References analysis of the Wikipedia article "Aritmogena kardiomiopatija" in the Serbian version

doi.org

„Report of the WHO/ISFC task force on the definition and classification of cardiomyopathies.”. Heart. 44 (6): 672—673. 1980-12-01. ISSN 1355-6037. doi:10.1136/hrt.44.6.672.

Beffagna G, Occhi G, Nava A, Vitiello L, Ditadi A, Basso C, Bauce B, Carraro G, Thiene G, Towbin JA, Danieli GA, Rampazzo A (фебруар 2005). „Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1”. Cardiovascular Research. 65 (2): 366—373. PMID 15639475. doi:10.1016/j.cardiores.2004.10.005 

Milting H, Lukas N, Klauke B, Körfer R, Perrot A, Osterziel KJ, Vogt J, Peters S, Thieleczek R, Varsányi M (август 2006). „Composite polymorphisms in the ryanodine receptor 2 gene associated with arrhythmogenic right ventricular cardiomyopathy”. Cardiovascular Research. 71 (3): 496—505. PMID 16769042. doi:10.1016/j.cardiores.2006.04.004 

Severini GM, Krajinovic M, Pinamonti B, Sinagra G, Fioretti P, Brunazzi MC, Falaschi A, Camerini F, Giacca M, Mestroni L (јануар 1996). „A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14”. Genomics. 31 (2): 193—200. PMID 8824801. doi:10.1006/geno.1996.0031. hdl:1765/58364.

Rampazzo A, Nava A, Miorin M, Fonderico P, Pope B, Tiso N, Livolsi B, Zimbello R, Thiene G, Danieli GA (октобар 1997). „ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm”. Genomics. 45 (2): 259—263. PMID 9344647. doi:10.1006/geno.1997.4927. hdl:11577/2461314.

Merner ND, Hodgkinson KA, Haywood AF, Connors S, French VM, Drenckhahn JD, Kupprion C, Ramadanova K, Thierfelder L, McKenna W, Gallagher B, Morris-Larkin L, Bassett AS, Parfrey PS, Young TL (април 2008). „Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene”. American Journal of Human Genetics. 82 (4): 809—821. PMC 2427209 

. PMID 18313022. doi:10.1016/j.ajhg.2008.01.010.

Christensen AH, Andersen CB, Tybjaerg-Hansen A, Haunso S, Svendsen JH (септембар 2011). „Mutation analysis and evaluation of the cardiac localization of TMEM43 in arrhythmogenic right ventricular cardiomyopathy”. Clinical Genetics. 80 (3): 256—264. PMID 21214875. S2CID 5617616. doi:10.1111/j.1399-0004.2011.01623.x.

Li D, Ahmad F, Gardner MJ, Weilbaecher D, Hill R, Karibe A, Gonzalez O, Tapscott T, Sharratt GP, Bachinski LL, Roberts R (јануар 2000). „The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14”. American Journal of Human Genetics. 66 (1): 148—156. PMC 1288320 

. PMID 10631146. doi:10.1086/302713.

Protonotarios A, Brodehl A, Asimaki A, Jager J, Quinn E, Stanasiuk C, Ratnavadivel S, Futema M, Akhtar MM, Gossios TD, Ashworth M, Savvatis K, Walhorn V, Anselmetti D, Elliott PM, Syrris P, Milting H, Lopes LR (јун 2021). „The Novel Desmin Variant p.Leu115Ile Is Associated With a Unique Form of Biventricular Arrhythmogenic Cardiomyopathy”. The Canadian Journal of Cardiology. 37 (6): 857—866. PMID 33290826. S2CID 228078648. doi:10.1016/j.cjca.2020.11.017.

Bermúdez-Jiménez FJ, Carriel V, Brodehl A, Alaminos M, Campos A, Schirmer I, Milting H, Abril BÁ, Álvarez M, López-Fernández S, García-Giustiniani D, Monserrat L, Tercedor L, Jiménez-Jáimez J (април 2018). „Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia”. Circulation. 137 (15): 1595—1610. PMID 29212896. doi:10.1161/CIRCULATIONAHA.117.028719 

. hdl:10481/89514 

Bauce B, Basso C, Rampazzo A, Beffagna G, Daliento L, Frigo G, Malacrida S, Settimo L, Danieli G, Thiene G, Nava A (август 2005). „Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations”. European Heart Journal. 26 (16): 1666—1675. PMID 15941723. doi:10.1093/eurheartj/ehi341 

