17
2021	10
2022	14
2023	7
2024	1

1

Two novel MYH7 proline substitutions cause Laing Distal Myopathy-like phenotypes with variable expressivity and neck extensor contracture.

Feinstein-Linial M, Buvoli M, Buvoli A, Sadeh M, Dabby R, Straussberg R, Shelef I, Dayan D, Leinwand LA, Birk OS. Feinstein-Linial M, et al. BMC Med Genet. 2016 Aug 12;17(1):57. doi: 10.1186/s12881-016-0315-1. BMC Med Genet. 2016. PMID: 27519903 Free PMC article.

2

Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation.

Overeem S, Schelhaas HJ, Blijham PJ, Grootscholten MI, ter Laak HJ, Timmermans J, van den Wijngaard A, Zwarts MJ. Overeem S, et al. Neuromuscul Disord. 2007 Jun;17(6):490-3. doi: 10.1016/j.nmd.2007.02.007. Epub 2007 Mar 23. Neuromuscul Disord. 2007. PMID: 17383184

3

Hereditary myosin myopathies.

Oldfors A. Oldfors A. Neuromuscul Disord. 2007 May;17(5):355-67. doi: 10.1016/j.nmd.2007.02.008. Epub 2007 Apr 16. Neuromuscul Disord. 2007. PMID: 17434305 Review.

4

Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report.

Bánfai Z, Hadzsiev K, Pál E, Komlósi K, Melegh M, Balikó L, Melegh B. Bánfai Z, et al. BMC Med Genet. 2017 Sep 19;18(1):105. doi: 10.1186/s12881-017-0463-y. BMC Med Genet. 2017. PMID: 28927399 Free PMC article.

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 mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7) distal myopathy.

Lamont PJ, Wallefeld W, Hilton-Jones D, Udd B, Argov Z, Barboi AC, Bonneman C, Boycott KM, Bushby K, Connolly AM, Davies N, Beggs AH, Cox GF, Dastgir J, DeChene ET, Gooding R, Jungbluth H, Muelas N, Palmio J, Penttilä S, Schmedding E, Suominen T, Straub V, Staples C, Van den Bergh PY, Vilchez JJ, Wagner KR, Wheeler PG, Wraige E, Laing NG. Lamont PJ, et al. Hum Mutat. 2014 Jul;35(7):868-79. doi: 10.1002/humu.22553. Epub 2014 May 21. Hum Mutat. 2014. PMID: 24664454 Free PMC article.

7

Exome sequencing identifies Laing distal myopathy MYH7 mutation in a Roma family previously diagnosed with distal neuronopathy.

Komlósi K, Hadzsiev K, Garbes L, Martínez Carrera LA, Pál E, Sigurðsson JH, Magnusson O, Melegh B, Wirth B. Komlósi K, et al. Neuromuscul Disord. 2014 Feb;24(2):156-61. doi: 10.1016/j.nmd.2013.10.010. Epub 2013 Nov 11. Neuromuscul Disord. 2014. PMID: 24300783

8

A novel MYH7 founder mutation causing Laing distal myopathy in Southern Spain.

Carbonell-Corvillo P, Tristán-Clavijo E, Cabrera-Serrano M, Servián-Morilla E, García-Martín G, Villarreal-Pérez L, Rivas-Infante E, Area-Gómez E, Chamorro-Muñoz MI, Gil-Gálvez A, Miranda-Vizuete A, Martinez-Mir A, Laing N, Paradas C. Carbonell-Corvillo P, et al. Neuromuscul Disord. 2018 Oct;28(10):828-836. doi: 10.1016/j.nmd.2018.07.006. Epub 2018 Jul 26. Neuromuscul Disord. 2018. PMID: 30166250 Free article.

9

Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsy.

Lamont PJ, Udd B, Mastaglia FL, de Visser M, Hedera P, Voit T, Bridges LR, Fabian V, Rozemuller A, Laing NG. Lamont PJ, et al. J Neurol Neurosurg Psychiatry. 2006 Feb;77(2):208-15. doi: 10.1136/jnnp.2005.073825. Epub 2005 Aug 15. J Neurol Neurosurg Psychiatry. 2006. PMID: 16103042 Free PMC article.

10

A rare mutation in MYH7 gene occurs with overlapping phenotype.

Ruggiero L, Fiorillo C, Gibertini S, De Stefano F, Manganelli F, Iodice R, Vitale F, Zanotti S, Galderisi M, Mora M, Santoro L. Ruggiero L, et al. Biochem Biophys Res Commun. 2015 Feb 13;457(3):262-6. doi: 10.1016/j.bbrc.2014.12.098. Epub 2015 Jan 7. Biochem Biophys Res Commun. 2015. PMID: 25576864

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