Results 31 to 40 of about 6,848,720 (280)

Interstitial Lung Disease in Common Variable Immunodeficiency

Frontiers in Immunology, 2021
Interstitial lung disease (ILD) is a common complication in patients with common variable immunodeficiency (CVID) and often associated with other features, such as bronchiectasis and autoimmunity.
Joao Pedro Lopes, Joao Pedro Lopes, Hsi-en Ho, Charlotte Cunningham-Rundles   +3 more
doaj   +1 more source

Common variable immunodeficiency - an update [PDF]

Arthritis Research & Therapy, 2012
Common variable immunodeficiency (CVID) describes a heterogeneous subset of hypogammaglobulinemias of unknown etiology. Typically, patients present with recurrent bacterial infections of the respiratory and gastrointestinal tract. A significant proportion of CVID patients develops additional autoimmune, inflammatory or lymphoproliferative complications.
Salzer, Ulrich, Warnatz, Klaus, Peter, Hans-Hartmut   +2 more
openaire   +3 more sources

Common variable immunodeficiency: difficulties in timely diagnosis (clinical case)

, 2022
Common variable immunodeficiency (CVID) belongs to the group of primary immunodeficiencies with a predominant deficiency in antibody synthesis and the most common diagnosis among clinically significant cases of primary immunodeficiency in adults.
Oksana V. Moskalets
core   +1 more source

Screening of functional and positional candidate genes in families with common variable immunodeficiency [PDF]

, 2008
Background: Common variable immunodeficiency (CVID) comprises a heterogeneous group of primary antibody deficiencies with complex clinical and immunological phenotypes.
Grimbacher, B, Thiel, J, Jung, J, Webster, A. David B., Webster, D, Schäffer, Alejandro A., Pan Hammarström, Q, Lougaris, V, Hammarström, L, Salzer, U, Hagena, Tina, Grimbacher, B., Jung, Johannes, Woellner, Cristina, MOSCHESE, VIVIANA, Schaffer, AA, Webster, DA, Birmelin, J, Pan-Hammarström, Qiang, Du, Likun, Schäffer, A, Birmelin, Jennifer, Woellner, C, Neumann, C, Salzer, Ulrich, Metin, A, Lougaris, Vassilios, Plebani, Alessandro, Hagena, T, Grimbacher, Bodo, Pan-Hammarstrom, Q, Du, L, Thiel, Jens, Hammarström, Lennart, Moschese, V, Hammarstroo, L, Metin, Ayse, Plebani, A, Neumann, Carla   +38 more
core   +1 more source

COMMON VARIABLE IMMUNODEFICIENCY AT ADULT AGE [PDF]

, 2021
Common Variable Immunodeficiency (CVID) is a heterogeneous group of diseases progressing with recurrent infections. This disease should be considered in cases experiencing recurrent lung infection, otitis media, rhinosinusitis, and urinary tract ...
Neslihan ÖZÇELİK, Dönmez, Halil, Özyurt, Songül, Ünal ŞAHİN, Şenol, Muzaffer, Özçelik, Neslihan, Halil DÖNMEZ, Aziz GÜMÜŞ, Muzaffer ŞENOL, Songül ÖZYURT, Gümüş, Aziz, Şahin, Ünal   +11 more
core   +1 more source

Autoimmunity in common variable immunodeficiency [PDF]

Current Allergy and Asthma Reports, 2009
Common variable immunodeficiency (CVID) is a primary immunodeficiency that is clinically heterogeneous, characterized by both infectious and noninfectious complications. Although the hallmark of disease presentation is commonly a history of recurrent sinopulmonary infections, autoimmunity and noninfectious inflammatory conditions are increasingly ...
Shradha, Agarwal, Charlotte, Cunningham-Rundles   +1 more
openaire   +4 more sources

Profound Perturbation : Immunopathological Mechanisms in Common Variable Immunodeficiency [PDF]

, 2005
The integrity of all organisms to injury is conserved through intricate mechanisms of response, but none more so than the immune system of the mammals. The complexity and potency of these mechanisms make them both difficult and intriguing to dissect, but
T Ueland, Fevang, Børre, S S Frøland, L Heggelund, A M Holm, P Aukrust, J K Damås, T E Mollnes, B Fevang   +8 more
core   +1 more source

Long-term follow-up and outcome of a large cohort of patients with common variable immunodeficiency

, 2007
Common Variable Immunodeficiency belongs to the group of rare diseases encompassing antibody deficiency syndromes of highly variable clinical presentation and outcome.
Claudio Pignata, Simona Donnanno, Franco Dammacco, A. M. Pesce, Network Within The Ipinet Italian Primary Immunodeficiency, Annarosa Soresina, QUINTI, Isabella, Carlo Agostini, Andrea Guerra, Silvana Martino, Alessandro Plebani, Roberto Rondelli, Giuseppe Spadaro, Federica Borghese   +13 more
core   +2 more sources

Common variable immunodeficiency

Allergologia et Immunopathologia, 2004
We describe a patient with common variable immunodeficiency who three times presented an anaphylactic reaction after intravenous immunoglobulin administration. These reactions were attributed to the total absence of IgG 2, 3 and 4.
L R, de Almeida Barry, W C N, Forte
openaire   +2 more sources

Non-functional immunoglobulin G transcripts in a case of hyper-immunoglobulin M syndrome similar to type 4 [PDF]

, 2004
86% of immunoglobulin G (IgG) heavy-chain gene transcripts were found to be non-functional in the peripheral blood B cells of a patient initially diagnosed with common variable immunodeficiency, who later developed raised IgM, whereas no non-functionally
Darlow, J.M., Farrell, A.M., John M. Darlow, David I. Stott, Stott, D.I., Alex M. Farrell   +5 more
core   +1 more source