Search Results

TLR8/TLR7 dysregulation due to a novel TLR8 mutation causes severe autoimmune hemolytic anemia and autoinflammation in identical twins.

• Authors : Fejtkova, Martina; Sukova, Martina; Hlozkova, Katerina

• Source: American Journal of Hematology; Mar2022, Vol. 97 Issue 3, p338-351, 14p

Record details

Novel Case of Homozygous Interferon Alpha/Beta Receptor Alpha Chain (IFNAR1) Deficiency With Hemophagocytic Lymphohistiocytosis.

• Authors : Gothe, Florian; Hatton, Catherine F; Truong, Linh

Subjects: HEMOPHAGOCYTIC lymphohistiocytosis; IMMUNIZATION; INFLAMMATION

• Source: Clinical Infectious Diseases; Jan2022, Vol. 74 Issue 1, p136-139, 4p

Record details

Clinical Outcomes, Immunogenicity, and Safety of BNT162b2 Vaccine in Primary Antibody Deficiency

• Authors : Milota, Tomas; Smetanova, Jitka; Skotnicova, Aneta

• Source: The Journal of Allergy and Clinical Immunology: In Practice; January 2023, Vol. 11 Issue: 1 p306-314.e2

Record details

Early-onset pulmonary and cutaneous vasculitis driven by constitutively active SRC-family kinase HCK.

• Authors : Kanderova, Veronika; Svobodova, Tamara; Borna, Simon

• Source: Journal of Allergy & Clinical Immunology; Apr2022, Vol. 149 Issue 4, p1464-1464, 1p

Record details

A Novel Case of Homozygous Interferon Alpha/Beta Receptor Alpha Chain (IFNAR1) Deficiency With Hemophagocytic Lymphohistiocytosis.

• Authors : Gothe F; Immunity and Inflammation Theme, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.; Department of Pediatrics, Dr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-Universität Munich, Munich, Germany.

Subjects: Lymphohistiocytosis, Hemophagocytic*/Lymphohistiocytosis, Hemophagocytic*/Lymphohistiocytosis, Hemophagocytic*/genetics; Homozygote ; Humans

• Source: Clinical infectious diseases : an official publication of the Infectious Diseases Society of America [Clin Infect Dis] 2022 Jan 07; Vol. 74 (1), pp. 136-139.Publisher: Oxford University Press Country of Publication: United States NLM ID: 9203213 Publication Model: Print Cited Medium: Internet ISSN:

Record details

Lymphoproliferation, immunodeficiency and early-onset inflammatory bowel disease associated with a novel mutation in Caspase 8.

• Authors : Kanderova V; Department of Pediatric Hematology and Oncology, 2 Faculty of Medicine, Charles University, and University Hospital Motol, Prague.; Grombirikova H

Subjects: Autoimmune Lymphoproliferative Syndrome*/Autoimmune Lymphoproliferative Syndrome*/Autoimmune Lymphoproliferative Syndrome*/enzymology ; Autoimmune Lymphoproliferative Syndrome*/Autoimmune Lymphoproliferative Syndrome*/Autoimmune Lymphoproliferative Syndrome*/genetics ; Autoimmune Lymphoproliferative Syndrome*/Autoimmune Lymphoproliferative Syndrome*/Autoimmune Lymphoproliferative Syndrome*/pathology

• Source: Haematologica [Haematologica] 2019 Jan; Vol. 104 (1), pp. e32-e34. Date of Electronic Publication: 2018 Oct 18.Publisher: Ferrata Storti Foundation Country of Publication: Italy NLM ID: 0417435 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details