- 5 resultaten
laagste prijs: € 60,82, hoogste prijs: € 554,79, gemiddelde prijs: € 200,50
1
bestellen
bij Biblio.co.uk
$ 188,38
(ongeveer € 173,03)
verzending: € 4,591
bestellenGesponsorde link
Author:

Inborn Metabolic Diseases: Diagnosis and Treatment Saudubray, Jean-Marie? Berghe, Georges van den; Walter, John H. - gebonden uitgave, pocketboek

2012, ISBN: 9783642157196

Springer, Auflage: 2nd ed. 2012. Auflage: 2nd ed. 2012. Hardcover. 5 x 17,8 x 25,5 cm. In its revised Second Edition, this book offers new and updated chapters and references, and unique… Meer...

DEU, THA - Verzendingskosten: EUR 4.59 BOOK-SERVICE Lars Lutzer - ANTIQUARIAN BOOKS - LITERATURE SEARCH *** BOOKSERVICE *** ANTIQUARIAN RESEARCH, TextbooksFast
2
Inborn Metabolic Diseases : Diagnosis and Treatment
bestellen
bij BetterWorldBooks.com
€ 60,82
bestellenGesponsorde link
Inborn Metabolic Diseases : Diagnosis and Treatment - gebruikt boek

ISBN: 9783642157196

Now in its 5th edition, this is the standard text for identification and management of patients with inborn errors of metabolism. Updates include newly discovered disorders and a chapter … Meer...

used in stock. Verzendingskosten:zzgl. Versandkosten., exclusief verzendingskosten
3
bestellen
bij Achtung-Buecher.de
€ 98,70
bestellenGesponsorde link
Saudubray, Jean-Marie; Berghe, Georges van den und Walter, John H.:
Inborn Metabolic Diseases: Diagnosis and Treatment. - gebruikt boek

ISBN: 364215719X

Mit Markierungen mit Leuchtstift auf Seite 278. Davon abgesehen exzellentes TOP Exemplar. Unbekannter Einband 2, [PU: Springer, Berlin/Heidelberg/New York, NY]

Verzendingskosten:Zzgl. Versandkosten., exclusief verzendingskosten Synca GmbH, 4325 Schupfart
4
bestellen
bij Biblio.co.uk
$ 611,49
(ongeveer € 554,79)
verzending: € 19,051
bestellenGesponsorde link
Jean-Marie Saudubray (Editor), Georges van den Berghe (Editor), John H. Walter (Editor):
Inborn Metabolic Diseases: Diagnosis and Treatment - gebonden uitgave, pocketboek

2012, ISBN: 9783642157196

Springer, 2012-01-20. 5th ed. 2012. Hardcover. Used:Good., Springer, 2012-01-20, 0

Verzendingskosten: EUR 19.05 Ergodebooks
5
Inborn Metabolic Diseases: Diagnosis and Treatment
bestellen
bij ZVAB.com
€ 115,17
verzending: € 4,681
bestellenGesponsorde link
Inborn Metabolic Diseases: Diagnosis and Treatment - gebonden uitgave, pocketboek

2012, ISBN: 364215719X

[EAN: 9783642157196], [SC: 4.68], [PU: Springer], Most items will be dispatched the same or the next working day., Books

Verzendingskosten: EUR 4.68 WeBuyBooks, Rossendale, LANCS, United Kingdom [50604927] [Rating: 5 (von 5)]

1Aangezien sommige platformen geen verzendingsvoorwaarden meedelen en deze kunnen afhangen van het land van levering, de aankoopprijs, het gewicht en de grootte van het artikel, een eventueel lidmaatschap van het platform, een rechtstreekse levering door het platform of via een derde aanbieder (Marktplaats), enz., is het mogelijk dat de door euro-boek.nl meegedeelde verzendingskosten niet overeenstemmen met deze van het aanbiedende platform.

Bibliografische gegevens van het best passende boek

Bijzonderheden over het boek
Inborn Metabolic Diseases: Diagnosis and Treatment

Being up to Date: Status Quo and Trends of Treatment For those involved in the identification and management of patients with inborn errors of metabolism, this book is now recognised as the standard textbook in this interdisciplinary field. It has proved to be indispensable for professionals in specialities ranging from pediatrics, neonatology, pathological biochemistry and genetics to neurology, internal medicine, nursing, dietetics and psychology. This 5th edition has been extensively revised and updated. What¿s new -          Additional chapter focusing on inborn errors affecting adults, particularly the late neurological presentations -          Numerous updates on diagnostic procedures and treatment -          Newly discovered disorders. As with previous editions, the book opens with a section presenting the clinical approach to inborn metabolic diseases for those cases in which a diagnosis is being sought. This now includes a chapter on the clinical presentation of metabolic diseases in the older age range, using an analogous structure. If a particular diagnosis is already suspected, the reader may refer to the following sections of the book containing general chapters on diagnostic procedures and treatment, and on specific groups of disorders. As with earlier editions, the chapters have been written by authors who are internationally recognised experts on their subjects. They provide information in a clear, relevant and concise manner using a coherent structure.

