UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 58

Sortiert nach

Assessment of Fetal Myocardial Performance Using Myocardial Deformation Analysis

The American journal of cardiology, 2007-04, Vol.99 (7), p.993-996

2007

Link zum Volltext

Verfügbarkeit prüfen

Amino-terminal pro-brain-type natriuretic peptide: heart or lung disease in pediatric respiratory distress?

Pediatrics (Evanston), 2005-05, Vol.115 (5), p.1347

2005

Link zum Volltext

Verfügbarkeit prüfen

A human laterality disorder caused by a homozygous deleterious mutation in MMP21

Journal of medical genetics, 2015-12, Vol.52 (12), p.840-847

2015

Link zum Volltext

Verfügbarkeit prüfen

Congenital valvular defects associated with deleterious mutations in the PLD1 gene

Journal of medical genetics, 2017-04, Vol.54 (4), p.278

2017

Link zum Volltext

Verfügbarkeit prüfen

A human laterality disorder associated with a homozygous WDR16 deletion

European journal of human genetics : EJHG, 2015-09, Vol.23 (9), p.1262-1265

2015

Link zum Volltext

Verfügbarkeit prüfen

Prevalence of Persistent Superior Vena Cava and Association With Congenital Heart Anomalies

The American journal of cardiology, 2013-10, Vol.112 (8), p.1214-1218

2013

Link zum Volltext

Verfügbarkeit prüfen

Comparison of N-terminal pro-B-type natriuretic peptide levels in critically ill children with sepsis versus acute left ventricular dysfunction

Pediatrics (Evanston), 2006-10, Vol.118 (4), p.e1165

2006

Link zum Volltext

Verfügbarkeit prüfen

Intracardiac Echogenic Foci Have No Hemodynamic Significance in the Fetus

Pediatric cardiology, 2010, Vol.31 (1), p.7-10

2010

Link zum Volltext

Verfügbarkeit prüfen

Tissue velocity Doppler assessment of atrial and ventricular electromechanical coupling and atrioventricular time intervals in normal subjects

The American journal of cardiology, 2003-12, Vol.92 (11), p.1347-1350

2003

Link zum Volltext

Verfügbarkeit prüfen

A human laterality disorder associated with recessive CCDC11 mutation

Journal of medical genetics, 2012-06, Vol.49 (6), p.386-390

2012

Link zum Volltext

Verfügbarkeit prüfen

Conotruncal malformations and absent thymus due to a deleterious NKX2-6 mutation

Journal of medical genetics, 2014-04, Vol.51 (4), p.268-270

2014

Link zum Volltext

Verfügbarkeit prüfen

Isolated truncus arteriosus associated with a mutation in the plexin-D1 gene

American journal of medical genetics. Part A, 2013-12, Vol.161A (12), p.3115-3120

2013

Link zum Volltext

Verfügbarkeit prüfen

Prevention of complete heart block in children of mothers with anti-SSA/Ro and anti-SSB/La autoantibodies: detection and treatment of first-degree atrioventricular block

Current opinion in rheumatology, 2009-09, Vol.21 (5), p.478-482

2009

Link zum Volltext

Verfügbarkeit prüfen

Analysis of Segmental and Global Function of the Fetal Heart Using Novel Automatic Functional Imaging

Journal of the American Society of Echocardiography, 2008-02, Vol.21 (2), p.146-150

2008

Link zum Volltext

Verfügbarkeit prüfen

Twin Pregnancy in a Patient after the Fontan Operation: Report of a Case

Congenital heart disease, 2013-11, Vol.8 (6), p.E196-E198

2013

Link zum Volltext

Verfügbarkeit prüfen

N-terminal-proB-type natriuretic peptide as a marker for acute anthracycline cardiotoxicity in children

Journal of pediatric hematology/oncology, 2007-07, Vol.29 (7), p.440-444

2007

Link zum Volltext

Verfügbarkeit prüfen

N-terminal pro-B–type natriuretic peptide levels in acute versus chronic left ventricular dysfunction

