Results 81 to 90 of about 8,104 (203)

Chronic Intestinal Pseudo-Obstruction and Lymphoproliferative Syndrome as a Novel Phenotype Associated With Tetratricopeptide Repeat Domain 7A Deficiency

Frontiers in Immunology, 2019
Mutations in the tetratricopeptide repeat domain 7A (TTC7A) gene cause very early onset inflammatory bowel diseases (VOIBD) or multiple intestinal atresia associated with immune deficiency of various severities, ranging from combined immune deficiency to
Marie-Thérèse El-Daher, Marie-Thérèse El-Daher, Julie Lemale, Julie Bruneau, Julie Bruneau, Claire Leveau, Claire Leveau, Frédéric Guerin, Frédéric Guerin, Nathalie Lambert, Jean-Sébastien Diana, Bénédicte Neven, Fernando E. Sepulveda, Fernando E. Sepulveda, Fernando E. Sepulveda, Aurore Coulomb-L'Hermine, Thierry Molina, Thierry Molina, Capucine Picard, Capucine Picard, Capucine Picard, Alain Fischer, Alain Fischer, Alain Fischer, Geneviève de Saint Basile, Geneviève de Saint Basile, Geneviève de Saint Basile   +26 more
doaj   +1 more source

Extranodal manifestation of Rosai-Dorfman disease with bilateral ocular involvement

Journal of Cytology, 2011
Rosai-Dorfman disease, that is, sinus histiocytosis with massive lymphadenopathy is a benign systemic proliferative disorder of histiocytes. The typical clinical presentation of the disease includes bilateral painless massive lymphadenopathy, fever and ...
Chayanika Kala, Asha Agarwal, Sanjay Kala   +2 more
doaj   +1 more source

Major histocompatibility complex class II hyperexpression on B cells in interleukin 4-transgenic mice does not lead to B cell proliferation and hypergammaglobulinemia.

, 1991
The murine interleukin 4 (IL4)-encoding cDNA expressed under the control of the immunoglobulin heavy chain enhancer/promoter was inserted into the mouse germ line.
Rajewsky, Klaus, Kühn, Ralf, Muller, Werner; id_orcid   +2 more
core   +2 more sources

A VERY RARE RELAPS TYPE IN MULTIPLE MYELOMA: LEPTOMENGEAL AND CRANIAL INVOLVEMENT

Hematology, Transfusion and Cell Therapy
Case report: Multiple myeloma is a hematological malignancy that develops as a result of clonal proliferation of plasma cells and progresses with remissions and relapses.
orhan Ayyildiz, Songul Beskisiz, Abdullah Karakus   +2 more
doaj   +1 more source

hypergammaglobulinemia

Citation: 'hypergammaglobulinemia' in the IUPAC Compendium of Chemical Terminology, 5th ed.; International Union of Pure and Applied Chemistry; 2025. Online version 5.0.0, 2025. 10.1351/goldbook.13237 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms ...
openaire   +1 more source

Cutaneous involvement in angioimmunoblastic T-cell lymphoma

Indian Journal of Dermatology, 2010
Angioimmunoblastic T-cell lymphoma (AITL) is an aggressive non-Hodgkin′s nodal peripheral T-cell lymphoma characterized by general lymphadenopathy, night sweats, fever, hepatosplenomegaly, polyclonal hypergammaglobulinemia, and cutaneous ...
Papadavid Evangelia, Panayiotides Ioannis, Dalamaga Marianna, Katoulis Alexandros, Economopoulos Theofanis, Stavrianeas Nikolaos   +5 more
doaj  

Visceral Leishmaniasis in the Republic of North Macedonia: A Retrospective Cohort Study

Mediterranean Journal of Infection, Microbes and Antimicrobials
Introduction: Visceral leishmaniasis (VL) is a systemic protozoan vector-borne disease and represents the most severe clinical form of leishmaniasis, with fatal outcomes if left untreated. This study aimed to evaluate the key epidemiological, clinical,
Mile Bosilkovski, Bachir Khezzani, Fadil Cana, Kostadin Poposki, Dejan Jakimovski, Jadranka Nikolic, Dajana Georgievska, Marija Dimzova   +7 more
doaj   +1 more source

A Comparison Study of Lymph Node Tuberculosis and Sarcoidosis Involvement to Facilitate Differential Diagnosis and to Establish a Predictive Score for Tuberculosis

Pathogens
Background: Tuberculosis (TB) and sarcoidosis are two common granulomatous diseases involving lymph nodes. Differential diagnosis is not always easy because pathogen demonstration in tuberculosis is not always possible and both diseases share clinical ...
Ellen Hoornaert, Halil Yildiz, Lucie Pothen, Julien De Greef, Olivier Gheysens, Alexandra Kozyreff, Diego Castanares-Zapatero, Jean Cyr Yombi   +7 more
doaj   +1 more source

Efeito dos antioxidantes ascorbato e n-acetil-cisteína associados à terapia antirretroviral em pacientes HIV positivos [PDF]

, 2005
Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciências de Saúde. Programa de Pós-Graduação em FarmáciaA infecção pelo vírus da imunodeficiência humana (HIV) resulta em alterações efetivas e complexas no sistema imunológico ...
Cunha, Joel da
core  

Case Report: two cases of idiopathic plasmacytic lymphadenopathy subtype of idiopathic multicentric Castleman disease with xanthelasma palpebrum from a Canadian center

Frontiers in Hematology
BackgroundIdiopathic plasmacytic lymphadenopathy is a newly recognized subtype of idiopathic multicentric Castleman disease (iMCD-IPL) and often mimics IgG4-related disease (IgG4-RD).
Andrew A. Y. Chen, Vivian T. Yin, Paula Blanco, Mark Trinder, Richard I. Crawford, Richard I. Crawford, Ryan Henrie, Stephen Parkin, Nasreen Khalil, Mollie Carruthers, Lu Zhang, Luke Y. C. Chen, Luke Y. C. Chen   +12 more
doaj   +1 more source