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Author Details
Full Name
Christoph Klein
Affiliation
Kinderklinik und Kinderpoliklinik der Ludwig-Maximilians-Universitat Munchen
ORCID
Career Start Year
1993
Papers
286
H Index
66
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34905786
["Child Life Specialist" Interventions in Clinical Pediatric Care: A Systematic Review of the Effects on Mental Health Outcomes of Children and Adolescents].
Gesundheitswesen
2023
37741518
C-terminal variants in CDC42 drive type I interferon-dependent autoinflammation in NOCARH syndrome reversible by ruxolitinib.
Clin Immunol
2023
37726493
Excellent outcome of stem cell transplantation for sickle cell disease.
Ann Hematol
2023
37351321
Implementing a psychosocial care approach in pediatric inpatient care: process evaluation of the pilot Child Life Specialist program at the University Hospital of Munich, Germany.
Front Pediatr
2023
37153356
<i>DNAH11</i> and a Novel Genetic Variant Associated with Situs Inversus: A Case Report and Review of the Literature.
Case Rep Med
2023
37098531
Transition for adolescents with a rare disease: results of a nationwide German project.
Orphanet J Rare Dis
2023
37228432
Changes in behavior and quality of life in German young children during the COVID-19 pandemic-results from the COVID kids bavaria study.
Front Pediatr
2023
36696755
Hematologically important mutations: Leukocyte adhesion deficiency (second update).
Blood Cells Mol Dis
2023
36853722
Analyzing mitochondrial respiration of human induced pluripotent stem cell-derived myeloid progenitors using Seahorse technology.
STAR Protoc
2023
36515678
Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency.
J Exp Med
2023
36462957
Human MD2 deficiency-an inborn error of immunity with pleiotropic features.
J Allergy Clin Immunol
2023
36462956
Biallelic TLR4 deficiency in humans.
J Allergy Clin Immunol
2023
36370291
Pathogenic Interleukin-10 Receptor Alpha Variants in Humans - Balancing Natural Selection and Clinical Implications.
J Clin Immunol
2023
35996251
Novel <i>DNMT3B</i> Mutation in a Patient with Immunodeficiency, Centromeric Instability, and Facial Anomalies (ICF) Syndrome and a Bronchopulmonary Collateral Artery.
Endocr Metab Immune Disord Drug Targets
2023
36223592
Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes.
Blood
2023
34800919
Combined multimodal ctDNA analysis and radiological imaging for tumor surveillance in Non-small cell lung cancer.
Transl Oncol
2022
35398861
The Mutation of CD27 Deficiency Presented With Familial Hodgkin Lymphoma and a Review of the Literature.
J Pediatr Hematol Oncol
2022
35499078
HAX1-dependent control of mitochondrial proteostasis governs neutrophil granulocyte differentiation.
J Clin Invest
2022
35748970
Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee.
J Clin Immunol
2022
36459971
Optimized human intestinal organoid model reveals interleukin-22-dependency of paneth cell formation.
Cell Stem Cell
2022
36002022
Optimized human intestinal organoid model reveals interleukin-22-dependency of paneth cell formation.
Cell Stem Cell
2022
36198931
The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity.
J Clin Immunol
2022
33560082
A Novel Intronic Mutation Reduces HAX1 Level and is Associated With Severe Congenital Neutropenia.
J Pediatr Hematol Oncol
2022
33634762
Novel Variants of DOCK8 Deficiency in a Case Series of Iranian Patients.
Endocr Metab Immune Disord Drug Targets
2022
33746097
A Systematic Review of Monogenic Inflammatory Bowel Disease.
Clin Gastroenterol Hepatol
2022
35100336
Hematopoietic stem cell transplantation for Wiskott-Aldrich syndrome: an EBMT Inborn Errors Working Party analysis.
Blood
2022
35273242
Valosin-containing protein-regulated endoplasmic reticulum stress causes NOD2-dependent inflammatory responses.
