about
Genetics of channelopathies associated with sudden cardiac deathDual fatty acid synthase and HER2 signaling blockade shows marked antitumor activity against breast cancer models resistant to anti-HER2 drugsUsefulness of Genetic Testing in Hypertrophic Cardiomyopathy: an Analysis Using Real-World Data.Syncope and polymorphic ventricular tachycardia in the setting of a febrile illness.Coexistence of epilepsy and Brugada syndrome in a family with SCN5A mutation.A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia.Short QT syndrome in pediatrics.Wolff-Parkinson-White Syndrome with Ventricular Hypertrophy in a Brazilian Family.Short QT and atrial fibrillation: A KCNQ1 mutation-specific disease. Late follow-up in three unrelated children.Stop-gain mutations in PKP2 are associated with a later age of onset of arrhythmogenic right ventricular cardiomyopathy.Sarcomeric gene mutations in sudden infant death syndrome (SIDS).A novel missense mutation, I890T, in the pore region of cardiac sodium channel causes Brugada syndromeIdentification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology.Genetic analysis, in silico prediction, and family segregation in long QT syndrome.Determining the pathogenicity of genetic variants associated with cardiac channelopathies.Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort.Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene.Large Genomic Imbalances in Brugada Syndrome.Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic InvestigationCardiovascular translational medicine (IV): The genetic basis of malignant arrhythmias and cardiomyopathies.Genetics of familial atrial fibrillation.Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic AdvancesGenetics and cardiac channelopathies.Genetics of sudden cardiac death in children and young athletes.Genetics of arrhythmogenic right ventricular cardiomyopathy.Negative autopsy and sudden cardiac death.Clinical interpretation of genetic variants in arrhythmogenic right ventricular cardiomyopathy.Brugada syndrome: clinical and genetic findings.Genetics of inherited arrhythmias in pediatrics.Sudden infant death syndrome caused by cardiac arrhythmias: only a matter of genes encoding ion channels?Medico-legal perspectives on sudden cardiac death in young athletes.Genetic basis of dilated cardiomyopathy.Familial dilated cardiomyopathy: A multidisciplinary entity, from basic screening to novel circulating biomarkers.Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death.Update about atrial fibrillation genetics.Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac DeathAdditional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy.A novel mutation in lamin a/c causing familial dilated cardiomyopathy associated with sudden cardiac death.Post-mortem genetic analysis in juvenile cases of sudden cardiac death.
P50
Q26777170-43318E6F-3F8D-4692-9B78-0E72FAB4FB81Q27303674-2BD4AC88-3FC0-4177-AB23-17C5D3635C26Q31158025-6E5AEE2B-9832-4A2D-9014-0A610046C45DQ33162554-7D4E4A67-6665-411F-B499-B3989B84F4BAQ33162565-109CB3F3-2578-4920-8AB5-BD759D1369D9Q33168032-E9D9F4A4-EA49-41B4-8668-50282B6C72B5Q33168420-32D3D884-88F0-4DAE-99C9-55EDB25E8AFCQ33168863-CC804E42-36C6-41B1-8321-5B9F71A6CC12Q33642565-B76495EF-FE33-46EF-87D5-323EA4EC7962Q33812341-9CA1C755-FDF0-43D5-AE8A-F809B04A8813Q34169191-616538DB-BFCD-4A4F-8288-7D23D245F98EQ34544772-2A5E2131-F205-49E4-BF3D-484467E54B05Q34672980-1E899264-1436-4561-9E7D-4A759EB13010Q34705080-B097044F-8118-4ED6-AEA1-ED5FCE459DDEQ34997072-B24A688D-3EFB-4F6D-A1B5-9D27508E0F42Q35691043-1BF784F4-B14B-4E77-962E-6D2091EC0F46Q35730438-2FC5D369-925F-4EB5-882F-7AA054C9779EQ36071394-E56679AF-7FCB-400C-B382-2A350FEF8CCBQ36148081-E6E7FA0B-CA44-4DAD-99C8-330E90E7AD7AQ36216129-0BF6C128-0480-4666-BC91-54751871A6EFQ37463403-31B7C2BB-8482-438A-BA8B-CB5AFDFC7B52Q37576796-9CCC59AB-1FB9-4CAA-B2A0-4D92354D78C5Q37728178-AC9EEABA-8623-45AA-81D1-61907E2BA083Q37729709-E69A356C-F120-4674-AB7A-614F07DBA654Q38028676-E10C6875-ECF7-47A3-A582-10E21F91D2FFQ38087285-7C722A3B-DF32-434D-8FA5-FE96677004B1Q38188482-A0F7928B-F070-475A-85EF-4FAB8D39A4D9Q38268280-4BBBD36D-994A-4DC8-9BAC-8840A7612A8CQ38438088-2588D190-EAB0-4E6F-87E2-1FD9BDBFEA08Q38587130-E2A0B682-9BF1-49CC-B78A-98867C478F39Q38731316-4E2E1801-49BA-418E-85EE-F284BD799A22Q38961073-AEC51114-6FA5-4534-ADC3-2ED08E2FB2AFQ38979662-3BE22FB1-9A4B-4325-BB6A-B24D96A61B10Q39020986-A6E1958D-A5B8-401A-88A1-99FF78B7DEFFQ39118099-053855BA-2EDD-4FF5-87D9-7A97641066CCQ39124450-E62B0BEF-716A-4CE1-9AEB-AB4E793A3276Q40375836-5DD409E2-EDED-48B4-A144-82B6E54BABADQ41237982-35576E21-0449-476A-9F1B-730873C4599EQ41700650-7BD09E71-E9B4-4E7B-89AA-687E5099621FQ41758739-3B7858EA-296E-4744-A61F-3994D435831C
P50
description
hulumtues
@sq
researcher
@en
ricercatore
@it
wetenschapper
@nl
հետազոտող
@hy
name
Oscar Campuzano
@ast
Oscar Campuzano
@en
Oscar Campuzano
@es
Oscar Campuzano
@nl
Oscar Campuzano
@sl
type
label
Oscar Campuzano
@ast
Oscar Campuzano
@en
Oscar Campuzano
@es
Oscar Campuzano
@nl
Oscar Campuzano
@sl
prefLabel
Oscar Campuzano
@ast
Oscar Campuzano
@en
Oscar Campuzano
@es
Oscar Campuzano
@nl
Oscar Campuzano
@sl
P108
P214
P1053
J-1968-2014
P106
P1153
26643853000
P21
P214
P31
P3829
P496
0000-0001-5298-5276
P734
P735
P7859
viaf-305871275