Gerull B, Heuser A, Wichter T, Paul M, Basson CT, McDermott DA, Lerman BB, Markowitz SM, Ellinor PT, MacRae CA, Peters S, Grossmann KS, Drenckhahn J, Michely B, Sasse-Klaassen S, Birchmeier W, Dietz R, Breithardt G, Schulze-Bahr E, Thierfelder L (новембар 2004). „Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy”. Nature Genetics. 36 (11): 1162—1164. PMID 15489853. doi:10.1038/ng1461 

Pilichou K, Nava A, Basso C, Beffagna G, Bauce B, Lorenzon A, Frigo G, Vettori A, Valente M, Towbin J, Thiene G, Danieli GA, Rampazzo A (март 2006). „Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy”. Circulation. 113 (9): 1171—1179. PMID 16505173. doi:10.1161/CIRCULATIONAHA.105.583674 

Awad MM, Dalal D, Cho E, Amat-Alarcon N, James C, Tichnell C, Tucker A, Russell SD, Bluemke DA, Dietz HC, Calkins H, Judge DP (јул 2006). „DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy”. American Journal of Human Genetics. 79 (1): 136—142. PMC 1474134 

. PMID 16773573. doi:10.1086/504393.

Brodehl A, Meshkov A, Myasnikov R, Kiseleva A, Kulikova O, Klauke B, Sotnikova E, Stanasiuk C, Divashuk M, Pohl GM, Kudryavtseva M, Klingel K, Gerull B, Zharikova A, Gummert J, Koretskiy S, Schubert S, Mershina E, Gärtner A, Pilus P, Laser KT, Sinitsyn V, Boytsov S, Drapkina O, Milting H (април 2021). „Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset”. International Journal of Molecular Sciences. 22 (7): 3786. PMC 8038858 

. PMID 33917638. doi:10.3390/ijms22073786 

Brodehl A, Weiss J, Debus JD, Stanasiuk C, Klauke B, Deutsch MA, Fox H, Bax J, Ebbinghaus H, Gärtner A, Tiesmeier J, Laser T, Peterschröder A, Gerull B, Gummert J, Paluszkiewicz L, Milting H (април 2020). „A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy”. Journal of Molecular and Cellular Cardiology. 141: 17—29. PMID 32201174. doi:10.1016/j.yjmcc.2020.03.006 

Heuser A, Plovie ER, Ellinor PT, Grossmann KS, Shin JT, Wichter T, Basson CT, Lerman BB, Sasse-Klaassen S, Thierfelder L, MacRae CA, Gerull B (децембар 2006). „Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy”. American Journal of Human Genetics. 79 (6): 1081—1088. PMC 1698714 

. PMID 17186466. doi:10.1086/509044.

Syrris P, Ward D, Evans A, Asimaki A, Gandjbakhch E, Sen-Chowdhry S, McKenna WJ (новембар 2006). „Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2”. American Journal of Human Genetics. 79 (5): 978—984. PMC 1698574 

. PMID 17033975. doi:10.1086/509122.

Antoniades L, Tsatsopoulou A, Anastasakis A, Syrris P, Asimaki A, Panagiotakos D, Zambartas C, Stefanadis C, McKenna WJ, Protonotarios N (септембар 2006). „Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis”. European Heart Journal. 27 (18): 2208—2216. PMID 16893920. doi:10.1093/eurheartj/ehl184.

Asimaki A, Syrris P, Wichter T, Matthias P, Saffitz JE, McKenna WJ (новембар 2007). „A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy”. American Journal of Human Genetics. 81 (5): 964—973. PMC 2265660 

. PMID 17924338. doi:10.1086/521633.

Brodehl A, Rezazadeh S, Williams T, Munsie NM, Liedtke D, Oh T, Ferrier R, Shen Y, Jones SJ, Stiegler AL, Boggon TJ, Duff HJ, Friedman JM, Gibson WT, Childs SJ, Gerull B (јун 2019). „Mutations in ILK, encoding integrin-linked kinase, are associated with arrhythmogenic cardiomyopathy”. Translational Research. 208: 15—29. PMC 7412573 

. PMID 30802431. doi:10.1016/j.trsl.2019.02.004.

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 (2015). „Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy”. PLOS ONE. 10 (4): e0121723. Bibcode:2015PLoSO..1021723F. PMC 4383583 

. PMID 25837155. doi:10.1371/journal.pone.0121723 

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