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Libros sobre el tema "Lysosomal storage diseases"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 9 de junio de 2025

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1

A, Barranger John, and Cabrera-Salazar Mario A, eds. Lysosomal storage disorders. New York: Springer, 2007.

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2

Mehta, Atul B., and Bryan Winchester. Lysosomal storage disorders: A practical guide. Chichester, West Sussex: Wiley-Blackwell, 2013.

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3

Mononen, Ilkka. Lysosomal storage disease--aspartylglycosaminuria. New York: Springer, 1997.

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4

Inc, ebrary, ed. Lysosomal storage disorders: Principles and practice. Singapore: World Scientific, 2010.

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5

Boelens, Jaap Jan, and Robert Wynn, eds. Stem Cell Therapy in Lysosomal Storage Diseases. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-8357-1.

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6

A, Gibbs Dorothy, ed. Lysosomal storage diseases: Biochemical and clinical aspects. London: Taylor & Francis, 1986.

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7

G, Thoene Jess, ed. Pathophysiology of lysosomal transport. Boca Raton: CRC Press, 1992.

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8

Al-Essa, Mohammed A. Atlas of common lysosomal and peroxisomal disorders. Riyadh, Saudi Arabia: Scientific Informations Office, Research Centre, King Faisal Specialist Hospital and Research Centre, 1999.

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9

Beck, M., Deborah Elstein, and Gheona Altarescu. Fabry disease. Dordrecht: Springer, 2010.

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10

1935-, Graucob E., ed. Hematologic cytology of storage diseases. Berlin: Springer-Verlag, 1985.

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11

1949-, Courtoy Pierre J., Dautry-Varsat Alice, and NATO-Advanced Research Workshop on Endocytosis (1990 : Paris, France), eds. Endocytosis: From cell biology to health, disease and therapy. Berlin: Springer-Verlag, 1992.

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12

Filosto, Massimiliano. Advances in diagnosis and management of glycogenosis II. Hauppauge, N.Y: Nova Science Publishers, 2011.

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13

A, Azzi, Drahota Z, Papa S, Unesco, and International Biomedical Institute, eds. Molecular basis of membrane-associated diseases. Berlin: Springer-Verlag, 1989.

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14

Anand, Geeta. The Cure. New York: HarperCollins, 2009.

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15

William, Krivit, Paul Natalie W, and March of Dimes Birth Defects Foundation., eds. Bone marrow transplantation for treatment of lysosomal storage diseases: Proceedings of a colloquium held May 7, 1985, Washington, D.C. New York: Liss, 1986.

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16

Tollefsbol, Trygve O. Biological aging: Methods and protocols. New York: Humana Press, 2013.

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17

Edward, Bittar E., and Bittar Neville, eds. Cellular organelles. Greenwich, Conn: JAI Press, 1995.

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18

Lysosomal Storage Diseases. Exon Publications, 2024. https://doi.org/10.36255/lysosomal-storage-diseases.

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Lysosomal Storage Diseases are a group of rare genetic disorders that affect the body’s ability to break down and recycle certain materials within cells, leading to their accumulation and progressive organ damage. This article provides a thorough guide to understanding these disorders, covering their causes, symptoms, and treatment options. It begins with an explanation of what Lysosomal Storage Diseases are, detailing how enzyme deficiencies in lysosomes disrupt normal cellular processes. The article explores the genetic basis of these conditions, focusing on their inheritance patterns and the role of specific genes. The guide outlines the different types of Lysosomal Storage Diseases, including Gaucher’s Disease, Fabry Disease, and Tay-Sachs Disease, highlighting how each condition affects the body uniquely. It describes the diagnostic process, including enzyme activity tests and genetic screening, and discusses treatment options such as enzyme replacement therapy, substrate reduction therapy, and emerging gene therapies. Practical advice for living with these conditions is provided, emphasizing the importance of regular medical care, supportive therapies, and emotional support. Organized to deliver clear and comprehensive information, this book ensures readers gain a solid understanding of Lysosomal Storage Diseases and how they can be managed effectively in daily life.
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19

Platt, Frances, and Nick Platt. Lysosomes and Lysosomal Diseases. Elsevier Science & Technology Books, 2015.

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20

Platt, Frances, and Nick Platt. Lysosomes and Lysosomal Diseases. Elsevier Science & Technology Books, 2015.

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21

Lysosomal storage disorders. New York: Springer, 2007.

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22

Cabrera-Salazar, Mario, and John A. Barranger. Lysosomal Storage Disorders. Springer, 2010.

