Prevention Of Thalassaemias And Other Haemoglobin Disorders
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Prevention Of Thalassaemias And Other Haemoglobin Disorders
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Author : Galanello Renzo
language : en
Publisher:
Release Date : 2003
Prevention Of Thalassaemias And Other Haemoglobin Disorders written by Galanello Renzo and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2003 with categories.
Volume 1 of the Prevention Book presents the principles of a programme for the prevention of the thalassaemia and other haemoglobin disorders, including a description of the various types of disorders requiring prenatal diagnosis, the strategies used for carrier screening, and a number of annexes listing upto date epidemiological and mutation data on thalassaemia. This book was written for use in combination with Volume 2, which describes many of the laboratory protocols in great detail.
The Thalassaemia Syndromes
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Author : David J. Weatherall
language : en
Publisher: John Wiley & Sons
Release Date : 2008-04-30
The Thalassaemia Syndromes written by David J. Weatherall and has been published by John Wiley & Sons this book supported file pdf, txt, epub, kindle and other format this book has been release on 2008-04-30 with Medical categories.
In the new edition of this successful and authoritative book, the thalassaemias are reviewed in detail with respect to their clinical features, cellular pathology, molecular genetics, prevention and treatment. It is aimed at specialists in haematology in the laboratory or clinical setting, particularly in areas where thalassaemia is common either in the native population or in immigrant communities. The fourth edition has been both updated and re-organized. Three new chapters have been added on the link between alpha-thalassaemia and mental retardation, on avoidance and population control and on global epidemiology. Considerable emphasis is placed on molecular pathology reflecting the huge burst of information to have come out of this field in the last few years.
Newborn Screening For Sickle Cell Disease And Other Haemoglobinopathies
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Author : Stephan Lobitz
language : en
Publisher: MDPI
Release Date : 2019-10-07
Newborn Screening For Sickle Cell Disease And Other Haemoglobinopathies written by Stephan Lobitz and has been published by MDPI this book supported file pdf, txt, epub, kindle and other format this book has been release on 2019-10-07 with Medical categories.
Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies is a Special Issue of the International Journal of Neonatal Screening. Sickle cell disease is one of the most common inherited blood disorders, with a huge impact on health care systems due to high morbidity and high mortality associated with the undiagnosed disease. Newborn screening helps to make the diagnosis early and to prevent fatal complications and diagnostic odysseys. This book gives an overview of diagnostic standards in newborn screening for sickle cell disease and examples of existing newborn screening programs.
Guidelines For The Clinical Management Of Thalassaemia
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Author : Maria-Domenica Cappellini
language : en
Publisher:
Release Date : 2008
Guidelines For The Clinical Management Of Thalassaemia written by Maria-Domenica Cappellini and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2008 with categories.
Thalassemia And Other Hemolytic Anemias
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Author : Isam Jaber Al-Zwaini
language : en
Publisher: BoD – Books on Demand
Release Date : 2018-07-11
Thalassemia And Other Hemolytic Anemias written by Isam Jaber Al-Zwaini and has been published by BoD – Books on Demand this book supported file pdf, txt, epub, kindle and other format this book has been release on 2018-07-11 with Medical categories.
Thalassemia is a very common disease first described by pediatrician Thomas Benton Cooley in 1925 who described it in a patient of Italian origin. At that time, it was designated as Cooley's anemia. George Hoyt Whipple, a Nobel prize winner, and W. L. Bradford, a professor of pediatrics at the University of Rochester, coined the term thalassemia in 1936, which in Greek means anemia of the sea (Thalassa means "sea", and emia means "blood"), due to the fact that it is very common in the area of the Mediterranean Sea. This name is actually misleading because it can occur everywhere in the world. Thalassemia is not a single disease; it is rather a group of hereditary disorders of the production of globulin chain of the hemoglobin. Throughout the world, thalassemia affects approximately 4.4 of every 10,000 live births. It represents a major social and emotional impact on the patient and his family and a major burden on health services where the prevalence is high.
Inherited Hemoglobin Disorders
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Author : Anjana Munshi
language : en
Publisher: BoD – Books on Demand
Release Date : 2015-11-11
Inherited Hemoglobin Disorders written by Anjana Munshi and has been published by BoD – Books on Demand this book supported file pdf, txt, epub, kindle and other format this book has been release on 2015-11-11 with Medical categories.