Gedetalleerde informatie over het boek. - Inborn Metabolic Diseases: Diagnosis and Treatment


EAN (ISBN-13): 9783642157196
ISBN (ISBN-10): 364215719X
Gebonden uitgave
Verschijningsjaar: 2012
Uitgever: Springer
656 Bladzijden
Gewicht: 1,573 kg
Taal: Englisch

Boek bevindt zich in het datenbestand sinds 2009-09-14T20:03:26+02:00 (Amsterdam)
Detailpagina laatst gewijzigd op 2023-08-23T12:04:14+02:00 (Amsterdam)
ISBN/EAN: 9783642157196

ISBN - alternatieve schrijfwijzen:
3-642-15719-X, 978-3-642-15719-6
alternatieve schrijfwijzen en verwante zoekwoorden:
Auteur van het boek: van den berghe, george van den bergh, georges jean, john bergh, van den berg, georg walter, aubourg, marie
Titel van het boek: the diagnosis and treatment diseases


Gegevens van de uitgever

Auteur: Jean-Marie Saudubray; Georges van den Berghe; John H. Walter
Titel: Inborn Metabolic Diseases - Diagnosis and Treatment
Uitgeverij: Springer; Springer Berlin
660 Bladzijden
Verschijningsjaar: 2011-11-23
Berlin; Heidelberg; DE
Gedrukt / Gemaakt in
Gewicht: 1,633 kg
Taal: Engels
197,94 € (DE)
203,49 € (AT)
203,50 CHF (CH)
Not available, publisher indicates OP

BB; Book; Hardcover, Softcover / Medizin/Klinische Fächer; Pädiatrie; Verstehen; Medizin, Gesundheit; disorders of metabolism; inborn errors of metabolism; neonatal screening; metabolic diseases; newborn screening; inherited metabolic diseases; B; Medicine; Pediatrics; Human Genetics; Endocrinology; Neurology; Genetik, Medizin; Endokrinologie; Neurologie und klinische Neurophysiologie; BB; BC; EA; BB

Part I: Diagnosis and Treatment: General Principles: Classification and clinical Approach to Inherited Metabolic Diseases in Pediatrics.- Clinical approach to Inherited Metabolic Diseases in Adulthood.- Newborn Screening for Inborn Errors of Metabolism.- Diagnostic Procedures and Postmortem Protocol.- Emergency Treatments.- Part II: Disorders of Carbohydrate Metabolism: Glycogen-Storage Diseases and Related Disorders.- Disorders of Galactose Metabolism.- Disorders of the Pentose Phosphate Pathway.- Disorders of Fructose Metabolism.- Persistent Hyperinsulinemic Hypoglycemia.- Disorders of Glucose Transport.- Part III: Disorders of Mitochondrial Energy Metabolism: Disorders of Pyruvate Metabolism and the Tricarboxylic Acid Cycle.- Disorders of Mitochondrial Fatty Acid Oxidation and Related Metabolic Pathways.- Disorders of Ketogenesis and Ketolysis.- Defects of the Respiratory Chain.- Creatine Deficiency Syndromes.- Part IV: Disorders of Amino Acid Metabolism and Transport: Hyperphenylalaninaemias.- Disorders of Tyrosine Metabolism.- Branched-Chain Organic Acidurias/Acidemias.- Disorders of the Urea Cycle and Related Enzymes.- Disorders of Sulfur Amino Acid Metabolism.- Disorders of Ornithine Metabolism.- Cerebral Organic Acid Disorders and other Disorders of Lysine Catabolism.- Nonketotic Hyperglycinemia (Glycine Encephalopathy).- Disorders of Proline and Serine Metabolism.- Transport Defects of Amino Acids at the Cell Membrane.- Part V : Vitamin-Responsive Disorders: Biotin-Responsive Multiple Carboxylase Deficiency.- Disorders of Cobalamin and Folate Transport and Metabolism.- Part VI: Neurotransmitter and Small Peptide Disorders: Disorders of Neurotransmission.- Disorders in the Metabolism of Glutathione and Imidazole Dipeptides.- Trimethylaminuria and Dimethylglycine Dehydrogenase Deficiency.- Part VII: Disorders of Lipid and Bile Acid Metabolism: Dyslipidemias.- Disorders of Cholesterol Synthesis.- Disorders of Bile Acid Synthesis.- Part VIII: Disorders of Nucleic Acid and Heme Metabolism: Disorders of Purine and Pyrimidine Metabolism.- Disorders of Heme Biosynthesis.- Part IX: Disorders of Metal Transport: Disorders in the Transport of Copper, Zinc and Magnesium.- Part X: Organelle-Related Disorders: Lysosomes, Peroxysomes, and Golgi and Pre-Golgi Systems: Disorders of Sphingolipid Metabolism and Ceroid lipofuscinosis.- Pompe Disease, Mucopolysaccharidoses, and Oligosacharidoses.- Peroxisomal Disorders.- Congenital Disorders of Glycosylation.- Cystinosis.

< naar Archief...