UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 52

Sortiert nach

Risk Estimation of Gestational Diabetes Mellitus in the First Trimester

The journal of clinical endocrinology and metabolism, 2023-10, Vol.108 (11), p.e1214-e1223

2023

Link zum Volltext

Verfügbarkeit prüfen

Decreased Expression of Placental Proteins in Recurrent Pregnancy Loss: Functional Relevance and Diagnostic Value

International journal of molecular sciences, 2024-02, Vol.25 (3), p.1865

2024

Link zum Volltext

Verfügbarkeit prüfen

An Ultra-Rare Manifestation of an X-Linked Recessive Disorder: Duchenne Muscular Dystrophy in a Female Patient

International journal of molecular sciences, 2022-11, Vol.23 (21), p.13076

2022

Link zum Volltext

Verfügbarkeit prüfen

Case report: Complex evaluation of coagulation, fibrinolysis and inflammatory cytokines in a SARS-CoV-2 infected pregnant woman with fetal loss

Frontiers in immunology, 2024-02, Vol.15, p.1329236

2024

Link zum Volltext

Verfügbarkeit prüfen

Early pathways, biomarkers, and four distinct molecular subclasses of preeclampsia: The intersection of clinical, pathological, and high-dimensional biology studies

Placenta (Eastbourne), 2022-07, Vol.125, p.10-19

2022

Link zum Volltext

Verfügbarkeit prüfen

Analysis of nationwide reflection of rising cesarean section rate in neonatal outcomes of Hungary

The journal of obstetrics and gynaecology research, 2021-02, Vol.47 (2), p.785-791

2021

Link zum Volltext

Verfügbarkeit prüfen

Classification of preeclampsia according to molecular clusters with the goal of achieving personalized prevention

Journal of reproductive immunology, 2024-02, Vol.161, p.104172-104172, Article 104172

2024

Link zum Volltext

Verfügbarkeit prüfen

Interfering effect of maternal cell contamination on invasive prenatal molecular genetic testing

Prenatal diagnosis, 2018-08, Vol.38 (9), p.713-719

2018

Link zum Volltext

Verfügbarkeit prüfen

Large fetal weight alone in Robson-1 parturients doesn’t translate into a risk of Caesarean delivery higher then that of a vaginal birth

European journal of obstetrics & gynecology and reproductive biology, 2019-08, Vol.239, p.7-10

2019

Link zum Volltext

Verfügbarkeit prüfen

Integrated Systems Biology Approach Identifies Novel Maternal and Placental Pathways of Preeclampsia

Frontiers in immunology, 2018-08, Vol.9, p.1661-1661

2018

Link zum Volltext

Verfügbarkeit prüfen

Prenatal diagnosis of the WAS R86H sequence variation in heterozygous twins

Clinical chemistry (Baltimore, Md.), 2006-05, Vol.52 (5), p.901-903

2006

Link zum Volltext

Verfügbarkeit prüfen

Inclusion of sex chromosomes in noninvasive prenatal testing in Asia, Australia, Europe and the USA: A survey study

Prenatal diagnosis, 2023-02, Vol.43 (2), p.144-155

2023

Link zum Volltext

Verfügbarkeit prüfen

Perinatal outcome in grand and great-grand multiparity: Effects of parity on obstetric risk factors

American journal of obstetrics and gynecology, 1999-09, Vol.181 (3), p.669-674

1999

Link zum Volltext

Verfügbarkeit prüfen

Variant type Glanzmann thrombasthenia caused by homozygous p.724R > X mutation in β3 integrin

Thrombosis research, 2010-05, Vol.125 (5), p.427-431

2010

Link zum Volltext

Verfügbarkeit prüfen

Variant type Glanzmann thrombasthenia caused by homozygous p.724R > X mutation in β 3 integrin

Thrombosis research, 2010, Vol.125 (5), p.427-431

2010

Link zum Volltext

Verfügbarkeit prüfen

Screening for preeclampsia in the first trimester of pregnancy in routine clinical practice in Hungary

Journal of biotechnology, 2019-07, Vol.300, p.11-19

2019

Link zum Volltext

Verfügbarkeit prüfen

Characterization of a new disease-causing mutation of SH2D1A in a family with X-linked lymphoproliferative disease

Human mutation, 2005-05, Vol.25 (5), p.506-506

2005

Link zum Volltext

Verfügbarkeit prüfen

Thyroglobulin level at week 16 of pregnancy is superior to urinary iodine concentration in revealing preconceptual and first trimester iodine supply

Maternal and child nutrition, 2018-01, Vol.14 (1), p.n/a

2018

Link zum Volltext

Verfügbarkeit prüfen

Fetal Aortic-cerebral Doppler Resistance Index Ratio: An Indicator of Physiologic Blood Flow Distribution