The book, Inherited Hemoglobin Disorders, describes the genetic defects of hemoglobins, disease complications, and therapeutic strategies. This book has two distinct sections. The first theme includes seven chapters devoted to the types of hemoglobinopathies, mutation spectrum, diagnostic methods, and disease complications, and the second theme includes three chapters focusing on various treatment strategies. The content of the chapters presented in the book is guided by the knowledge and experience of the contributing authors. This book serves as an important resource and review to the researchers in the field of hemoglobinopathies.
Neonatal Hematology
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Author : Pedro A. de Alarcón
language : en
Publisher: Cambridge University Press
Release Date : 2021-02-18
Neonatal Hematology written by Pedro A. de Alarcón and has been published by Cambridge University Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2021-02-18 with Medical categories.
An essential guide to the pathogenesis, diagnosis and management of hematologic problems in the neonate, covering erythrocyte disorders, leukocyte disorders, immunologic disorders and hemostatic disorders. Guidance is practical, including blood test interpretation, advice on transfusions and reference ranges for hematological values.
Hemoglobin Disorders
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Author : Ronald L. Nagel
language : en
Publisher: Springer Science & Business Media
Release Date : 2008-02-01
Hemoglobin Disorders written by Ronald L. Nagel and has been published by Springer Science & Business Media this book supported file pdf, txt, epub, kindle and other format this book has been release on 2008-02-01 with Medical categories.
Hemoglobin and Hemoglobinologists This volume, Hemoglobin Disorders: Molecular Methods and Protocols, will be introduced with a review of the great milestones in the field, and the scientists responsible for those achievements. The history of hemoglobin can be divided into three periods: the Classical period, the Modern period, and the Post-Modern period. I am inclined to include as the four major members of the classical period Francis Roughton, Quentin Gibson, Jeffries Wyman, and Linus Pauling, not only because of their achievements, but also because of the superb scientists they trained and/or influenced. Francis John Worsely Roughton (1899–1972) (Fig. 1), in his laboratory at Trinity College in Cambridge, England, made the first measurements of the rapid reaction of oxygen with hemoglobin at the millisecond scale, at first by flow-mixing methods and later by flash photolysis. He not only opened an era of molecular research of hemoglobin, but also invented the methodology for fast reactions through the use of laser technology, which was later improved by others so that even faster reactions could be detected. Another contribution of Roughton was the education of Quentin H. Gibson (Fig. 2), his favorite s- dent, who, in his laboratory in Sheffield, continued to expand the horizon of ligand binding to hemoglobin, defining the oxygen binding constants for each of the hemes of hemoglobin. Though this did not, as expected, solve the und- lying mechanism of ligand cooperativity as discussed below, it was nonet- less an important milestone.
Haemoglobinopathy Diagnosis
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Author : Barbara J. Bain
language : en
Publisher: John Wiley & Sons
Release Date : 2008-04-15
Haemoglobinopathy Diagnosis written by Barbara J. Bain and has been published by John Wiley & Sons this book supported file pdf, txt, epub, kindle and other format this book has been release on 2008-04-15 with Medical categories.
This unique book is written by Barbara Bain, a leadinghaematologist with a reputation for her educational prowess in thefield. It provides a concise overview of the haemoglobinopathies andfocuses on the selection, performance, and interpretation ofrelevant laboratory tests. The tests dealt with are mainly thosedone regularly in diagnostic haematology laboratories. Where morespecialist tests are required, the reader is given an overview ofwhat the specialist centre will do, with guidance on what theresult will imply. This book is extremely practical in orientation and is anessential reference volume in the haematology laboratory. Haemoglobinopathy Diagnosis is ideal for: Trainees and residents in haematology Hematologists in practice Laboratory scientists Why Buy This Book? New Edition - Fully updated, with 43 new pictures and 37 pagesof illustrated clinical cases to use for teaching andself-evaluation Essential reference volume for the haematology laboratory Focuses on diagnosis Very practical in its approach In addition to the self-assessment case studies, contains "testyour knowledge" sections at the end of every chapter Remarkably comprehensive for a compact book
The Haemoglobinopathies
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Author : David John Weatherall
language : en
Publisher:
Release Date : 1993
The Haemoglobinopathies written by David John Weatherall and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1993 with Hemoglobinopathy categories.