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Person

Kaan Boztug (1977-)

Arzt

Name	Kaan Boztug
Zeit	1977- (Lebensdaten)
Ort	Eregli, Türkei (Geburtsort) Hannover (2005-2010) (Wirkungsort) Wien (2011-) (Wirkungsort) Türkei Deutschland Österreich
Geschlecht	männlich
Akademischer Grad bzw. Titel	Prof. Dr.
Beruf	Arzt (charakteristischer Beruf) Kinderarzt Hochschullehrer
Variante	K. Boztug
Beziehung	Universitäts-Klinik für Kinder- und Jugendheilkunde (Wien) (2011-) Medizinische Hochschule Hannover (2005-2010) Forschungszentrum für Molekulare Medizin GmbH (2011-)
Quelle	https://www.meduniwien.ac.at/web/ueber-uns/news/2021/news-im-dezember-2021/kaan-boztug-uebernimmt-professur-im-fachbereich-kinderheilkunde-und-entzuendungsforschung/ (Stand: 07.02.2022) https://cemm.at/research/adjunct-pis/kaan-boztug-director-lbi-rud (Stand: 07.02.2022)
Datensatztyp	Person
GND-Nummer	13006985X
Datensatz-ID	13006985X
Beteiligt an alle anzeigen Very-early-onset Inflammatory Bowel Disease in an Infant with a Partial RIPK1 Deletion Rapamycin Controls Lymphoproliferation and Reverses T-Cell Responses in a Patient with a Novel STIM1 Loss-of-Function Deletion A Novel Homozygous Six Base Pair Deletion Found in the NFATC2 Gene in a Patient with EBV-Associated Lymphoproliferation Author Correction: GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway Treatment and management of primary antibody deficiency: German interdisciplinary evidence‐based consensus guideline Novel PGM3 mutation in two siblings with combined immunodeficiency and childhood bullous pemphigoid: a case report and review of the literature Chronische oder schwere Darmerkrankung und Immundefekt: Manchmal ist es doch ein Kolibri Low Density Granulocytes and Dysregulated Neutrophils Driving Autoinflammatory Manifestations in NEMO Deficiency Curation and expansion of human phenotype ontology for defined groups of inborn errors of immunity Distinct prognostic value of different portal hypertension-associated features in patients with primary biliary cholangitis Immunologisch relevante Aspekte der neuen COVID-19-Impfstoffe : Ein Positionspapier der Österreichischen Gesellschaft für Allergologie und Immunologie (ÖGAI) und des Ärzteverbands Deutscher Allergologen (AeDA) Immunologically relevant aspects of the new COVID-19 vaccines—an ÖGAI (Austrian Society for Allergology and Immunology) and AeDA (German Society for Applied Allergology) position paper Genomic Spectrum and Phenotypic Heterogeneity of Human IL-21 Receptor Deficiency Occurrence of autoimmune pancreatitis after chronic immune thrombocytopenia in a Caucasian adolescent Immunologically relevant aspects of the new COVID-19 vaccines—an ÖGAI (Austrian Society for Allergology and Immunology) and AeDA (German Society for Applied Allergology) position paper Treatment and management of primary antibody deficiency: German interdisciplinary evidence‐based consensus guideline Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis Germline biallelic PIK3CG mutations in a multifaceted immunodeficiency with immune dysregulation : : letter to the editor Treatment and management of primary antibody deficiency: German interdisciplinary evidence‐based consensus guideline Unreported Missense Mutation in the Dimerization Domain of ADA2 Leads to ADA2 Deficiency Associated with Severe Oral Ulcers and Neutropenia in a Female Somalian Patient—Addendum to the Genotype-Phenotype Puzzle Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis Publisher correction: Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis CEBPE-mutant specific granule deficiency correlates with aberrant granule organization and substantial proteome alterations in neutrophils Current Understanding and Future Research Priorities in Malignancy Associated With Inborn Errors of Immunity and DNA Repair Disorders: The Perspective of an Interdisciplinary Working Group The Phenotype and Treatment of WIP Deficiency: Literature Synopsis and Review of a Patient With Pre-transplant Serial Donor Lymphocyte Infusions to Eliminate CMV Mutations outside the N-terminal part of RBCK1 may cause polyglucosan body myopathy with immunological dysfunction: expanding the genotype–phenotype spectrum Multiple Presentations of LRBA Deficiency: a Single-Center Experience Variant PIK3R1 Hypermorphic Mutation and Clinical Phenotypes in a Family with Short Statures, Mild Immunodeficiency and Lymphoma Protein Kinase C δ: a Gatekeeper of Immune Homeostasis NF-κB1 Haploinsufficiency Causing Immunodeficiency and EBV-Driven Lymphoproliferation Potentially Beneficial Effect of Hydroxychloroquine in a Patient with a Novel Mutation in Protein Kinase Cδ Deficiency Molekulare Pädiatrie in der postgenomischen Ära : von der molekularen Genetik und Pathophysiologie zu gentherapeutischen Behandlungsstrategien Neuropathological characterization of transgenic mice with astrocyte-directed production of the CXC chemokine ligand 10 = Neuropathologische Charakterisierung eines transgenen Mausmodells mit Produktion des CXC-Chemokinliganden 10 durch Astrozyten

