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Muscular dystrophy : (Record no. 91417)

MARC details
000 -LEADER
fixed length control field 05688cam a2200625 i 4500
001 - CONTROL NUMBER
control field ocn868950997
003 - CONTROL NUMBER IDENTIFIER
control field OCoLC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20240729131342.0
006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS--GENERAL INFORMATION
fixed length control field m d
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
fixed length control field cr |||||||||||
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 130312s2013 nyua ob 001 0 eng
010 ## - LIBRARY OF CONGRESS CONTROL NUMBER
LC control number 2020678387
040 ## - CATALOGING SOURCE
Original cataloging agency DLC
019 ## -
-- 923548920
-- 923670323
-- 928194354
-- 929143286
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 9781626185098
Qualifying information (eBook)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 1626185093
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Cancelled/invalid ISBN 1626184607
Qualifying information (hardback)
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Cancelled/invalid ISBN 9781626184602
Qualifying information (hardback)
035 ## - SYSTEM CONTROL NUMBER
System control number 635078
-- (N$T)
035 ## - SYSTEM CONTROL NUMBER
System control number (OCoLC)868950997
Canceled/invalid control number (OCoLC)923548920
-- (OCoLC)923670323
-- (OCoLC)928194354
-- (OCoLC)929143286
072 #7 - SUBJECT CATEGORY CODE
Subject category code HEA
Subject category code subdivision 039000
Source bisacsh
072 #7 - SUBJECT CATEGORY CODE
Subject category code MED
Subject category code subdivision 014000
Source bisacsh
072 #7 - SUBJECT CATEGORY CODE
Subject category code MED
Subject category code subdivision 022000
Source bisacsh
072 #7 - SUBJECT CATEGORY CODE
Subject category code MED
Subject category code subdivision 112000
Source bisacsh
072 #7 - SUBJECT CATEGORY CODE
Subject category code MED
Subject category code subdivision 045000
Source bisacsh
049 ## - LOCAL HOLDINGS (OCLC)
Holding library MAIN
245 00 - TITLE STATEMENT
Title Muscular dystrophy :
Subtitle causes and management
Statement of responsibility, etc
Medium [E-Book]
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture New York :
Name of producer, publisher, distributor, manufacturer Nova Biomedical,
Date of production, publication, distribution, manufacture, or copyright notice [2013]
300 ## - PHYSICAL DESCRIPTION
Physical description 1 online resource.
336 ## - CONTENT TYPE
Content type term text
Content type code txt
Source rdacontent
337 ## - MEDIA TYPE
Media type term computer
Media type code c
Source rdamedia
338 ## - CARRIER TYPE
Carrier type term online resource
Carrier type code cr
Source rdacarrier
490 1# - SERIES TITLE
Series statement Neurodegenerative diseases--laboratory and clinical research
490 1# - SERIES TITLE
Series statement Muscular System - Anatomy, Functions and Injuries
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc Includes bibliographical references and index.
505 0# - CONTENTS
Contents ""MUSCULAR DYSTROPHY. CAUSES AND MANAGEMENT""; ""MUSCULAR DYSTROPHY. CAUSES AND MANAGEMENT""; ""Library of Congress Cataloging-in-Publication Data""; ""Contents""; ""Preface""; ""Section 1. Genetic, Environmental Interactions and Evaluation""; ""Chapter 1: Muscular Dystrophy: The Present and Future""; ""Abstract""; ""The Present""; ""The Future""; ""Genetic and Environmental Interaction""; ""References""; ""Chapter 2: History and Pathogenesis of Muscular Dystrophy""; ""Introduction""; ""Muscular Dystrophy: Recognition of Different Forms""; ""Recognition of Severe X-Linked Muscular Dystrophy""
505 8# - CONTENTS
Contents ""The Nosographic Era: The Recognition of Limb-Girdle Dystrophies""""The Recognition of Facio-Scapulo Humeral Dystrophy (FSHD)""; ""Therapeutical Trials in DMD""; ""The Molecular Era""; ""References""; ""Chapter 3: Biomarkers and Genetic Risks""; ""Abstract""; ""Defining Biomarkers""; ""Biomarkers in Muscular Dystrophies""; ""Emerging Biomarkers""; ""Critical Parameters for the Choice of Biomarker Assay""; ""Conclusion""; ""References""; ""Chapter 4: Inflammation in Duchenne Muscular Dystrophy""; ""Introduction""; ""General Aspects of Dystrophic Muscle and the Immune Response""
