Da: Majestic Books, Hounslow, Regno Unito
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Condizione: New. pp. 182 1st Edition.
Da: Biblios, Frankfurt am main, HESSE, Germania
EUR 28,00
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Aggiungi al carrelloCondizione: New. pp. 182.
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Aggiungi al carrelloOkart. , deutsch, 795 S., 24 X 21,5 cm, Mit 349 vorwiegend farbigen Abbildungen, 280 Tabellen u. 69 Fallbeispielen. Ecken u. Kanten leicht berieben. Unterer Schnitt m. Mängelexemplarzeichen. , 2.
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Aggiungi al carrelloCondizione: good. Befriedigend/Good: Durchschnittlich erhaltenes Buch bzw. Schutzumschlag mit Gebrauchsspuren, aber vollständigen Seiten. / Describes the average WORN book or dust jacket that has all the pages present.
Editore: Mediscript, M?nchen 1982,, 1982
Da: Antiquariat Petri, Jena, Germania
EUR 12,00
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Aggiungi al carrelloSC. Condizione: Gut. originalgetreuer Einband (Faks,), (Br.)., 4?,230s, in gutem Zustand, [GSA7,1a] Deu 700g.
Da: Romtrade Corp., STERLING HEIGHTS, MI, U.S.A.
Condizione: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.
EUR 124,09
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Aggiungi al carrelloCondizione: As New. Unread book in perfect condition.
Da: Ria Christie Collections, Uxbridge, Regno Unito
EUR 113,79
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Da: Ria Christie Collections, Uxbridge, Regno Unito
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EUR 129,12
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Da: GreatBookPricesUK, Woodford Green, Regno Unito
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Aggiungi al carrelloPaperback. Condizione: Brand New. reprint edition. 168 pages. 8.10x5.40x0.40 inches. In Stock.
Da: Revaluation Books, Exeter, Regno Unito
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. Urate Deposition in Man and its Clinical Consequences | Ursula Gresser (u. a.) | Taschenbuch | x | Englisch | 2012 | Springer | EAN 9783642844935 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.
Da: preigu, Osnabrück, Germania
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. Molecular Genetics, Biochemistry and Clinical Aspects of Inherited Disorders of Purine and Pyrimidine Metabolism | Ursula Gresser | Taschenbuch | xiv | Englisch | 2011 | Springer Vieweg | EAN 9783642849640 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.
Lingua: Inglese
Editore: Springer Berlin Heidelberg, 2012
ISBN 10: 3642844936 ISBN 13: 9783642844935
Da: AHA-BUCH GmbH, Einbeck, Germania
EUR 106,99
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - One person in four in the industrialized countries suffersfrom hyperuricemia and is therefore at risk of developinggouty arthritis, nephrolithiasis, or any of the otherconsequences of urate deposition.At present, far too little is known about urate depositionand the mechanisms by which it occurs, as well as about itsclinical consequences, which include formation of toph; overthe helix of the ear or in bones close to joints that havenever exhibited an attack, development of bursitis, chronictendovaginitis leading to carpal tunnel syndrome, and goutyparaplegia. Information on these matters is needed toestimate the risks of hyperuricemia and to determine whentherapeutic intervention is indicated. The contributions anddiscussions in this book, resulting from an internationalsymposium held in December 1990 in the MedizinischePoliklinik in Munich, provide an up-to-date source ofcurrent knowledge about hyperuricemia in man and itsclinical consequences.
Lingua: Inglese
Editore: Springer Berlin Heidelberg, 2011
ISBN 10: 3642849644 ISBN 13: 9783642849640
Da: AHA-BUCH GmbH, Einbeck, Germania
EUR 106,99
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - Inherited disorders of purine and pyrimidine metabolism inman lead to severe diseases. At the 2nd M}nchnerAdventssymposium the state of the art as to the geneticbasis, clinical aspects, and the biochemical basis has beengiven by leading experts in the fields concerning thefollowing diseases: Hypoxanthine phosphoribosyltransferasedeficiency (HGPRT-deficieny), adeninephosphoribosyltransferase deficiency (APRT-deficiency),hyperuricemia and gout, adenosine deaminase deficiency(ADA-deficiency, purine nucleoside phosphorylase deficiency(PNP-deficiency). All contributions of the symposium arepublished within this volume thus giving and overview ofthis most interesting field.
