156 related articles for article (PubMed ID: 36031908)
1. Muscle MRI as a Diagnostic Challenge in Emery-Dreifuss Muscular Dystrophy.
Pinto MJ; Fromes Y; Ackermann-Bonan I; Leturcq F; Verebi C; Romero NB; Stojkovic T
J Neuromuscul Dis; 2022; 9(5):649-654. PubMed ID: 36031908
[TBL] [Abstract][Full Text] [Related]
2. 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
Neuropediatrics; 2023 Dec; 54(6):426-429. PubMed ID: 37257496
[TBL] [Abstract][Full Text] [Related]
3. X-linked Emery-Dreifuss muscular dystrophy manifesting with adult onset axial weakness, camptocormia, and minimal joint contractures.
Brisset M; Ben Yaou R; Carlier RY; Chanut A; Nicolas G; Romero NB; Wahbi K; Decrocq C; Leturcq F; Laforêt P; Malfatti E
Neuromuscul Disord; 2019 Sep; 29(9):678-683. PubMed ID: 31474437
[TBL] [Abstract][Full Text] [Related]
4. [A case of Emery-Dreifuss muscular dystrophy with slight joint contracture].
Fujii S; Eguchi K; Sato C; Saito Y; Indrawati LA; Shirai S; Nishino I; Yabe I
Rinsho Shinkeigaku; 2020 Aug; 60(8):554-559. PubMed ID: 32641626
[TBL] [Abstract][Full Text] [Related]
5. Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery-Dreifuss muscular dystrophy.
Meinke P; Schneiderat P; Srsen V; Korfali N; Lê Thành P; Cowan GJ; Cavanagh DR; Wehnert M; Schirmer EC; Walter MC
Neuromuscul Disord; 2015 Feb; 25(2):127-36. PubMed ID: 25454731
[TBL] [Abstract][Full Text] [Related]
6. A novel emerin gene mutation in Emery Dreifuss muscular dystrophy patient with spontaneous chordae tendinae rupture.
Pancheri E; Bozzetti S; Rimessi P; Macchione F; Barillari M; Venturoli A; Guglielmi V; Fortunato F; Tonin P; Vattemi G
Clin Neurol Neurosurg; 2019 Nov; 186():105536. PubMed ID: 31574358
[TBL] [Abstract][Full Text] [Related]
7. Muscle Magnetic Resonance Imaging in Patients with Various Clinical Subtypes of
Lin HT; Liu X; Zhang W; Liu J; Zuo YH; Xiao JX; Zhu Y; Yuan Y; Wang ZX
Chin Med J (Engl); 2018 Jun; 131(12):1472-1479. PubMed ID: 29893365
[TBL] [Abstract][Full Text] [Related]
8. Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner pattern.
Deconinck N; Dion E; Ben Yaou R; Ferreiro A; Eymard B; Briñas L; Payan C; Voit T; Guicheney P; Richard P; Allamand V; Bonne G; Stojkovic T
Neuromuscul Disord; 2010 Aug; 20(8):517-23. PubMed ID: 20576434
[TBL] [Abstract][Full Text] [Related]
9. Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy.
Mercuri E; Counsell S; Allsop J; Jungbluth H; Kinali M; Bonne G; Schwartz K; Bydder G; Dubowitz V; Muntoni F
Neuropediatrics; 2002 Feb; 33(1):10-4. PubMed ID: 11930270
[TBL] [Abstract][Full Text] [Related]
10. 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
Eur Heart J; 2023 Dec; 44(48):5064-5073. PubMed ID: 37639473
[TBL] [Abstract][Full Text] [Related]
11. 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
Neuromuscul Disord; 2022 Sep; 32(9):718-727. PubMed ID: 35922275
[TBL] [Abstract][Full Text] [Related]
12. A novel mutation in human EMD gene and mitochondrial dysfunction in emerin knockdown cardiomyocytes.
Du Z; Zhu T; Lin M; Bao Y; Qiao J; Lv G; Xie Y; Li Q; Quan J; Xu C; Xie Y; Wang L; Yang W; Wang S; Wu L; Yin T; Xie Y
J Cell Mol Med; 2022 Oct; 26(19):5054-5066. PubMed ID: 36106556
[TBL] [Abstract][Full Text] [Related]
13. 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
BMC Pediatr; 2022 Oct; 22(1):601. PubMed ID: 36253810
[TBL] [Abstract][Full Text] [Related]
14. Three novel FHL1 variants cause a mild phenotype of Emery-Dreifuss muscular dystrophy.
Borch JDS; Krag T; Holm-Yildiz SD; Cetin H; Solheim TA; Fornander F; Straub V; Duno M; Vissing J
Hum Mutat; 2022 Sep; 43(9):1234-1238. PubMed ID: 35607917
[TBL] [Abstract][Full Text] [Related]
15. Emery-Dreifuss muscular dystrophy.
Zacharias AS; Wagener ME; Warren ST; Hopkins LC
Semin Neurol; 1999; 19(1):67-79. PubMed ID: 10711990
[TBL] [Abstract][Full Text] [Related]
16. Cardiac dysrhythmias,cardiomyopathy and muscular dystrophy in patients with Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy type 1B.
Hong JS; Ki CS; Kim JW; Suh YL; Kim JS; Baek KK; Kim BJ; Ahn KJ; Kim DK
J Korean Med Sci; 2005 Apr; 20(2):283-90. PubMed ID: 15832002
[TBL] [Abstract][Full Text] [Related]
17. Early onset, autosomal recessive muscular dystrophy with Emery-Dreifuss phenotype and normal emerin expression.
Taylor J; Sewry CA; Dubowitz V; Muntoni F
Neurology; 1998 Oct; 51(4):1116-20. PubMed ID: 9781539
[TBL] [Abstract][Full Text] [Related]
18. Emery-Dreifuss muscular dystrophy.
Heller SA; Shih R; Kalra R; Kang PB
Muscle Nerve; 2020 Apr; 61(4):436-448. PubMed ID: 31840275
[TBL] [Abstract][Full Text] [Related]
19. [Emery-Dreifuss muscular dystrophy: case report].
Saraiva F; Rodrigues D; Andrade H; Negrão L; Gonçalves L; Marinho A; Providência LA
Rev Port Cardiol; 2012 Mar; 31(3):241-5. PubMed ID: 22284682
[TBL] [Abstract][Full Text] [Related]
20. EDMD-Causing Emerin Mutant Myogenic Progenitors Exhibit Impaired Differentiation Using Similar Mechanisms.
Iyer A; Holaska JM
Cells; 2020 Jun; 9(6):. PubMed ID: 32549231
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]