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Items: 1 to 20 of 134

1.

Occurrence of Emery-Dreifuss muscular dystrophy in a rural setting of Cameroon: a case report and review of the literature.

Ekabe CJ, Kehbila J, Sama CB, Kadia BM, Abanda MH, Monekosso GL.

BMC Res Notes. 2017 Jan 9;10(1):36. doi: 10.1186/s13104-016-2363-1. Review.

2.

Diagnosis and management of adult hereditary cardio-neuromuscular disorders: A model for the multidisciplinary care of complex genetic disorders.

Sommerville RB, Vincenti MG, Winborn K, Casey A, Stitziel NO, Connolly AM, Mann DL.

Trends Cardiovasc Med. 2017 Jan;27(1):51-58. doi: 10.1016/j.tcm.2016.06.005. Epub 2016 Jun 14. Review.

PMID:
27452966
3.

Prenatal diagnosis of congenital myopathies and muscular dystrophies.

Massalska D, Zimowski JG, Bijok J, Kucińska-Chahwan A, Łusakowska A, Jakiel G, Roszkowski T.

Clin Genet. 2016 Sep;90(3):199-210. doi: 10.1111/cge.12801. Epub 2016 Jun 2. Review.

PMID:
27197572
4.

Emery-Dreifuss muscular dystrophy: the most recognizable laminopathy.

Madej-Pilarczyk A, Kochański A.

Folia Neuropathol. 2016;54(1):1-8. Review.

5.

Biology and Regulatory Roles of Nuclear Lamins in Cellular Function and Dysfunction.

Khadija SG, Chen F, Hadden T, Commissaris RL, Kowluru A.

Recent Pat Endocr Metab Immune Drug Discov. 2015;9(2):111-20. Review.

PMID:
26453024
6.

Diverse lamin-dependent mechanisms interact to control chromatin dynamics. Focus on laminopathies.

Camozzi D, Capanni C, Cenni V, Mattioli E, Columbaro M, Squarzoni S, Lattanzi G.

Nucleus. 2014 Sep-Oct;5(5):427-40. doi: 10.4161/nucl.36289. Review.

7.

Emerin in health and disease.

Koch AJ, Holaska JM.

Semin Cell Dev Biol. 2014 May;29:95-106. doi: 10.1016/j.semcdb.2013.12.008. Epub 2013 Dec 21. Review.

8.

The muscular dystrophies.

Wicklund MP.

Continuum (Minneap Minn). 2013 Dec;19(6 Muscle Disease):1535-70. doi: 10.1212/01.CON.0000440659.41675.8b. Review. Erratum in: Continuum (Minneap Minn). 2014 Jun;20(3 Neurology of Systemic Disease):520.

PMID:
24305447
9.

The nuclear envelope LEM-domain protein emerin.

Berk JM, Tifft KE, Wilson KL.

Nucleus. 2013 Jul-Aug;4(4):298-314. doi: 10.4161/nucl.25751. Epub 2013 Jul 17. Review.

10.

Advances in basic and clinical research in laminopathies.

Politano L, Carboni N, Madej-Pilarczyk A, Marchel M, Nigro G, Fidziaóska A, Opolski G, Hausmanowa-Petrusewicz I.

Acta Myol. 2013 May;32(1):18-22. Review.

11.

Emery-Dreifuss muscular dystrophy, laminopathies, and other nuclear envelopathies.

Bonne G, Quijano-Roy S.

Handb Clin Neurol. 2013;113:1367-76. doi: 10.1016/B978-0-444-59565-2.00007-1. Review.

12.

Scapuloperoneal muscular dystrophy phenotype due to TRIM32-sarcotubular myopathy in South Dakota Hutterite.

Liewluck T, Tracy JA, Sorenson EJ, Engel AG.

Neuromuscul Disord. 2013 Feb;23(2):133-8. doi: 10.1016/j.nmd.2012.09.010. Epub 2012 Nov 9. Review.

PMID:
23142638
13.

Cardiac management in neuromuscular diseases.

Allen HD, Thrush PT, Hoffman TM, Flanigan KM, Mendell JR.

Phys Med Rehabil Clin N Am. 2012 Nov;23(4):855-68. doi: 10.1016/j.pmr.2012.08.001. Review.

PMID:
23137741
14.

Nuclear lamins: functions and clinical implications.

Cortelli P, Terlizzi R, Capellari S, Benarroch E.

Neurology. 2012 Oct 16;79(16):1726-31. doi: 10.1212/WNL.0b013e31826ea887. Review. No abstract available.

PMID:
23071165
15.

External and internal influences on muscle pathology.

McKeever PE, Camelo-Piragua S, Dowling J.

Arch Pathol Lab Med. 2012 Aug;136(8):927-34. doi: 10.5858/arpa.2012-0232-CR. Review.

PMID:
22849742
16.

Arrhythmias in the muscular dystrophies.

Groh WJ.

Heart Rhythm. 2012 Nov;9(11):1890-5. doi: 10.1016/j.hrthm.2012.06.038. Epub 2012 Jun 30. Review.

PMID:
22760083
17.

Arrhythmia-related workup in hereditary myopathies.

Finsterer J, Stöllberger C, Keller H.

J Electrocardiol. 2012 Jul-Aug;45(4):376-84. doi: 10.1016/j.jelectrocard.2012.02.003. Epub 2012 Mar 14. Review.

PMID:
22424849
18.

Reducing body myopathy and other FHL1-related muscular disorders.

Schessl J, Feldkirchner S, Kubny C, Schoser B.

Semin Pediatr Neurol. 2011 Dec;18(4):257-63. doi: 10.1016/j.spen.2011.10.007. Review.

PMID:
22172421
19.

The LINC complex and human disease.

Meinke P, Nguyen TD, Wehnert MS.

Biochem Soc Trans. 2011 Dec;39(6):1693-7. doi: 10.1042/BST20110658. Review.

PMID:
22103509
20.

[Laminopathies. Nuclear lamina diseases].

Méndez-López I.

Med Clin (Barc). 2012 Mar 3;138(5):208-14. doi: 10.1016/j.medcli.2011.03.032. Epub 2011 May 31. Review. Spanish.

PMID:
21632068

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