UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 53

Sortiert nach

CD4 and IL-2 mediated NK cell responses after COVID-19 infection and mRNA vaccination in adults

Immunobiology (1979), 2023-01, Vol.228 (1), p.152304-152304, Article 152304

2023

Volltextzugriff (PDF)

Serum Phosphorus, Serum Bicarbonate, and Renal Function in Relation to Liver CYP1A2 Activity

Diagnostics (Basel), 2023-09, Vol.13 (18), p.2996

2023

Volltextzugriff (PDF)

Advantages of the Meso-Rex Bypass Compared with Portosystemic Shunts in the Management of Extrahepatic Portal Vein Obstruction in Children

Journal of the American College of Surgeons, 2013, Vol.216 (1), p.83-89

2013

Volltextzugriff (PDF)

Spina Bifida Outcome: A 25-Year Prospective

Pediatric neurosurgery, 2001-03, Vol.34 (3), p.114-120

2001

Volltextzugriff (PDF)

Amniotic fluid biomarkers of fetal stress response to cardiac dysfunction in twin-twin transfusion syndrome

American journal of obstetrics and gynecology, 2023-01, Vol.228 (1), p.S397-S397

2023

Volltextzugriff (PDF)

Factors associated with abortion completion among people with a fetus affected with myelomeningocele

American journal of obstetrics and gynecology, 2023-01, Vol.228 (1), p.S244-S245

2023

Volltextzugriff (PDF)

120 Association between distance to fetal treatment center and abortion consideration among people with fetal myelomeningocele

American journal of obstetrics and gynecology, 2024-01, Vol.230 (1), p.S81-S82

2024

Volltextzugriff (PDF)

894 Neighborhood deprivation is not associated with abortion consideration or completion in patients with fetal myelomeningocele

American journal of obstetrics and gynecology, 2024-01, Vol.230 (1), p.S473-S473

2024

Volltextzugriff (PDF)

Magnetic Resonance Imaging: A Personalized Approach to Understanding Fatty Liver Disease

Journal of pediatric gastroenterology and nutrition, 2019-06, Vol.68 (6), p.777-781

2019

Volltextzugriff (PDF)

Magnetic Resonance Imaging

Journal of pediatric gastroenterology and nutrition, 2019-06, Vol.68 (6), p.777-781

2019

Volltextzugriff (PDF)

Cold Exposures in Relation to Dysmenorrhea among Asian and White Women

International journal of environmental research and public health, 2023-12, Vol.21 (1), p.56

2023

Volltextzugriff (PDF)

Tethered cord release: a long-term study in 114 patients

Journal of neurosurgery. Pediatrics, 2009-03, Vol.3 (3), p.181

2009

Volltextzugriff (PDF)

In Children With Nonalcoholic Fatty Liver Disease, Zone 1 Steatosis Is Associated With Advanced Fibrosis

Clinical gastroenterology and hepatology, 2018-03, Vol.16 (3), p.438-446.e1

2018

Volltextzugriff (PDF)

Metabolic profile of children with extrahepatic portal vein obstruction undergoing meso-Rex bypass

The Journal of surgical research, 2018-03, Vol.223, p.109-114

2018

Volltextzugriff (PDF)

Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects

Birth defects research. A Clinical and molecular teratology, 2008-10, Vol.82 (10), p.662-669

2008

Volltextzugriff (PDF)

Exome sequencing of an adolescent with nonalcoholic fatty liver disease identifies a clinically actionable case of Wilson disease

Cold Spring Harbor molecular case studies, 2018-10, Vol.4 (5), p.1

2018

Volltextzugriff (PDF)

Exome sequencing of an adolescent with nonalcoholic fatty liver disease identifies a clinically actionable case of Wilson disease

Cold Spring Harbor molecular case studies, 2018-10, Vol.4 (5), p.a003087

2018

Volltextzugriff (PDF)

Refinement of 2q and 7p loci in a large multiplex NTD family

Birth defects research. A Clinical and molecular teratology, 2008-06, Vol.82 (6), p.441-452

