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Barranger, John A.

Lysosomal Storage Disorders

Barranger, John A. - Lysosomal Storage Disorders, ebook

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Ebook, PDF with Adobe DRM
ISBN: 9780387709093
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Table of contents

1. From Lysosomes to Storage Diseases and Back: A Personal Reminiscence
Christian Duve

2. Lysosomal Biogenesis and Disease
Doug Brooks, Emma Parkinson-Lawrence

3. The Concept of Treatment in Lysosomal Storage Diseases
Roscoe O. Brady

4. Complex Lipid Catabolism
Roscoe O. Brady, Roscoe O. Brady

5. Retroviral Vectors for Gene Therapy
Seon-Hee Kim, Paul D. Robbins

6. Adenovirus in Gene Therapy
Angela Montecalvo, Andrea Gambotto, Leonardo D’Aiuto

7. Setting Back the Clock: Adenoviral-Mediated Gene Therapy for Lysosomal Storage Disorders
Dolan Sondhi, Neil R. Hackett, Stephen M. Kaminksy, Ronald G. Crystal

8. Adeno-Associated Viral-Mediated Gene Therapy of Lysosomal Storage Disorders
Mario A. Cabrera-Salazar, Seng H. Cheng

9. Herpes Simplex Virus Vectors for Gene Therapy of Lysosomal Storage Disorders
Edward A. Burton, Joseph C. Glorioso

10. Gene Therapy of Lysosomal Storage Disorders by Lentiviral Vectors
Alessandra Biffi, Luigi Naldini

11. Substrate Reduction Therapy
Frances M. Platt, Terry D. Butters

12. Newborn Screening for Lysosomal Storage Disorders
C. Ronald Scott, Frantisek Turecek, Michael H. Gelb

13. Genetic Counseling for Lysosomal Storage Diseases
Erin O'Rourke, Dawn Laney, Cindy Morgan, Kim Mooney, Jennifer Sullivan

14. Neural Stem Cell Therapy in Lysosomal Storage Disorders
Jean-Pyo Lee, Dan Clark, Mylvaganam Jeyakumar, Rodolfo Gonzalez, Scott Mckercher, Franz-Josef Muller, Rahul Jandial, Rosanne M. Taylor, Kook Park, Thomas N. Seyfried, Frances M. Platt, Evan Y. Snyder

15. The GM1 Gangliosidoses
Gustavo Charria-Ortiz

16. The GM2 Gangliosidoses
Gustavo A. Charria-Ortiz

17. Acid Sphingomyelinase-Deficient Niemann–Pick Disease
Edward H. Schuchmann, Margaret McGovern, Calogera M. Simonaro, Melissa P. Wasserstein, Robert J. Desnick

18. Krabbe Disease (Globoid Cell Leukodystrophy)
Junko Matsuda, Kunihiko Suzuki

19. Metachromatic Leukodystrophy
Volkmar Gieselmann

20. Fabry Disease
Roscoe O. Brady

21. Gaucher Disease: Review and Perspectives on Treatment
Mario A. Cabrera-Salazar, John A. Barranger

22. Therapeutic Goals in the Treatment of Gaucher Disease
Neal Weinreb

23. The Neuronal Ceroid Lipofuscinoses: Clinical Features and Molecular Basis of Disease
Beverly L. Davidson, Mario A. Cabrera-Salazar, David A. Pearce

24. Mucopolysaccharidosis I
Lorne A. Clarke

25. Mucopolysaccharidosis II (Hunter Syndrome)
Lorne A. Clarke

26. Sanfilippo Syndrome: Clinical Genetic Diagnosis and Therapies
John J. Hopwood

27. Mucopolysaccharidosis IV (Morquio Syndrome)
Shunji Tomatsu, Adriana M. Montaño, Tatsuo Nishioka, Tadao Orii

28. Mucopolysaccharidosis Type VI (Maroteaux–Lamy Syndrome)
James. E. Wraith

29. Mucopolysaccharidosis Type VII (Sly Disease): Clinical, Genetic Diagnosis and Therapies
Denise J. Norato

30. Pompe Disease-Glycogenosis Type II: Acid Maltase Deficiency
Arnold Reuser, Marian Kroos

31. Lysosomal Free Sialic Acid Storage Disorders: Salla Disease and ISSD
Amanda Helip-Wooley, Robert Kleta, William A. Gahl

32. Cystinosis
Amanda Helip-Wooley, Robert Kleta, William A. Gahl

33. I-Cell Disease
Doug Brooks, Chris Turner, Viv Muller, John J. Hopwood, Peter Meikle

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Printing: not available
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Keywords: TECHNOLOGY & ENGINEERING / Biomedical TEC059000

Author(s)
 
Publisher
Springer
Publication year
2008
Language
en
Edition
1
Category
Medicine, Health Care, Mode
Format
Ebook
eISBN (PDF)
9780387709093

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