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Katalog der Deutschen Nationalbibliothek

Kaan Boztug (1977-)

Very-early-onset Inflammatory Bowel Disease in an Infant with a Partial RIPK1 Deletion

Rapamycin Controls Lymphoproliferation and Reverses T-Cell Responses in a Patient with a Novel STIM1 Loss-of-Function Deletion

A Novel Homozygous Six Base Pair Deletion Found in the NFATC2 Gene in a Patient with EBV-Associated Lymphoproliferation

Author Correction: GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway

Treatment and management of primary antibody deficiency: German interdisciplinary evidence‐based consensus guideline

Novel PGM3 mutation in two siblings with combined immunodeficiency and childhood bullous pemphigoid: a case report and review of the literature

Chronische oder schwere Darmerkrankung und Immundefekt: Manchmal ist es doch ein Kolibri

Low Density Granulocytes and Dysregulated Neutrophils Driving Autoinflammatory Manifestations in NEMO Deficiency

Curation and expansion of human phenotype ontology for defined groups of inborn errors of immunity

Distinct prognostic value of different portal hypertension-associated features in patients with primary biliary cholangitis

Immunologisch relevante Aspekte der neuen COVID-19-Impfstoffe : Ein Positionspapier der Österreichischen Gesellschaft für Allergologie und Immunologie (ÖGAI) und des Ärzteverbands Deutscher Allergologen (AeDA)

Immunologically relevant aspects of the new COVID-19 vaccines—an ÖGAI (Austrian Society for Allergology and Immunology) and AeDA (German Society for Applied Allergology) position paper

Genomic Spectrum and Phenotypic Heterogeneity of Human IL-21 Receptor Deficiency

Occurrence of autoimmune pancreatitis after chronic immune thrombocytopenia in a Caucasian adolescent

Immunologically relevant aspects of the new COVID-19 vaccines—an ÖGAI (Austrian Society for Allergology and Immunology) and AeDA (German Society for Applied Allergology) position paper

Treatment and management of primary antibody deficiency: German interdisciplinary evidence‐based consensus guideline

Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis

Germline biallelic PIK3CG mutations in a multifaceted immunodeficiency with immune dysregulation : : letter to the editor

Treatment and management of primary antibody deficiency: German interdisciplinary evidence‐based consensus guideline

Unreported Missense Mutation in the Dimerization Domain of ADA2 Leads to ADA2 Deficiency Associated with Severe Oral Ulcers and Neutropenia in a Female Somalian Patient—Addendum to the Genotype-Phenotype Puzzle

Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis

Publisher correction: Human DEF6 deficiency underlies an immunodeficiency syndrome with systemic autoimmunity and aberrant CTLA-4 homeostasis

CEBPE-mutant specific granule deficiency correlates with aberrant granule organization and substantial proteome alterations in neutrophils

Current Understanding and Future Research Priorities in Malignancy Associated With Inborn Errors of Immunity and DNA Repair Disorders: The Perspective of an Interdisciplinary Working Group

The Phenotype and Treatment of WIP Deficiency: Literature Synopsis and Review of a Patient With Pre-transplant Serial Donor Lymphocyte Infusions to Eliminate CMV

Mutations outside the N-terminal part of RBCK1 may cause polyglucosan body myopathy with immunological dysfunction: expanding the genotype–phenotype spectrum

Multiple Presentations of LRBA Deficiency: a Single-Center Experience

Variant PIK3R1 Hypermorphic Mutation and Clinical Phenotypes in a Family with Short Statures, Mild Immunodeficiency and Lymphoma

Protein Kinase C δ: a Gatekeeper of Immune Homeostasis

NF-κB1 Haploinsufficiency Causing Immunodeficiency and EBV-Driven Lymphoproliferation

Potentially Beneficial Effect of Hydroxychloroquine in a Patient with a Novel Mutation in Protein Kinase Cδ Deficiency

Molekulare Pädiatrie in der postgenomischen Ära : von der molekularen Genetik und Pathophysiologie zu gentherapeutischen Behandlungsstrategien

Neuropathological characterization of transgenic mice with astrocyte-directed production of the CXC chemokine ligand 10 = Neuropathologische Charakterisierung eines transgenen Mausmodells mit Produktion des CXC-Chemokinliganden 10 durch Astrozyten