233 related articles for article (PubMed ID: 36968203)
1. Characterization of cardiac involvement in children with
Cesar S; Campuzano O; Cruzalegui J; Fiol V; Moll I; Martínez-Barrios E; Zschaeck I; Natera-de Benito D; Ortez C; Carrera L; Expósito J; Berrueco R; Bautista-Rodriguez C; Dabaj I; Gómez García-de-la-Banda M; Quijano-Roy S; Brugada J; Nascimento A; Sarquella-Brugada G
Front Cell Dev Biol; 2023; 11():1142937. PubMed ID: 36968203
[No Abstract] [Full Text] [Related]
2.
Cesar S; Coll M; Fiol V; Fernandez-Falgueras A; Cruzalegui J; Iglesias A; Moll I; Perez-Serra A; Martínez-Barrios E; Ferrer-Costa C; Del Olmo B; Puigmulè M; Alcalde M; Lopez L; Pico F; Berrueco R; Brugada J; Zschaeck I; Natera-de Benito D; Carrera-García L; Exposito-Escudero J; Ortez C; Nascimento A; Brugada R; Sarquella-Brugada G; Campuzano O
Front Genet; 2023; 14():1135438. PubMed ID: 37035729
[No Abstract] [Full Text] [Related]
3. 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]
4. Clinical spectrum and genetic variations of
Fan Y; Tan D; Song D; Zhang X; Chang X; Wang Z; Zhang C; Chan SH; Wu Q; Wu L; Wang S; Yan H; Ge L; Yang H; Mao B; Bönnemann C; Liu J; Wang S; Yuan Y; Wu X; Zhang H; Xiong H
J Med Genet; 2021 May; 58(5):326-333. PubMed ID: 32571898
[TBL] [Abstract][Full Text] [Related]
5. Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations.
Scharner J; Brown CA; Bower M; Iannaccone ST; Khatri IA; Escolar D; Gordon E; Felice K; Crowe CA; Grosmann C; Meriggioli MN; Asamoah A; Gordon O; Gnocchi VF; Ellis JA; Mendell JR; Zammit PS
Hum Mutat; 2011 Feb; 32(2):152-67. PubMed ID: 20848652
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Cardiac manifestations of congenital LMNA-related muscular dystrophy in children: three case reports and recommendations for care.
Heller F; Dabaj I; Mah JK; Bergounioux J; Essid A; Bönnemann CG; Rutkowski A; Bonne G; Quijano-Roy S; Wahbi K
Cardiol Young; 2017 Aug; 27(6):1076-1082. PubMed ID: 27938454
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.
Bonne G; Mercuri E; Muchir A; Urtizberea A; Bécane HM; Recan D; Merlini L; Wehnert M; Boor R; Reuner U; Vorgerd M; Wicklein EM; Eymard B; Duboc D; Penisson-Besnier I; Cuisset JM; Ferrer X; Desguerre I; Lacombe D; Bushby K; Pollitt C; Toniolo D; Fardeau M; Schwartz K; Muntoni F
Ann Neurol; 2000 Aug; 48(2):170-80. PubMed ID: 10939567
[TBL] [Abstract][Full Text] [Related]
10. Congenital LMNA-Related Muscular Dystrophy in Paediatrics: Cardiac Management in Monozygotic Twins.
Martínez Olorón P; Alegría I; Cesar S; Del Olmo B; Martínez-Barrios E; Carrera-García L; Natera-de Benito D; Nascimento A; Campuzano O; Sarquella-Brugada G
Int J Mol Sci; 2024 May; 25(11):. PubMed ID: 38892025
[TBL] [Abstract][Full Text] [Related]
11. Cardiac features of Emery-Dreifuss muscular dystrophy caused by lamin A/C gene mutations.
Sanna T; Dello Russo A; Toniolo D; Vytopil M; Pelargonio G; De Martino G; Ricci E; Silvestri G; Giglio V; Messano L; Zachara E; Bellocci F
Eur Heart J; 2003 Dec; 24(24):2227-36. PubMed ID: 14659775
[TBL] [Abstract][Full Text] [Related]
12. Emery-Dreifuss muscular dystrophy, laminopathies, and other nuclear envelopathies.
Bonne G; Quijano-Roy S
Handb Clin Neurol; 2013; 113():1367-76. PubMed ID: 23622360
[TBL] [Abstract][Full Text] [Related]
13. Lamin A/C Cardiomyopathies: Current Understanding and Novel Treatment Strategies.
Wang X; Zabell A; Koh W; Tang WH
Curr Treat Options Cardiovasc Med; 2017 Mar; 19(3):21. PubMed ID: 28299614
[TBL] [Abstract][Full Text] [Related]
14. [Clinical, genealogical and molecular genetic study of Emery-Dreifuss muscular dystrophy].
Rudenskaia GE; Tverskaia SM; Chukhrova AL; Zakliaz'minskaia EV; Kuropatkina IuV; Dadali EL; Perminov VS; Poliakov AV
Zh Nevrol Psikhiatr Im S S Korsakova; 2006; 106(10):58-65. PubMed ID: 17117676
[TBL] [Abstract][Full Text] [Related]
15. Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth.
Owens DJ; Messéant J; Moog S; Viggars M; Ferry A; Mamchaoui K; Lacène E; Roméro N; Brull A; Bonne G; Butler-Browne G; Coirault C
Int J Mol Sci; 2020 Dec; 22(1):. PubMed ID: 33396724
[TBL] [Abstract][Full Text] [Related]
16. Laminopathies affecting skeletal and cardiac muscles: clinical and pathophysiological aspects.
Decostre V; Ben Yaou R; Bonne G
Acta Myol; 2005 Oct; 24(2):104-9. PubMed ID: 16550926
[TBL] [Abstract][Full Text] [Related]
17. Early-Onset LMNA-Associated Muscular Dystrophy with Later Involvement of Contracture.
Lee Y; Lee JH; Park HJ; Choi YC
J Clin Neurol; 2017 Oct; 13(4):405-410. PubMed ID: 29057633
[TBL] [Abstract][Full Text] [Related]
18. Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B).
Muchir A; Bonne G; van der Kooi AJ; van Meegen M; Baas F; Bolhuis PA; de Visser M; Schwartz K
Hum Mol Genet; 2000 May; 9(9):1453-9. PubMed ID: 10814726
[TBL] [Abstract][Full Text] [Related]
19. Identification of lamin A/C ( LMNA) gene mutations in Korean patients with autosomal dominant Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy 1B.
Ki CS; Hong JS; Jeong GY; Ahn KJ; Choi KM; Kim DK; Kim JW
J Hum Genet; 2002; 47(5):225-8. PubMed ID: 12032588
[TBL] [Abstract][Full Text] [Related]
20. Phenotype-Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy.
Tan D; Yang H; Yuan Y; Bonnemann C; Chang X; Wang S; Wu Y; Wu X; Xiong H
PLoS One; 2015; 10(6):e0129699. PubMed ID: 26098624
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
