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  1. AU="Tendera, Michal"
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  1. Book ; Conference proceedings: Past, present and future of ACE inhibitors

    Tendera, Michał

    proceedings of a satellite symposium held during the European Society of Cardiology congress ; Vienna, Austria, September 1, 2007

    (European heart journal : Supplements ; 9E)

    2007  

    Institution European Society of Cardiology
    Author's details ed. by Michal Tendera
    Series title European heart journal : Supplements ; 9E
    European heart journal
    European heart journal ; Supplements
    Collection European heart journal
    European heart journal ; Supplements
    Language English
    Size E29 S. : Ill., graph. Darst.
    Publisher Saunders
    Publishing place London u.a.
    Publishing country Great Britain
    Document type Book ; Conference proceedings
    HBZ-ID HT015292956
    Database Catalogue ZB MED Medicine, Health

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  2. Article ; Online: Medicine of the future: a look through the keyhole.

    Tendera, Michal

    European heart journal

    2022  Volume 43, Issue 44, Page(s) 4606–4608

    Language English
    Publishing date 2022-09-23
    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/ehac523
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Book: Zastosowanie sieci internet w kardiologii

    Tendera, Michał

    praktyczny przewodnik dla lekarzy

    (Kardiologia polska ; 49, Supl. 3)

    1998  

    Institution Polskie Towarzystwo Kardiologiczne
    Author's details Polish Cardiac Society. Red. supl. Michał Tendera
    Series title Kardiologia polska ; 49, Supl. 3
    Collection
    Language Polish
    Size 144 S. : Ill.
    Publishing place Warszawa
    Publishing country Poland
    Document type Book
    HBZ-ID HT010091514
    Database Catalogue ZB MED Medicine, Health

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  4. Book ; Online: Diastolic Heart Failure

    Smiseth, Otto A. / Tendera, Michał

    2008  

    Author's details edited by Otto A. Smiseth, Michał Tendera
    Keywords Cardiology ; Diabetes ; Internal medicine
    Language English
    Publisher Springer-Verlag London Limited
    Publishing place London
    Document type Book ; Online
    HBZ-ID TT050387269
    ISBN 978-1-8462-8890-6 ; 978-1-8462-8891-3 ; 1-8462-8890-8 ; 1-8462-8891-6
    DOI 10.1007/978-1-84628-891-3
    Database ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture

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  5. Article ; Online: Profesor Lars Ryden — doktor honoris causa Śląskiego Uniwersytetu Medycznego w Katowicach.

    Tendera, Michał

    Kardiologia polska

    2011  Volume 69, Issue 2, Page(s) 200–201

    Title translation Professor Lars Ryden - doctor honoris causa of the Medical University of Silesia in Katowice, Poland.
    MeSH term(s) Cardiology/history ; History, 20th Century ; History, 21st Century ; Humans ; Poland
    Language Polish
    Publishing date 2011
    Publishing country Poland
    Document type Historical Article ; Journal Article
    ZDB-ID 411492-9
    ISSN 1897-4279 ; 0022-9032
    ISSN (online) 1897-4279
    ISSN 0022-9032
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Lekarz pierwszego kontaktu a niewydolność serca.

    Tendera, Michał

    Kardiologia polska

    2011  Volume 69, Issue 1, Page(s) 32

    Title translation Primary care physician and heart failure.
    MeSH term(s) Adrenergic beta-Antagonists/therapeutic use ; Angiotensin-Converting Enzyme Inhibitors/therapeutic use ; Cardiovascular Agents/therapeutic use ; Female ; Heart Failure/epidemiology ; Humans ; Male
    Chemical Substances Adrenergic beta-Antagonists ; Angiotensin-Converting Enzyme Inhibitors ; Cardiovascular Agents
    Language Polish
    Publishing date 2011
    Publishing country Poland
    Document type Comment ; Journal Article
    ZDB-ID 411492-9
    ISSN 1897-4279 ; 0022-9032
    ISSN (online) 1897-4279
    ISSN 0022-9032
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Rodzinna kardiomiopatia rozstrzeniowa - poszukiwanie tozsamości.

    Tendera, Michał

    Kardiologia polska

    2009  Volume 67, Issue 3, Page(s) 242

    Title translation Familial idiopathic dilated cardiomyopathy - search for identity.
    MeSH term(s) Adult ; Aged ; Cardiomyopathy, Dilated/genetics ; Female ; Gene Frequency ; Genetic Predisposition to Disease ; Humans ; Male ; Middle Aged ; Phenotype ; Poland ; Polymorphism, Genetic ; Polymorphism, Restriction Fragment Length ; Receptors, Adrenergic, beta-1/genetics ; Receptors, Adrenergic, beta-2/genetics ; Risk Assessment ; Ventricular Function, Left/genetics
    Chemical Substances Receptors, Adrenergic, beta-1 ; Receptors, Adrenergic, beta-2
    Language Polish
    Publishing date 2009-03
    Publishing country Poland
    Document type Comment ; Journal Article
    ZDB-ID 411492-9
    ISSN 0022-9032
    ISSN 0022-9032
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Artificial Intelligence Can Improve Patient Management at the Time of a Pandemic: The Role of Voice Technology.

    Jadczyk, Tomasz / Wojakowski, Wojciech / Tendera, Michal / Henry, Timothy D / Egnaczyk, Gregory / Shreenivas, Satya

    Journal of medical Internet research

    2021  Volume 23, Issue 5, Page(s) e22959

    Abstract: Artificial intelligence-driven voice technology deployed on mobile phones and smart speakers has the potential to improve patient management and organizational workflow. Voice chatbots have been already implemented in health care-leveraging innovative ... ...

