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Lysosomal Storage Disorders

our understanding of both the scientific and the clinical basis of these diseases. Lysosomal Storage Disorders: A Practical Guide is the fruit;

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Stem Cell Therapy in Lysosomal Storage Diseases

Stem Cell therapy for lysosomal diseases (LSDs) is developing rapidly. This volume discusses the history, current practice and future;

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Neurochemistry of Metabolic Diseases

abnormalities is useful to interpret possible targets in these diseases. This book reveals what factors contribute in lysosomal storage diseases;

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Glycobiology and Human Diseases

urinary glycans as a possible method for the diagnosis of lysosomal storage diseases, glycobiology of human milk (biological roles and diseases;

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Glycobiology and Human Diseases

urinary glycans as a possible method for the diagnosis of lysosomal storage diseases, glycobiology of human milk (biological roles and diseases;

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Clinical Neurogenetics, An Issue of Neurologic Clinics

; Autism/ASD; Fragile X Tremor Ataxia Syndrome (FXTAS); Lysosomal Storage Diseases; Psychiatric Disorders; Dominant Spinocerebellar Ataxias;

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Lysosomal Storage Diseases

description of the various pathophysiologic changes associated with the lysosomal storage disorders. Therapeutic considerations and aspects relating;

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Lysosomes and Lysosomal Diseases

This new volume of Methods in Cell Biology looks at methods for lysosomes and lysosomal diseases. Chapters focus upon practical;

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Lysosomal Storage Diseases

diseases (LSDs), transforming many of them from dire, untreatable progressive diseases to conditions that allow for possible cure or mitigation;

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Chemical Diagnostics

Screening: About Both Small Molecular Diseases and Lysosomal Storage Diseases, by W.-L. Hwu, Y.-H. Chien, N.-C. Lee, S.-F. Wang, S.-C. Chiang, L.-W;

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Neurochemistry of Metabolic Diseases

. Several new developments on metabolic diseases research have been emerging. Gaucher disease is a lysosomal storage disorder caused by;

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Inborn Errors of Metabolism, An Issue of Pediatric Clinics of North America

storage diseases and gluconeogenesis defects; Inborn errors of metabolism with myopathy: defects of fatty acid oxidation and carnitine transport;

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Lysosomal Storage Disorders

This book presents an overview of lysosomal storage disorders, and provides the reader with an understanding of clinical features;

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Autophagy of the Nervous System

, ischemia/hypoxia and lysosomal storage diseases, will be discussed along with current drug development strategies targeting autophagy.;

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Pharmaceutical Biocatalysis

treatment of thromboembolic diseases, and the molecular mechanisms for statin pleiotropy and its clinical relevance in cardiovascular diseases. The;

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Gaucher Disease

Book Competition! Although rare in the general population, Gaucher disease is the most prevalent of the lysosomal storage disorders, making;

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Gaucher Disease

Book Competition! Although rare in the general population, Gaucher disease is the most prevalent of the lysosomal storage disorders, making;

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Rare Diseases

highlighted and we look at enzyme replacement therapy in lysosomal storage diseases. This work is part of a series, produced with the involvement;

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Recent Advances in iPSC Disease Modeling

Recent Advances in iPSC Disease Modeling, Volume One addresses how induced pluripotent stem cells can be used to model various diseases;

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Progranulin and Central Nervous System Disorders

targeting the recovery of lysosomal function appear to hold particular promise in patients with neurodegenerative diseases resulting from PGRN;

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Progranulin and Central Nervous System Disorders

targeting the recovery of lysosomal function appear to hold particular promise in patients with neurodegenerative diseases resulting from PGRN;

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Biometals in Neurodegenerative Diseases

Biometals in Neurodegenerative Diseases: Mechanisms and Therapeutics is an authoritative and timely resource bringing together the;

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Metabolic Encephalopathies

, urea cycle defects, lysosomal storage and peroxylsomal disorders. Finally, a discussion of long term follow-up and family related issues also;

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Charnolophagy in Health and Disease

je de site van RIVM.This book introduces charnolophagy (CP) as energy-driven, lysosomal-dependent mitochondrial inclusion;

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Metal Chelation in Medicine

therapy for treating diseases caused by toxic and heavy metal poisoning, chelating agents are capable of binding to toxic metal ions to form;

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The Ubiquitin-proteasome System

to the discoverers of ubiquitin as a cofactor for intracellular non-lysosomal proteolysis. There is a voluminous literature showing that;

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Nathan and Oski's Hematology and Oncology of Infancy and Childhood, 2-Volume Set

> thanks to new and revised chapters covering topics such as paroxysmal nocturnal hemoglobinuria, lysosomal storage diseases, childhood genetic;

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