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Physician’s Guide to the Treatment and Follow-Up of Metabolic Diseases (Record no. 501920)

000 -LEADER
fixed length control field 04767nam a22005655i 4500
001 - CONTROL NUMBER
control field 978-3-540-28962-3
003 - CONTROL NUMBER IDENTIFIER
control field DE-He213
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20161121230641.0
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
fixed length control field cr nn 008mamaa
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 100301s2006 gw | s |||| 0|eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9783540289623
-- 978-3-540-28962-3
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1007/3-540-28962-3
Source of number or code doi
050 #4 - LIBRARY OF CONGRESS CALL NUMBER
Classification number RC627.5-632
072 #7 - SUBJECT CATEGORY CODE
Subject category code MFGM
Source bicssc
072 #7 - SUBJECT CATEGORY CODE
Subject category code MED027000
Source bisacsh
082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 616.39
Edition number 23
245 10 - TITLE STATEMENT
Title Physician’s Guide to the Treatment and Follow-Up of Metabolic Diseases
Medium [electronic resource] /
Statement of responsibility, etc. edited by Nenad Blau, James Leonard, Georg F. Hoffmann, Joe T. R. Clarke.
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture Berlin, Heidelberg :
Name of producer, publisher, distributor, manufacturer Springer Berlin Heidelberg,
Date of production, publication, distribution, manufacture, or copyright notice 2006.
300 ## - PHYSICAL DESCRIPTION
Extent XVIII, 416 p. 13 illus.
Other physical details 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
347 ## - DIGITAL FILE CHARACTERISTICS
File type text file
Encoding format PDF
Source rda
505 0# - FORMATTED CONTENTS NOTE
Formatted contents note Emergency Management of Metabolic Diseases -- The Role of Communication in the Treatment of Inborn Metabolic Diseases -- Disorders of Phenylalanine and Tetrahydrobiopterin Metabolism -- Disorders of Neurotransmission -- Disorders of GABA, Glycine, Serine, and Proline -- Disorders of Tyrosine Degradation -- Disorders of Histidine Metabolism -- Disorders of Leucine Metabolism -- Disorders of Valine-Isoleucine Metabolism -- Various Organic Acidurias -- Disorders of the ?-Glutamyl Cycle -- Disorders of Sulfur Amino Acid Metabolism -- Inherited Hyperammonaemias -- Disorders of Ornithine, Lysine, and Tryptophan -- Defective Transcellular Transport of Amino Acids -- Disorders of Mitochondrial Fatty Acid Oxidation and Ketone Body Metabolism -- Disorders of Carbohydrate and Glycogen Metabolism -- Disorders of Glucose Transport -- Disorders of Glycerol Metabolism -- The Mucopolysaccharidoses -- Oligosaccharidoses and Related Disorders -- Congenital Disorders of Glycosylation -- Cystinosis -- Other Storage Disorders -- Inborn Errors of Purine and Pyrimidine Metabolism -- Disorders of Creatine Metabolism -- Peroxisomal Disorders -- Hyperoxaluria -- Mitochondrial Energy Metabolism -- Genetic Dyslipoproteinemias -- Disorders of Steroid Synthesis and Metabolism -- Inborn Errors of Cholesterol Biosynthesis -- The Porphyrias -- Disorders of Bile Acid Synthesis -- Disorders of Copper, Zinc, and Iron Metabolism -- Leukotrienes -- Hyperinsulinism of Infancy -- Other Metabolic Disorders.
520 ## - SUMMARY, ETC.
Summary, etc. The greatest dif?culty in life is to make knowledge effective, to convert it into practical wisdom. Sir William Osler. The inborn errors of metabolism, as a group of metabolic diseases, are re- tively rare and are sometimes called “orphan diseases. ” As a group, they account for about 1 in 2,500 births (Applegarth et al. 2000) and, as a cumulative group reaching 20 years of age, their prevalence is about 40 cases per 100,000 popu- tion. In terms of patient days of continuous supervision and care, hundreds of thousands of such days are involved per generation of these patients. Although experience with these diseases as a class may be small and people expert in their management may be relatively few, in the years to come many caregivers will become involved. This book offers help to them. Until the mid-twentieth century, hereditary metabolic and other genetic diseases were considered to be purely “genetic” problems. Destiny would take its course, treatment did not exist, and genetic counseling about recurrence risks was virtually all that could be offered. Phenylketonuria (PKU) was then shown to be a treatable genetic disease in which early diagnosis and effective treatment prevented the disease (mental retardation) in PKU. Other genetic diseases for which an environmental experience was an essential component of cause (e. g. , exposure to a dietary component or a drug) were then seen to yield to treatment.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Medicine.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Human genetics.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element General practice (Medicine).
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Internal medicine.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Metabolic diseases.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Pathology.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Pediatrics.
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Medicine & Public Health.
650 24 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Metabolic Diseases.
650 24 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Pediatrics.
650 24 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Human Genetics.
650 24 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Internal Medicine.
650 24 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Pathology.
650 24 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element General Practice / Family Medicine.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Blau, Nenad.
Relator term editor.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Leonard, James.
Relator term editor.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Hoffmann, Georg F.
Relator term editor.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Clarke, Joe T. R.
Relator term editor.
710 2# - ADDED ENTRY--CORPORATE NAME
Corporate name or jurisdiction name as entry element SpringerLink (Online service)
773 0# - HOST ITEM ENTRY
Title Springer eBooks
776 08 - ADDITIONAL PHYSICAL FORM ENTRY
Relationship information Printed edition:
International Standard Book Number 9783540229544
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier http://dx.doi.org/10.1007/3-540-28962-3
912 ## -
-- ZDB-2-SME
Holdings
Withdrawn status Lost status Damaged status Not for loan Permanent Location Current Location Date acquired Barcode Date last seen Price effective from Koha item type
        PK Kelkar Library, IIT Kanpur PK Kelkar Library, IIT Kanpur 2016-11-21 EBK2207 2016-11-21 2016-11-21 E books

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