175 related articles for article (PubMed ID: 37035729)
21. Up-regulation of Toll-like receptors 7 and 9 and its potential implications in the pathogenic mechanisms of LMNA-related myopathies.
Cappelletti C; Salerno F; Canioni E; Mora M; Mantegazza R; Bernasconi P; Maggi L
Nucleus; 2018; 9(1):398-409. PubMed ID: 29895224
[TBL] [Abstract][Full Text] [Related]
22. Emery-Dreifuss dystrophy: a 4-year follow-up on a laminopathy of special interest.
Hausmanowa-Petrusewicz I; Madej-Pilarczyk A; Marchel M; Opolski G
Neurol Neurochir Pol; 2009; 43(5):415-20. PubMed ID: 20054742
[TBL] [Abstract][Full Text] [Related]
23. Genetic Patterns of Selected Muscular Dystrophies in the Muscular Dystrophy Surveillance, Tracking, and Research Network.
Kang PB; Jorand-Fletcher M; Zhang W; McDermott SW; Berry R; Chambers C; Wong KN; Mohamed Y; Thomas S; Venkatesh YS; Westfield C; Whitehead N; Johnson NE;
Neurol Genet; 2023 Dec; 9(6):e200113. PubMed ID: 38045992
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. International retrospective natural history study of
Ben Yaou R; Yun P; Dabaj I; Norato G; Donkervoort S; Xiong H; Nascimento A; Maggi L; Sarkozy A; Monges S; Bertoli M; Komaki H; Mayer M; Mercuri E; Zanoteli E; Castiglioni C; Marini-Bettolo C; D'Amico A; Deconinck N; Desguerre I; Erazo-Torricelli R; Gurgel-Giannetti J; Ishiyama A; Kleinsteuber KS; Lagrue E; Laugel V; Mercier S; Messina S; Politano L; Ryan MM; Sabouraud P; Schara U; Siciliano G; Vercelli L; Voit T; Yoon G; Alvarez R; Muntoni F; Pierson TM; Gómez-Andrés D; Reghan Foley A; Quijano-Roy S; Bönnemann CG; Bonne G
Brain Commun; 2021 Jul; 3(3):fcab075. PubMed ID: 34240052
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B.
Park YE; Hayashi YK; Goto K; Komaki H; Hayashi Y; Inuzuka T; Noguchi S; Nonaka I; Nishino I
Neuromuscul Disord; 2009 Jan; 19(1):29-36. PubMed ID: 19070492
[TBL] [Abstract][Full Text] [Related]
29. The Influence of a Genetic Variant in
Mohar NP; Cox EM; Adelizzi E; Moore SA; Mathews KD; Darbro BW; Wallrath LL
Int J Mol Sci; 2024 Apr; 25(9):. PubMed ID: 38732148
[TBL] [Abstract][Full Text] [Related]
30. Skeletal Muscle Laminopathies: A Review of Clinical and Molecular Features.
Maggi L; Carboni N; Bernasconi P
Cells; 2016 Aug; 5(3):. PubMed ID: 27529282
[TBL] [Abstract][Full Text] [Related]
31.
Perepelina K; Zaytseva A; Khudiakov A; Neganova I; Vasichkina E; Malashicheva A; Kostareva A
Front Cardiovasc Med; 2022; 9():932956. PubMed ID: 35935653
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. 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]
34. 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]
35. 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]
36. The nuclear muscular dystrophies.
Wehnert MS; Bonne G
Semin Pediatr Neurol; 2002 Jun; 9(2):100-7. PubMed ID: 12138994
[TBL] [Abstract][Full Text] [Related]
37. Predictors of mortality and cardiovascular outcomes in Emery-Dreifuss muscular dystrophy in a long-term follow-up.
Marchel M; Madej-Pilarczyk A; Steckiewicz R; Stolarz P; Peller M; Tymińska A; Ostrowska E; Ozierański K; Balsam P; Grabowski M; Opolski G
Kardiol Pol; 2021; 79(12):1335-1342. PubMed ID: 34783354
[TBL] [Abstract][Full Text] [Related]
38. Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophy.
Walter MC; Witt TN; Weigel BS; Reilich P; Richard P; Pongratz D; Bonne G; Wehnert MS; Lochmüller H
Neuromuscul Disord; 2005 Jan; 15(1):40-4. PubMed ID: 15639119
[TBL] [Abstract][Full Text] [Related]
39. Effect of genetic background on the cardiac phenotype in a mouse model of Emery-Dreifuss muscular dystrophy.
Vignier N; Mougenot N; Bonne G; Muchir A
Biochem Biophys Rep; 2019 Sep; 19():100664. PubMed ID: 31341969
[TBL] [Abstract][Full Text] [Related]
40. Genetics of laminopathies.
Ben Yaou R; Muchir A; Arimura T; Massart C; Demay L; Richard P; Bonne G
Novartis Found Symp; 2005; 264():81-90; discussion 90-97, 227-30. PubMed ID: 15773749
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
