PMC Articles for MedGen (Select 811441) - PMC

Select item 90778681.

Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality

Jia Chen, Yuting Ma, Hong Li, Zhuo Lin, Zhe Yang, Qin Zhang, Feng Wang, Yanping Lin, Zebing Ye, Yubi Lin

Orphanet J Rare Dis. 2022; 17: 183. Published online 2022 May 7. doi: 10.1186/s13023-022-02348-z

PMCID:: PMC9077868

Abstract Article PDF–2.1M

Select item 72166482.

A case report of one vasovagal syncope patient with third-degree atrioventricular block caused by SCN5A gene mutation and literature review

Lu Gao, Xia Yu, Hongxia Li, Yue Yuan

BMC Pediatr. 2020; 20: 211. Published online 2020 May 12. doi: 10.1186/s12887-020-02123-8

PMCID:: PMC7216648

Abstract Article PDF–706K

Select item 34180503.

The Ca²⁺-stimulated adenylyl cyclase AC1 generates efficient biological pacing as single gene therapy and in combination with HCN2

Gerard J. J. Boink, Bruce D. Nearing, Iryna N. Shlapakova, Lian Duan, Yelena Kryukova, Eugene Bobkov, Hanno L. Tan, Ira S. Cohen, Peter Danilo, Jr., Richard B. Robinson, Richard L. Verrier, Michael R. Rosen

Circulation. Author manuscript; available in PMC 2013 Jul 31.

Published in final edited form as: Circulation. 2012 Jul 31; 126(5): 528–536. Published online 2012 Jun 29. doi: 10.1161/CIRCULATIONAHA.111.083584

PMCID:: PMC3418050

Abstract Article PDF–1.8M

Select item 26958484.

Severe infantile-onset cardiomyopathy associated with a homozygous deletion in desmin

Gerard Piñol-Ripoll, Alexey Shatunov, Ana Cabello, Pilar Larrodé, Iris de la Puerta, Juana Pelegrín, Feliciano J Ramos, Montse Olivé, Lev G Goldfarb

Neuromuscul Disord. Author manuscript; available in PMC 2010 Jun 1.

Published in final edited form as: Neuromuscul Disord. 2009 Jun; 19(6): 418–422. Published online 2009 May 9. doi: 10.1016/j.nmd.2009.04.004

PMCID:: PMC2695848

Abstract Article PDF–506K

Select item 4815695.

Disturbances of cardiac rhythm and conduction in familial amyloidosis with polyneuropathy.

P Eriksson, K Karp, P Bjerle, B O Olofsson

Br Heart J. 1984 Jun; 51(6): 658–662. doi: 10.1136/hrt.51.6.658

PMCID:: PMC481569

Summary Page Browse PDF–704K

Select item 4814816.

Complete heart block in HLA B27 associated disease. Electrophysiological and clinical characteristics.

L Bergfeldt, H Vallin, O Edhag

Br Heart J. 1984 Feb; 51(2): 184–188. doi: 10.1136/hrt.51.2.184

PMCID:: PMC481481

Summary Page Browse PDF–778K

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