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List of works by Jana Pachlopnik Schmid

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 Coll

scientific article published on March 2016

Allergic manifestations as the results of a conditional autoimmune response.

scientific article

Angeborene hämophagozytische Lymphohistiozytose (HLH).

scientific article published on 10 May 2010

Antigen interaction and heat inactivation expose new epitopes on human IgE

scientific article published on 01 December 1998

Causes of low neonatal T-cell receptor excision circles: A systematic review.

scientific article published on 27 March 2017

Conditional Autoantibodies in Urticaria Patients: A Unifying Hypothesis ⬇️

scientific article published on November 1, 2001

Conditional autoimmunity mediated by human natural anti‐FcεRIα autoantibodies? ⬇️

scientific article published on October 1, 2001

Development of new classification criteria for macrophage activation syndrome complicating systemic juvenile idiopathic arthritis.

scientific article

Distinct molecular response patterns of activating STAT3 mutations associate with penetrance of lymphoproliferation and autoimmunity

scientific article published on 23 November 2019

Distinct severity of HLH in both human and murine mutants with complete loss of cytotoxic effector PRF1, RAB27A, and STX11

scientific article published on 16 November 2012

Eosinophilia during Psoriasis Treatment with TNF Antagonists

article

Expert consensus on dynamics of laboratory tests for diagnosis of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis.

scientific article published on 19 January 2016

Febrile ulceronecrotic Mucha-Habermann disease mimicking Kawasaki disease

scientific article published on 09 December 2019

Hemolytic uremic syndrome linked to infectious mononucleosis.

scientific article

Interaction of human IgE with Fc epsilon RI alpha exposes hidden epitopes on IgE

scientific article published on 01 December 1999

Life-Threatening Primary Varicella Zoster Virus Infection With Hemophagocytic Lymphohistiocytosis-Like Disease in GATA2 Haploinsufficiency Accompanied by Expansion of Double Negative T-Lymphocytes

scientific article published on 03 December 2018

MHC-II Deficiency Among Egyptians: Novel Mutations and Unique Phenotypes

scientific article published on 28 August 2018

Maternal Tobacco Smoking and Decreased Leukocytes, Including Dendritic Cells, in Neonates

scientific article published on 01 April 2007

Microangiopathic anemia without thrombocytopenia and kidney disease in a child with diarrhea caused by Shiga toxin-producing Escherichia coli.

scientific article

Modern management of primary T-cell immunodeficiencies.

scientific article published on 03 January 2014

Natural anti-FcepsilonRIalpha autoantibodies isolated from healthy donors and chronic idiopathic urticaria patients reveal a restricted repertoire and autoreactivity on human basophils.

scientific article

Non-lethal fetal toxicity of the angiotensin receptor blocker candesartan

scientific article published on 29 June 2006

Persistent mammalian orthoreovirus, coxsackievirus and adenovirus co-infection in a child with a primary immunodeficiency detected by metagenomic sequencing: a case report.

scientific article published on 11 January 2018

Phenotypic Heterogeneity in RAG-deficient Patients from a Highly Consanguineous Population

scientific article published on 04 November 2018

Premature birth, respiratory distress, intracerebral hemorrhage, and silvery-gray hair: differential diagnosis of the 3 types of Griscelli syndrome

scientific article published on 01 August 2010

Recurrent inflammatory disease caused by a heterozygous mutation in CD48

scientific article published on 13 August 2019

Transient hemophagocytosis with deficient cellular cytotoxicity, monoclonal immunoglobulin M gammopathy, increased T-cell numbers, and hypomorphic NEMO mutation

scientific article published on 24 April 2006

Unusual dermatological presentation and immune phenotype in SCID due to anIL7Rmutation: the value of whole-exome sequencing and the potential benefit of newborn screening

scientific article published on 05 September 2016

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