Results 101 to 110 of about 7,183,098 (196)

Intravenous immunoglobulin (IVIG) efficiency in women with common variable immunodeficiency (CVID) decreases significantly during pregnancy

, 2018
Immunoglobulin replacement therapy, including intravenous immunoglobulin (IVIG), is essential for pregnant women with common variable immunodeficiency (CVID) since it prevents infection and improves the health of the newborn.
Kohsuke Imai (5060816), Makiko Egawa (5461937), Hirokazu Kanegane (5461934), Naoyuki Miyasaka (3692545), Tomohiro Morio (200076)   +4 more
core   +1 more source

Analysis of rare genetic variants in All of Us cohort patients with common variable immunodeficiency

Frontiers in Genetics
Common variable immunodeficiency (CVID) is a group of genetic disorders involving more than a dozen genetic loci and characterized by a deficiency in specific antibody isotypes leading to poor immune responses and recurrent infection.
Troy von Beck, Meera Patel, Niraj C. Patel, Joshy Jacob   +3 more
doaj   +1 more source

Management of common variable immunodeficiency by subcutaneous IgG self‐administration during pregnancy – a case report

Clinical Case Reports, 2017
Key Clinical Message Patients with common variable immunodeficiency are prone to infections, and this poses a particular challenge during pregnancy, when the requirement for immunoglobulin (Ig) replacement therapy is even more demanding so as to achieve ...
Carolina Marasco, Alberta Venturelli, Luigia Rao, Angelo Vacca, Maria Rosaria Carratù   +4 more
doaj   +1 more source

A Broad Spectrum of Liver Manifestations in Common Variable Immunodeficiency Syndrome—Two Case Reports and a Literature Overview

Diagnostics
Background and Clinical Significance: Common variable immunodeficiency (CVID) is a primary B-cell immunodeficiency disorder, characterized by severe hypogammaglobulinemia and disturbed antibody production.
Eva Supovec, Jan Drnovšek
doaj   +1 more source

The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID). [PDF]

Sci Rep, 2021
Bisgin A, Sonmezler O, Boga I, Yilmaz M.
europepmc   +1 more source

Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients.

, 2013
Splenectomy has been used in patients with common variable immunodeficiency disorders (CVID), mainly in the context of refractory autoimmune cytopenia and suspected lymphoma, but there are understandable concerns about the potential of compounding an ...
LOUGARIS, Vassilios, Alecsandru D, Vidaller A, Schmidt RE, Grimbacher B, Baumann U, Contreras R, Ibrahim MA, Jones A, Martini H, Hammarstrom L, Chapel H, Wong GK, Lucas M, Clinical Working Party of the European Society for Immunodeficiencies, Kutukculer N, Ernst D, Litzman J, McEwen D, Winterhalter C, Gonzalez Granado LI, Quinti I, Carbone J, Goldacker S, Warnatz K, Gaspar HB, PLEBANI, Alessandro, Kiani Alikhan S, Fernandez Cruz E, Espanol T, Huissoon AP   +30 more
core  

Relapsing polychondritis in a child with common variable immunodeficiency

, 2009
Common variable immunodeficiency (CVID) is associated with recurrent infections and autoimmunity. The most common autoimmune conditions are idiopathic thrombocytopenic purpura, autoimmune hemolytic anemia, chronic arthritis, and gastrointestinal ...
Gulez, Nesrin, Yildiz, Basak, Kutukculer, Necil, Turk, Bengu, Dereli, Tugrul, Karaca, Neslihan Edeer, Aksu, Guzide   +6 more
core   +1 more source

The Genetic Heterogeneity of Common Variable Immunodeficiency (CVID): An Update

Journal of Vaccines & Vaccination, 2014
B cells are generated in the bone marrow and then enter the periphery, where the maturation process takes place leading to the formation of an effective humoral immune response. Defects in this highly regulated process in the periphery have been considered to be responsible for the pathogenesis of Common Variable Immunodeficiency (CVID) for more than 6
openaire   +1 more source

Common variable immunodeficiency-associated heterozygous transcription factor 3 (TCF3) gene mutations in two pediatric cases

Common variable immunodeficiency (CVID) is one of the predominant antibody deficiencies and the most common symptomatic inborn error of immunity (IEI). However, in most cases, the genetic background of the disease cannot be identified.
Ümmügülsüm Dikici, Öner Özdemir, Murat Hakkı Yarar   +2 more
core   +1 more source

Investigating serum free light chains in patients with common variable immunodeficiency disorder in compare with other immunodeficiency diseases

Scientific Reports
Serum free light chains (sFLCs) have recently been introduced as a diagnostic biomarker in common variable immunodeficiency (CVID) patients. Most patients with CVID have undetectable or lower levels of sFLCs compared to people with other types of immune ...
Mohammad Hassan Bemanian, Majid Khoshmirsafa, Mina Ahmadi, Mohamad Nabavi, Saba Arshi, Zahra Chavoshzadeh, Sima Shokri, Morteza Fallahpour, Negin Jafariaghdam, Fatemeh Afrashteh, Samane Asefi, Mehrnaz Mesdaghi, Samin Sharafian   +12 more
doaj   +1 more source