Results 91 to 100 of about 19,833 (230)

Rituximab and hypogammaglobulinemia [PDF]

, 2015
El rituximab (RTX), un anticuerpo quimérico anti-CD20 que induce la depleción de linfocitos B, es utilizado para el tratamiento de enfermedades linfoproliferativas y autoinmunes.
Fernández Romero, Diego S., Juri, María Cristina, Larrauri, Blas J., Malbran, Eloisa, Malbrán, Alejandro, Torre, María Gabriela   +5 more
core  

TACI mutations and impaired B-cell function in subjects with CVID and healthy heterozygotes [PDF]

, 2012
Mutations in the gene coding for the transmembrane activator and calcium-modulating cyclophilin ligand interactor (TACI) are found in 8% to 10% of subjects with common variable immunodeficiency (CVID).
Bonhomme, Bossen, Castigli, Castigli, Chapel, Chinen, Cunningham-Rundles, Garibyan, Goldacker, Grimbacher, He, Hymowitz, Ingold, Kaur, Kuijpers, Lee, Lee, Mackay, Martinez-Pomar, Ochtrop, Orange, Pan-Hammarström, Resnick, Salzer, Salzer, Schneider, Schroeder, Thiel, van Zelm, van Zelm, Vorechovsky, Warnatz, Warnatz, Zhang   +33 more
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Hypogammaglobulinemia and Poor Performance Status are Predisposing Factors for Vancomycin-Resistant Enterococcus Colonization in Patients with Hematological Malignancies

Turkish Journal of Hematology, 2017
Objective: Vancomycin-resistant enterococci (VRE) are common pathogens of hospital-acquired infection. Long hospitalization periods, use of broadspectrum antibiotics, and immunosuppression are major risks for VRE colonization.
Elif Gülsüm Ümit, Figen Kuloglu, Ahmet Muzaffer Demir   +2 more
doaj   +1 more source

Cytomegalovirus infection does not impact on survival or time to first treatment in patients with chronic lymphocytic leukemia [PDF]

, 2016
Human cytomegalovirus (HCMV) is a widely prevalent herpes virus which establishes a state of chronic infection. The establishment of CMV‐specific immunity controls viral reactivation and leads to the accumulation of very large numbers of virus‐specific T
Adami, Bate, Callea, Cannon, Chidrawar, Derhovanessian, Dewald, Dollard, Elmaagacli, Forconi, Hadrup, Hecker, Ito, Jelinek, Katrinakis, Kilgour, Lopo, Mackus, Nunes, Olsson, Pachnio, Parry, Pourgheysari, Riches, Roberts, Savva, Shanafelt, Shanafelt, Slobedman, Steininger, Strandberg, te Raa, Trzonkowski, Trzonkowski, Vanura, Vyse, Weaver, Wikby, Wikby   +38 more
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Noninvasive Urinary Monitoring of Progression in IgA Nephropathy. [PDF]

, 2019
Standard methods for detecting and monitoring of IgA nephropathy (IgAN) have conventionally required kidney biopsies or suffer from poor sensitivity and specificity.
Fervenza, Fernando C, Lafayette, Richard A, Sarwal, Minnie M, Sarwal, Reuben D, Yang, Joshua YC   +4 more
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When Autoimmunity Meets Malignancy: A Rare Case of Concomitant Systemic Lupus and Multiple Myeloma

Clinical Case Reports
The association between systemic lupus erythematosus (SLE) and multiple myeloma (MM) is rare, with fewer than 20 cases reported in the literature, raising questions about the link between chronic immune dysregulation and oncogenesis.
Solohery Jean Noël Ratsimbazafy, Havantsoa Nomena Fandresena Andrianarisambatra, Rajo Païdia Radinasoa, Hitsy Andraina Razafindrazaka, Tahianasoa Randriamampianina, Rija Mikhaël Miandrisoa, Fidiarivony Ralison, Hanta Marie Danielle Vololontiana   +7 more
doaj   +1 more source

The lung in primary immunodeficiencies: new concepts in infection and inflammation [PDF]

, 2018
Immunoglobulin replacement therapy (IGRT) has contributed critically to the management of primary antibody deficiencies (PAD) and the decrease in pneumonia rate.
Baumann, Ulrich, Jolles, Stephen, Routes, John M., Soler-Palacín, Pere, Universitat Autònoma de Barcelona   +4 more
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A Late-Diagnosed Case of Common Variable Immunodeficiency

Ahi Evran Medical Journal
Common Variable Immunodeficiency (CVID) is the most common form of primary immunodeficiency (PID). CVID is characterized by decreased serum immunoglobulin levels, decreased or absent antibody production, and normal or low B-lymphocyte counts.
Coşkun Doğan, Nurhan Kasap, Cihan Örçen   +2 more
doaj   +1 more source

Multisystem disorder associated with a pathogenic variant in CLCN7 in the absence of osteopetrosis

Molecular Genetics & Genomic Medicine
Background We clinically and genetically evaluated a Taiwanese boy presenting with developmental delay, organomegaly, hypogammaglobulinemia and hypopigmentation without osteopetrosis.
Chung‐Lin Lee, Yeun‐Wen Chang, Hsiang‐Yu Lin, Hung‐Chang Lee, Ting‐Chi Yeh, Li‐Ching Fang, Ni‐Chung Lee, Jeng‐Daw Tsai, Shuan‐Pei Lin   +8 more
doaj   +1 more source

Effect of monomeric immunoglobulin G (IgG) on the clearance of soluble aggregates of IgG in man [PDF]

, 1991
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Breedveld, F.C., Cohen, A., Daha, M.R., Es, L.A. van, Evers-Schouten, J.H., Furth, R. van, Halma, C., Meer, J.W.M. van der, Pauwels, E.K.J.   +8 more
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