Results 201 to 210 of about 109,095 (245)

Neuropsychiatric‐Led Presentation of Late‐Onset Parkin‐Related Parkinson's Disease

Movement Disorders Clinical Practice, EarlyView.
Sarah Fullam, Shane Lyons, Martha Finnegan, Richard Walsh, Sean O'Dowd   +4 more
wiley   +1 more source

Utility of serum cytokine testing to differentiate complicated common variable immunodeficiency in resource limited settings. [PDF]

J Allergy Clin Immunol Glob
Jogdand A, Gilbert KM, Hong JS, Pak AJ, Liu K, Kamau U, Khairnar NV, Ssemaganda HC, DiGiacomo D, Barmettler S, Ong MS, Farmer JR.   +11 more
europepmc   +1 more source

Common Variable Immunodeficiency Clinical Manifestations Are Shaped by Presence and Type of Heterozygous NFKB1 Variants. [PDF]

J Allergy Clin Immunol Pract
Yin J, Hayes KM, Ong MS, Mizgerd JP, Cunningham-Rundles C, Dominguez I, Barmettler S, Farmer JR, Maglione PJ.   +8 more
europepmc   +1 more source

Monogenic Common Variable Immunodeficiency (Mo-CVID) Score for Optimizing the Genetic Diagnosis in Pediatric CVID Cohort. [PDF]

Eur J Immunol
Barbati F, Lodi L, Boscia S, Cortimiglia M, Calistri E, Quaranta F, Maggi L, Mazzoni A, Palterer B, Annunziato F, Azzari C, Ricci S.   +11 more
europepmc   +1 more source

Common Variable Immunodeficiency Disorder: A Decade of Insights from a Cohort of 150 Patients in India and the Use of Machine Learning Algorithms to Predict Severity. [PDF]

J Clin Immunol
Bargir UA, Setia P, Desai M, S C, Dalvi A, Shinde S, Gupta M, Jodhawat N, Jose A, Goriwale M, Yadav RM, Vedpathak D, Temkar L, Shabrish S, Hule G, Gowri V, Taur P, Athavale A, Jijina F, Bhatia S, Shukla A, Kalra M, Sivasankaran M, Balaji S, Jain P, Sharma S, Gangadharan H, Narula G, Sharma R, Kini P, Mangalani M, Zanwar A, Chaudhary H, Chaudhary NK, Khurana U, Bavdekar A, Subramaniam G, Raj R, Saniyal S, Shah N, Petiwala T, Kumar P, Pai V, Bhattad S, Sengupta A, Soneja M, Upase D, Ganapule A, Talukdar I, Madkaikar M.   +49 more
europepmc   +1 more source

The Presentation, Diagnosis, and Management of Autosomal Dominant Common Variable Immunodeficiency Type XII with NFKB1 Mutation and Autoimmune Neutropenia Treated with Allogenic Stem Cell Transplantation. [PDF]

Hematol Rep
Gold M, Kannan C, Schofield A, Rogers A, Weeks CJ, Dontu S, Suchomski J, Ghani N, Doss S, Boccucci J, Zheng M, Keruakous A.   +11 more
europepmc   +1 more source

First‐Trimester Bilateral Choanal Atresia as a Marker of a De Novo Pathogenic KMT2D Variant Associated With BCAHH Syndrome

Prenatal Diagnosis, EarlyView.
Patrik Šimják, Jan Král, Dagmar Rašková, Monika Koudová, David Stejskal   +4 more
wiley   +1 more source

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Common Variable Immunodeficiency

The Indian Journal of Pediatrics, 2016
Common variable immunodeficiency (CVID) is the most common primary immunodeficiency of young adolescents and adults which also affects the children. The disease remains largely under-diagnosed in India and Southeast Asian countries. Although in majority of cases it is sporadic, disease may be inherited in a autosomal recessive pattern and rarely, in ...
Biman, Saikia, Sudhir, Gupta
openaire   +2 more sources

Common variable immunodeficiency

Current Allergy and Asthma Reports, 2001
Common variable immunodeficiency (CVID) is a common primary immnodeficiency disease, the hallmark of which is hypogammaglobulinemia. Due to the lack of antibodies, patients usually have recurrent bacterial infections, but there are a number of other puzzling manifestations, including inflammatory conditions, autoimmune disease, and the development of ...
  +6 more sources

Hepatitis in common variable immunodeficiency

Human Pathology, 2009
Common variable immunodeficiency is an important form of primary immunodeficiency disease. The most recognized histologic manifestation of common variable immunodeficiency is a paucity of plasma cells in gut biopsies. However, chronic inflammation can affect other organs including the liver.
Jason A, Daniels, Michael, Torbenson, Perumal, Vivekanandan, Robert A, Anders, John K, Boitnott   +4 more
openaire   +2 more sources