UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Application of Whole Exome Sequencing in the Clinical Diagnosis and Management of Inherited Cardiovascular Diseases in Adults

Circulation. Cardiovascular genetics, 2017-02, Vol.10 (1)

2017

Volltextzugriff (PDF)

Metabolic syndrome: genetic insights into disease pathogenesis

Current opinion in lipidology, 2016-04, Vol.27 (2), p.162-171

2016

Volltextzugriff (PDF)

Dyrk1b promotes autophagy during skeletal muscle differentiation by upregulating 4e-bp1

Cellular signalling, 2022-02, Vol.90, p.110186-110186, Article 110186

2022

Volltextzugriff (PDF)

Nurse-led theory-based educational intervention improves glycemic and metabolic parameters in South Asian patients with type II diabetes: a randomized controlled trial

Diabetology international, 2017-03, Vol.8 (1), p.95-103

2017

Volltextzugriff (PDF)

Epistatic interaction of PDE4DIP and DES mutations in familial atrial fibrillation with slow conduction

Human mutation, 2021-10, Vol.42 (10), p.1279-1293

2021

Volltextzugriff (PDF)

Severe extra-glandular involvement and pleural effusions complicating primary Sjogren’s syndrome: a case report

Journal of medical case reports, 2022-10, Vol.16 (1), p.1-374, Article 374

2022

Volltextzugriff (PDF)

The interplay of canonical and noncanonical Wnt signaling in metabolic syndrome

Nutrition research (New York, N.Y.), 2019-10, Vol.70, p.18-25

2019

Volltextzugriff (PDF)

Wnt signaling, a novel pathway regulating blood pressure? State of the art review

Atherosclerosis, 2017-07, Vol.262, p.171-178

2017

Volltextzugriff (PDF)

Pulmonary Embolism and Atrial Fibrillation: Two Sides of the Same Coin? A Systematic Review

Seminars in thrombosis and hemostasis, 2017-11, Vol.43 (8), p.849-863

2017

Volltextzugriff (PDF)

Prevalence of the Apolipoprotein E Arg145Cys Dyslipidemia At-Risk Polymorphism in African-Derived Populations

The American journal of cardiology, 2014-01, Vol.113 (2), p.302-308

2014

Volltextzugriff (PDF)

Tachyarrhythmia Onset Captured on Telemetry Deciphers the Diagnosis

JAMA internal medicine, 2017-11, Vol.177 (11), p.1673

2017

Volltextzugriff (PDF)

Beware of Limb Lead Reversal—Reply

JAMA internal medicine, 2018-03, Vol.178 (3), p.435

2018

Volltextzugriff (PDF)

Severe extra-glandular involvement and pleural effusions complicating primary Sjogren’s syndrome: a case report

Journal of medical case reports, 2022-10, Vol.16

2022

Volltextzugriff (PDF)

The Value of the History and Physical Examination--Sailing Through Medicine With Modern Tools: A Teachable Moment

JAMA internal medicine, 2015-12, Vol.175 (12), p.1901

2015

Volltextzugriff (PDF)

Erratum: Pulmonary Embolism and Atrial Fibrillation: Two Sides of the Same Coin? A Systematic Review

Seminars in thrombosis and hemostasis, 2017-12, Vol.43 (8), p.e1-e1

2017

Volltextzugriff (PDF)

DELETERIOUS MUTATIONS IN SCN10A ARE ASSOCIATED WITH LONG QT SYNDROME

Journal of the American College of Cardiology, 2017-03, Vol.69 (11), p.509-509

2017

Volltextzugriff (PDF)

Collaborative leadership: organisational structure and institutional investment to multiply innovative educational efforts among trainees

BMJ leader, 2021-03, Vol.5 (1), p.55-58

2021

Volltextzugriff (PDF)

PO-657-07 SPONTANEOUS RESTORATION OF SINUS RHYTHM AFTER INTER ATRIAL SHUNT PLACEMENT IN A PATIENT WITH LONGSTANDING PERSISTENT ATRIAL FIBRILLATION

Heart rhythm, 2022-05, Vol.19 (5), p.S273-S274

2022

Volltextzugriff (PDF)

The interplay of Canonical and Non-canonical Wnt Signaling in Metabolic Syndrome1

Nutrition research (New York, N.Y.), 2018-07, Vol.70, p.18-25

2018

Volltextzugriff (PDF)

Abstract 17195: Hydroxychloroquine Associated Electrocardiographic Changes in Patients With COVID-19 Extend Beyond QTc Prolongation and Are Accentuated in Those With Myocardial Injury

Circulation (New York, N.Y.), 2020-11, Vol.142 (Suppl_3 Suppl 3), p.A17195-A17195

2020

Volltextzugriff (PDF)

