Global systematic review of primary immunodeficiency registries

H Abolhassani, G Azizi, L Sharifi… - Expert review of …, 2020 - Taylor & Francis
Introduction During the last 4 decades, registration of patients with primary
immunodeficiencies (PID) has played an essential role in different aspects of these diseases …

Gene therapy on the move

KB Kaufmann, H Büning, A Galy… - EMBO molecular …, 2013 - embopress.org
The first gene therapy clinical trials were initiated more than two decades ago. In the early
days, gene therapy shared the fate of many experimental medicine approaches and was …

How I treat common variable immune deficiency

C Cunningham-Rundles - Blood, The Journal of the American …, 2010 - ashpublications.org
Common variable immunodeficiency is a rare immune deficiency, characterized by low
levels of serum immunoglobulin G, A, and/or M with loss of antibody production. The …

The enteropathy associated with common variable immunodeficiency: the delineated frontiers with celiac disease

G Malamut, V Verkarre, F Suarez… - Official journal of the …, 2010 - journals.lww.com
OBJECTIVES: The enteropathy associated with common variable immunodeficiency (CVID)
is poorly characterized, and its possible relationships with well-defined causes of …

Clinical features that identify children with primary immunodeficiency diseases

A Subbarayan, G Colarusso, SM Hughes… - …, 2011 - publications.aap.org
BACKGROUND: The 10 warning signs of primary immunodeficiency diseases (PID) have
been promoted by various organizations in Europe and the United States to predict PID …

Use of combination chemotherapy for treatment of granulomatous and lymphocytic interstitial lung disease (GLILD) in patients with common variable …

NM Chase, JW Verbsky, MK Hintermeyer… - Journal of clinical …, 2013 - Springer
Purpose A subset of patients with common variable immunodeficiency (CVID) develops
granulomatous and lymphocytic interstitial lung disease (GLILD), a restrictive lung disease …

The hyper IgM syndromes: Epidemiology, pathogenesis, clinical manifestations, diagnosis and management

R Yazdani, S Fekrvand, S Shahkarami, G Azizi… - Clinical …, 2019 - Elsevier
Abstract Hyper Immunoglobulin M syndrome (HIGM) is a rare primary immunodeficiency
disorder characterized by low or absent levels of serum IgG, IgA, IgE and normal or …

When to initiate immunoglobulin replacement therapy (IGRT) in antibody deficiency: a practical approach

S Jolles, H Chapel, J Litzman - Clinical & Experimental …, 2017 - academic.oup.com
Primary antibody deficiencies (PAD) constitute the majority of all primary immunodeficiency
diseases (PID) and immunoglobulin replacement forms the mainstay of therapy for many …

“A rose is a rose is a rose,” but CVID is not CVID: common variable immune deficiency (CVID), what do we know in 2011?

PFK Yong, JED Thaventhiran, B Grimbacher - Advances in immunology, 2011 - Elsevier
Common variable immune deficiency (CVID) is the commonest symptomatic primary
immunodeficiency and represents a heterogenous collection of disorders resulting mostly in …

Prevalence and morbidity of primary immunodeficiency diseases, United States 2001–2007

L Kobrynski, RW Powell, S Bowen - Journal of clinical immunology, 2014 - Springer
Purpose Few studies have estimated population prevalence and morbidity of primary
immunodeficiency diseases (PIDD). We used administrative healthcare databases to …