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المؤلفون: Marshall Heradien, Felix Mahfoud, Christeman Greyling, Lucas Lauder, Pieter van der Bijl, Douglas A. Hettrick, Warren Stilwaney, Siyolise Sibeko, Rene Jansen van Rensburg, Dale Peterson, Bonke Khwinani, Althea Goosen, Jan A. Saaiman, Christian Ukena, Michael Böhm, Paul A. Brink
المصدر: Heart rhythm.
مصطلحات موضوعية: Physiology (medical), Cardiology and Cardiovascular Medicine
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2
المؤلفون: Giulia Girardengo, Alfred L. George, Lia Crotti, Alberto Porta, Althea Goosen, Paul A. Brink, Peter J. Schwartz, Vlasta Bari
المساهمون: Porta, A, Girardengo, G, Bari, V, George, A, Brink, P, Goosen, A, Crotti, L, Schwartz, P
المصدر: J. Am. Coll. Cardiol. 65, 367-374 (2015)
مصطلحات موضوعية: Adult, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Sympathetic Nervous System, Romano-Ward Syndrome, Long QT syndrome, Adrenergic beta-Antagonists, QT interval, Article, Electrocardiography, Internal medicine, Heart rate, medicine, Humans, Heart rate variability, cardiovascular diseases, beta-blocker therapy, cardiovascular control, QT variability, medicine.diagnostic_test, business.industry, autonomic nervous system, Case-control study, heart rate variability, Adrenergic beta-Antagonist, Vagus Nerve, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, medicine.disease, Circadian Rhythm, Romano–Ward syndrome, Autonomic nervous system, Case-Control Studies, KCNQ1 Potassium Channel, Cardiology, Case-Control Studie, business, Cardiology and Cardiovascular Medicine, Qt Variability, Autonomic Nervous System, Beta-blocker Therapy, Cardiovascular Control, Heart Rate Variability, Human
وصف الملف: STAMPA; application/pdf
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المؤلفون: Durrheim Ga, Valerie A. Corfield, Birgitte Støvring, Paula L. Hedley, Cathrine Jespersgaard, Paul A. Brink, Michael Christiansen, Tam Thanh Pham, Althea Goosen, Firzana Hendricks
المصدر: Cardiovascular Journal Of Africa. 24:231-237
مصطلحات موضوعية: Genetics, congenital, hereditary, and neonatal diseases and abnormalities, Genetic diversity, medicine.diagnostic_test, biology, business.industry, Long QT syndrome, Genetic disorder, KCNE2, General Medicine, medicine.disease, Sudden death, Mutation (genetic algorithm), medicine, biology.protein, Cardiology and Cardiovascular Medicine, business, Genetic testing, Founder effect
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المؤلفون: Maria Teresa La Rovere, Lia Crotti, Marshall Heradien, Paul A. Brink, Federica Dagradi, Carla Spazzolini, Peter J. Schwartz, Alessandro Vicentini, Erika Taravelli, Barbara Petracci, Alessandra P. Porretta, Alfred L. George, Althea Goosen, Matteo Pedrazzini, Emilio Vanoli
المصدر: Journal of the American College of Cardiology. 60:2515-2524
مصطلحات موضوعية: medicine.medical_specialty, medicine.diagnostic_test, business.industry, Long QT syndrome, medicine.disease, Sudden death, Vagus nerve, Autonomic nervous system, Internal medicine, Heart rate, Physical therapy, medicine, Cardiology, Reflex, Cardiology and Cardiovascular Medicine, business, Risk assessment, Electrocardiography
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المؤلفون: Carla Spazzolini, Thomas Meitinger, Althea Goosen, Marshall Heradien, Gianfranco Parati, Peter J. Schwartz, Caterina Morassutto, Paul A. Brink, Elisa Mastantuono, Heikki Swan, Annukka M. Lahtinen, Peter Lichtner, Kimmo Kontula, Mari Cristina A Monti, Lia Crotti
