The year in human and medical genetics

inborn errors of immunity I

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Last edited by MARC Bot
September 22, 2020 | History

The year in human and medical genetics

inborn errors of immunity I

The genetic dissection of human primary immunodeficiency is expanding at full speed, in at least two directions. Some investigators pursue the dissection of well-known clinical phenotypes, for which the count of genetic etiologies seems to be endless, whereas others begin the search for inborn errors underlying new phenotypes, infectious and otherwise. The field of primary immunodeficiency is also expanding in other ways, with new therapeutic approaches, and with the care of patients in regions of the world where these diseases were unheard of less than a decade ago. The volume provides an overview of the field of medical genetics and its progress in 2011. Volume I opens with a dialog between the volume editors on the definition of "primary immunodeficiencies (PIDs)"; additional papers in this volume focus on PIDs in Latin America, Eastern and Central Europe, North Africa, Turkey, Asia, Iran, and the South Pacific--

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Edition Availability
Cover of: Year in Human and Medical Genetics
Year in Human and Medical Genetics: Inborn Errors of Immunity III
2012, Wiley & Sons, Incorporated, John
in English
Cover of: The year in human and medical genetics
The year in human and medical genetics: inborn errors of immunity I
2011, Published by Blackwell Pub. on behalf of the New York Academy of Sciences
in English

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Book Details


Table of Contents

Definition of primary immunodeficiency in 2011 : a "trialogue" among friends / Mary Ellen Conley, Luigi D. Notarangelo, and Jean-Laurent Casanova
Ten warning signs of primary immunodeficiency : a new paradigm is needed for the 21st century / Peter D. Arkwright and Andrew R. Gennery
Thirty years of primary immunodeficiencies in Turkey / Ozden Sanal and Ilhan Tezcan
The demographics of primary immunodeficiency diseases across the unique ethnic groups in Iran, and approaches to diagnosis and treatment / Nima Rezaei, Payam Mohammadinejad, and Asghar Aghamohammadi
Improving care, education, and research : the Asian primary immunodeficiency network / Pamela Pui-Wah Lee and Yu-Lung Lau
Primary immunodeficiencies in highly consanguineous North African populations / Mohamed-Ridha Barbouche ... [et al.]
Primary immune deficiency disorders in the South Pacific : the clinical utility of a customized genetic testing program in New Zealand / Rohan Ameratunga ... [et al.]
The creation and progress of the J Project in Eastern and Central Europe / Lá́szló Maródi, the J Project Study Group
Immunodeficiency due to defects in store-operated calcium entry / Stefan Feske
Type I interferonopathies : a novel set of inborn errors of immunity / Yanick J. Crow
Newborn screening for SCID : three years of experience / Nicole M. Chase, James W. Verbsky, and John M. Routes
Familial hemophagocytic lymphohistiocytosis and X-linked lymphoproliferative disease / Rebecca A. Marsh and Alexandra H. Filipovich
Hematopoietic stem cell transplantation for primary immunodeficiency diseases / Mary A. Slatter and Andrew J. Cant
Regulation of mucosal IgA responses : lessons from primary immunodeficiencies / Andrea Cerutti ... [et al.].

Edition Notes

Cover title.

Includes bibliographical references.

Published in
Boston, Mass
Series
Annals of the New York Academy of Sciences -- v. 1238, Annals of the New York Academy of Sciences -- v. 1238.
Other Titles
Inborn errors of immunity I, Inborn errors of immunity one

Classifications

Dewey Decimal Class
616.042
Library of Congress
QR188.35 .Y42 2011, QH431

The Physical Object

Pagination
144 p. :
Number of pages
144

Edition Identifiers

Open Library
OL25292454M
ISBN 10
1573318493
ISBN 13
9781573318495
LCCN
2012392450
OCLC/WorldCat
751856848

Work Identifiers

Work ID
OL16609474W

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