UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 85

Sortiert nach

Cardiac Genetic Predisposition in Sudden Infant Death Syndrome

Journal of the American College of Cardiology, 2018-03, Vol.71 (11), p.1217-1227

2018

Volltextzugriff (PDF)

Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome

The Journal of pediatrics, 2018-12, Vol.203, p.423-428.e11

2018

Volltextzugriff (PDF)

Impact of clinical and genetic findings on the management of young patients with Brugada syndrome

Heart rhythm, 2016-06, Vol.13 (6), p.1274-1282

2016

Volltextzugriff (PDF)

Cardiac Evaluation of Pediatric Relatives in Sudden Arrhythmic Death Syndrome: A 2-Center Experience

Circulation. Arrhythmia and electrophysiology, 2014-10, Vol.7 (5), p.800-806

2014

Volltextzugriff (PDF)

Sudden unexplained death in infants and children: the role of undiagnosed inherited cardiac conditions

Europace (London, England), 2014-12, Vol.16 (12), p.1706-1713

2014

Volltextzugriff (PDF)

Noncardiac genetic predisposition in sudden infant death syndrome

Genetics in medicine, 2019-03, Vol.21 (3), p.641-649

2019

Volltextzugriff (PDF)

Early-onset cardiac arrest, prolonged QT interval, and left ventricular hypertrophy: Phenotypic manifestations of a pathogenic de novo calmodulin variant

HeartRhythm case reports, 2023-12, Vol.9 (12), p.858-862

2023

Volltextzugriff (PDF)

Acquired long QT syndrome: as risky as congenital long QT syndrome?

Europace (London, England), 2012-03, Vol.14 (3), p.310-311

2012

Volltextzugriff (PDF)

Familial cardiological evaluation in sudden arrhythmic death syndrome: essential but challenging

Europace (London, England), 2013-07, Vol.15 (7), p.924-926

2013

Volltextzugriff (PDF)

Computed tomography may demonstrate pseudosubarachnoid hemorrhage in diffuse cerebral edema after cardiorespiratory arrest

Pediatric critical care medicine, 2011-09, Vol.12 (5), p.e208-e210

2011

Volltextzugriff (PDF)

Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study

The Lancet (British edition), 2018-04, Vol.391 (10129), p.1483-1492

2018

Volltextzugriff (PDF)

Author's reply: To PMID 24585884

Europace (London, England), 2015-11, Vol.17 (11), p.1739-1740

2015

Volltextzugriff (PDF)

Outcomes From Pediatric Ablation: A Review of 20 Years of National Data

JACC. Clinical electrophysiology, 2021-11, Vol.7 (11), p.1358-1365

2021

Volltextzugriff (PDF)

Outcomes From Pediatric Ablation

JACC. Clinical electrophysiology, 2021-11, Vol.7 (11), p.1358-1365

2021

Volltextzugriff (PDF)

Abstract 18543: Whole Exome Sequencing in Sudden Infant Death Syndrome Identifies a High Proportion of Putative Pathogenic and Functionally Significant Rare Variants Related to Inherited Cardiac Conditions

Circulation (New York, N.Y.), 2014-11, Vol.130 (suppl_2)

2014

Volltextzugriff (PDF)

SCN5A mutations in 442 neonates and children: Genotype-phenotype correlation and identification of higher-risk subgroups

Archives of Cardiovascular Diseases Supplements, 2019-09, Vol.11 (4), p.e381-e382

2019

Volltextzugriff (PDF)

Early-onset cardiac arrest, prolonged QT interval, and left ventricular hypertrophy: Phenotypic manifestations of a pathogenic de novo calmodulin variant

HeartRhythm case reports, 2023, Vol.9 (12), p.858-862

2023

Volltextzugriff (PDF)

VPS13C regulates phospho-Rab10-mediated lysosomal function in human dopaminergic neurons

The Journal of cell biology, 2024-05, Vol.223 (5)

2024

Volltextzugriff (PDF)

Gain-of-Function RHOA Mutations Promote Focal Adhesion Kinase Activation and Dependency in Diffuse Gastric Cancer

