PubMed for id: 413212

Year	Number of Results
1999	2
2000	8
2001	6
2002	9
2003	3
2004	7
2005	14
2006	10
2007	11
2008	12
2009	7
2010	9
2011	9
2012	11
2013	12
2014	7
2015	10
2016	7
2017	6
2018	11
2019	12
2020	15
2021	13
2022	5
2023	6
2024	0

1

Skeletal and Cardiac Muscle Disorders Caused by Mutations in Genes Encoding Intermediate Filament Proteins.

Maggi L, Mavroidis M, Psarras S, Capetanaki Y, Lattanzi G. Maggi L, et al. Int J Mol Sci. 2021 Apr 20;22(8):4256. doi: 10.3390/ijms22084256. Int J Mol Sci. 2021. PMID: 33923914 Free PMC article. Review.

2

COMPREHENSIVE CARDIOVASCULAR THERAPY IN EMERY-DREIFUSS MUSCULAR DYSTROPHY: A CASE REPORT.

Chendey TV, Rishko MV, Chendey VI. Chendey TV, et al. Wiad Lek. 2023;76(11):2531-2534. doi: 10.36740/WLek202311130. Wiad Lek. 2023. PMID: 38112376

3

Emerin deficiency does not exacerbate cardiomyopathy in a murine model of Emery-Dreifuss muscular dystrophy caused by an LMNA gene mutation.

Wada E, Matsumoto K, Susumu N, Kato M, Hayashi YK. Wada E, et al. J Physiol Sci. 2023 Nov 8;73(1):27. doi: 10.1186/s12576-023-00886-0. J Physiol Sci. 2023. PMID: 37940872 Free PMC article.

4

Emery-Dreifuss muscular dystrophy Type 1 is associated with a high risk of malignant ventricular arrhythmias and end-stage heart failure.

Cannie DE, Syrris P, Protonotarios A, Bakalakos A, Pruny JF, Ditaranto R, Martinez-Veira C, Larrañaga-Moreira JM, Medo K, Bermúdez-Jiménez FJ, Ben Yaou R, Leturcq F, Mezcua AR, Marini-Bettolo C, Cabrera E, Reuter C, Limeres Freire J, Rodríguez-Palomares JF, Mestroni L, Taylor MRG, Parikh VN, Ashley EA, Barriales-Villa R, Jiménez-Jáimez J, Garcia-Pavia P, Charron P, Biagini E, García Pinilla JM, Bourke J, Savvatis K, Wahbi K, Elliott PM. Cannie DE, et al. Eur Heart J. 2023 Dec 21;44(48):5064-5073. doi: 10.1093/eurheartj/ehad561. Eur Heart J. 2023. PMID: 37639473 Free PMC article.

5

Early Muscle MRI Findings in a Pediatric Case of Emery-Dreifuss Muscular Dystrophy Type 1.

Panicucci C, Casalini S, Traverso M, Brolatti N, Baratto S, Raffaghello L, Pedemonte M, Doglio L, Derchi M, Tasca G, Damasio BM, Fiorillo C, Bruno C. Panicucci C, et al. Neuropediatrics. 2023 Dec;54(6):426-429. doi: 10.1055/s-0043-1768989. Epub 2023 May 31. Neuropediatrics. 2023. PMID: 37257496 Free article. Review.

6

Drosophila Models Reveal Properties of Mutant Lamins That Give Rise to Distinct Diseases.

Walker SG, Langland CJ, Viles J, Hecker LA, Wallrath LL. Walker SG, et al. Cells. 2023 Apr 12;12(8):1142. doi: 10.3390/cells12081142. Cells. 2023. PMID: 37190051 Free PMC article.

7

Detection of gonosomal mosaicism by ultra-deep sequencing and droplet digital PCR in patients with Emery-Dreifuss muscular dystrophy.

Xie Y, Luo J, Zhong J, Liu X, Tang J, Lan D. Xie Y, et al. Mol Genet Genomic Med. 2023 Jun;11(6):e2161. doi: 10.1002/mgg3.2161. Epub 2023 Mar 10. Mol Genet Genomic Med. 2023. PMID: 36897110 Free PMC article.

8

Autosomal dominant Emery-Dreifuss muscular dystrophy caused by a mutation in the lamin A/C gene identified by exome sequencing: a case report.

Iskandar K, Sunartini, Astari FN, Gumilang RA, Ilma N, Shartyanie NP, Adistyawan G, Tan G, Gunadi, Lai PS. Iskandar K, et al. BMC Pediatr. 2022 Oct 17;22(1):601. doi: 10.1186/s12887-022-03662-y. BMC Pediatr. 2022. PMID: 36253810 Free PMC article.

9

Clinical and genetic characteristics of Emery-Dreifuss muscular dystrophy patients from Turkey: 30 years longitudinal follow-up study.

Yunisova G, Ceylaner S, Oflazer P, Deymeer F, Parman YG, Durmus H. Yunisova G, et al. Neuromuscul Disord. 2022 Sep;32(9):718-727. doi: 10.1016/j.nmd.2022.07.397. Epub 2022 Jul 13. Neuromuscul Disord. 2022. PMID: 35922275

10

Genetics and muscle pathology in the diagnosis of muscular dystrophies: An update.

Narasimhaiah D, Uppin MS, Ranganath P. Narasimhaiah D, et al. Indian J Pathol Microbiol. 2022 May;65(Supplement):S259-S270. doi: 10.4103/ijpm.ijpm_1074_21. Indian J Pathol Microbiol. 2022. PMID: 35562158 Free article. Review.

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