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  1. Article ; Online: From gene-specific to function-specific risk stratification in long QT syndrome Type 2: implications for clinical management.

    Crotti, Lia

    Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology

    2023  Volume 25, Issue 4, Page(s) 1320–1322

    MeSH term(s) Humans ; Long QT Syndrome/diagnosis ; Long QT Syndrome/genetics ; Long QT Syndrome/therapy ; Death, Sudden, Cardiac ; Risk Assessment ; ERG1 Potassium Channel
    Chemical Substances KCNH2 protein, human ; ERG1 Potassium Channel
    Language English
    Publishing date 2023-05-09
    Publishing country England
    Document type Editorial ; Comment
    ZDB-ID 1449879-0
    ISSN 1532-2092 ; 1099-5129
    ISSN (online) 1532-2092
    ISSN 1099-5129
    DOI 10.1093/europace/euad035
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 5434: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (2.OG)
    ab Jg. 2022: Lesesaal (EG)

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  2. Article ; Online: Calmodulin, sudden death, and the Folbigg case: genes in court.

    Schwartz, Peter J / Crotti, Lia / Nyegaard, Mette / Overgaard, Michael Toft

    European heart journal

    2024  

    Language English
    Publishing date 2024-04-09
    Publishing country England
    Document type Journal Article
    ZDB-ID 603098-1
    ISSN 1522-9645 ; 0195-668X
    ISSN (online) 1522-9645
    ISSN 0195-668X
    DOI 10.1093/eurheartj/ehae152
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    Zs.A 1563: Show issues Location:
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    Zs.MO 640: Show issues

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  3. Article: Diagnostic and prognostic electrocardiographic features in patients with hypertrophic cardiomyopathy.

    Bernardini, Andrea / Crotti, Lia / Olivotto, Iacopo / Cecchi, Franco

    European heart journal supplements : journal of the European Society of Cardiology

    2023  Volume 25, Issue Suppl C, Page(s) C173–C178

    Abstract: The standard 12-lead electrocardiogram (ECG) represents a cornerstone for the diagnosis and evaluation of hypertrophic cardiomyopathy (HCM), the most common genetically determined heart muscle disease, due to its cost-effectiveness and wide availability. ...

    Abstract The standard 12-lead electrocardiogram (ECG) represents a cornerstone for the diagnosis and evaluation of hypertrophic cardiomyopathy (HCM), the most common genetically determined heart muscle disease, due to its cost-effectiveness and wide availability. The ECG may surprisingly look normal in 4-6% of adult patients, and in less than 3% of paediatric patients, but it is abnormal in the vast majority of the remaining patients. 'Specific' features comprise pathological Q-waves, deep S-waves in V1-V3, or high R-waves in V4-V6 due to left ventricular hypertrophy with T-wave (TW) depression or negative TWs. Negative giant TWs are often found in apical HCM. However, in many patients, the ECG may only show non-specific ST-T changes with diphasic or flat TWs. An isolated inverted TW in lateral leads (usually aVL) may be the only marker for HCM in some patients. Electrocardiogram helps to diagnose sarcomeric HCM and distinguish it from different phenocopies, such as cardiac amyloidosis, glycogen storage, or Fabry disease. Electrocardiogram may also have a prognostic role, identifying high-risk features that could impact the clinical outcome.
    Language English
    Publishing date 2023-04-26
    Publishing country England
    Document type Journal Article
    ZDB-ID 1463769-8
    ISSN 1554-2815 ; 1520-765X
    ISSN (online) 1554-2815
    ISSN 1520-765X
    DOI 10.1093/eurheartjsupp/suad074
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    Zs.A 1563 -Suppl.-: Show issues Location:
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  4. Article ; Online: COVID-19 treatments, QT interval, and arrhythmic risk: The need for an international registry on arrhythmias.

    Crotti, Lia / Arbelo, Elena

    Heart rhythm

    2020  Volume 17, Issue 9, Page(s) 1423–1424

    MeSH term(s) Arrhythmias, Cardiac ; Betacoronavirus ; COVID-19 ; Coronavirus ; Coronavirus Infections/drug therapy ; Electrocardiography ; Humans ; Pandemics ; Pneumonia, Viral ; Registries ; SARS-CoV-2 ; COVID-19 Drug Treatment
    Keywords covid19
    Language English
    Publishing date 2020-05-26
    Publishing country United States
    Document type Editorial ; Comment
    ZDB-ID 2229357-7
    ISSN 1556-3871 ; 1547-5271
    ISSN (online) 1556-3871
    ISSN 1547-5271
    DOI 10.1016/j.hrthm.2020.05.024
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    Zs.A 6278: Show issues Location:
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  5. Article ; Online: COVID-19 pandemia and inherited cardiomyopathies and channelopathies: a short term and long term perspective.

    Limongelli, Giuseppe / Crotti, Lia

    Orphanet journal of rare diseases

    2020  Volume 15, Issue 1, Page(s) 157

    Abstract: Inherited heart disease represent a very heterogenous group of cardiac disorders, characterized by inherited, acquired, and often rare disorders affecting the heart muscle (cardiomyopathies) or the cardiac electrical system (ion channel disease). They ... ...