المساهمون: Crotti, L, Lahtinen, A, Spazzolini, C, Mastantuono, E, Monti, M, Morassutto, C, Parati, G, Heradien, M, Goosen, A, Lichtner, P, Meitinger, T, Brink, P, Kontula, K, Swan, H, Schwartz, P
مصطلحات موضوعية: 0301 basic medicine, Untranslated region, Long QT syndrome, Population, Single-nucleotide polymorphism, BIO/18 - GENETICA, 030204 cardiovascular system & hematology, Biology, medicine.disease_cause, 03 medical and health sciences, 0302 clinical medicine, Genetic, Genetics, medicine, long QT syndrome, education, Genetics (clinical), Mutation, education.field_of_study, genetic modifier, KCNQ1, Three prime untranslated region, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, medicine.disease, 030104 developmental biology, Haploinsufficiency, Cardiology and Cardiovascular Medicine
وصف الملف: STAMPA
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1adc902dc4611b98cc694af022a8b575
http://hdl.handle.net/10281/148488 -
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المؤلفون: Lia Crotti, Althea Goosen, Heikki Swan, Paul A. Brink, Marshall Heradien, Kimmo Kontula, Elisa Mastantuono, Peter J. Schwartz, Caterina Morassutto, Gianfranco Parati, Annukka M. Lahtinen, Thomas Meitinger, Maria Cristina Monti, Peter Lichtner, Carla Spazzolini
المساهمون: Crotti, L, Lahtinen, A, Spazzolini, C, Mastantuono, E, Monti, M, Morassutto, C, Parati, G, Heradien, M, Goosen, A, Lichtner, P, Meitinger, T, Brink, P, Kontula, K, Swan, H, Schwartz, P
مصطلحات موضوعية: Male, 0301 basic medicine, Heredity, Romano-Ward Syndrome, Long QT syndrome, Population, Single-nucleotide polymorphism, BIO/18 - GENETICA, 030204 cardiovascular system & hematology, Biology, Bioinformatics, arrhythmia, Polymorphism, Single Nucleotide, Severity of Illness Index, QT interval, Linkage Disequilibrium, untranslated region, South Africa, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, Risk Factors, medicine, Genetics, Humans, SNP, Genetic Predisposition to Disease, education, 3' Untranslated Regions, Allele frequency, Genetic Association Studies, Genetics (clinical), MED/01 - STATISTICA MEDICA, education.field_of_study, Haplotype, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, medicine.disease, Pedigree, long-QT syndrome, Europe, Phenotype, 030104 developmental biology, KCNQ1 potassium channel, Haplotypes, genes, modifier, Mutation (genetic algorithm), Female, Cardiology and Cardiovascular Medicine
وصف الملف: STAMPA
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a6427bb92b381e9ed78386590987a32
http://hdl.handle.net/10281/131754 -
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المؤلفون: Althea Goosen, Paul A. Brink, Johanna C. Moolman-Smook, M. Revera, Jomien Mouton, L. van der Merwe, Craig J. Kinnear
المصدر: Human genetics. 135(5)
مصطلحات موضوعية: 0301 basic medicine, Adult, Male, TNNT2, DNA Mutational Analysis, Single-nucleotide polymorphism, Cardiomegaly, macromolecular substances, 030204 cardiovascular system & hematology, Biology, Left ventricular hypertrophy, Muscle hypertrophy, Pathogenesis, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, Humans, Genetic Testing, Genetics (clinical), Polymorphism, Genetic, Hypertrophic cardiomyopathy, Cardiomyopathy, Hypertrophic, Middle Aged, medicine.disease, Prognosis, 3. Good health, Cytoskeletal Proteins, 030104 developmental biology, Myosin binding, Mutation, cardiovascular system, MYH7, Female, Follow-Up Studies
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المؤلفون: Paul A. Brink, Marshall Heradien, Nadia Carstens, Johanna C. Moolman-Smook, Miriam Revera, Lize van der Merwe, Althea Goosen
المصدر: Journal of the Renin-Angiotensin-Aldosterone System, Vol 12 (2011)
