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Lysosomal Storage Disorders

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Cover of 'Lysosomal Storage Disorders'

Table of Contents

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    Book Overview
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    Chapter 1 From Lysosomes to Storage Diseases and Back: A Personal Reminiscence
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    Chapter 2 Lysosomal Biogenesis and Disease
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    Chapter 3 The Concept of Treatment in Lysosomal Storage Diseases
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    Chapter 4 Complex Lipid Catabolism
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    Chapter 5 Retroviral Vectors for Gene Therapy
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    Chapter 6 Adenovirus in Gene Therapy
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    Chapter 7 Setting Back the Clock: Adenoviral-Mediated Gene Therapy for Lysosomal Storage Disorders
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    Chapter 8 Adeno-Associated Viral-Mediated Gene Therapy of Lysosomal Storage Disorders
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    Chapter 9 Herpes Simplex Virus Vectors for Gene Therapy of Lysosomal Storage Disorders
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    Chapter 10 Gene Therapy of Lysosomal Storage Disorders by Lentiviral Vectors
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    Chapter 11 Substrate Reduction Therapy
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    Chapter 12 Newborn Screening for Lysosomal Storage Disorders
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    Chapter 13 Genetic Counseling for Lysosomal Storage Diseases
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    Chapter 14 Neural Stem Cell Therapy in Lysosomal Storage Disorders
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    Chapter 15 The GM1 Gangliosidoses
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    Chapter 16 The GM2 Gangliosidoses
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    Chapter 17 Acid Sphingomyelinase-Deficient Niemann–Pick Disease
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    Chapter 18 Krabbe Disease (Globoid Cell Leukodystrophy)
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    Chapter 19 Metachromatic Leukodystrophy
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    Chapter 20 Fabry Disease
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    Chapter 21 Gaucher Disease: Review and Perspectives on Treatment
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    Chapter 22 Therapeutic Goals in the Treatment of Gaucher Disease
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    Chapter 23 The Neuronal Ceroid Lipofuscinoses: Clinical Features and Molecular Basis of Disease
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    Chapter 24 Mucopolysaccharidosis I
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    Chapter 25 Mucopolysaccharidosis II (Hunter Syndrome)
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    Chapter 26 Sanfilippo Syndrome: Clinical Genetic Diagnosis and Therapies
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    Chapter 27 Mucopolysaccharidosis IV (Morquio Syndrome)
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    Chapter 28 Mucopolysaccharidosis Type VI (Maroteaux–Lamy Syndrome)
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    Chapter 29 Mucopolysaccharidosis Type VII (Sly Disease): Clinical, Genetic Diagnosis and Therapies
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    Chapter 30 Pompe Disease-Glycogenosis Type II: Acid Maltase Deficiency
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    Chapter 31 Lysosomal Free Sialic Acid Storage Disorders: Salla Disease and ISSD
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    Chapter 32 Cystinosis
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    Chapter 33 I-Cell Disease
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Title
Lysosomal Storage Disorders
Published by
Springer US, October 2007
DOI 10.1007/978-0-387-70909-3
ISBNs
978-0-387-70908-6, 978-0-387-70909-3
Authors

Barranger, John A., Cabrera-Salazar, Mario A.

X Demographics

X Demographics

The data shown below were collected from the profiles of 2 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 31 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
India 2 6%
Unknown 29 94%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 9 29%
Student > Bachelor 6 19%
Professor 3 10%
Student > Master 3 10%
Researcher 2 6%
Other 3 10%
Unknown 5 16%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 11 35%
Agricultural and Biological Sciences 11 35%
Veterinary Science and Veterinary Medicine 1 3%
Medicine and Dentistry 1 3%
Chemistry 1 3%
Other 1 3%
Unknown 5 16%