These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
47 related articles for article (PubMed ID: 22006699)
1. Dilated cardiomyopathy with conduction defects in a patient with partial merosin deficiency due to mutations in the laminin-α2-chain gene: a chance association or a novel phenotype? Carboni N; Marrosu G; Porcu M; Mateddu A; Solla E; Cocco E; Maioli MA; Oppo V; Piras R; Marrosu MG Muscle Nerve; 2011 Nov; 44(5):826-8. PubMed ID: 22006699 [TBL] [Abstract][Full Text] [Related]
2. Many roads lead to a broken heart: the genetics of dilated cardiomyopathy. Schönberger J; Seidman CE Am J Hum Genet; 2001 Aug; 69(2):249-60. PubMed ID: 11443548 [No Abstract] [Full Text] [Related]
3. Dilated Cardiomyopathy: New Distinct Phenotypes or Temporal Phases of Disease? Hershberger RE; Zareba KM J Am Coll Cardiol; 2022 Jun; 79(22):2233-2235. PubMed ID: 35654494 [No Abstract] [Full Text] [Related]
4. Atypical phenotype in two patients with LAMA2 mutations. Marques J; Duarte ST; Costa S; Jacinto S; Oliveira J; Oliveira ME; Santos R; Bronze-da-Rocha E; Silvestre AR; Calado E; Evangelista T Neuromuscul Disord; 2014 May; 24(5):419-24. PubMed ID: 24534542 [TBL] [Abstract][Full Text] [Related]
5. Genetic blueprint of congenital muscular dystrophies with brain malformations in Egypt: A report of 11 families. Safwat S; Flannery KP; El Beheiry AA; Mokhtar MM; Abdalla E; Manzini MC Neurogenetics; 2024 Apr; 25(2):93-102. PubMed ID: 38296890 [TBL] [Abstract][Full Text] [Related]
6. Nerve pathology is prevented by linker proteins in mouse models for Reinhard JR; Porrello E; Lin S; Pelczar P; Previtali SC; Rüegg MA PNAS Nexus; 2023 Apr; 2(4):pgad083. PubMed ID: 37038437 [No Abstract] [Full Text] [Related]
7. The role of basement membranes in cardiac biology and disease. Boland E; Quondamatteo F; Van Agtmael T Biosci Rep; 2021 Aug; 41(8):. PubMed ID: 34382650 [TBL] [Abstract][Full Text] [Related]
8. NMRK2 Gene Is Upregulated in Dilated Cardiomyopathy and Required for Cardiac Function and NAD Levels during Aging. Tannous C; Deloux R; Karoui A; Mougenot N; Burkin D; Blanc J; Coletti D; Lavery G; Li Z; Mericskay M Int J Mol Sci; 2021 Mar; 22(7):. PubMed ID: 33805532 [TBL] [Abstract][Full Text] [Related]
9. Patients with coronary heart disease, dilated cardiomyopathy and idiopathic ventricular tachycardia share overlapping patterns of pathogenic variation in cardiac risk genes. Guelly C; Abilova Z; Nuralinov O; Panzitt K; Akhmetova A; Rakhimova S; Kozhamkulov U; Kairov U; Molkenov A; Seisenova A; Trajanoski S; Abildinova Rashbayeva G; Kaussova G; Windpassinger C; Lee JH; Zhumadilov Z; Bekbossynova M; Akilzhanova A PeerJ; 2021; 9():e10711. PubMed ID: 33552729 [TBL] [Abstract][Full Text] [Related]
10. LAMA2-related muscular dystrophy: Natural history of a large pediatric cohort. Zambon AA; Ridout D; Main M; Mein R; Phadke R; Muntoni F; Sarkozy A Ann Clin Transl Neurol; 2020 Oct; 7(10):1870-1882. PubMed ID: 32910545 [TBL] [Abstract][Full Text] [Related]
11. Limb girdle muscular dystrophy due to Magri F; Brusa R; Bello L; Peverelli L; Del Bo R; Govoni A; Cinnante C; Colombo I; Fortunato F; Tironi R; Corti S; Grimoldi N; Sciacco M; Bresolin N; Pegoraro E; Moggio M; Comi GP Acta Myol; 2020 Jun; 39(2):67-82. PubMed ID: 32904964 [TBL] [