Results 81 to 90 of about 8,688 (201)

Increased serum BAFF levels in patients with active chronic sarcoidosis correlates with serum hypergammaglobulinemia.

, 2013
(A) Increased serum BAFF levels in active sarcoidosis patients. Scatter plots show the serum BAFF concentrations in 18 healthy donors (healthy), 18 active chronic sarcoidosis patients (active) and 15 inactive sarcoidosis patients (inactive).
Martine Bagot (310513), Anne Saussine (310501), Michel Rybojad (310505), Valérie Dessirier (310510), Fatiha Bouhidel (310511), Abdellatif Tazi (72203), Séverine Feuillet (310504), Anne Bergeron (20268), Armand Bensussan (214677), Anne Janin (187607), Jean-David Bouaziz (310514), Caroline Juillard (310507)   +11 more
core   +1 more source

Antibody to the ligand for CD40 (gp39) inhibits murine AIDS-associated splenomegaly, hypergammaglobulinemia, and immunodeficiency in disease-susceptible C57/BL/6 mice [PDF]

, 1996
Infection of genetically susceptible C57BL/6 mice with the LP-BM5 isolate of murine retroviruses cause profound splenomegaly, hypergammaglobulinemia, lymphadenopathy, and an immunodeficiency syndrome which includes the development of terminal B-cell ...
Laman, J.D., Noelle, R.J., Foy, T.M., Green, K.A., Crassi, K.M., Green, W.R., Schoneveld, A., Strawbridge, R.R.   +7 more
core   +1 more source

Immunodeficiencies with hypergammaglobulinemia: a review [PDF]

LymphoSign Journal, 2015
Primary immunodeficiencies (PID) can present with recurrent infections, autoimmunity, inflammation, or malignancy and each of these conditions can be associated with elevated immunoglobulin. A high level of immunoglobulin G (IgG) is an uncommon finding, especially in pediatrics, and does not rule out primary immunodeficiency.
openaire   +1 more source

A Familial TRAPS Phenotype Masquerading as Autoimmune Disease: The Pitfalls of Polyclonal Hypergammaglobulinemia and Low-Titer ANA in Diagnosis

Autoimmune and autoinflammatory disorders can exhibit significant clinical and immunological overlap, often leading to diagnostic delays and therapeutic misdirection.
G Khellaf, A Benziane
core   +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

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

Enzyme replacement therapy decreases hypergammaglobulinemia in Gaucher's disease

Haematologica, 1998
We report the effects of enzyme replacement therapy in a patient with Gaucher's disease associated with a monoclonal gammopathy. Alglucerase induces a linear decline in immunoglobulin and beta 2-microglobulin levels.
J Deibener, P Kaminsky, C Jacob, B Dousset, M Klein, M Duc   +5 more
doaj  

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

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