Fabry Disease - Erstausgabe
2010, ISBN: 9789048190324
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[ED: Hardcover], [PU: Springer / Springer Netherlands], Fabry disease is an X-linked inborn error of metabolism wherein deficiency of a lysosomal enzyme results in systemic deposition of … Mehr…
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2010, ISBN: 9048190320
[EAN: 9789048190324], Neubuch, [SC: 0.0], [PU: Springer Netherlands], METABOLISMUS; STOFFWECHSEL - FETTSTOFFWECHSEL; BLOODVESSEL; BONE; CELLS; ENDOTHELIUM; GENETICS; SMOOTHMUSCLE; METABOL… Mehr…
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Fabry disease is an X-linked inborn error of metabolism wherein deficiency of a lysosomal enzyme results in systemic deposition of glycosphingolipids. Storage deposition, and hence pathol… Mehr…
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ISBN: 9789048190324
Fabry disease is an X-linked inborn error of metabolism wherein deficiency of a lysosomal enzyme results in systemic deposition of glycosphingolipids. Storage deposition, and hence pathol… Mehr…
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Fabry Disease - gebunden oder broschiert
2010, ISBN: 9048190320
2010 Gebundene Ausgabe Metabolismus, Stoffwechsel - Fettstoffwechsel, Krankheiten und Störungen, bloodvessel; Bone; Cells; endothelium; Genetics; smoothmuscle; metabolicdisease, mit Sch… Mehr…
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Fabry Disease - Erstausgabe
2010, ISBN: 9789048190324
Gebundene Ausgabe
[ED: Hardcover], [PU: Springer / Springer Netherlands], Fabry disease is an X-linked inborn error of metabolism wherein deficiency of a lysosomal enzyme results in systemic deposition of … Mehr…
Deborah Elstein:
Fabry Disease - gebunden oder broschiert2010, ISBN: 9048190320
[EAN: 9789048190324], Neubuch, [SC: 0.0], [PU: Springer Netherlands], METABOLISMUS; STOFFWECHSEL - FETTSTOFFWECHSEL; BLOODVESSEL; BONE; CELLS; ENDOTHELIUM; GENETICS; SMOOTHMUSCLE; METABOL… Mehr…
ISBN: 9789048190324
Fabry disease is an X-linked inborn error of metabolism wherein deficiency of a lysosomal enzyme results in systemic deposition of glycosphingolipids. Storage deposition, and hence pathol… Mehr…
ISBN: 9789048190324
Fabry disease is an X-linked inborn error of metabolism wherein deficiency of a lysosomal enzyme results in systemic deposition of glycosphingolipids. Storage deposition, and hence pathol… Mehr…
Fabry Disease - gebunden oder broschiert
2010, ISBN: 9048190320
2010 Gebundene Ausgabe Metabolismus, Stoffwechsel - Fettstoffwechsel, Krankheiten und Störungen, bloodvessel; Bone; Cells; endothelium; Genetics; smoothmuscle; metabolicdisease, mit Sch… Mehr…
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Detailangaben zum Buch - Fabry Disease
EAN (ISBN-13): 9789048190324
ISBN (ISBN-10): 9048190320
Gebundene Ausgabe
Erscheinungsjahr: 2010
Herausgeber: Springer Netherlands Core >2 >T
512 Seiten
Gewicht: 1,083 kg
Sprache: eng/Englisch
Buch in der Datenbank seit 2008-11-05T21:37:24+01:00 (Berlin)
Detailseite zuletzt geändert am 2024-05-14T06:48:26+02:00 (Berlin)
ISBN/EAN: 9048190320
ISBN - alternative Schreibweisen:
90-481-9032-0, 978-90-481-9032-4
Alternative Schreibweisen und verwandte Suchbegriffe:
Autor des Buches: elste, gheon, michael beck
Daten vom Verlag:
Autor/in: Deborah Elstein; Gheona Altarescu; Michael Beck
Titel: Fabry Disease
Verlag: Springer; Springer Netherland
512 Seiten
Erscheinungsjahr: 2010-08-12
Dordrecht; NL
Gedruckt / Hergestellt in Niederlande.
Sprache: Englisch
246,09 € (DE)
252,99 € (AT)
271,50 CHF (CH)
POD
XXXVII, 512 p.
BB; Hardcover, Softcover / Medizin/Klinische Fächer; Krankheiten und Störungen; Verstehen; blood vessel; bone; cells; endothelium; genetics; smooth muscle; metabolic disease; Diseases; Medical Genetics; Genetik, Medizin; EA; BC
Fabry disease is an X-linked inborn error of metabolism wherein deficiency of a lysosomal enzyme results in systemic deposition of glycosphingolipids. Storage deposition, and hence pathological disease, occurs preferentially in renal glomerular and tubular epithelial cells, myocardial cells, heart valve fibrocytes, neurons of dorsal root ganglia, and in endothelial smooth muscle cells of blood vessels. Thus, Fabry disease is a multi-system disorder, albeit with considerable phenotypic heterogeneity in onset and in severity; however, it is progressive, exhibits extensive morbidity, and is life-threatening. Within the past two decades, there has been a radical change in the natural course Fabry disease by virtue of the availability of specific enzyme replacement therapy. Moreover, there has been a concerted effort to better understand the underlying pathology and equally to identify patients prior to the onset of irreversible end-organ damage. It is to be hoped that the future for patients with Fabry disease can be viewed with greater, albeit guarded, optimism. This state-of-the-art textbook attempts to bridge the span of pre-clinical studies, clinical finding, and management options in a readable but comprehensive manner for the medical practitioner as well as the interested non-medical reader.first full-length textbook about Fabry disease includes chapters on the therapeutic management options complete and stat-of-the-art range of pre-clinical studies comprehensive chapters on clinical findings all authors are experts with many years of clinical and research experience
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9789400798847 Fabry Disease (Elstein, Deborah (Herausgeber); Beck, Michael (Herausgeber); Altarescu, Gheona (Herausgeber))
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