Sci Rep
2022
34964150
Severe congenital neutropenia due to G6PC3 deficiency: Case series of five patients and literature review.
Scand J Immunol
2022
35333544
Gain-of-function <i>IKZF1</i> variants in humans cause immune dysregulation associated with abnormal T/B cell late differentiation.
Sci Immunol
2022
35134932
Novel CD55 Mutation Associated With Severe Small Bowel Ulceration Mimicking Inflammatory Bowel Disease in a Pair of Siblings.
Inflamm Bowel Dis
2022
35105298
A 3-Year-Old Boy with an Xp21 Deletion Syndrome: A Case Report.
Endocr Metab Immune Disord Drug Targets
2022
34987219
Author Correction: Gain-of-function variants in SYK cause immune dysregulation and systemic inflammation in humans and mice.
Nat Genet
2022
34472204
Influence of professional dental hygiene on oral and general health of retirement home residents: A comparative study.
Clin Exp Dent Res
2022
34780721
An Integrated Taxonomy for Monogenic Inflammatory Bowel Disease.
Gastroenterology
2022
32205782
Refractory and Fatal Presentation of Severe Autoimmune Hemolytic Anemia in a Child With the DNASE1L3 Mutation Complicated With an Additional DOCK8 Variant.
J Pediatr Hematol Oncol
2021
33683986
New Findings of Immunodysregulation, Polyendocrinopathy, and Enteropathy X-linked Syndrome (IPEX); Granulomas in Lung and Duodenum.
Pediatr Dev Pathol
2021
33598806
The Ever-Increasing Array of Novel Inborn Errors of Immunity: an Interim Update by the IUIS Committee.
J Clin Immunol
2021
33875794
Correction: Generation and characterization of a novel hematopoietic progenitor cell line with DC differentiation potential.
Leukemia
2021
33512427
Mammalian VPS45 orchestrates trafficking through the endosomal system.
Blood
2021
33504943
Correction: Generation and characterization of a novel hematopoietic progenitor cell line with DC differentiation potential.
Leukemia
2021
33891011
Variants in STXBP3 are Associated with Very Early Onset Inflammatory Bowel Disease, Bilateral Sensorineural Hearing Loss and Immune Dysregulation.
J Crohns Colitis
2021
33804706
Genetic Correction of IL-10RB Deficiency Reconstitutes Anti-Inflammatory Regulation in iPSC-Derived Macrophages.
J Pers Med
2021
33723309
Novel CARMIL2 loss-of-function variants are associated with pediatric inflammatory bowel disease.
Sci Rep
2021
35003119
Rubella Virus Infected Macrophages and Neutrophils Define Patterns of Granulomatous Inflammation in Inborn and Acquired Errors of Immunity.
Front Immunol
2021
34739342
Deficiency in X-linked inhibitor of apoptosis protein promotes susceptibility to microbial triggers of intestinal inflammation.
Sci Immunol
2021
34785797
Publisher Correction: Comprehensive genomic characterization of gene therapy-induced T-cell acute lymphoblastic leukemia.
Leukemia
2021
34486458
Chronic neutropenia: how best to assess severity and approach management?
Expert Rev Hematol
2021
34390440
Genetic Analysis of a Cohort of 275 Patients with Hyper-IgE Syndromes and/or Chronic Mucocutaneous Candidiasis.
J Clin Immunol
2021
34772435
An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Federal Joint Committee.
Orphanet J Rare Dis
2021
34386911
NBAS Variants Are Associated with Quantitative and Qualitative NK and B Cell Deficiency.
J Clin Immunol
2021
1 - 50 of 286
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Co-authored papers
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Eric E Schadt
Icahn School of Medicine at Mount Sinai
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Gerhard Kindle
Center for Chronic Immunodeficiency (CCI), Medical Center, University of Freiburg
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Matthias Griese
University of Munich, German Center for Lung Research (DZL)
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Maximilian Hastreiter
Dr. von Hauner Children's Hospital
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Joshua D Milner
Columbia University
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William A Gahl
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