مصطلحات موضوعية: Adult, Male, Medicine (General), medicine.medical_specialty, Heart Ventricles, Cardiomyopathy, Blood Pressure, Single-nucleotide polymorphism, Left ventricular hypertrophy, Polymorphism, Single Nucleotide, Receptor, Angiotensin, Type 2, Muscle hypertrophy, Cohort Studies, R5-920, Endocrinology, Gene Frequency, Internal medicine, Renin–angiotensin system, Internal Medicine, medicine, Humans, Genetic Predisposition to Disease, cardiovascular diseases, Allele, Principal Component Analysis, Angiotensin II receptor type 1, business.industry, Hypertrophic cardiomyopathy, Cardiomyopathy, Hypertrophic, Middle Aged, medicine.disease, cardiovascular system, Cardiology, Female, Hypertrophy, Left Ventricular, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::324cdb1e0be83f7fc3b44a2f470512d8
https://doi.org/10.1177/1470320310390725 -
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المؤلفون: Marshall Heradien, Bongani M. Mayosi, Valerie A. Corfield, Lize van der Merwe, Johanna C. Moolman-Smook, Paul A. Brink, Althea Goosen, Miriam Revera
المصدر: Heart Rhythm
مصطلحات موضوعية: Male, CR, chronotropic response, HCM, hypertrophic cardiomyopathy, Survival, TNNT2, Blood Pressure, TNNT2, cardiac troponin T gene, Genetic mutation, 030204 cardiovascular system & hematology, Sudden cardiac death, 0302 clinical medicine, Heart Rate, Risk Factors, Medicine, 0303 health sciences, HR, heart rate, Troponin T, Hypertrophic cardiomyopathy, Ca2+, calcium, Middle Aged, MYH7, beta cardiac myosin heavy chain gene, maxLVWT, maximum left ventricular wall thickness, Echocardiography, Cardiology, Female, LVM, left ventricular mass, METs, metabolic equivalents, Cardiology and Cardiovascular Medicine, Adult, Heterozygote, medicine.medical_specialty, Adolescent, DBP, diastolic blood pressure, Article, Young Adult, 03 medical and health sciences, Internal medicine, Physiology (medical), Heart rate, Humans, Abnormal blood pressure response, Aged, 030304 developmental biology, business.industry, SBP, systolic blood pressure, Odds ratio, Cardiomyopathy, Hypertrophic, medicine.disease, LV, left ventricle, Death, Sudden, Cardiac, Blood pressure, SCD, sudden cardiac death, Mutation, Exercise Test, ECG, electrocardiogram, Beta-myosin, MYH7, business, Cardiac Myosins
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المؤلفون: Peter J. Schwartz, Paul A. Brink, Roberto Insolia, Maria Cristina Monti, Lia Crotti, Althea Goosen, David A. Greenberg, Anna L. Peljto, Alfred L. George
المساهمون: Crotti, L, Monti, M, Insolia, R, Peljto, A, Goosen, A, Brink, P, Greenberg, D, Schwartz, P, George, A
المصدر: Circulation. 120:1657-1663
مصطلحات موضوعية: Genetic Markers, Male, medicine.medical_specialty, Long QT syndrome, Population, Sudden death, QT interval, Article, Sudden cardiac death, Death, Sudden, Risk Factors, Physiology (medical), Internal medicine, medicine, Humans, education, Adaptor Proteins, Signal Transducing, Genetic association, Genetics, education.field_of_study, long qt syndrome, genetic modifier, NOS1AP, Genetic heterogeneity, business.industry, Genetic Variation, Arrhythmias, Cardiac, MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE, medicine.disease, Long QT Syndrome, Mutation, SECS-S/01 - STATISTICA, Mutation (genetic algorithm), Cardiology, Female, Cardiology and Cardiovascular Medicine, business
وصف الملف: STAMPA
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2efb810340e638398f1379874f84309
https://doi.org/10.1161/circulationaha.109.879643
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