505 8# - CONTENTS
Contents ""Hypothesis on a Putative Link between Functional Concepts of the Immune Response and Development of Fibrosis in DMD""""A View on Pathogenesis in DMD with Emphasis on Fibrosis and Inflammation""; ""Modeling DMD, Mediators and Drivers of the Immune Process �a�? What Can We Learn from the Mouse?""; ""Therapy Targeting Immune Processes""; ""Conclusion""; ""References""; ""Chapter 5: MRI Imaging in Muscular Dystrophies""; ""Abstract""; ""Introduction""; ""MRI Scoring and Interpretation""; ""Duchenne Muscular Dystrophy (DMD)""; ""Limb Girdle Muscular Dystrophies""; ""LGMD2A (Calpainopathy)""
505 8# - CONTENTS
Contents ""LGMD 2B (Dysferlinopathy)""""LGMD2I (FKRP Defect)""; ""Myotonic Dystrophy Type 1 (DM1)""; ""PROMM or Myotonic Dystrophy Type 2 (DM2)""; ""Congenital Muscular Dystrophies (CMD)""; ""Hyaline Body Myopathy (Scapulo-Peroneal Syndrome)""; ""Emery�a�?Dreifuss Muscular Dystrophy""; ""Bethlem Myopathy""; ""Future Perspectives""; ""References""; ""Chapter 6: Clinical Scales for the Evaluation of Neuromuscular Patients""; ""Abstract""; ""Motor Function""; ""Quality of Life""; ""References""; ""Section 2. Specific Dystrophies""; ""Chapter 7: Dystrophinopathies""; ""Abstract""
505 8# - CONTENTS
Contents ""Introduction: An Overview of Dystrophinopathies""""Clinical Description of DMD""; ""Clinical Description of BMD""; ""Clinical Description of Carriers""; ""Molecular Bases of Dystrophinopathies: The DMD Gene""; ""Molecular Bases of Dystrophinopathy: The Dystrophin Protein""; ""Molecular Bases of Dystrophinopathy: Pathogenesis""; ""Diagnosis of Dystrophinopathy""; ""Genetic Counseling and Prevention""; ""Treatment""; ""References""; ""Chapter 8: Scapulo-peroneal Syndromes""; ""Introduction""; ""Case Presentation""; ""Historical Perspective""; ""1. Scapuloperoneal Muscular Dystrophy (SPMD)""
520 ## - ABSTRACT
Abstract Muscular Dystrophies include a heterogeneous series of diseases that range from childhood to adult onset cases, of difficult diagnosis and treatment. This book presents the state of the art in muscular dystrophies, after the molecular revolution. In the field of patients' diagnosis, several advances have been done by recognizing new entities. New techniques such as biochemical, molecular advancements, and the use of muscle MRI are collected that allow rapid diagnosis. Also, advances in therapy and therapeutical trials are presented in Duchenne and other muscular dystrophies and some novel trea.
590 ## - LOCAL NOTE (RLIN)
Local note Master record variable field(s) change: 050, 082
650 #0 - SUBJECT HEADINGS
Subject term Muscular dystrophy.
9 (RLIN) 7054
700 1# - ADDED PERSONAL NAME
Added personal author Angelini, C.
Relator term editor.
830 #0 - SERIES ADDED ENTRY--UNIFORM TITLE
Uniform title Neurodegenerative diseases--laboratory and clinical research.
830 #0 - SERIES ADDED ENTRY--UNIFORM TITLE
Uniform title Muscular system--anatomy, functions, and injuries series.
856 ## - ONLINE RESOURCE
Uniform Resource Identifier <a href="#gotoholdings">#gotoholdings</a>
Link text Access resource
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Suppress in OPAC Do not Suppress in OPAC
588 ## - SOURCE OF DESCRIPTION NOTE
Source of description note Description based on print version record.
938 ## -
-- YBP Library Services
-- YANK
-- 11120189
938 ## -
-- EBSCOhost
-- EBSC
-- 635078
938 ## -
-- ebrary
-- EBRY
-- ebr10752217
938 ## -
-- ProQuest Ebook Central
-- EBLB
-- EBL2194161
994 ## -
-- 92
-- N$T
Holdings
Withdrawn status Lost status Damaged status Not for loan Home library Current library Shelving location Date acquired Source of acquisition Total Checkouts Date last seen Uniform Resource Identifier Price effective from Koha item type
        Stenhouse Library (Kingston Hospital) Stenhouse Library (Kingston Hospital) Online 28/11/2022 eBook EBSCO clinical collection   28/11/2022 https://search.ebscohost.com/login.aspx?custid=ns123844&authtype=ip,shib&direct=true&scope=site&db=nlebk&db=nlabk&AN=635078 28/11/2022 Electronic book
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