    Abstract Inherited heart disease represent a very heterogenous group of cardiac disorders, characterized by inherited, acquired, and often rare disorders affecting the heart muscle (cardiomyopathies) or the cardiac electrical system (ion channel disease). They are often familial diseases, and are among the leading cause of juvenile sudden death and heart failure. The aim of this paper is to give a perspective on how to run a clinical service during an epidemic or pandemic emergency and to describe the potential COVID-19 associated risks for patients affected by inherited heart diseases.
    MeSH term(s) Betacoronavirus ; COVID-19 ; Cardiomyopathies/complications ; Cardiomyopathies/genetics ; Channelopathies/complications ; Channelopathies/genetics ; Coronavirus Infections/complications ; Coronavirus Infections/epidemiology ; Coronavirus Infections/prevention & control ; Genetic Predisposition to Disease ; Humans ; Outpatient Clinics, Hospital/organization & administration ; Pandemics/prevention & control ; Pneumonia, Viral/complications ; Pneumonia, Viral/epidemiology ; Pneumonia, Viral/prevention & control ; Rare Diseases/complications ; Risk Factors ; SARS-CoV-2 ; Telemedicine/organization & administration
    Keywords covid19
    Language English
    Publishing date 2020-06-22
    Publishing country England
    Document type Letter
    ISSN 1750-1172
    ISSN (online) 1750-1172
    DOI 10.1186/s13023-020-01444-2
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  6. Article: Current gaps in knowledge in inherited arrhythmia syndromes.

    Peltenburg, Puck J / Crotti, Lia / Roston, Thomas M / van der Werf, Christian

    Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation

    2023  Volume 31, Issue 7-8, Page(s) 272–281

    Abstract: The 3 most common inherited arrhythmia syndromes-Brugada syndrome, congenital long QT syndrome and catecholaminergic polymorphic ventricular tachycardia-were initially described in the previous century. Since then, research has evolved, which has enabled ...

    Abstract The 3 most common inherited arrhythmia syndromes-Brugada syndrome, congenital long QT syndrome and catecholaminergic polymorphic ventricular tachycardia-were initially described in the previous century. Since then, research has evolved, which has enabled us to identify patients prior to the onset of potentially life-threatening symptoms. However, there are significant gaps in knowledge that complicate clinical management of these patients today. With this review paper, we aim to highlight the most important knowledge gaps in clinical research of these inherited arrhythmia syndromes.
    Language English
    Publishing date 2023-07-06
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 2211468-3
    ISSN 1876-6250 ; 1568-5888 ; 0929-7456
    ISSN (online) 1876-6250
    ISSN 1568-5888 ; 0929-7456
    DOI 10.1007/s12471-023-01797-w
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    Zs.A 6216: Show issues Location:
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  7. Article ; Online: To be, or not to be engaged in sport activities, that is the amletic question for patients with coronary artery disease.

    Castelletti, Silvia / Crotti, Lia

    European journal of preventive cardiology

    2019  Volume 27, Issue 7, Page(s) 767–769

    MeSH term(s) Athletes ; Cardiology ; Coronary Artery Disease/epidemiology ; Humans ; Leisure Activities ; Sports
    Language English
    Publishing date 2019-10-04
    Publishing country England
    Document type Editorial ; Comment
    ZDB-ID 2626011-6
    ISSN 2047-4881 ; 2047-4873
    ISSN (online) 2047-4881
    ISSN 2047-4873
    DOI 10.1177/2047487319877701
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    Zs.A 4686: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
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  8. Article ; Online: COVID-19 pandemia and inherited cardiomyopathies and channelopathies

    Giuseppe Limongelli / Lia Crotti

    Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-

    a short term and long term perspective

    2020  Volume 7

    Abstract: Abstract Inherited heart disease represent a very heterogenous group of cardiac disorders, characterized by inherited, acquired, and often rare disorders affecting the heart muscle (cardiomyopathies) or the cardiac electrical system (ion channel disease). ...

    Abstract Abstract Inherited heart disease represent a very heterogenous group of cardiac disorders, characterized by inherited, acquired, and often rare disorders affecting the heart muscle (cardiomyopathies) or the cardiac electrical system (ion channel disease). They are often familial diseases, and are among the leading cause of juvenile sudden death and heart failure. The aim of this paper is to give a perspective on how to run a clinical service during an epidemic or pandemic emergency and to describe the potential COVID-19 associated risks for patients affected by inherited heart diseases.
    Keywords Inherited and rare heart disease ; Cardiomyopathies ; Channellopathies ; COVID-19 ; Medicine ; R ; covid19
    Language English
    Publishing date 2020-06-01T00:00:00Z
    Publisher BMC
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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    Inter-library loan at ZB MED

    Your chosen title can be delivered directly to ZB MED Cologne location if you are registered as a user at ZB MED Cologne.

  10. Article ; Online: COVID-19 treatments, QT interval, and arrhythmic risk

    Crotti, Lia / Arbelo, Elena

    Heart Rhythm

    The need for an international registry on arrhythmias

    2020  Volume 17, Issue 9, Page(s) 1423–1424

    Keywords Physiology (medical) ; Cardiology and Cardiovascular Medicine ; covid19
    Language English
    Publisher Elsevier BV
    Publishing country us
    Document type Article ; Online
    ZDB-ID 2229357-7
    ISSN 1556-3871 ; 1547-5271
    ISSN (online) 1556-3871
    ISSN 1547-5271
    DOI 10.1016/j.hrthm.2020.05.024
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

    Full text online

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 6278: Show issues Location:
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