The expanding field of secondary antibody deficiency: causes, diagnosis, and management
SY Patel, J Carbone, S Jolles - Frontiers in immunology, 2019 - frontiersin.org
Antibody deficiency or hypogammaglobulinemia can have primary or secondary etiologies.
Primary antibody deficiency (PAD) is the result of intrinsic genetic defects, whereas …
Primary antibody deficiency (PAD) is the result of intrinsic genetic defects, whereas …
Common variable immunodeficiency: epidemiology, pathogenesis, clinical manifestations, diagnosis, classification, and management.
Common variable immunodeficiency (CVID) is a heterogeneous disorder characterized by
hypogammaglobulinemia and increased susceptibility to recurrent bacterial infections. It is …
hypogammaglobulinemia and increased susceptibility to recurrent bacterial infections. It is …
Autoimmunity in common variable immunodeficiency: epidemiology, pathophysiology and management
Introduction: Common variable immunodeficiency (CVID) comprises a large heterogeneous
group of patients with primary antibody deficiency. Areas covered: The affected patients are …
group of patients with primary antibody deficiency. Areas covered: The affected patients are …
[PDF][PDF] T-cell abnormalities in common variable immunodeficiency.
Common variable immunodeficiency (CVID) is the most common clinical primary
immunodeficiency. It is characterized by a defect in B-cell differentiation to plasma and …
immunodeficiency. It is characterized by a defect in B-cell differentiation to plasma and …
Acute abdomen in the immunocompromised patient: WSES, SIS-E, WSIS, AAST, and GAIS guidelines
Immunocompromised patients are a heterogeneous and diffuse category frequently
presenting to the emergency department with acute surgical diseases. Diagnosis and …
presenting to the emergency department with acute surgical diseases. Diagnosis and …
Autoimmune lymphoproliferative syndrome: an overview
DR Matson, DT Yang - Archives of pathology & laboratory …, 2020 - meridian.allenpress.com
Autoimmune lymphoproliferative syndrome (ALPS) is an inherited nonmalignant
lymphoproliferative disorder characterized by heterozygous mutations within the first …
lymphoproliferative disorder characterized by heterozygous mutations within the first …
Epidemiology and pathophysiology of malignancy in common variable immunodeficiency?
Common variable immunodeficiency (CVID) is a diagnostic category of primary
immunodeficiency (PID) which may present with heterogeneous disorders including …
immunodeficiency (PID) which may present with heterogeneous disorders including …
Approach to the management of autoimmunity in primary immunodeficiency
Primary immunodeficiency diseases (PID s) consist of a genetically heterogeneous group of
immune disorders that affect distinct elements of the immune system. PID patients are more …
immune disorders that affect distinct elements of the immune system. PID patients are more …
Mechanisms and management of refractory coeliac disease
T Van Gils, P Nijeboer, RL Van Wanrooij… - Nature reviews …, 2015 - nature.com
A small subset of patients with coeliac disease become refractory to a gluten-free diet with
persistent malabsorption and intestinal villous atrophy. The most common cause of this …
persistent malabsorption and intestinal villous atrophy. The most common cause of this …
Clinical phenotype classification for selective immunoglobulin A deficiency
R Yazdani, AH Latif, F Tabassomi… - Expert review of …, 2015 - Taylor & Francis
Selective immunoglobulin A deficiency (SIgAD) is the most common predominantly antibody
deficiency, with a wide range of presentations from asymptomatic to severe manifestations …
deficiency, with a wide range of presentations from asymptomatic to severe manifestations …