about
Natural anti-FcepsilonRIalpha autoantibodies isolated from healthy donors and chronic idiopathic urticaria patients reveal a restricted repertoire and autoreactivity on human basophils.Allergic manifestations as the results of a conditional autoimmune response.Hemolytic uremic syndrome linked to infectious mononucleosis.Microangiopathic anemia without thrombocytopenia and kidney disease in a child with diarrhea caused by Shiga toxin-producing Escherichia coli.Expert consensus on dynamics of laboratory tests for diagnosis of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis.Angeborene hämophagozytische Lymphohistiozytose (HLH).Modern management of primary T-cell immunodeficiencies.2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation CollCauses of low neonatal T-cell receptor excision circles: A systematic review.Development of new classification criteria for macrophage activation syndrome complicating systemic juvenile idiopathic arthritis.Persistent mammalian orthoreovirus, coxsackievirus and adenovirus co-infection in a child with a primary immunodeficiency detected by metagenomic sequencing: a case report.Eosinophilia during Psoriasis Treatment with TNF AntagonistsPhenotypic Heterogeneity in RAG-deficient Patients from a Highly Consanguineous PopulationMaternal Tobacco Smoking and Decreased Leukocytes, Including Dendritic Cells, in NeonatesLife-Threatening Primary Varicella Zoster Virus Infection With Hemophagocytic Lymphohistiocytosis-Like Disease in GATA2 Haploinsufficiency Accompanied by Expansion of Double Negative T-LymphocytesUnusual dermatological presentation and immune phenotype in SCID due to anIL7Rmutation: the value of whole-exome sequencing and the potential benefit of newborn screeningInteraction of human IgE with Fc epsilon RI alpha exposes hidden epitopes on IgEAntigen interaction and heat inactivation expose new epitopes on human IgENon-lethal fetal toxicity of the angiotensin receptor blocker candesartanTransient hemophagocytosis with deficient cellular cytotoxicity, monoclonal immunoglobulin M gammopathy, increased T-cell numbers, and hypomorphic NEMO mutationPremature birth, respiratory distress, intracerebral hemorrhage, and silvery-gray hair: differential diagnosis of the 3 types of Griscelli syndromeDistinct severity of HLH in both human and murine mutants with complete loss of cytotoxic effector PRF1, RAB27A, and STX11MHC-II Deficiency Among Egyptians: Novel Mutations and Unique PhenotypesDistinct molecular response patterns of activating STAT3 mutations associate with penetrance of lymphoproliferation and autoimmunityFebrile ulceronecrotic Mucha-Habermann disease mimicking Kawasaki diseaseRecurrent inflammatory disease caused by a heterozygous mutation in CD48
P50
Q30813778-647A974F-3464-4AFB-8AFD-A7C725AF8D17Q30986929-E69A9ABC-B084-4881-80C6-EF3935CF1EFCQ33352812-36A19DF0-157F-4431-86B9-5831CEF8C3BFQ33358593-AC170754-01DA-47DE-895A-9F6718D01DC9Q36517235-493226D6-9659-487A-AD0E-39C26EAE91FAQ37748641-51484BB7-E578-4301-8DB9-E7FC8694DE44Q38175191-76373F4F-2C19-403A-AAA9-D855D00662CEQ38729149-DB48DFF8-8896-479D-8124-66D82ECA34E9Q39209382-E83AC853-2233-4FF8-A847-A93F1673C65EQ45840736-2196BE90-511D-4D8B-A7EA-226B0A1982ABQ47555023-10787532-9111-4595-B76F-5F4FEEB6A115Q56747640-805CAC7F-56E0-4666-883A-7DFFFCBEA75CQ57280244-440EA973-B936-415A-9800-27431E298476Q57661245-3BE2BB9D-0CE6-4940-8E39-E54AF77198A4Q60047530-0EA4543B-78E7-4E8D-B5C0-5825AFC4705DQ62658421-421B0AAC-2454-4885-AB88-725B5A82C99AQ73368529-A1934D66-4DF4-4FE1-825A-817F624ED9E6Q77755700-43DB10E8-6AD5-4459-8F20-DF2195640D18Q79811384-1E06D7AA-C654-4F37-850F-7F8D23927D81Q83195019-2C77BFFC-C961-4F9A-B1C2-EE41A2681BB1Q84596384-B1771C01-B196-49A7-92F2-A13924B287FCQ85474057-E4639992-27DE-4F39-879A-3C66CF105576Q91251139-A19A2CF8-460A-4536-BE6F-E7AE62DD0476Q91465677-CB3819DD-CB0C-4AE2-9126-61A5536C3016Q91785771-F484A5C7-4418-495C-86CA-D573980E1F45Q92662676-BF0875AC-7E49-4E89-90D0-648D6BBA9C6C
P50
description
researcher
@en
wetenschapper
@nl
name
J M Pachlopnik
@en
J M Pachlopnik
@nl
type
label
J M Pachlopnik
@en
J M Pachlopnik
@nl
prefLabel
J M Pachlopnik
@en
J M Pachlopnik
@nl
P106
P31
P496
0000-0002-6653-9047