Da: Mispah books, Redhill, SURRE, Regno Unito
EUR 221,82
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Aggiungi al carrelloPaperback. Condizione: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.
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Aggiungi al carrelloPF. Condizione: New.
Editore: Urban u. Fischer, Mchn., 1996
ISBN 10: 388320188X ISBN 13: 9783883201887
Da: DER COMICWURM - Ralf Heinig, Hohnhorst, DE, Germania
EUR 27,48
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Aggiungi al carrelloBroschiert. Condizione: Gut. ALTERSBEDINGTE GEBRAUCHSSPUREN!!!Es können auch Mängelexemplare sein---. nein.
Da: Revaluation Books, Exeter, Regno Unito
EUR 107,39
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Aggiungi al carrelloPaperback. Condizione: Brand New. 2nd edition. 570 pages. German language. 8.19x5.43x1.26 inches. In Stock.
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EUR 38,17
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Aggiungi al carrelloPAP. Condizione: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.
Da: PBShop.store UK, Fairford, GLOS, Regno Unito
EUR 36,29
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Aggiungi al carrelloPAP. Condizione: New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.
Da: Brook Bookstore On Demand, Napoli, NA, Italia
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Aggiungi al carrelloCondizione: new. Questo è un articolo print on demand.
Da: Brook Bookstore On Demand, Napoli, NA, Italia
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Aggiungi al carrelloCondizione: new. Questo è un articolo print on demand.
Lingua: Inglese
Editore: Springer, Springer Berlin Heidelberg Jan 2012, 2012
ISBN 10: 3642844936 ISBN 13: 9783642844935
Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Germania
EUR 106,99
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Aggiungi al carrelloTaschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -One person in four in the industrialized countries suffersfrom hyperuricemia and is therefore at risk of developinggouty arthritis, nephrolithiasis, or any of the otherconsequences of urate deposition.At present, far too little is known about urate depositionand the mechanisms by which it occurs, as well as about itsclinical consequences, which include formation of toph; overthe helix of the ear or in bones close to joints that havenever exhibited an attack, development of bursitis, chronictendovaginitis leading to carpal tunnel syndrome, and goutyparaplegia. Information on these matters is needed toestimate the risks of hyperuricemia and to determine whentherapeutic intervention is indicated. The contributions anddiscussions in this book, resulting from an internationalsymposium held in December 1990 in the MedizinischePoliklinik in Munich, provide an up-to-date source ofcurrent knowledge about hyperuricemia in man and itsclinical consequences. 172 pp. Englisch.
Lingua: Inglese
Editore: Springer Berlin Heidelberg, Springer Berlin Heidelberg Dez 2011, 2011
ISBN 10: 3642849644 ISBN 13: 9783642849640
Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Germania
EUR 106,99
Quantità: 2 disponibili
Aggiungi al carrelloTaschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Inherited disorders of purine and pyrimidine metabolism inman lead to severe diseases. At the 2nd M}nchnerAdventssymposium the state of the art as to the geneticbasis, clinical aspects, and the biochemical basis has beengiven by leading experts in the fields concerning thefollowing diseases: Hypoxanthine phosphoribosyltransferasedeficiency (HGPRT-deficieny), adeninephosphoribosyltransferase deficiency (APRT-deficiency),hyperuricemia and gout, adenosine deaminase deficiency(ADA-deficiency, purine nucleoside phosphorylase deficiency(PNP-deficiency). All contributions of the symposium arepublished within this volume thus giving and overview ofthis most interesting field. 200 pp. Englisch.
Lingua: Inglese
Editore: Springer Berlin Heidelberg, 2011
ISBN 10: 3642849644 ISBN 13: 9783642849640
Da: moluna, Greven, Germania
EUR 92,27
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Aggiungi al carrelloCondizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. I Purine Salvage Enzymes.- IA Hypoxanthine Guanine Phosphoribosyltransferase (HGPRT) Deficiency 3.- 1 Introductory Remarks.- 2 The Clinical Aspects of HGPRT Deficiency.- 3 The Biochemical Basis of HGPRT Deficiency.- 4 Prenatal Diagnosis of Lesch-Nyhan Syndr.