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...

Total anomalous pulmonary venous connection: Influence of heterotaxy and venous obstruction on outcomes

The Journal of thoracic and cardiovascular surgery, 2022-02, Vol.163 (2), p.387-395.e3

2022

Volltextzugriff (PDF)

Fetal heterotaxy: Should we still categorize?

Archives of Cardiovascular Diseases Supplements, 2021-09, Vol.13 (4), p.306-306

2021

Volltextzugriff (PDF)

Long-term survival and phenotypic spectrum in heterotaxy syndrome: A 25-year follow-up experience

International journal of cardiology, 2018-10, Vol.268, p.100-105

2018

Volltextzugriff (PDF)

Commentary: Total anomalous pulmonary venous connection, heterotaxy and pulmonary vein obstruction: The relentless pursuit of imperfection

The Journal of thoracic and cardiovascular surgery, 2022-02, Vol.163 (2), p.397-398

2022

Volltextzugriff (PDF)

Outcomes Of Multistage Palliation Of Infants With Functional Single Ventricle And Heterotaxy Syndrome

The Journal of thoracic and cardiovascular surgery, 2016-05, Vol.151 (5), p.1369-1377.e2

2016

Volltextzugriff (PDF)

Increased mortality, morbidities, and costs after heart transplantation in heterotaxy syndrome and other complex situs arrangements

The Journal of thoracic and cardiovascular surgery, 2019-02, Vol.157 (2), p.730-740.e11

2019

Volltextzugriff (PDF)

Three-Dimensional Modeling Prior to Stage 1 Palliation in a Patient With Heterotaxy Syndrome: Planning for the Future

Circulation. Cardiovascular imaging, 2022-09, Vol.15 (9), p.e014260-e014260

2022

Volltextzugriff (PDF)

Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia

Developmental cell, 2016-09, Vol.38 (5), p.478-492

2016

Volltextzugriff (PDF)

Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis

The Journal of clinical investigation, 2019-07, Vol.129 (7), p.2841-2855

2019

Volltextzugriff (PDF)

Inflammation, Active Fibroplasia, and End-stage Fibrosis in 172 Biliary Atresia Remnants Correlate Poorly With Age at Kasai Portoenterostomy, Visceral Heterotaxy, and Outcome

The American journal of surgical pathology, 2018-12, Vol.42 (12), p.1625-1635

2018

Volltextzugriff (PDF)

Malrotation is not associated with adverse outcomes after cardiac surgery in patients with heterotaxy syndrome

Journal of pediatric surgery, 2018-08, Vol.53 (8), p.1494-1498

2018

Volltextzugriff (PDF)

Interventions on residual lesions in patients with heterotaxy syndrome following orthotropic heart transplantation: A single‐center experience

Pediatric transplantation, 2024-05, Vol.28 (3), p.e14706-n/a

2024

Volltextzugriff (PDF)

Extracardiac anomalies in prenatally diagnosed heterotaxy syndrome

Ultrasound in obstetrics & gynecology, 2016-04, Vol.47 (4), p.443-449

2016

Volltextzugriff (PDF)

Human Heterotaxy Syndrome: From Molecular Genetics to Clinical Features, Management, and Prognosis

Circulation Journal, 2012, Vol.76(9), pp.2066-2075

2012

Volltextzugriff (PDF)

Outcomes After Ladd Procedures for Intestinal Malrotation in Newborns with Heterotaxy Syndrome

Journal of pediatric surgery, 2023-06, Vol.58 (6), p.1095-1100

2023

Volltextzugriff (PDF)

Risk factors for death or heart transplantation in single-ventricle physiology (tricuspid atresia, pulmonary atresia, and heterotaxy): A systematic review and meta-analysis

The Journal of heart and lung transplantation, 2019-07, Vol.38 (7), p.739-747

2019

Volltextzugriff (PDF)

Cardiac surgical outcomes of patients with heterotaxy syndromeCentral MessagePerspective

JTCVS open, 2023-03, Vol.13, p.292-306

2023

Volltextzugriff (PDF)

Abnormalities of Fetal Situs: An Overview and Literature Review

Obstetrical & gynecological survey, 2016-01, Vol.71 (1), p.33-38

2016

Volltextzugriff (PDF)

High Prevalence of Respiratory Ciliary Dysfunction in Congenital Heart Disease Patients With Heterotaxy

Circulation (New York, N.Y.), 2012-05, Vol.125 (18), p.2232-2242

2012

Volltextzugriff (PDF)

A Rare Case of Heterotaxy Syndrome With Left Isomerism

Clinical gastroenterology and hepatology, 2022-02, Vol.20 (2), p.e11-e11

2022

Volltextzugriff (PDF)