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23

(Editor), John A. Barranger, and Mario Cabrera (Editor), eds. Lysosomal Storage Disorders. Springer, 2007.

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24

Mehta, Atul B., and Bryan Winchester. Lysosomal Storage Disorders: A Practical Guide. Wiley & Sons, Incorporated, John, 2012.

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25

Mehta, Atul B., and Bryan Winchester. Lysosomal Storage Disorders: A Practical Guide. Wiley & Sons, Incorporated, John, 2022.

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26

Mehta, Atul B., and Bryan Winchester. Lysosomal Storage Disorders: A Practical Guide. Wiley & Sons, Incorporated, John, 2012.

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27

Mehta, Atul B., and Bryan Winchester. Lysosomal Storage Disorders: A Practical Guide. Wiley & Sons, Incorporated, John, 2022.

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28

Mehta, Atul B., and Bryan Winchester. Lysosomal Storage Disorders: A Practical Guide. Wiley & Sons, Incorporated, John, 2012.

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29

Mehta, Atul B., and Bryan Winchester. Lysosomal Storage Disorders: A Practical Guide. Wiley & Sons, Incorporated, John, 2022.

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30

Mehta, Atul B., and Bryan Winchester. Lysosomal Storage Disorders: A Practical Guide. Wiley & Sons, Limited, John, 2012.

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31

Lysosomal Storage Disorders: A Practical Guide. Wiley & Sons, Limited, John, 2022.

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32

Lysosomal storage disease: Aspartylglycosaminuria. New York: Chapman & Hall, 1997.

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33

Johnson, Karl Frank. Characterization of [alpha]-L-fucosidase and its related lysosomal storage disease fucosidosis. 1988.

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34

Neurochemistry of metabolic diseases: Lysosomal storage diseases, phenylketonuria, and Canavan disease. New York: Nova Science Publishers, 2012.

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35

Surendran, Sankar. Neurochemistry of Metabolic Diseases: Lysosomal Storage Diseases, Phenylketonuria, and Canavan Disease. Nova Science Publishers, Incorporated, 2020.

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36

Surendran, Sankar. Neurochemistry of Metabolic Diseases: Lysosomal Storage Diseases, Phenylketonuria, and Canavan Disease. Nova Science Publishers, Incorporated, 2020.

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37

Wynn, Robert, and Jaap Jan Boelens. Stem Cell Therapy in Lysosomal Storage Diseases. Humana Press, 2013.

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38

Bennett, Lunawati. Frontiers in Lysosomal Storage Diseases (LSD) Treatments. Nova Science Publishers, Incorporated, 2023.

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39

Wynn, Robert, and Jaap Jan Boelens. Stem Cell Therapy in Lysosomal Storage Diseases. Humana, 2016.

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40

Pastores, Gregory M. Lysosomal Storage Diseases: Pathobiology and Therapeutic Consideration. Nova Science Publishers, Incorporated, 2016.

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41

Pastores, Gregory M. Lysosomal Storage Disorders: Principles and Practice. World Scientific Publishing Co Pte Ltd, 2009.

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42

Neurochemistry of metabolic diseases: Lysosomal storage diseases, phenylketonuria and Canavan disease, 2007. Kerala, India: Transworld Research Network, 2007.

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43

Gaucher Disease. UNI-MED Verlag AG, 2006.

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44

Parini, Rossella, and Generoso Andria. Lysosomal Storage Diseases: Early Diagnosis and New Treatments. Editions John Libbey Eurotext, 2010.

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45

Azzi, Angelo, Sergio Papa, and Zdenek Drahota. Molecular Basis of Membrane-Associated Diseases. Springer, 2011.

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46

Azzi, Angelo, Sergio Papa, and Zdenek Drahota. Molecular Basis of Membrane-Associated Diseases. Springer London, Limited, 2012.

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47

Ahern-Rindell, Amelia Julia. The genetic and biochemical characterization of an inherited ovine lysosomal storage disease. 1988.

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48

KRIVIT, W. Krivit Bone Marrow Transplantation for Treatment of Lysosomal Storage Diseases. John Wiley & Sons Inc, 1986.

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49

Baydakova, Galina. Biomarkers in diagnostics and therapy monitoring of lysosomal storage diseases. Triumph Publishing, 2025. https://doi.org/10.29039/978-5-94472-257-7-4-2025.

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50

Murnane, Robert Daniel. Pathologic characterization and progress towards preimplantation diagnosis of an ovine lysosomal storage disease. 1989.

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