2008

Volltextzugriff (PDF)

Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2

Birth defects research. A Clinical and molecular teratology, 2005-11, Vol.73 (11), p.868-875

2005

Volltextzugriff (PDF)

SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects

Human genetics, 2005-07, Vol.117 (2-3), p.133-142

2005

Volltextzugriff (PDF)

High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35

Birth defects research. A Clinical and molecular teratology, 2006-06, Vol.76 (6), p.499-505

2006

Volltextzugriff (PDF)

Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects

Clinical genetics, 2003-03, Vol.63 (3), p.210-214

2003

Volltextzugriff (PDF)

Disbanding a multidisciplinary clinic: effects on the health care of myelomeningocele patients

Pediatric neurosurgery, 1994, Vol.21 (1), p.36

1994

Volltextzugriff (PDF)

TERC is not a major gene in human neural tube defects

Birth defects research. A Clinical and molecular teratology, 2004-08, Vol.70 (8), p.531-533

2004

Volltextzugriff (PDF)

A Novel Mutation in the Gene Encoding Noggin is Not Causative in Human Neural Tube Defects

Journal of neurogenetics, 2002, Vol.16 (1), p.65-71

2002

Volltextzugriff (PDF)

1 – 25 von 53

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(51)
Mit Volltextzugriff
(49)

Publikationsform

Sprache

Englisch
(53)
Japanisch
(7)

Erscheinungsjahr

n.n

Thema

Science & Technology
(32)
Life Sciences & Biomedicine
(23)
Humans
(18)
Male
(10)
Female
(9)
Biological And Medical Sciences
(7)
Neural Tube Defects
(7)
Medical Sciences
(6)
Science & Technology - Other Topics
(6)
Developmental Biology
(5)
Neural Tube Defects - Genetics
(5)
Physical Sciences
(5)
Toxicology
(5)
Adolescent
(4)
Animals
(4)
Child, Preschool
(4)
Diseases Of The Osteoarticular System
(4)
Multidisciplinary Sciences
(4)
Mutation
(4)
Neurons
(4)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

CD4 and IL-2 mediated NK cell responses after COVID-19 infection and mRNA vaccination in adults

Serum Phosphorus, Serum Bicarbonate, and Renal Function in Relation to Liver CYP1A2 Activity

Advantages of the Meso-Rex Bypass Compared with Portosystemic Shunts in the Management of Extrahepatic Portal Vein Obstruction in Children

Spina Bifida Outcome: A 25-Year Prospective

Amniotic fluid biomarkers of fetal stress response to cardiac dysfunction in twin-twin transfusion syndrome

Factors associated with abortion completion among people with a fetus affected with myelomeningocele

120 Association between distance to fetal treatment center and abortion consideration among people with fetal myelomeningocele

894 Neighborhood deprivation is not associated with abortion consideration or completion in patients with fetal myelomeningocele

Magnetic Resonance Imaging: A Personalized Approach to Understanding Fatty Liver Disease

Magnetic Resonance Imaging

Cold Exposures in Relation to Dysmenorrhea among Asian and White Women

Tethered cord release: a long-term study in 114 patients

In Children With Nonalcoholic Fatty Liver Disease, Zone 1 Steatosis Is Associated With Advanced Fibrosis

Metabolic profile of children with extrahepatic portal vein obstruction undergoing meso-Rex bypass

Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects

Exome sequencing of an adolescent with nonalcoholic fatty liver disease identifies a clinically actionable case of Wilson disease

Exome sequencing of an adolescent with nonalcoholic fatty liver disease identifies a clinically actionable case of Wilson disease

Refinement of 2q and 7p loci in a large multiplex NTD family

Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2

SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects

High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35

Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects

Disbanding a multidisciplinary clinic: effects on the health care of myelomeningocele patients

TERC is not a major gene in human neural tube defects

A Novel Mutation in the Gene Encoding Noggin is Not Causative in Human Neural Tube Defects

Suchergebnisse filtern