Trends in Infant Mortality After TAPVR Repair over 18 Years in Texas and Impact of Hospital Surgical Volume

Pediatric cardiology, 2020, Vol.41 (1), p.77-87

2020

Volltextzugriff (PDF)

Successful biventricular repair in a 14‐year‐old patient of asplenia with congenital heart disease syndrome

Journal of cardiac surgery, 2022-12, Vol.37 (12), p.5626-5629

2022

Volltextzugriff (PDF)

Contemporary Outcomes of Surgical Repair of Total Anomalous Pulmonary Venous Connection in Patients With Heterotaxy Syndrome

The Annals of thoracic surgery, 2015-06, Vol.99 (6), p.2134-2140

2015

Volltextzugriff (PDF)

Loss of ciliary transition zone protein TMEM107 leads to heterotaxy in mice

Developmental biology, 2020-04, Vol.460 (2), p.187-199

2020

Volltextzugriff (PDF)

Predicting Cardiac Anatomy, Physiology, and Surgical Management Based on Fetal Echocardiography in Heterotaxy Syndrome

American journal of perinatology, 2023-07, Vol.40 (10), p.1081-1087

2023

Volltextzugriff (PDF)

1 – 25 von 1.016

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(826)
Mit Volltextzugriff
(852)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

10 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(736)
Life Sciences & Biomedicine
(731)
Humans
(652)
Heterotaxy
(396)
Female
(343)
Cardiac & Cardiovascular Systems
(322)
Cardiovascular System & Cardiology
(322)
Heterotaxy Syndrome
(301)
Male
(285)
Pediatrics
(189)
Infant
(151)
Surgery
(136)
Infant, Newborn
(134)
Congenital Heart Disease
(133)
Child
(128)
Heterotaxy Syndrome - Complications
(123)
Adult
(116)
Child, Preschool
(114)
Heterotaxy Syndrome - Surgery
(114)
Retrospective Studies
(104)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(7)

Menü

Weitere Dienste

Einstellungen

Total anomalous pulmonary venous connection: Influence of heterotaxy and venous obstruction on outcomes

Fetal heterotaxy: Should we still categorize?

Long-term survival and phenotypic spectrum in heterotaxy syndrome: A 25-year follow-up experience

Commentary: Total anomalous pulmonary venous connection, heterotaxy and pulmonary vein obstruction: The relentless pursuit of imperfection

Outcomes Of Multistage Palliation Of Infants With Functional Single Ventricle And Heterotaxy Syndrome

Increased mortality, morbidities, and costs after heart transplantation in heterotaxy syndrome and other complex situs arrangements

Three-Dimensional Modeling Prior to Stage 1 Palliation in a Patient With Heterotaxy Syndrome: Planning for the Future

Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia

Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis

Inflammation, Active Fibroplasia, and End-stage Fibrosis in 172 Biliary Atresia Remnants Correlate Poorly With Age at Kasai Portoenterostomy, Visceral Heterotaxy, and Outcome

Malrotation is not associated with adverse outcomes after cardiac surgery in patients with heterotaxy syndrome

Interventions on residual lesions in patients with heterotaxy syndrome following orthotropic heart transplantation: A single‐center experience

Extracardiac anomalies in prenatally diagnosed heterotaxy syndrome

Human Heterotaxy Syndrome: From Molecular Genetics to Clinical Features, Management, and Prognosis

Outcomes After Ladd Procedures for Intestinal Malrotation in Newborns with Heterotaxy Syndrome

Risk factors for death or heart transplantation in single-ventricle physiology (tricuspid atresia, pulmonary atresia, and heterotaxy): A systematic review and meta-analysis

Cardiac surgical outcomes of patients with heterotaxy syndromeCentral MessagePerspective

Abnormalities of Fetal Situs: An Overview and Literature Review

High Prevalence of Respiratory Ciliary Dysfunction in Congenital Heart Disease Patients With Heterotaxy

A Rare Case of Heterotaxy Syndrome With Left Isomerism

Trends in Infant Mortality After TAPVR Repair over 18 Years in Texas and Impact of Hospital Surgical Volume

Successful biventricular repair in a 14‐year‐old patient of asplenia with congenital heart disease syndrome

Contemporary Outcomes of Surgical Repair of Total Anomalous Pulmonary Venous Connection in Patients With Heterotaxy Syndrome

Loss of ciliary transition zone protein TMEM107 leads to heterotaxy in mice

Predicting Cardiac Anatomy, Physiology, and Surgical Management Based on Fetal Echocardiography in Heterotaxy Syndrome

Suchergebnisse filtern