125 related articles for article (PubMed ID: 38892025)
1. 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]
2. Floppy infant syndrome as a first manifestation of LMNA-related congenital muscular dystrophy.
Jędrzejowska M; Potulska-Chromik A; Gos M; Gambin T; Dębek E; Rosiak E; Stępień A; Szymańczak R; Wojtaś B; Gielniewski B; Ciara E; Sobczyńska A; Chrzanowska K; Kostera-Pruszczyk A; Madej-Pilarczyk A
Eur J Paediatr Neurol; 2021 May; 32():115-121. PubMed ID: 33940562
[TBL] [Abstract][Full Text] [Related]
3. The most severe form of LMNA-associated congenital muscular dystrophy.
Murofushi Y; Hayakawa I; Abe Y; Nakao H; Ono H; Kubota M
Brain Dev; 2022 Oct; 44(9):650-654. PubMed ID: 35729056
[TBL] [Abstract][Full Text] [Related]
4.
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]
5. 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]
6. Importance of early diagnosis in LMNA-related muscular dystrophy for cardiac surveillance.
Choi SA; Cho A; Kim SY; Kim WJ; Shim YK; Lee JS; Jang SS; Lim BC; Kim H; Hwang H; Choi JE; Kim KJ; Kim MJ; Seong MW; Chae JH
Muscle Nerve; 2019 Dec; 60(6):668-672. PubMed ID: 31498906
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophy.
Menezes MP; Waddell LB; Evesson FJ; Cooper S; Webster R; Jones K; Mowat D; Kiernan MC; Johnston HM; Corbett A; Harbord M; North KN; Clarke NF
Neurology; 2012 Apr; 78(16):1258-63. PubMed ID: 22491857
[TBL] [Abstract][Full Text] [Related]
9. De novo LMNA mutations cause a new form of congenital muscular dystrophy.
Quijano-Roy S; Mbieleu B; Bönnemann CG; Jeannet PY; Colomer J; Clarke NF; Cuisset JM; Roper H; De Meirleir L; D'Amico A; Ben Yaou R; Nascimento A; Barois A; Demay L; Bertini E; Ferreiro A; Sewry CA; Romero NB; Ryan M; Muntoni F; Guicheney P; Richard P; Bonne G; Estournet B
Ann Neurol; 2008 Aug; 64(2):177-86. PubMed ID: 18551513
[TBL] [Abstract][Full Text] [Related]
10. Germinal mosaicism for LMNA mimics autosomal recessive congenital muscular dystrophy.
Makri S; Clarke NF; Richard P; Maugenre S; Demay L; Bonne G; Guicheney P
Neuromuscul Disord; 2009 Jan; 19(1):26-8. PubMed ID: 19084400
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy.
Forleo C; Carmosino M; Resta N; Rampazzo A; Valecce R; Sorrentino S; Iacoviello M; Pisani F; Procino G; Gerbino A; Scardapane A; Simone C; Calore M; Torretta S; Svelto M; Favale S
PLoS One; 2015; 10(4):e0121723. PubMed ID: 25837155
[TBL] [Abstract][Full Text] [Related]
13. Congenital muscular dystrophy with dropped head linked to the LMNA gene in a Brazilian cohort.
Pasqualin LM; Reed UC; Costa TV; Quedas E; Albuquerque MA; Resende MB; Rutkowski A; Chadi G; Zanoteli E
Pediatr Neurol; 2014 Apr; 50(4):400-6. PubMed ID: 24508248
[TBL] [Abstract][Full Text] [Related]
14. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics.
van Tintelen JP; Hofstra RM; Katerberg H; Rossenbacker T; Wiesfeld AC; du Marchie Sarvaas GJ; Wilde AA; van Langen IM; Nannenberg EA; van der Kooi AJ; Kraak M; van Gelder IC; van Veldhuisen DJ; Vos Y; van den Berg MP;
Am Heart J; 2007 Dec; 154(6):1130-9. PubMed ID: 18035086
[TBL] [Abstract][Full Text] [Related]
15. Novel LMNA mutation presenting as severe congenital muscular dystrophy.
Prigogine C; Richard P; Van den Bergh P; Groswasser J; Deconinck N
Pediatr Neurol; 2010 Oct; 43(4):283-6. PubMed ID: 20837309
[TBL] [Abstract][Full Text] [Related]
16. LMNA-associated myopathies: the Italian experience in a large cohort of patients.
Maggi L; D'Amico A; Pini A; Sivo S; Pane M; Ricci G; Vercelli L; D'Ambrosio P; Travaglini L; Sala S; Brenna G; Kapetis D; Scarlato M; Pegoraro E; Ferrari M; Toscano A; Benedetti S; Bernasconi P; Colleoni L; Lattanzi G; Bertini E; Mercuri E; Siciliano G; Rodolico C; Mongini T; Politano L; Previtali SC; Carboni N; Mantegazza R; Morandi L
Neurology; 2014 Oct; 83(18):1634-44. PubMed ID: 25274841
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. LMNA-Related Muscular Dystrophy with Clinical Intrafamilial Variability.
Cotta A; Paim JF; Carvalho E; Valicek J; da Cunha Junior AL; Navarro MM; Vargas AP; Lima MI; de Almeida CF; Takata RI; Vainzof M
J Mol Neurosci; 2019 Dec; 69(4):623-627. PubMed ID: 31410651
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Cardiac effects of the c.1583 C→G LMNA mutation in two families with Emery-Dreifuss muscular dystrophy.
Zhang L; Shen H; Zhao Z; Bing Q; Hu J
Mol Med Rep; 2015 Oct; 12(4):5065-71. PubMed ID: 26165385
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