    Abstract Artificial intelligence-driven voice technology deployed on mobile phones and smart speakers has the potential to improve patient management and organizational workflow. Voice chatbots have been already implemented in health care-leveraging innovative telehealth solutions during the COVID-19 pandemic. They allow for automatic acute care triaging and chronic disease management, including remote monitoring, preventive care, patient intake, and referral assistance. This paper focuses on the current clinical needs and applications of artificial intelligence-driven voice chatbots to drive operational effectiveness and improve patient experience and outcomes.
    MeSH term(s) Artificial Intelligence ; COVID-19 ; Cell Phone ; Chronic Disease/therapy ; Communication ; Critical Care/methods ; Delivery of Health Care/methods ; Humans ; Pandemics ; Referral and Consultation ; Speech Recognition Software ; Telemedicine/methods ; Triage ; Voice
    Language English
    Publishing date 2021-05-25
    Publishing country Canada
    Document type Journal Article
    ZDB-ID 2028830-X
    ISSN 1438-8871 ; 1439-4456
    ISSN (online) 1438-8871
    ISSN 1439-4456
    DOI 10.2196/22959
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Book ; Conference proceedings: Past, present, and future of ACE inhibitors

    Tendera, Michał

    proceedings of a satellite symposium held during the European Society of Cardiology Congress, Vienna, Austria, September 1, 2007

    (European heart journal supplements, ; v. 9, suppl. E)

    2007  

    Institution European Society of Cardiology.
    European Society of Cardiology. / Congress
    Author's details edited by Michal Tendera
    Series title European heart journal supplements, ; v. 9, suppl. E
    MeSH term(s) Angiotensin-Converting Enzyme Inhibitors/therapeutic use ; Perindopril/therapeutic use
    Language English
    Size 29 p. :, ill.
    Publisher Oxford University Press
    Publishing place Oxford
    Document type Book ; Conference proceedings
    Database Catalogue of the US National Library of Medicine (NLM)

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  10. Article ; Online: Cardiomyopathies in children and adolescents: aetiology, management, and outcomes in the European Society of Cardiology EURObservational Research Programme Cardiomyopathy and Myocarditis Registry.

    Kaski, Juan Pablo / Norrish, Gabrielle / Gimeno Blanes, Juan Ramon / Charron, Philippe / Elliott, Perry / Tavazzi, Luigi / Tendera, Michal / Laroche, Cécile / Maggioni, Aldo P / Baban, Anwar / Khraiche, Diala / Ziolkowska, Lidia / Limongelli, Giuseppe / Ojala, Tiina / Gorenflo, Matthias / Anastasakis, Aris / Mostafa, Shaimaa / Caforio, Alida L P

    European heart journal

    2024  Volume 45, Issue 16, Page(s) 1443–1454

    Abstract: Background and aims: Childhood-onset cardiomyopathies are rare and poorly characterized. This study examined the baseline characteristics and 1-year follow-up of children with cardiomyopathy in the first European Cardiomyopathy Registry.: Methods: ... ...

    Abstract Background and aims: Childhood-onset cardiomyopathies are rare and poorly characterized. This study examined the baseline characteristics and 1-year follow-up of children with cardiomyopathy in the first European Cardiomyopathy Registry.
    Methods: Prospective data were collected on individuals aged 1-<18 years enrolled in the European Society of Cardiology EURObservational Research Programme Cardiomyopathy and Myocarditis long-term registry (June 2014-December 2016).
    Results: A total of 633 individuals aged ≤18 years with hypertrophic [HCM; n = 388 (61.3%)], dilated [DCM; n = 206 (32.5%)], restrictive [RCM; n = 28 (4.4%)], and arrhythmogenic right ventricular cardiomyopathy [ARVC; n = 11 (1.7%)] were enrolled by 23 referral centres in 14 countries. Median age at diagnosis was 4.0 [interquartile range (IQR) 0-10] years, and there was a male predominance [n = 372 (58.8%)] across all subtypes, with the exception of DCM diagnosed <10 years of age; 621 (98.1%) patients were receiving cardiac medication and 80 (12.6%) had an implantable cardioverter-defibrillator. A total of 253 patients (253/535, 47.3%) had familial disease. Genetic testing was performed in 414 (67.8%) patients with a pathogenic or likely pathogenic variant reported in 250 (60.4%). Rare disease phenocopies were reported in 177 patients (28.0%) and were most frequent in patients under 10 years [142 (30.9%) vs. 35 (19.6%); P = .003]. Over a median follow-up of 12.5 months (IQR 11.3-15.3 months), 18 patients (3.3%) died [HCM n = 9 (2.6%), DCM n = 5 (3.0%), RCM n = 4 (16.0%)]. Heart failure events were most frequent in RCM patients (36.0%).
    Conclusions: The findings confirm the heterogeneous aetiology of childhood cardiomyopathies and show a high frequency of familial disease. Outcomes differed by cardiomyopathy subtype, highlighting a need for disease-specific evaluation and treatment.
    MeSH term(s) Child ; Humans ; Male ; Adolescent ; Infant, Newborn ; Infant ; Child, Preschool ; Female ; Myocarditis/epidemiology ; Myocarditis/etiology ; Myocarditis/therapy ; Prospective Studies ; Cardiomyopathies/epidemiology ; Cardiomyopathies/genetics ; Cardiomyopathies/therapy ; Cardiology ; Registries ; Cardiomyopathy, Hypertrophic/diagnosis
    Language English
    Publishing date 2024-03-01
    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/ehae109
    Database MEDical Literature Analysis and Retrieval System OnLINE

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