The Journal of pediatrics, 2006-07, Vol.149 (1), p.28-31

2006

Link zum Volltext

Verfügbarkeit prüfen

Significance of a Cardiac Murmur as the Sole Clinical Sign in the Newborn

Clinical pediatrics, 2000-09, Vol.39 (9), p.511-520

2000

Link zum Volltext

Verfügbarkeit prüfen

Myocardial Infarction Due to Coronary Compression by a Rhabdomyoma

The Israel Medical Association journal, 2023-09, Vol.25 (9), p.631-632

2023

Link zum Volltext

Verfügbarkeit prüfen

Absent Ductus venosus in the Fetus: Review of the Literature and First Report of Direct Umbilical Venous Drainage to the Coronary Sinus

Fetal diagnosis and therapy, 2003-07, Vol.18 (4), p.247-251

2003

Link zum Volltext

Verfügbarkeit prüfen

Cardiovascular abnormalities associated with the Stuve–Wiedemann syndrome

American journal of medical genetics, 2003-08, Vol.121A (2), p.156-158

2003

Link zum Volltext

Verfügbarkeit prüfen

The natriuretic peptides as biomarkers for adults with congenital heart disease

Biomarkers in medicine, 2012-12, Vol.6 (6), p.827-837

2012

Link zum Volltext

Verfügbarkeit prüfen

Symptomatic myocardial bridging in a child without hypertrophic cardiomyopathy

Pediatrics (Evanston), 2006-02, Vol.117 (2), p.e333

2006

Link zum Volltext

Verfügbarkeit prüfen

Left heart obstructive lesions and left ventricular growth in the midtrimester fetus : a longitudinal study

Circulation (New York, N.Y.), 1995-09, Vol.92 (6), p.1531-1538

1995

Link zum Volltext

Verfügbarkeit prüfen

Clinical, echocardiographic and humoral status of patients following repair of tetralogy of Fallot: comparison of the second to the first decade

The Israel Medical Association journal, 2007-12, Vol.9 (12), p.843-846

2007

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 58

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(51)
Mit Volltextzugriff
(51)

Publikationsform

Artikel
(57)
Berichte
(1)

Sprache

Englisch
(58)
Japanisch
(6)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Assessment of Fetal Myocardial Performance Using Myocardial Deformation Analysis

Amino-terminal pro-brain-type natriuretic peptide: heart or lung disease in pediatric respiratory distress?

A human laterality disorder caused by a homozygous deleterious mutation in MMP21

Congenital valvular defects associated with deleterious mutations in the PLD1 gene

A human laterality disorder associated with a homozygous WDR16 deletion

Prevalence of Persistent Superior Vena Cava and Association With Congenital Heart Anomalies

Comparison of N-terminal pro-B-type natriuretic peptide levels in critically ill children with sepsis versus acute left ventricular dysfunction

Intracardiac Echogenic Foci Have No Hemodynamic Significance in the Fetus

Tissue velocity Doppler assessment of atrial and ventricular electromechanical coupling and atrioventricular time intervals in normal subjects

A human laterality disorder associated with recessive CCDC11 mutation

Conotruncal malformations and absent thymus due to a deleterious NKX2-6 mutation

Isolated truncus arteriosus associated with a mutation in the plexin-D1 gene

Prevention of complete heart block in children of mothers with anti-SSA/Ro and anti-SSB/La autoantibodies: detection and treatment of first-degree atrioventricular block

Analysis of Segmental and Global Function of the Fetal Heart Using Novel Automatic Functional Imaging

Twin Pregnancy in a Patient after the Fontan Operation: Report of a Case

N-terminal-proB-type natriuretic peptide as a marker for acute anthracycline cardiotoxicity in children

N-terminal pro-B–type natriuretic peptide levels in acute versus chronic left ventricular dysfunction

Significance of a Cardiac Murmur as the Sole Clinical Sign in the Newborn

Myocardial Infarction Due to Coronary Compression by a Rhabdomyoma

Absent Ductus venosus in the Fetus: Review of the Literature and First Report of Direct Umbilical Venous Drainage to the Coronary Sinus

Cardiovascular abnormalities associated with the Stuve–Wiedemann syndrome

The natriuretic peptides as biomarkers for adults with congenital heart disease

Symptomatic myocardial bridging in a child without hypertrophic cardiomyopathy

Left heart obstructive lesions and left ventricular growth in the midtrimester fetus : a longitudinal study

Clinical, echocardiographic and humoral status of patients following repair of tetralogy of Fallot: comparison of the second to the first decade

Suchergebnisse filtern