UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 421

Sortiert nach

Protein-Losing Enteropathy in Patients With Congenital Heart Disease

Journal of the American College of Cardiology, 2017-06, Vol.69 (24), p.2929-2937

2017

Link zum Volltext

Verfügbarkeit prüfen

Autoimmune Pancreatitis in Children: Characteristic Features, Diagnosis, and Management

The American journal of gastroenterology, 2017-10, Vol.112 (10), p.1604-1611

2017

Link zum Volltext

Verfügbarkeit prüfen

Evaluating the biocontrol potential of Canadian strain Bacillus velezensis 1B-23 via its surfactin production at various pHs and temperatures

BMC biotechnology, 2021-04, Vol.21 (1), p.31-31, Article 31

2021

Link zum Volltext

Verfügbarkeit prüfen

Moyamoya Syndrome Associated with Alagille Syndrome: Outcome after Surgical Revascularization

The Journal of pediatrics, 2015-02, Vol.166 (2), p.470-473

2015

Link zum Volltext

Verfügbarkeit prüfen

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

Nature genetics, 1997-07, Vol.16 (3), p.235-242

1997

Link zum Volltext

Verfügbarkeit prüfen

Incidence of perforation in pediatric GI endoscopy and colonoscopy: an 11-year experience

Gastrointestinal endoscopy, 2013-06, Vol.77 (6), p.960-966

2013

Link zum Volltext

Verfügbarkeit prüfen

Reply: The Need to Define Treatment Goals for Protein-Losing Enteropathy in Fontan Care and Research

Journal of the American College of Cardiology, 2017-11, Vol.70 (20), p.2603-2603

2017

Link zum Volltext

Verfügbarkeit prüfen

Intrahepatic dynamic contrast MR lymphangiography: initial experience with a new technique for the assessment of liver lymphatics

European radiology, 2019-10, Vol.29 (10), p.5190-5196

2019

Link zum Volltext

Verfügbarkeit prüfen

Alagille syndrome mutation update: Comprehensive overview of JAG1 and NOTCH2 mutation frequencies and insight into missense variant classification

Human mutation, 2019-12, Vol.40 (12), p.2197-2220

2019

Link zum Volltext

Verfügbarkeit prüfen

NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway

American journal of human genetics, 2006-07, Vol.79 (1), p.169-173

2006

Link zum Volltext

Verfügbarkeit prüfen

Erratum to: A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case report

BMC gastroenterology, 2015-12, Vol.15 (179), p.179-179, Article 179

2015

Link zum Volltext

Verfügbarkeit prüfen

Severe Eosinophilic Gastroenteritis in a Crohn's Disease Patient Treated With Infliximab and Adalimumab

The American journal of gastroenterology, 2016-03, Vol.111 (3), p.437-438

2016

Link zum Volltext

Verfügbarkeit prüfen

Pathology of Pediatric Gastrointestinal and Liver Disease

Second edition., 2014

Link zum Volltext

Verfügbarkeit prüfen

Bone geometry and microarchitecture deficits in children with Alagille syndrome

Bone (New York, N.Y.), 2020-12, Vol.141, p.115576-115576, Article 115576

2020

Link zum Volltext

Verfügbarkeit prüfen

NOTCH2 mutations in Alagille syndrome

Journal of medical genetics, 2012-02, Vol.49 (2), p.138-144

2012

Link zum Volltext

Verfügbarkeit prüfen

Dynamic Contrast Magnetic Resonance Lymphangiography Localizes Lymphatic Leak to the Duodenum in Protein‐Losing Enteropathy

Journal of pediatric gastroenterology and nutrition, 2022-01, Vol.74 (1), p.38-45

2022

Link zum Volltext

Verfügbarkeit prüfen

Vedolizumab Therapy in Severe Pediatric Inflammatory Bowel Disease

Inflammatory bowel diseases, 2016-10, Vol.22 (10), p.2425-2431

2016

Link zum Volltext

Verfügbarkeit prüfen

Vedolizumab Therapy in Severe Pediatric Inflammatory Bowel Disease

Inflammatory bowel diseases, , Vol.22 (10), p.2425-2431

Link zum Volltext

Verfügbarkeit prüfen

Alagille syndrome and risk for hepatocellular carcinoma: Need for increased surveillance in adults with mild liver phenotypes

American journal of medical genetics. Part A, 2021-03, Vol.185 (3), p.719-731

2021

Link zum Volltext

Verfügbarkeit prüfen

Genome sequencing increases diagnostic yield in clinically diagnosed Alagille syndrome patients with previously negative test results