PO-05-102 CHARACTERISTICS AND ABLATION OF VENTRICULAR ARRHYTHMIAS FROM THE POSTERIOR SUPERIOR PROCESS OF THE LEFT VENTRICLE

Heart rhythm, 2023-05, Vol.20 (5), p.S645-S646

2023

Volltextzugriff (PDF)

Deleterious protein‐altering mutations in the SCN10A voltage‐gated sodium channel gene are associated with prolonged QT

Clinical genetics, 2018-04, Vol.93 (4), p.741-751

2018

Volltextzugriff (PDF)

PO-669-03 MACHINE LEARNING BASED ONE-YEAR MORTALITY PREDICTION IN PATIENTS UNDERGOING PRIMARY PREVENTION CARDIOVERTER DEFIBRILLATOR IMPLANTATION: A RETROSPECTIVE COHORT STUDY

Heart rhythm, 2022-05, Vol.19 (5), p.S316-S317

2022

Volltextzugriff (PDF)

B-AB13-03 NOVEL ROLE OF PDE4DIP IN FAMILIAL ATRIAL FIBRILLATION WITH SLOW VENTRICULAR RESPONSE

Heart rhythm, 2021-08, Vol.18 (8), p.S26-S26

2021

Volltextzugriff (PDF)

Rare mutation in the SLC26A3 transporter causes life-long diarrhoea with metabolic alkalosis

BMJ case reports, 2015-01, Vol.2015, p.bcr2014206849

2015

Volltextzugriff (PDF)

1 – 25 von 27

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(27)
Mit Volltextzugriff
(19)

Publikationsform

Artikel
(27)

Sprache

Englisch
(27)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Application of Whole Exome Sequencing in the Clinical Diagnosis and Management of Inherited Cardiovascular Diseases in Adults

Metabolic syndrome: genetic insights into disease pathogenesis

Dyrk1b promotes autophagy during skeletal muscle differentiation by upregulating 4e-bp1

Nurse-led theory-based educational intervention improves glycemic and metabolic parameters in South Asian patients with type II diabetes: a randomized controlled trial

Epistatic interaction of PDE4DIP and DES mutations in familial atrial fibrillation with slow conduction

Severe extra-glandular involvement and pleural effusions complicating primary Sjogren’s syndrome: a case report

The interplay of canonical and noncanonical Wnt signaling in metabolic syndrome

Wnt signaling, a novel pathway regulating blood pressure? State of the art review

Pulmonary Embolism and Atrial Fibrillation: Two Sides of the Same Coin? A Systematic Review

Prevalence of the Apolipoprotein E Arg145Cys Dyslipidemia At-Risk Polymorphism in African-Derived Populations

Tachyarrhythmia Onset Captured on Telemetry Deciphers the Diagnosis

Beware of Limb Lead Reversal—Reply

Severe extra-glandular involvement and pleural effusions complicating primary Sjogren’s syndrome: a case report

The Value of the History and Physical Examination--Sailing Through Medicine With Modern Tools: A Teachable Moment

Erratum: Pulmonary Embolism and Atrial Fibrillation: Two Sides of the Same Coin? A Systematic Review

DELETERIOUS MUTATIONS IN SCN10A ARE ASSOCIATED WITH LONG QT SYNDROME

Collaborative leadership: organisational structure and institutional investment to multiply innovative educational efforts among trainees

PO-657-07 SPONTANEOUS RESTORATION OF SINUS RHYTHM AFTER INTER ATRIAL SHUNT PLACEMENT IN A PATIENT WITH LONGSTANDING PERSISTENT ATRIAL FIBRILLATION

The interplay of Canonical and Non-canonical Wnt Signaling in Metabolic Syndrome1

Abstract 17195: Hydroxychloroquine Associated Electrocardiographic Changes in Patients With COVID-19 Extend Beyond QTc Prolongation and Are Accentuated in Those With Myocardial Injury

PO-05-102 CHARACTERISTICS AND ABLATION OF VENTRICULAR ARRHYTHMIAS FROM THE POSTERIOR SUPERIOR PROCESS OF THE LEFT VENTRICLE

Deleterious protein‐altering mutations in the SCN10A voltage‐gated sodium channel gene are associated with prolonged QT

PO-669-03 MACHINE LEARNING BASED ONE-YEAR MORTALITY PREDICTION IN PATIENTS UNDERGOING PRIMARY PREVENTION CARDIOVERTER DEFIBRILLATOR IMPLANTATION: A RETROSPECTIVE COHORT STUDY

B-AB13-03 NOVEL ROLE OF PDE4DIP IN FAMILIAL ATRIAL FIBRILLATION WITH SLOW VENTRICULAR RESPONSE

Rare mutation in the SLC26A3 transporter causes life-long diarrhoea with metabolic alkalosis

Suchergebnisse filtern