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Monday, May 11, 2020 | History

5 edition of Disorders of Hemoglobin found in the catalog.

Disorders of Hemoglobin

Genetics, Pathophysiology and Clinical Management

  • 398 Want to read
  • 29 Currently reading

Published by Cambridge University Press .
Written in English

    Subjects:
  • Haematology,
  • Medical Hematology,
  • Hemoglobinopathies,
  • Molecular Genetics,
  • Oncology,
  • Medical / Nursing,
  • Medical,
  • Hemoglobinopathy,
  • Hematology,
  • Reference,
  • Medical / Oncology,
  • Life Sciences - Genetics & Genomics,
  • Thalassemia,
  • Anemia, Sickle Cell

  • Edition Notes

    ContributionsH. Franklin Bunn (Foreword), Martin H. Steinberg (Editor), Bernard G. Forget (Editor), Douglas R. Higgs (Editor), Ronald L. Nagel (Editor)
    The Physical Object
    FormatHardcover
    Number of Pages1268
    ID Numbers
    Open LibraryOL7749460M
    ISBN 100521632668
    ISBN 109780521632669

    This book is a completely revised new edition of the definitive reference on disorders of hemoglobin. Authored by world-renowned experts, the book focuses on basic science aspects and clinical. Hemoglobin disorders can be broadly classified into two general categories (as listed in Table 1): Those in which there is a quantitative defect in the production of one of the globin subunits, either total absence or marked reduction. These are called the thalassemia syndromes.

    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 .   The book opens with a review of the scientific underpinnings. Pathophysiology of common hemoglobin disorders is discussed next in an entirely new section devoted to vascular biology, the erythrocyte membrane, nitric oxide biology, and hemolysis. Four sections deal with α and β thalassemia, sickle cell disease, and related conditions, Brand: Cambridge University Press.

    Hemoglobin Disorders: Molecular Methods and Protocols (Methods in Molecular Medicine) Content 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 . This book is a completely revised new edition of the definitive reference on disorders of hemoglobin. Authored by world-renowned experts, the book focuses on basic science aspects and clinical features of hemoglobinopathies, covering diagnosis, treatment, and future applications of current research.


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Disorders of Hemoglobin Download PDF EPUB FB2

This book is a completely revised new edition of the definitive reference on disorders of hemoglobin. Authored by world-renowned experts, the book focuses on basic science aspects and clinical features of hemoglobinopathies, covering diagnosis, treatment, and future applications of current by:   This book is a completely revised new edition of the definitive reference on disorders of hemoglobin.

Authored by world-renowned experts, the book focuses on basic science aspects and clinical features of hemoglobinopathies, covering diagnosis, treatment, and 4/5(1).

Disorders of Hemoglobin by Howard Franklin Bunn,available at Book Depository with free delivery worldwide.4/5(1). DISORDERS OF HEMOGLOBIN Genetics, Pathophysiology, and Clinical Management SECOND EDITION This book is a completely revised new edition of the defini-tive reference on disorders of hemoglobin.

Authored by world-renowned experts, the book focuses on basic sci-ence aspects and clinical features of hemoglobinopathies. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management (Cambridge Medicine) Pdf Kindle Free Download.

Free Torrent Download Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management (Cambridge Medicine) Pdf ebook. Among these disorders, sickle cell syndromes and thalassemias constitute a major public health problem.

A glutamic acid to valine substitution at the sixth amino acid of the β -globin chain of human hemoglobin (HbA) results in formation of sickle hemoglobin (HbS). The book, Inherited Hemoglobin Disorders of Hemoglobin book, 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.

GENERAL CLASSIFICATION OF HEMOGLOBIN DISORDERS Hemoglobin disorders can be broadly classified into two general categories (as listed in Table 1): 1.

Those in which there is a quantitative defect in the production of one of the globin sub-units, either total absence or marked reduc-tion. These are called the thalassemia syn-dromes.

GENERAL CLASSIFICATION OF HEMOGLOBIN DISORDERS. Hemoglobin disorders can be broadly classified into two general categories (as listed in Table 1): Those in which there is a quantitative defect in the production of one of the globin subunits, either total absence or marked reduction.

These are called the thalassemia by: Category of Impairments, Hematological Disorders Hemolytic anemias, including sickle cell disease, thalassemia, and their variants (see C), with: Documented painful (vaso-occlusive) crises requiring parenteral (intravenous or intramuscular) narcotic medication, occurring at least six times within a month period with at least.

About the e-Book Hemoglobin Disorders: Molecular Methods and Protocols Pdf 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. Hemoglobinopathies are the most common single gene disorders worldwide with a considerable frequency in certain area particularly Mediterranean and Middle Eastern countries. Hemoglobinopathies include structural variants of hemoglobin (Hb S, Hb C, HbE,) and thalassaemias which are inherited defects in the globin chains synthesis.

The present study was conducted to determine the prevalence Author: Mehrdad Payandeh, Masoud Sadeghi. Disorders of Hemoglobin provides a comprehensive review of both the scientific and the clinical aspects of human erythropoiesis and its disorders.

It offers a collection of well written chapters by leading international investigators, many of whom are able to refer to the contribution their own research work has made to the by: 3. Pathophysiology of common hemoglobin disorders is discussed next in an entirely new section devoted to vascular biology, the erythrocyte membrane, nitric oxide biology, and hemolysis.

Four sections deal with α and β thalassemia, sickle cell disease, and related conditions. Cambridge Core - Hematology - Disorders of Hemoglobin - by Martin H. SteinbergAuthor: Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs, David J.

Weatherall. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management and a great selection of related books, art and collectibles available now at Hemoglobinopathy is the medical term for a group of blood disorders and diseases that affect red blood cells.

It can be a kind of genetic defect that results in abnormal structure of one of the globin chains of the hemoglobin molecule. Hemoglobinopathies are inherited single-gene disorders; in most cases, they are inherited as autosomal co-dominant lty: Hematology. Disorders of Hemoglobin. Genetics, Pathophysiology, and Clinical Management, 2nd ed.

Cambridge University Press, New York, • Color Altas of Hemoglobin Disorders: A compendium Based on Proficiency Testing (), updated in File Size: 1MB. Hemoglobinopathies are disorders affecting the structure, function, or production of hemoglobin.

These conditions are usually inherited and range in severity from asymptomatic laboratory abnormalities. Disorders of Hemoglobin is the first comprehensive reference on the genetic and acquired disorders of hemoglobin in over a decade.

It stands as the definitive work on the genetics, pathophysiology, and clinical management of this wide range of disorders. Drs.4/5(2). 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 Author: Anjana Munshi.

The striking blood film entitled, “Homozygous hemoglobin C disease,” and the accompanying case report in Blood Work (Blood ;), is unlikely to represent homozygosity for hemoglobin C (HbC). 1 To establish this diagnosis, either informative family studies or DNA analysis of the β-globin genes are needed.

Hemoglobin electrophoresis cannot differentiate homozygosity for. Access to society journal content varies across our titles. If you have access to a journal via a society or association membership, please browse to your society journal, select an article to view, and follow the instructions in this by: 3.