Genetics in medicine, 2021-02, Vol.23 (2), p.323-330

2021

Link zum Volltext

Verfügbarkeit prüfen

Immune Response to Influenza Vaccine in Pediatric Patients With Inflammatory Bowel Disease

Clinical gastroenterology and hepatology, 2007-07, Vol.5 (7), p.851-856

2007

Link zum Volltext

Verfügbarkeit prüfen

Protein‐elongating mutations in MYH11 are implicated in a dominantly inherited smooth muscle dysmotility syndrome with severe esophageal, gastric, and intestinal disease

Human mutation, 2020-05, Vol.41 (5), p.973-982

2020

Link zum Volltext

Verfügbarkeit prüfen

Recommendations for Diagnosis and Management of Autoimmune Pancreatitis in Childhood: Consensus From INSPPIRE

Journal of pediatric gastroenterology and nutrition, 2018-08, Vol.67 (2), p.232-236

2018

Link zum Volltext

Verfügbarkeit prüfen

Medical Management of Alagille Syndrome

Journal of pediatric gastroenterology and nutrition, 2010-06, Vol.50 (6), p.580-586

2010

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 421

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(305)
Mit Volltextzugriff
(283)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(207)
Life Sciences & Biomedicine
(190)
Humans
(169)
Male
(89)
Pediatrics
(89)
Female
(87)
Biological And Medical Sciences
(74)
Child
(72)
Medical Sciences
(70)
Gastroenterology & Hepatology
(69)
Gastroenterology
(61)
Adolescent
(58)
Child, Preschool
(52)
Adult
(43)
Pathology
(43)
Paediatric Medicine
(42)
Infant
(38)
Alagille Syndrome
(33)
Retrospective Studies
(30)
Gastroenterology. Liver. Pancreas. Abdomen
(29)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

Ingenta
(186)
MEDLINE
(180)
Journals@Ovid Complete
(174)
EZB Electronic Journals Library
(145)
Wiley Online Library
(106)
IngentaConnect Journals
(103)
NUS Single-Journal Subscriptions
(103)
Ebook Central Perpetual and DDA
(91)
eBooks on EBSCOhost
(91)
Elsevier ScienceDirect Journals Complete
(82)
ScienceDirect eBooks
(48)
Wiley Online Library
(44)
Springer Books
(44)
Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
(31)
Nature Journals
(25)
SpringerNature Journals
(24)
Oxford journals
(22)
Oxford Journals 2020 Medicine
(21)
Nexis
(13)
SpringerLINK Contemporary (Konsortium Baden-Württemberg)
(11)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Protein-Losing Enteropathy in Patients With Congenital Heart Disease

Autoimmune Pancreatitis in Children: Characteristic Features, Diagnosis, and Management

Evaluating the biocontrol potential of Canadian strain Bacillus velezensis 1B-23 via its surfactin production at various pHs and temperatures

Moyamoya Syndrome Associated with Alagille Syndrome: Outcome after Surgical Revascularization

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

Incidence of perforation in pediatric GI endoscopy and colonoscopy: an 11-year experience

Reply: The Need to Define Treatment Goals for Protein-Losing Enteropathy in Fontan Care and Research

Intrahepatic dynamic contrast MR lymphangiography: initial experience with a new technique for the assessment of liver lymphatics

Alagille syndrome mutation update: Comprehensive overview of JAG1 and NOTCH2 mutation frequencies and insight into missense variant classification

NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway

Erratum to: A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case report

Severe Eosinophilic Gastroenteritis in a Crohn's Disease Patient Treated With Infliximab and Adalimumab

Pathology of Pediatric Gastrointestinal and Liver Disease

Bone geometry and microarchitecture deficits in children with Alagille syndrome

NOTCH2 mutations in Alagille syndrome

Dynamic Contrast Magnetic Resonance Lymphangiography Localizes Lymphatic Leak to the Duodenum in Protein‐Losing Enteropathy

Vedolizumab Therapy in Severe Pediatric Inflammatory Bowel Disease

Vedolizumab Therapy in Severe Pediatric Inflammatory Bowel Disease

Alagille syndrome and risk for hepatocellular carcinoma: Need for increased surveillance in adults with mild liver phenotypes

Genome sequencing increases diagnostic yield in clinically diagnosed Alagille syndrome patients with previously negative test results

Immune Response to Influenza Vaccine in Pediatric Patients With Inflammatory Bowel Disease

Protein‐elongating mutations in MYH11 are implicated in a dominantly inherited smooth muscle dysmotility syndrome with severe esophageal, gastric, and intestinal disease

Recommendations for Diagnosis and Management of Autoimmune Pancreatitis in Childhood: Consensus From INSPPIRE

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

Medical Management of Alagille Syndrome

Suchergebnisse filtern