Duchenne muscular dystrophy : (Record no. 92172)

MARC details
000 -LEADER
fixed length control field 05556cam a2200601 i 4500
001 - CONTROL NUMBER
control field ocn908550524
003 - CONTROL NUMBER IDENTIFIER
control field OCoLC
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20221128212902.0
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 150126s2015 nyua ob 001 0 eng
010 ## - LIBRARY OF CONGRESS CONTROL NUMBER
LC control number 2020678711
040 ## - CATALOGING SOURCE
Original cataloging agency DLC
019 ## -
-- 911247050
-- 923678445
-- 928197735
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 9781634821971
Qualifying information ebook
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
ISBN 1634821971
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Cancelled/invalid ISBN 163482153X
Qualifying information hbk.
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Cancelled/invalid ISBN 9781634821537
Qualifying information hbk.
035 ## - SYSTEM CONTROL NUMBER
System control number 986704
-- (N$T)
035 ## - SYSTEM CONTROL NUMBER
System control number (OCoLC)908550524
Canceled/invalid control number (OCoLC)911247050
-- (OCoLC)923678445
-- (OCoLC)928197735
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 Duchenne muscular dystrophy :
Subtitle symptoms, management and prognosis
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 [2015]
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 Neuroscience research progress series
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc Includes bibliographical references and index.
505 0# - CONTENTS
Contents DUCHENNE MUSCULAR DYSTROPHY: SYMPTOMS, MANAGEMENT AND PROGNOSIS; DUCHENNE MUSCULAR DYSTROPHY: SYMPTOMS, MANAGEMENT AND PROGNOSIS; Library of Congress Cataloging-in-Publication Data; Contents; Preface; Chapter 1: Yoga and Duchenne; Abstract; Introduction; Respiratory Complications in Patients with Duchenne Muscular Dystrophy; Yoga; Yoga and Breathing; The Exercises Chosen to Be Applied to Children with Duchenne; Pulmonary Function and Respiratory Pressures; The Choice of the Boys (Series) for Our Investigation; Teaching Schedule and Technical; Practice; Pulmonary Function Test.
505 8# - CONTENTS
Contents Evaluation of Respiratory PressuresResults; FVC and FEV1; EMS; IMS; Conclusion; References; Chapter 2: Physical Activity in Duchenne Muscular Dystrophy; Abstract; Introduction; Exercising in the Water; Important Considerations before Exercising; Land Based Exercises; References; Chapter 3: Functional Evaluation Scale for Duchenne Muscular Dystrophy (FES-DMD); Abstract; Introduction; The Scale FES-DMD; FES-DMD-Domain 1 (D1); FES-DMD-Domain 2 (D2); FES-DMD-Domain 3 (D3); FES-DMD-Domain 4 (D4); References; Chapter 4: Physiotherapy and Duchenne Muscular Dystrophy; Abstract; Introduction.
505 8# - CONTENTS
Contents WeaknessMuscle Strength Assessment; Functional Testing; Muscle Strengthening and Improvement of Function; Contractures; Gait; Functional Capacity; Physical Activity and Exercise Training; Respiratory Issues; Pulmonary Function Assessment; Respiratory Muscles (Inspiration and Expiration): Assessment, Training and Fatigue; Airway Clearance; Non-Invasive Ventilation; Pain Management; References; Chapter 5: Age-Dependent Proteomics of Duchenne Muscular Dystrophy in Human Myoblasts; Abstract; Introduction; Methods; Materials; Human Myoblasts; Reagents; Experimental Set Up; Cell Culture.
505 8# - CONTENTS
Contents Protein Extraction and PurificationSample Preparation for Mass Spectrometry; Peptide Labelling with iTRAQ(Reporter Tags; Fractionation of Peptides; Mass Spectrometric Analysis; Software and Statistics; Results; Cytoskeletal Proteins; Metabolism-Associated Proteins; Antioxidative Proteins; Stress-Related and Degradation Proteins; Calcium-Dependent Proteins; Vesicle Trafficking-Associated Proteins; Gene Expression Associated Proteins; Signalling-Associated Proteins; Conclusion; Acknowledgments; References.
505 8# - CONTENTS
Contents Chapter 6: Molecular Studies in Duchenne/Becker Muscular Dystrophies of Argentine PatientsAbstract; Introduction; Cl�inical Characterization of DMD/DMB; Relation of Dystrophin with Cognitive Impairment; Symptomatic Females; Molecular Studies; Objectives of Our Reported Publications; Methods; Subjects; PCR Assays; MLPA Analysis; Segregation Analysis of STR Loci; Risk Estimates; Neuropsychological Assessment; Statistical Method; X-Chromosome Inactivation Pattern Analysis (HUMARA Assay); Results; Deletion Pattern in DMD/BMD Patients in the Dystrophin Gene.
520 ## - ABSTRACT
Abstract A child with Duchenne Muscular Dystrophy (DMD) faces a childhood and adolescence with a disability that develops gradually. This book intends to expose the problems of children with DMD. The authors discuss situations related to the disease in an attempt to provide some quality and improvement of life for those affected since DMD is a degenerative disease which affects muscle. This book offers a historical study of muscular dystrophy. It also shows some profiles of excellent clinicians and scientists that have contributed to this book with a description of muscular dystrophy from the clinical.
590 ## - LOCAL NOTE (RLIN)
Local note Master record variable field(s) change: 050, 082
650 #0 - SUBJECT HEADINGS
Subject term Duchenne muscular dystrophy.
650 #0 - SUBJECT HEADINGS
Subject term Duchenne muscular dystrophy
General subdivision Treatment.
700 1# - ADDED PERSONAL NAME
Added personal author H�onorio, Samuel Alexandre Almeida,
Relator term editor.
830 #0 - SERIES ADDED ENTRY--UNIFORM TITLE
Uniform title Neuroscience research progress series.
856 40 - ONLINE RESOURCE
Uniform Resource Identifier <a href="https://search.ebscohost.com/login.aspx?custid=ns123844&authtype=ip,shib&direct=true&scope=site&db=nlebk&db=nlabk&AN=986704">https://search.ebscohost.com/login.aspx?custid=ns123844&authtype=ip,shib&direct=true&scope=site&db=nlebk&db=nlabk&AN=986704</a>
Link text Kingston Hospital NHS Foundation Trust OpenAthens account holders click here for access
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Suppress in OPAC Do not Suppress in OPAC
938 ## -
-- YBP Library Services
-- YANK
-- 12257692
938 ## -
-- EBSCOhost
-- EBSC
-- 986704
938 ## -
-- ebrary
-- EBRY
-- ebr11050188
938 ## -
-- ProQuest Ebook Central
-- EBLB
-- EBL2070938
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 Stenhouse Library   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=986704 28/11/2022 Electronic book
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