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Biomedical Sciences Immunology. Free Preview. Designed as a practical, awareness-raising guide for the clinician Provides key information relevant to the diagnosis and management of each primary immunodeficiency PID Comprises a series of case-oriented problems drawn from typical patient scenarios Enables prompt recognition of PIDs, thereby helping to avoid delayed diagnosis and its consequences see more benefits.

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FAQ Policy. About this book Primary immunodeficiency diseases PIDs are a heterogeneous group of inherited disorders characterized by different defects in the development and function of the immune system. Show all.

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Show next xx. Primary immunodeficiency diseases : definition, diagnosis, and management by Nima Rezaei 25 editions published between and in English and German and held by WorldCat member libraries worldwide Primary immunodeficiency diseases PIDs are a group of inborn disorders of the immune system, characterized by increased susceptibility to infections, autoimmunity, and cancers.

Although PIDs were previously considered rare conditions, the number of diagnosed cases is growing rapidly, and about different forms of PIDs have already been recognized.


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Nevertheless, because of inadequate medical awareness, misdiagnosis or late diagnosis occurs in a significant number of patients, leading to avoidable morbidity and mortality. The first edition of this practical reference textbook was widely welcomed by scientists and clinicians from around the world.

Clinical Cases in Primary Immunodeficiency Diseases

This new edition has been extensively revised to reflect advances in knowledge and includes various PIDs not previously covered. For each disease, information is provided on definition, etiology, clinical manifestations, diagnosis, and management. Every effort has been made to ensure that, throughout, the text is easy to read and readily comprehensible.

Clinical Cases in Primary Immunodeficiency Diseases A Problem Solving Approach

The book will represent an ideal resource for specialists when engaging in diagnosis, clinical decision-making, and treatment planning. It will also prove invaluable for doctors in training and other physicians and nurses who wish to learn more about PIDs.

Clinical Cases in Primary Immunodeficiency Diseases

Clinical cases in primary immunodeficiency diseases : a problem-solving approach by Asghar Aghamohammadi 15 editions published between and in English and held by WorldCat member libraries worldwide Recurrent infections -- Combined T- and B-cell immunodeficiencies -- Primary Antibody Deficiencies -- Disorders of Phagocytic Cells -- Immune dysregulation diseases -- Defects in Innate immunity: Receptors and Signaling Components -- Autoinflammatory disorders -- Complement deficiencies -- Other well-defined immunodeficiency syndromes.

Role of apoptosis in common variable immunodeficiency and selective immunoglobulin A deficiency 1 edition published in in English and held by 1 WorldCat member library worldwide Highlights: B and T-cells from CVID patients undergo increased spontaneous apoptosis.

Both diseases share clinical manifestation and molecular defects. Elevated apoptosis in this disorder leads to defective long-term survival of B-cells, reduced antibody production, decreased lymphocyte proliferation and defective cytokine secretion.

Background

Evaluation of infectious and non-infectious complications in patients with primary immunodeficiency 1 edition published in in English and held by 1 WorldCat member library worldwide. The patients have a variety of clinical symptoms including hypogammaglobulinemia, recurrent infections, autoimmunity, and enteropathy.

destmondsinmo.tk For all patients, demographic information, clinical records, laboratory, and molecular data were collected. Result: Hypogammaglobulinemia was reported in 14