المؤلفون: Mayosi, B, Fish, M, Shaboodien, G, Mastantuono, E, Kraus, S, Wieland, T, Kotta, M, Chin, A, Laing, N, Ntusi, N, Chong, M, Horsfall, C, Pimstone, S, Gentilini, D, Parati, G, Strom, T, Meitinger, T, Pare, G, Schwartz, P, CROTTI, LIA

المساهمون: Mayosi, B, Fish, M, Shaboodien, G, Mastantuono, E, Kraus, S, Wieland, T, Kotta, M, Chin, A, Laing, N, Ntusi, N, Chong, M, Horsfall, C, Pimstone, S, Gentilini, D, Parati, G, Strom, T, Meitinger, T, Pare, G, Schwartz, P, Crotti, L

مصطلحات موضوعية: arrhythmogenic right ventricular dysplasia, cadherin, cardiomyopathie, genetic, mutation, Adolescent, Adult, Amino Acid Substitution, Antigens, CD, Female, Human, Male, Exome, Missense, Cardiology and Cardiovascular Medicine, Genetics (clinical), MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, MED/03 - GENETICA MEDICA

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/28280076; info:eu-repo/semantics/altIdentifier/wos/WOS:000397822400003; volume:10; issue:2; journal:CIRCULATION, CARDIOVASCULAR GENETICS; http://hdl.handle.net/10281/171722Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85018214956; http://circgenetics.ahajournals.orgTest/

الإتاحة: https://doi.org/10.1161/CIRCGENETICS.116.001605Test
http://hdl.handle.net/10281/171722Test
http://circgenetics.ahajournals.orgTest/

المؤلفون: Crotti L., Johnson CN., Graf E., De Ferrari G., Cuneo BF., Ovadia M., Papagiannis J., Feldkamp MD., Rathi SG., Kunic JD., Pedrazzini M., Wieland T., Lichtner P., Beckmann BM., Clark T., Shaffer C., Benson DW., Kääb S., Meitinger T., Strom TM., Chazin WJ., Schwartz P, George AL Jr.

المساهمون: Crotti, L, Johnson, C, Graf, E, De Ferrari, G, Cuneo, B, Ovadia, M, Papagiannis, J, Feldkamp, M, Rathi, S, Kunic, J, Pedrazzini, M, Wieland, T, Lichtner, P, Beckmann, B, Clark, T, Shaffer, C, Benson, D, Kääb, S, Meitinger, T, Strom, T, Chazin, W, Schwartz, P, George AL, J

مصطلحات موضوعية: arrhythmia, calcium signaling, death, sudden, cardiac, exome, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, BIO/18 - GENETICA

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23388215; info:eu-repo/semantics/altIdentifier/wos/WOS:000315804800015; volume:127; issue:9; firstpage:1009; lastpage:1017; numberofpages:9; journal:CIRCULATION; http://hdl.handle.net/10281/189535Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84874664698; https://www.ncbi.nlm.nih.gov/pubmed/?term=23388215Test

الإتاحة: https://doi.org/10.1161/CIRCULATIONAHA.112.001216Test
http://hdl.handle.net/10281/189535Test
https://www.ncbi.nlm.nih.gov/pubmed/?term=23388215Test

المؤلفون: Nakita Laing, Simon N. Pimstone, Thomas Meitinger, Ashley Chin, Ntobeko B A Ntusi, Tim Matthias Strom, Thomas Wieland, Maryam Fish, Maria Christina Kotta, Gasnat Shaboodien, Sarah Kraus, Peter J. Schwartz, Bongani M. Mayosi, Davide Gentilini, Gianfranco Parati, Guillaume Paré, Elisa Mastantuono, Lia Crotti, Christopher Horsfall, Michael Chong

المساهمون: Mayosi, B, Fish, M, Shaboodien, G, Mastantuono, E, Kraus, S, Wieland, T, Kotta, M, Chin, A, Laing, N, Ntusi, N, Chong, M, Horsfall, C, Pimstone, S, Gentilini, D, Parati, G, Strom, T, Meitinger, T, Pare, G, Schwartz, P, Crotti, L

المصدر: Circ. Cardiovasc. Genet. 10:e001605 (2017)

مصطلحات موضوعية: 0301 basic medicine, arrhythmogenic right ventricular dysplasia, Adult, Male, Pathology, medicine.medical_specialty, Adolescent, MED/03 - GENETICA MEDICA, Mutation, Missense, 030204 cardiovascular system & hematology, Biology, medicine.disease_cause, CDH2, Right ventricular cardiomyopathy, 03 medical and health sciences, 0302 clinical medicine, Genetic, Antigens, CD, Genetics, medicine, Exome, Exome sequencing, Genetics (clinical), Mutation, cardiomyopathie, Arrhythmogenic Right Ventricular Dysplasia, Cadherins, Cardiomyopathies, Genetic heterogeneity, Cadherin, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, medicine.disease, Molecular biology, Arrhythmogenic right ventricular dysplasia, 030104 developmental biology, cadherin, Amino Acid Substitution, Female, mutation, Cardiology and Cardiovascular Medicine, Human

وصف الملف: STAMPA; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9e0ec143230e15cedff076d95c4033eTest
http://hdl.handle.net/10281/171722Test

المؤلفون: Peter J. Schwartz, Travis Clark, Christopher N. Johnson, Tim M. Strom, Christian M. Shaffer, Thomas Meitinger, Subodh Rathi, D. Woodrow Benson, Gaetano M. De Ferrari, John Papagiannis, Elisabeth Graf, Michael D. Feldkamp, Britt M. Beckmann, Thomas Wieland, Marc Ovadia, Alfred L. George, Jennifer D. Kunic, Lia Crotti, Peter Lichtner, Matteo Pedrazzini, Walter J. Chazin, Stefan Kääb, Bettina F. Cuneo

المساهمون: Crotti, L, Johnson, C, Graf, E, De Ferrari, G, Cuneo, B, Ovadia, M, Papagiannis, J, Feldkamp, M, Rathi, S, Kunic, J, Pedrazzini, M, Wieland, T, Lichtner, P, Beckmann, B, Clark, T, Shaffer, C, Benson, D, Kääb, S, Meitinger, T, Strom, T, Chazin, W, Schwartz, P, George AL, J

المصدر: Circulation 127, 1009-1017 (2013)
Circulation
Circulation; Vol 127

مصطلحات موضوعية: Proband, Male, Candidate gene, 030204 cardiovascular system & hematology, Bioinformatics, medicine.disease_cause, Cohort Studies, 0302 clinical medicine, Arrhythmia, Calcium Signaling, Death, Sudden, Cardiac, Exome, Recurrence, Medicine, Exome sequencing, Genetics, 0303 health sciences, Mutation, 3. Good health, Pedigree, Long QT Syndrome, Child, Preschool, Cohort, Female, Cardiology and Cardiovascular Medicine, arrhythmia, calcium signaling, death, sudden, cardiac, exome, Long QT syndrome, Molecular Sequence Data, BIO/18 - GENETICA, 03 medical and health sciences, Calmodulin, Physiology (medical), Humans, Amino Acid Sequence, Gene, Genetic Association Studies, 030304 developmental biology, business.industry, Infant, Newborn, Infant, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, medicine.disease, Heart Arrest, business, Follow-Up Studies

وصف الملف: STAMPA; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20a020965a06a38ff46aa85a4729503fTest
http://hdl.handle.net/10281/189535Test