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02866nam a22003615i 4500 |
| 001 |
978-0-387-70909-3 |
| 005 |
20191026153110.0 |
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cr nn 008mamaa |
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100301s2007 xxu| s |||| 0|eng d |
| 020 |
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|a 9780387709093
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| 024 |
7 |
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|a 10.1007/978-0-387-70909-3
|2 doi
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| 040 |
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|a Sistema de Bibliotecas del Tecnológico de Costa Rica
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| 245 |
1 |
0 |
|a Lysosomal Storage Disorders
|c edited by John A. Barranger, Mario Cabrera-Salazar.
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| 250 |
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|a 1st ed. 2007.
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| 260 |
# |
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|a New York, NY :
|b Springer US :
|b Imprint: Springer,
|c 2007.
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| 300 |
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|a XX, 564 p.
|b online resource.
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| 336 |
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|a text
|b txt
|2 rdacontent
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| 337 |
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|a computer
|b c
|2 rdamedia
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| 338 |
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|a online resource
|b cr
|2 rdacarrier
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| 505 |
0 |
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|a From Lysosomes to Storage Diseases and Back: A Personal Reminiscence -- Lysosomal Biogenesis and Disease -- The Concept of Treatment in Lysosomal Storage Diseases -- Complex Lipid Catabolism -- Retroviral Vectors for Gene Therapy -- Adenovirus in Gene Therapy -- Setting Back the Clock: Adenoviral-Mediated Gene Therapy for Lysosomal Storage Disorders -- Adeno-Associated Viral-Mediated Gene Therapy of Lysosomal Storage Disorders -- Herpes Simplex Virus Vectors for Gene Therapy of Lysosomal Storage Disorders -- Gene Therapy of Lysosomal Storage Disorders by Lentiviral Vectors -- Substrate Reduction Therapy -- Newborn Screening for Lysosomal Storage Disorders -- Genetic Counseling for Lysosomal Storage Diseases -- Neural Stem Cell Therapy in Lysosomal Storage Disorders -- The GM1 Gangliosidoses -- The GM2 Gangliosidoses -- Acid Sphingomyelinase-Deficient Niemann-Pick Disease -- Krabbe Disease (Globoid Cell Leukodystrophy) -- Metachromatic Leukodystrophy -- Fabry Disease -- Gaucher Disease: Review and Perspectives on Treatment -- Therapeutic Goals in the Treatment of Gaucher Disease -- The Neuronal Ceroid Lipofuscinoses: Clinical Features and Molecular Basis of Disease -- Mucopolysaccharidosis I -- Mucopolysaccharidosis II (Hunter Syndrome) -- Sanfilippo Syndrome: Clinical Genetic Diagnosis and Therapies -- Mucopolysaccharidosis IV (Morquio Syndrome) -- Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome) -- Mucopolysaccharidosis Type VII (Sly Disease): Clinical, Genetic Diagnosis and Therapies -- Pompe Disease-Glycogenosis Type II: Acid Maltase Deficiency -- Lysosomal Free Sialic Acid Storage Disorders: Salla Disease and ISSD -- Cystinosis -- I-Cell Disease.
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| 650 |
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|a Cell biology.
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| 650 |
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0 |
|a Human genetics.
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| 650 |
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0 |
|a Epidemiology.
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| 650 |
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0 |
|a Biochemistry.
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| 650 |
1 |
4 |
|a Cell Biology.
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| 650 |
2 |
4 |
|a Human Genetics.
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| 650 |
2 |
4 |
|a Epidemiology.
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| 650 |
2 |
4 |
|a Biochemistry, general.
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| 700 |
1 |
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|a Barranger, John A.
|e editor.
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| 700 |
1 |
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|a Cabrera-Salazar, Mario.
|e editor.
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| 710 |
2 |
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|a SpringerLink (Online service)
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| 773 |
0 |
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|t Springer eBooks
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| 856 |
4 |
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|u https://doi.org/10.1007/978-0-387-70909-3
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