The diagnostic approach to monogenic very early onset inflammatory bowel disease - Wikidata - wikimedia - TriplyDB

The diagnostic approach to monogenic very early onset inflammatory bowel disease

The diagnostic approach to monogenic very early onset inflammatory bowel disease

http://www.wikidata.org/entity/Q27015077

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Genetics and Therapeutics in Pediatric Ulcerative Colitis: the Past, Present and Future Host-microbiome interaction in Crohn's disease: A familiar or familial issue?Genetic disorders coupled to ROS deficiency Viral Infection of the Central Nervous System Exacerbates Interleukin-10 Receptor Deficiency-Mediated Colitis in SJL Mice Current issues of pediatric inflammatory bowel disease in Korea.Genetics of inflammatory bowel disease from multifactorial to monogenic forms Early-onset autoimmune disease as a manifestation of primary immunodeficiency Early-onset Crohn's disease and autoimmunity associated with a variant in CTLA-4 Recent advances in clinical practice: a systematic review of isolated colonic Crohn's disease: the third IBD?The incidence of Crohn's disease and ulcerative colitis since 1995 in Danish children and adolescents <17 years - based on nationwide registry data.An inflammatory bowel disease-risk variant in INAVA decreases pattern recognition receptor-induced outcomes A Nationwide Study of Severe and Protracted Diarrhoea in Patients with Primary Immunodeficiency Diseases Inflammatory bowel disease in pediatric patients: Characteristics of newly diagnosed patients from the CEDATA-GPGE Registry.Mutations in Plasmalemma Vesicle Associated Protein Result in Sieving Protein-Losing Enteropathy Characterized by Hypoproteinemia, Hypoalbuminemia, and Hypertriglyceridemia Host lysozyme-mediated lysis of Lactococcus lactis facilitates delivery of colitis-attenuating superoxide dismutase to inflamed colons.The diagnostic challenge of very early-onset enterocolitis in an infant with XIAP deficiency Clinical course and outcomes of diagnosing Inflammatory Bowel Disease in children 10 years and under: retrospective cohort study from two tertiary centres in the United Kingdom and in Italy Defects in NADPH Oxidase Genes NOX1 and DUOX2 in Very Early Onset Inflammatory Bowel Disease Maintaining intestinal health: the genetics and immunology of very early onset inflammatory bowel disease.Is Whole Exome Sequencing Clinically Practical in the Management of Pediatric Crohn's Disease?Prevalence of paediatric inflammatory bowel disease in Sweden: a nationwide population-based register study Analysis of the human monocyte-derived macrophage transcriptome and response to lipopolysaccharide provides new insights into genetic aetiology of inflammatory bowel disease.Identifying Mutations of the Tetratricopeptide Repeat Domain 37 (TTC37) Gene in Infants With Intractable Diarrhea and a Comparison of Asian and Non-Asian Phenotype and Genotype: A Global Case-report Study of a Well-Defined Syndrome With Immunodefici Ginseng Berry Extract Attenuates Dextran Sodium Sulfate-Induced Acute and Chronic Colitis.Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease.Is There a Role for the Enteral Administration of Serum-Derived Immunoglobulins in Human Gastrointestinal Disease and Pediatric Critical Care Nutrition?Comprehensive mutation screening for 10 genes in Chinese patients suffering very early onset inflammatory bowel disease.Clinical Pattern of Early-Onset Inflammatory Bowel Disease in Saudi Arabia: A Multicenter National Study Defining the microbial transcriptional response to colitis through integrated host and microbiome profiling Paneth cell defects in Crohn's disease patients promote dysbiosis.Altered pattern of tumor necrosis factor-alpha production in peripheral blood monocytes from Crohn's disease.Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population.Variable outcome in infantile-onset inflammatory bowel disease in an Asian cohort.Resetting microbiota by Lactobacillus reuteri inhibits T reg deficiency-induced autoimmunity via adenosine A2A receptors.Making sense of the cause of Crohn's - a new look at an old disease.The plethora, clinical manifestations and treatment options of autoimmunity in patients with primary immunodeficiency.A Potential Role of Salmonella Infection in the Onset of Inflammatory Bowel Diseases Curcumin and inflammatory bowel disease: potential and limits of innovative treatments.The genetics of Crohn's disease and ulcerative colitis--status quo and beyond.Immune deficiency vs. immune excess in inflammatory bowel diseases-STAT3 as a rheo-STAT of intestinal homeostasis.

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The diagnostic approach to monogenic very early onset inflammatory bowel disease

http://www.wikidata.org/entity/Q27015077

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2014 nî lūn-bûn

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2014 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2014 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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The diagnostic approach to monogenic very early onset inflammatory bowel disease

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The diagnostic approach to monogenic very early onset inflammatory bowel disease

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The diagnostic approach to monogenic very early onset inflammatory bowel disease

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The diagnostic approach to monogenic very early onset inflammatory bowel disease

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The diagnostic approach to monogenic very early onset inflammatory bowel disease

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The diagnostic approach to monogenic very early onset inflammatory bowel disease

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The diagnostic approach to monogenic very early onset inflammatory bowel disease

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The diagnostic approach to monogenic very early onset inflammatory bowel disease

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The diagnostic approach to monogenic very early onset inflammatory bowel disease

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J.GASTRO.2014.07.023

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Gastroenterology

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The diagnostic approach to monogenic very early onset inflammatory bowel disease

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Abdul Elkadri

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Aleixo M. Muise

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Christoph Klein

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Dan Turner

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David C. Wilson

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Jochen Kammermeier

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Jodie Ouahed

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Neil Shah

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Scott B. Snapper

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P2860

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

Defective human interleukin 2 receptor gamma chain in an atypical X chromosome-linked severe combined immunodeficiency with peripheral T cells

Common variants at five new loci associated with early-onset inflammatory bowel disease

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

Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity

Unexplained aplastic anaemia, immunodeficiency, and cerebellar hypoplasia (Hoyeraal-Hreidarsson syndrome) due to mutations in the dyskeratosis congenita gene, DKC1

NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant in NCF2 that results in reduced binding to RAC2

XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome

Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease

Guidelines for investigating causality of sequence variants in human disease

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264201451

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Very early onset inflammatory bowel disease

inflammatory bowel diseases

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