Donald School journal of ultrasound in obstetrics and gynecology, 2009-09, Vol.3 (3), p.91-96

2009

Link zum Volltext

Verfügbarkeit prüfen

Characterization of a new disease-causing mutation of SH2D1A in a family with X-linked lymphoproliferative disease: MUTATIONS IN BRIEF

Human mutation, 2005-05, Vol.25 (5), p.506-506

2005

Link zum Volltext

Verfügbarkeit prüfen

Measuring expression levels of small regulatory RNA molecules from body fluids and formalin-fixed, paraffin-embedded samples

Methods in molecular biology (Clifton, N.J.), 2014, Vol.1182, p.105

2014

Link zum Volltext

Verfügbarkeit prüfen

Variant type Glanzmann thrombasthenia caused by homozygous p.724R>X mutation in beta3 integrin

Thrombosis research, 2010-05, Vol.125 (5), p.427-431

2010

Link zum Volltext

Verfügbarkeit prüfen

In utero incarceration of congenital diaphragmatic hernia

Journal of pediatric surgery, 2011-03, Vol.46 (3), p.551-553

2011

Link zum Volltext

Verfügbarkeit prüfen

Case report: Complex evaluation of coagulation, fibrinolysis and inflammatory cytokines in a SARS-CoV-2 infected pregnant woman with fetal loss

Frontiers in immunology, 2024, Vol.15, p.1329236-1329236

2024

Link zum Volltext

Verfügbarkeit prüfen

Quality Assurance in Obstetric and Gynecologic Ultrasound: The Hungarian Model

Annals of the New York Academy of Sciences, 1998-06, Vol.847 (1), p.99-102

1998

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 52

Suche als RSS-Feed

Aktive Filter

SpracheUngarisch

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(47)
Mit Volltextzugriff
(50)

Publikationsform

Sprache

Englisch
(52)
Japanisch
(2)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Risk Estimation of Gestational Diabetes Mellitus in the First Trimester

Decreased Expression of Placental Proteins in Recurrent Pregnancy Loss: Functional Relevance and Diagnostic Value

An Ultra-Rare Manifestation of an X-Linked Recessive Disorder: Duchenne Muscular Dystrophy in a Female Patient

Case report: Complex evaluation of coagulation, fibrinolysis and inflammatory cytokines in a SARS-CoV-2 infected pregnant woman with fetal loss

Early pathways, biomarkers, and four distinct molecular subclasses of preeclampsia: The intersection of clinical, pathological, and high-dimensional biology studies

Analysis of nationwide reflection of rising cesarean section rate in neonatal outcomes of Hungary

Classification of preeclampsia according to molecular clusters with the goal of achieving personalized prevention

Interfering effect of maternal cell contamination on invasive prenatal molecular genetic testing

Large fetal weight alone in Robson-1 parturients doesn’t translate into a risk of Caesarean delivery higher then that of a vaginal birth

Integrated Systems Biology Approach Identifies Novel Maternal and Placental Pathways of Preeclampsia

Prenatal diagnosis of the WAS R86H sequence variation in heterozygous twins

Inclusion of sex chromosomes in noninvasive prenatal testing in Asia, Australia, Europe and the USA: A survey study

Perinatal outcome in grand and great-grand multiparity: Effects of parity on obstetric risk factors

Variant type Glanzmann thrombasthenia caused by homozygous p.724R > X mutation in β3 integrin

Variant type Glanzmann thrombasthenia caused by homozygous p.724R > X mutation in β 3 integrin

Screening for preeclampsia in the first trimester of pregnancy in routine clinical practice in Hungary

Characterization of a new disease-causing mutation of SH2D1A in a family with X-linked lymphoproliferative disease

Thyroglobulin level at week 16 of pregnancy is superior to urinary iodine concentration in revealing preconceptual and first trimester iodine supply

Fetal Aortic-cerebral Doppler Resistance Index Ratio: An Indicator of Physiologic Blood Flow Distribution

Characterization of a new disease-causing mutation of SH2D1A in a family with X-linked lymphoproliferative disease: MUTATIONS IN BRIEF

Measuring expression levels of small regulatory RNA molecules from body fluids and formalin-fixed, paraffin-embedded samples

Variant type Glanzmann thrombasthenia caused by homozygous p.724R>X mutation in beta3 integrin

In utero incarceration of congenital diaphragmatic hernia

Case report: Complex evaluation of coagulation, fibrinolysis and inflammatory cytokines in a SARS-CoV-2 infected pregnant woman with fetal loss

Quality Assurance in Obstetric and Gynecologic Ultrasound: The Hungarian Model

Aktive Filter

Suchergebnisse filtern