Results 71 to 80 of about 4,202 (211)

Development of multiple gallstones in a child with lipopolysaccharide-responsive beige-like anchor protein mutation

Central European Journal of Immunology, 2019
A defect in the lipopolysaccharide-responsive beige-like anchor protein (LRBA) gene is a newly defined rare cause of primary immunodeficiency diseases, which manifests as immune dysregulation and humoral immune deficiency.
Şeyhan Kutluǧ, Kaan Boztuǧ, Alişan Yıldıran   +2 more
doaj   +1 more source

Thymic Carcinoma Associated with Cerebellar Degeneration [PDF]

, 2017
We present the case of a 57-year-old man with ataxia and clinical and radiological features of cerebellar degeneration. A computed tomography showed a mediastinal mass. The patient was diagnosed of thymic carcinoma. paraneoplastic cerebellar degeneration
García Cuartero, Irene, García del Pozo, Julián Solís, Pérez Pinar, Montserrat, Rodríguez Galdeano, Mónica   +3 more
core   +2 more sources

Risk of persistent hypogammaglobulinaemia in children with autoimmune bullous dermatoses treated with rituximab

Journal of the European Academy of Dermatology and Venereology, EarlyView.
S. Benkimoun, A. Welfringer‐Morin, V. Barlogis, R. Gravier Dumonceau, E. Bourrat, C. Chiaverini, C. Léauté‐Labrèze, P. Joly, B. Tedbirt, A.‐C. Bursztejn, G. Font, C. Bodemer, M.‐A. Richard, S. Mallet, Groupe Bulles of the French Society of Dermatology; Clinical Research Group of the French Society of Pediatric Dermatology   +14 more
wiley   +1 more source

The effect of plasma donation frequency on total serum protein, immunoglobulin G and donor safety: A non‐inferiority randomized controlled trial

Vox Sanguinis, Volume 120, Issue 12, Page 1205-1215, December 2025.
Abstract Background and Objectives The safety of varying plasma donation frequencies remains unclear. This non‐inferiority randomized controlled trial investigated the effect of plasma donation frequency on total serum protein (TSP), immunoglobulin G (IgG) concentrations, additional biomarkers, adverse events (AEs) and psychological distress. Materials
Morten Haugen, Lise Sofie Haug Nissen‐Meyer, Tor A. Strand, Karin Magnussen   +3 more
wiley   +1 more source

Diffuse large B-cell lymphoma chemotherapy reveals a combined immunodeficiency syndrome in cartilage hair hypoplasia

Swiss Medical Weekly, 2018
Cartilage hair hypoplasia (CHH) is a rare autosomal recessive ribosomopathy characterised by skeletal and integumentary system manifestations. It may also present with varied forms and intensities of haematopoietic and/or immune disorders.
Alexandre Nguyen, Nicolas Martin-Silva, Hubert de Boysson, Damaj Gandhi, Achille Aouba   +4 more
doaj   +1 more source

Common variable immunodeficiency with granulomatous-lymphocytic interstitial lung disease and preceding neurological involvement: a case-report

BMC Pulmonary Medicine, 2020
Background Common variable immunodeficiency (CVID) is a group of heterogeneous primary immunodeficiencies characterised by a dysregulated and impaired immune response.
Jake E. Cowen, James Stevenson, Madhusudan Paravasthu, James Darroch, Anu Jacob, Salaheddin Tueger, John R. Gosney, Anneliese Simons, Lisa G. Spencer, Eoin P. Judge   +9 more
doaj   +1 more source

DiGeorge syndrome presenting as hypocalcaemia-induced seizures in adulthood [PDF]

, 2013
Introduction. DiGeorge syndrome is a developmental defect commonly caused by a microdeletion on the long arm of chromosome 22 or less frequently by a deletion of the short arm of chromosome 10.
Attard, Alex, Grech Marguerat, Deborah, Psaila, Josephine, Zammit, Adrian   +3 more
core   +3 more sources

Oral lichenoid lesions in CTLA‐4 haploinsufficiency: Targeting IFN‐γ‐driven mucosal immunopathology

Journal of the European Academy of Dermatology and Venereology, EarlyView.
Chen Wang, Laurie Brenchley, Teresa Greenwell‐Wild, Vasileios Ionas Theofilou, Timothy G. Myers, Chi A. Ma, Katherine Howe, Stefania Pittaluga, Steven M. Holland, Niki M. Moutsopoulos, David Fraser, Gulbu Uzel   +11 more
wiley   +1 more source

Outcomes following exposure to drug interactions with ibrutinib in patients with chronic lymphocytic leukaemia

British Journal of Haematology, Volume 207, Issue 5, Page 1893-1901, November 2025.
Summary Ibrutinib is metabolized by cytochrome P450 3A (CYP3A) and poses challenges with drug interactions. We conducted a population‐based cohort study of Ontario residents aged ≥66 years who initiated ibrutinib for chronic lymphocytic leukaemia (CLL) to evaluate the frequency of potential drug interactions involving moderate/strong CYP3A inhibitors ...
Tuan Hoang, Matthew C. Cheung, David N. Juurlink, Kelvin K. W. Chan, Cindy Lau, Ning Liu, Husam Abdel‐Qadir, Anca Prica, Annette E. Hay, Abi Vijenthira, Lee Mozessohn   +10 more
wiley   +1 more source

Humoral immune response to filarial antigens in chyluria [PDF]

, 1984
Humoral immune parameters like total immunoglobulins and specific antibody levels in serum were studied in filarial chyluria patients. Mean serum IgG was significantly reduced in this group compared to normal controls, while IgA and IgM levels ...
A. Date, A. Raja, A. Tandon, A. Voller, Alamelu Raja, D. Rowe, J. Takahashi, K. J. Turner, K. Mehta, K. Saha, O. H. Lowry, P. R. Narayanan, P. R. Narayanan, R. G. Hamilton, R. Hussain, R. Prabhakar, R. S. Desowitz, R. S. Paranjape, Rabia Hussain, S. Dissanayake, W. Strober   +20 more
core   +1 more source