Cargando…

Primary Sjögren's syndrome and high type I interferon signalling in a kindred with C2 deficiency

Detalles Bibliográficos
Autores principales:	Willemsen, Mathijs, Van Nieuwenhove, Erika, Seyed Tabib, Nasim Sadat, Staels, Frederik, Schrijvers, Rik, De Somer, Lien, Liston, Adrian, Humblet-Baron, Stephanie, Wouters, Carine
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2022
Materias:	Letter to the Editor (Case report)
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8969662/ https://www.ncbi.nlm.nih.gov/pubmed/35368972 http://dx.doi.org/10.1093/rap/rkac018

Ejemplares similares

Monogenic Adult-Onset Inborn Errors of Immunity
por: Staels, Frederik, et al.
Publicado: (2021)

Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations
por: Staels, Frederik, et al.
Publicado: (2022)

Adult-Onset ANCA-Associated Vasculitis in SAVI: Extension of the Phenotypic Spectrum, Case Report and Review of the Literature
por: Staels, Frederik, et al.
Publicado: (2020)

A Novel Homozygous Stop Mutation in IL23R Causes Mendelian Susceptibility to Mycobacterial Disease
por: Staels, Frederik, et al.
Publicado: (2022)

Author Correction: Disrupted Ca(2+) homeostasis and immunodeficiency in patients with functional IP(3) receptor subtype 3 defects
por: Neumann, Julika, et al.
Publicado: (2022)

Disrupted Ca(2+) homeostasis and immunodeficiency in patients with functional IP(3) receptor subtype 3 defects
por: Neumann, Julika, et al.
Publicado: (2022)

Case Report: VEXAS Syndrome: From Mild Symptoms to Life-Threatening Macrophage Activation Syndrome
por: Staels, Frederik, et al.
Publicado: (2021)

CTLA4-Ig Effectively Controls Clinical Deterioration and Immune Condition in a Murine Model of Foxp3 Deficiency
por: Gerbaux, Margaux, et al.
Publicado: (2023)

Case report: Myocarditis in congenital STAT1 gain-of function
por: Staels, Frederik, et al.
Publicado: (2023)

Gain-of-function mutation in IFIH1 can cause both aicardi-goutières syndrome and systemic lupus erythematosus with IgA-deficiency
por: Van Eyck, Lien, et al.
Publicado: (2014)

Rituximab and improved nodular regenerative hyperplasia-associated non-cirrhotic liver disease in common variable immunodeficiency: a case report and literature study
por: Roosens, Willem, et al.
Publicado: (2023)

Kindred spirits?
por: Gamson, Joshua
Publicado: (2018)

Total body MRI, a guide to diagnosis in patients with osteo-articular pain and inflammation
por: De Somer, Lien, et al.
Publicado: (2014)

NFIL3 mutations alter immune homeostasis and sensitise for arthritis pathology
por: Schlenner, Susan, et al.
Publicado: (2019)

Evaluation of immune suppressive mechanisms in a murine model of familial hemophagocytic lymphohistiocytosis
por: Humblet-Baron, Stéphanie, et al.
Publicado: (2011)

Gonorrhœa and Kindred Affections
Publicado: (1931)

Bronchitis, and Kindred Diseases
Publicado: (1854)

Bronchitis, and Kindred Diseases
por: Hall, W. W.
Publicado: (1868)

The Audiphone and Kindred Instruments
por: Holmes, E. L.
Publicado: (1880)

Bronchitis, and Kindred Diseases
por: Hall, W. W.
Publicado: (1864)

Bronchitis, and Kindred Diseases
por: Hall, W. W.
Publicado: (1867)

Amalgam and Kindred Poisons
por: Sheffield, Henry
Publicado: (1896)

The Audiphone and Kindred Instruments
por: Holmes, E. L.
Publicado: (1880)

A Narrative Review of the Neurological Manifestations of Human Adenosine Deaminase 2 Deficiency
por: Dzhus, Mariia, et al.
Publicado: (2023)

A companion text for Kindred
por: Giannotti, Janet
Publicado: (1999)

Pseudohypoparathyroidism: phenotypic spectrum in kindred
por: Natino, Antonette A A, et al.
Publicado: (2015)

Treatment of Blenorrhœa and Kindred Affections
Publicado: (1861)

Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia
por: Van Nieuwenhove, Erika, et al.
Publicado: (2020)

The Prevention of Cholera Infantum and Kindred Diseases
por: Vaughan, Victor C.
Publicado: (1887)

Fear and Anxiety—Distinct or “Kindred” Phenomena?
por: Domschke, Katharina
Publicado: (2022)

The Homœopathic Treatment of Rheumatism and Kindred Diseases
Publicado: (1888)

Interferons and Dry Eye in Sjögren’s Syndrome
por: Ogawa, Yoko, et al.
Publicado: (2018)

The accusative with infinitive and some kindred constructions in english
por: Zeitlin, Jacob 1883-
Publicado: (1908)

Importance of Age of Onset in Pancreatic Cancer Kindreds
por: Brune, Kieran A., et al.
Publicado: (2010)

Precautions against Fire in Hospitals and Kindred Institutions
Publicado: (1904)

Familial Creutzfeldt-Jakob Disease in an Indian Kindred
por: Katrak, Sarosh M., et al.
Publicado: (2019)

Clinical Lecture on Conjugal Onanism and Kindred Sins
por: Goodell, William
Publicado: (1872)

Amenorrhea, Dysmenorrhea and Kindred Disorders Treated with Ergoapiol
Publicado: (1901)

Models of Aire-Dependent Gene Regulation for Thymic Negative Selection
por: Danso-Abeam, Dina, et al.
Publicado: (2011)

Dry synovitis, a rare entity distinct from juvenile idiopathic arthritis
por: De Somer, Lien, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_bs7qmsbihik165q1u95k0hai8q