Cancer discovery, 2020-02, Vol.10 (2), p.288-305

2020

Volltextzugriff (PDF)

Conceptual Modeling Enables Systems Thinking in Sustainable Chemistry and Chemical Engineering

Journal of chemical education, 2023-12, Vol.100 (12), p.4577-4584

2023

Volltextzugriff (PDF)

Relative hyperglycemia is associated with complications following an acute myocardial infarction: a post-hoc analysis of HI-5 data

Cardiovascular diabetology, 2017-12, Vol.16 (1), p.157-157, Article 157

2017

Volltextzugriff (PDF)

Parkin regulates amino acid homeostasis at mitochondria-lysosome (M/L) contact sites in Parkinson's disease

Science advances, 2023-07, Vol.9 (29), p.eadh3347

2023

Volltextzugriff (PDF)

Early intensive care sedation predicts long-term mortality in ventilated critically ill patients

American journal of respiratory and critical care medicine, 2012-10, Vol.186 (8), p.724-731

2012

Volltextzugriff (PDF)

1 – 25 von 85

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(72)
Mit Volltextzugriff
(81)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(57)
Life Sciences & Biomedicine
(38)
Humans
(32)
Female
(18)
Male
(17)
Technology
(16)
Computer Science
(12)
Child
(10)
Computer Science, Theory & Methods
(10)
Authenticated Encryption
(9)
Cardiac & Cardiovascular Systems
(9)
Cardiovascular System & Cardiology
(9)
Computer Science, Information Systems
(9)
Pediatrics
(9)
Adult
(8)
Infant
(8)
Encryption
(7)
Middle Aged
(7)
Stream Cipher
(7)
Adolescent
(6)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Cardiac Genetic Predisposition in Sudden Infant Death Syndrome

Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome

Impact of clinical and genetic findings on the management of young patients with Brugada syndrome

Cardiac Evaluation of Pediatric Relatives in Sudden Arrhythmic Death Syndrome: A 2-Center Experience

Sudden unexplained death in infants and children: the role of undiagnosed inherited cardiac conditions

Noncardiac genetic predisposition in sudden infant death syndrome

Early-onset cardiac arrest, prolonged QT interval, and left ventricular hypertrophy: Phenotypic manifestations of a pathogenic de novo calmodulin variant

Acquired long QT syndrome: as risky as congenital long QT syndrome?

Familial cardiological evaluation in sudden arrhythmic death syndrome: essential but challenging

Computed tomography may demonstrate pseudosubarachnoid hemorrhage in diffuse cerebral edema after cardiorespiratory arrest

The Impact of Clinical and Genetic Findings on The Management of Young Brugada Syndrome Patients

Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study

Author's reply: To PMID 24585884

Outcomes From Pediatric Ablation: A Review of 20 Years of National Data

Outcomes From Pediatric Ablation

Abstract 18543: Whole Exome Sequencing in Sudden Infant Death Syndrome Identifies a High Proportion of Putative Pathogenic and Functionally Significant Rare Variants Related to Inherited Cardiac Conditions

SCN5A mutations in 442 neonates and children: Genotype-phenotype correlation and identification of higher-risk subgroups

Early-onset cardiac arrest, prolonged QT interval, and left ventricular hypertrophy: Phenotypic manifestations of a pathogenic de novo calmodulin variant

VPS13C regulates phospho-Rab10-mediated lysosomal function in human dopaminergic neurons

Gain-of-Function RHOA Mutations Promote Focal Adhesion Kinase Activation and Dependency in Diffuse Gastric Cancer

Conceptual Modeling Enables Systems Thinking in Sustainable Chemistry and Chemical Engineering

Relative hyperglycemia is associated with complications following an acute myocardial infarction: a post-hoc analysis of HI-5 data

Cardiovascular Effects of Stimulant and Non-Stimulant Medication for Children and Adolescents with ADHD: A Systematic Review and Meta-Analysis of Trials of Methylphenidate, Amphetamines and Atomoxetine

Parkin regulates amino acid homeostasis at mitochondria-lysosome (M/L) contact sites in Parkinson's disease

Early intensive care sedation predicts long-term mortality in ventilated critically ill patients

Suchergebnisse filtern