Coverart for item
The Resource Physician's guide to the treatment and follow-up of metabolic diseases, Nenad Blau [and others] (eds.) ; foreword by C.R. Scriver

Physician's guide to the treatment and follow-up of metabolic diseases, Nenad Blau [and others] (eds.) ; foreword by C.R. Scriver

Label
Physician's guide to the treatment and follow-up of metabolic diseases
Title
Physician's guide to the treatment and follow-up of metabolic diseases
Statement of responsibility
Nenad Blau [and others] (eds.) ; foreword by C.R. Scriver
Contributor
Subject
Language
eng
Cataloging source
OHX
Illustrations
illustrations
Index
index present
Literary form
non fiction
Nature of contents
bibliography
http://library.link/vocab/relatedWorkOrContributorDate
1946-
http://library.link/vocab/relatedWorkOrContributorName
Blau, N.
http://library.link/vocab/subjectName
  • Metabolic Diseases
  • Metabolism, Inborn Errors
Label
Physician's guide to the treatment and follow-up of metabolic diseases, Nenad Blau [and others] (eds.) ; foreword by C.R. Scriver
Instantiates
Publication
Note
CD-ROM contains entire contents of volume in Adobe pdf format
Accompanying material
1 CD-ROM (4 3/4 in.).
Bibliography note
Includes bibliographical references and indexes
Carrier category
volume
Carrier category code
  • nc
Carrier MARC source
rdacarrier
Content category
text
Content type code
  • txt
Content type MARC source
rdacontent
Contents
Part one: initial approaches -- Emergency management of metabolic diseases -- Role of communication in the treatment of inborn metabolic diseases -- Part two: approach to treatment -- 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 Þ-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 -- Mucopolysaccharidoses -- Oligosaccharidoses and related disorders -- Congenital disorders of glycosylation -- Cystinosis -- Other storage disorders -- Inborn errors of purineand 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 -- Porphyrias -- Disorders of bile acid synthesis -- Disorders of copper, zinc, and iron metabolism -- Leukotrienes -- Hyperinsulinism of infancy -- Other metabolic disorders
Control code
61714582
Dimensions
25 cm +
Extent
xviii, 415 pages
Isbn
9783540229544
Isbn Type
(hd.bd.)
Lccn
2004110452
Media category
unmediated
Media MARC source
rdamedia
Media type code
  • n
Other control number
9783540229544
Other physical details
illustrations
Label
Physician's guide to the treatment and follow-up of metabolic diseases, Nenad Blau [and others] (eds.) ; foreword by C.R. Scriver
Publication
Note
CD-ROM contains entire contents of volume in Adobe pdf format
Accompanying material
1 CD-ROM (4 3/4 in.).
Bibliography note
Includes bibliographical references and indexes
Carrier category
volume
Carrier category code
  • nc
Carrier MARC source
rdacarrier
Content category
text
Content type code
  • txt
Content type MARC source
rdacontent
Contents
Part one: initial approaches -- Emergency management of metabolic diseases -- Role of communication in the treatment of inborn metabolic diseases -- Part two: approach to treatment -- 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 Þ-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 -- Mucopolysaccharidoses -- Oligosaccharidoses and related disorders -- Congenital disorders of glycosylation -- Cystinosis -- Other storage disorders -- Inborn errors of purineand 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 -- Porphyrias -- Disorders of bile acid synthesis -- Disorders of copper, zinc, and iron metabolism -- Leukotrienes -- Hyperinsulinism of infancy -- Other metabolic disorders
Control code
61714582
Dimensions
25 cm +
Extent
xviii, 415 pages
Isbn
9783540229544
Isbn Type
(hd.bd.)
Lccn
2004110452
Media category
unmediated
Media MARC source
rdamedia
Media type code
  • n
Other control number
9783540229544
Other physical details
illustrations

Library Locations

    • J. Otto Lottes Health Sciences LibraryBorrow it
      1 Hospital Dr, Columbia, MO, 65201, US
      38.939544 -92.328377
    • University of Missouri Libraries DepositoryBorrow it
      2908 Lemone Blvd, Columbia, MO, 65211, US
      38.919360 -92.291620
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