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Deformation Characteristics of Geomaterials
  • Language: en
  • Pages: 1382

Deformation Characteristics of Geomaterials

  • Type: Book
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  • Published: 2011
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  • Publisher: IOS Press

This book is the international edition of the proceedings of IS-Seoul 2011, the Fifth International Symposium on Deformation Characteristics of Geomaterials, held in Seoul, South Korea, in September 2011.The book includes 7 invited lectures, as well as 158 technical papers selected from the 182 submitted. The symposium explored ideas about the complex load-deformation response in geomaterials, including laboratory methods for small and large strains; anisotropy and localization; time-dependent responses in soils; characteristics of treated, unsaturated, and natural geomaterials; applications in field methods; evaluation of field performance in geotechnical structures; and physical and numeri...

Humoral Primary Immunodeficiencies
  • Language: en
  • Pages: 383

Humoral Primary Immunodeficiencies

  • Type: Book
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  • Published: 2018-12-29
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  • Publisher: Springer

This book presents detailed state of the art knowledge on the humoral primary immunodeficiencies (PIDs), i.e., disorders arising from impaired antibody production due to defects intrinsic to B cells or defective interaction between B and T cells. There is extensive coverage of both basic science discoveries and the latest clinical advances in the field. The book is structured in accordance with the most recent classification of PIDs and also covers updates on the B cell immunological synapse. Readers will find comprehensive, in-depth descriptions of novel humoral PID genes and related clinical applications, mucosal B cells, and the various clinical phenotypes of humoral PIDs. Aspects such as differential diagnosis, clinical management in children and adults, and the role of vaccines are also addressed. The authors are all recognized experts from Europe, Australia, and the United States. Humoral Primary Immunodeficiencies will be of high value for immunologists, pediatricians, rheumatologists, oncologists, internists, and infectious disease specialists and will also be informative for MD and PhD students.

Etiopathogenesis of Systemic Sclerosis: An Update
  • Language: en
  • Pages: 119

Etiopathogenesis of Systemic Sclerosis: An Update

description not available right now.

Immunoglobulin Therapy in the 21st Century: The Dark Side of the Moon
  • Language: en
  • Pages: 126

Immunoglobulin Therapy in the 21st Century: The Dark Side of the Moon

In the early decades since the introduction in the early '80s of immunoglobulin therapy many studies tried to identify which clinical indications might benefit from the therapy, which treatment’s schedules are effective and safe. It is universally accepted that immunoglobulin therapy is a life-saving treatment in patients with PID. The rise of new indications for further different clinical conditions resulted in a steady increase in demand for immunoglobulins. Currently the consumption of immunoglobulin for PID represents a small fraction of the market. In the recent past we have been observing: 1) An increase in the demand for plasma and in the consequent need to increase the number of do...

Autoimmune Vasculitis: Advances in Pathogenesis and Therapies
  • Language: en
  • Pages: 321

Autoimmune Vasculitis: Advances in Pathogenesis and Therapies

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Identifying Novel Inborn Errors of the Immune System
  • Language: en
  • Pages: 91

Identifying Novel Inborn Errors of the Immune System

  • Type: Book
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  • Published: 2017-01-03
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  • Publisher: Springer

In her study Elisabeth Salzer describes three novel monogenic diseases. For CD27 deficiency Elisabeth Salzer describes a large cohort of patients. Although all patients shared the same causative missense mutation, they displayed diverse clinical presentations. In another patient she was able to identify a mutation in PRKCD resulting in a primary immunodeficiency with severe Lupus-like autoimmunity. The patient exhibited increased mRNA levels of IL6. Therefore, treatment with Tocilizumab, a humanized anti-IL-6 receptor monoclonal antibody was suggested. In a family with a history of deaths due to inflammatory bowel disease she identified a missense mutation in IL21. She produced wild type and mutated IL-21 protein and demonstrated a loss of function phenotype. As IL-21 is in clinical trials, she proposed a potentially curative treatment option. These discoveries contributed to the understanding of the multifaceted regulatory mechanisms of the immune system and highlighted essential players in these complex signaling networks.

Autoimmune blistering diseases, volume II
  • Language: en
  • Pages: 372

Autoimmune blistering diseases, volume II

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Autoimmunity, Part B
  • Language: en
  • Pages: 742

Autoimmunity, Part B

The incidence of autoimmune diseases is increasing worldwide, and the search for better management of these diseases and even for a cure is being pursued by scientists from many disciplines. Tools from the areas of genetics, neuroscience, cell biology, virology, and infectious disease are being applied to the problem and are yielding useful results. This is the second volume of a series of four on autoimmunity, and findings related to particular organs, organ systems, and diseases are presented. The focus in Part B is on genetics and advances in treatment. Part A presents new principles in autoimmunity and new diagnostic tools. See Parts C and D for clinical venues in autoimmunity. NOTE: Annals volumes are available for sale as individual books or as a journal. For information on institutional journal subscriptions, please visit www.blackwellpublishing.com/nyas. ACADEMY MEMBERS: Please contact the New York Academy of Sciences directly to place your order (www.nyas.org). Members of the New York Academy of Science receive full-text access to the Annals online and discounts on print volumes. Please visit www.nyas.org/membership/main.asp for more information about becoming a member.

The Journal of Immunology
  • Language: en
  • Pages: 716

The Journal of Immunology

  • Type: Book
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  • Published: 2008-12
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  • Publisher: Unknown

description not available right now.