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Fabry Disease by Deborah Elstein: New

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eBay-objectnummer:282936317483
Laatst bijgewerkt op 18 dec 2023 20:34:47 CETAlle herzieningen bekijkenAlle herzieningen bekijken

Specificaties

Objectstaat
Nieuw: Een nieuw, ongelezen en ongebruikt boek in perfecte staat waarin geen bladzijden ontbreken of ...
ISBN
9048190320
EAN
9789048190324
Book Title
Fabry Disease
Item Length
9.3 in
Publisher
Springer Netherlands
Publication Year
2010
Type
Textbook
Format
Hardcover
Language
English
Illustrator
Yes
Author
Gheona Altarescu
Genre
Science, Medical
Topic
Life Sciences / Biochemistry, Endocrinology & Metabolism, Genetics, Diseases
Item Width
6.1 in
Item Weight
38.3 Oz
Number of Pages
Xxxvii, 512 Pages

Over dit product

Product Information

This is the first full-length textbook about Fabry disease. It covers pre-clinical studies, clinical findings, and management options. These are comprehensively presented for the medical practitioner as well as the interested non-medical reader.

Product Identifiers

Publisher
Springer Netherlands
ISBN-10
9048190320
ISBN-13
9789048190324
eBay Product ID (ePID)
109308489

Product Key Features

Author
Gheona Altarescu
Book Title
Fabry Disease
Format
Hardcover
Language
English
Topic
Life Sciences / Biochemistry, Endocrinology & Metabolism, Genetics, Diseases
Publication Year
2010
Type
Textbook
Illustrator
Yes
Genre
Science, Medical
Number of Pages
Xxxvii, 512 Pages

Dimensions

Item Length
9.3 in
Item Width
6.1 in
Item Weight
38.3 Oz

Additional Product Features

Intended Audience
Scholarly & Professional
Number of Volumes
1 Vol.
Lc Classification Number
Rc1-1245
Reviews
From the reviews: "As the first book dedicated to Fabry Disease, this provides an extensive, detailed review of all current information about this rare disorder. ... The information presented here will serve genetics specialists in the evaluation, surveillance, and management of affected patients with this rare disorder. ... It is also a well-written and informative tool for families affected by this disorder, helping them understand its natural course and available treatment. ... This highly specialized, unique book on this rare disorder has no comparison." (Luis F. Escobar, Doody's Review Service, March, 2012), From the reviews:As the first book dedicated to Fabry Disease, this provides an extensive, detailed review of all current information about this rare disorder. … The information presented here will serve genetics specialists in the evaluation, surveillance, and management of affected patients with this rare disorder. … It is also a well-written and informative tool for families affected by this disorder, helping them understand its natural course and available treatment. … This highly specialized, unique book on this rare disorder has no comparison. (Luis F. Escobar, Doody's Review Service, March, 2012), From the reviews: "As the first book dedicated to Fabry Disease, this provides an extensive, detailed review of all current information about this rare disorder. ... The information presented here will serve genetics specialists in the evaluation, surveillance, and management of affected patients with this rare disorder.  ... It is also a well-written and informative tool for families affected by this disorder, helping them understand its natural course and available treatment. ... This highly specialized, unique book on this rare disorder has no comparison." (Luis F. Escobar, Doody's Review Service, March, 2012)
Table of Content
Pre-Clinical.- Molecular Genetics of Fabry Disease and Genotype-Phenotype Correlation.- The Structure of Human ?-Galactosidase A and Implications for Fabry Disease.- Subcellular, Cellular and Organ Pathology of Fabry Disease.- Biochemistry of Fabry Disease.- Clinically Relevant Examples of Genotype-Phenotype Correlation.- Laboratory Diagnosis of Fabry Disease.- Biomarkers for Fabry Disease.- Fabry Disease Case Finding Studies in High-Risk Populations.- Small Molecule Drug Discovery for Fabry Disease.- Clinical.- Clinical Manifestations of Fabry Disease: An Overview.- The Heart in Fabry Disease - from Pathogenesis to Enzyme Replacement Therapy.- Renal Manifestations of Fabry Disease.- Neurological Manifestations in Fabry Disease.- Dermatological Manifestations of Fabry Disease.- Histopathology of Skin in Fabry Disease.- Bone and Muscle Involvement in Fabry Disease.- The Eye in Fabry Disease.- Pulmonary, Ear and Less Commonly Appreciated Manifestations.- Neuropsychiatric Manifestations of AFD.- Genetic Counseling and Psychosocial Issues for Individuals and Their Families with Fabry Disease.- Fabry Disease in Females.- Fabry Disease in Pediatric Patients.- Experimental Studies in Mice on the Vasculopathy of Fabry Disease.- Management.- Overview.- Agalsidase Alfa in the Treatment of Anderson-Fabry Disease.- Agalsidase Beta Clinical Trials and Long Term Experience.- Analyses of Agalsidase Alfa and Agalsidase Beta for the Treatment of Fabry Disease.- Enzyme Replacement Therapy in Children with Fabry Disease.- Pharmacological Chaperone Therapy for Fabry Disease.- Potential Factors Influencing Treatment Outcomes.- Symptomatic and Ancillary Therapy.- The Price of Care Versus the Cost of Caring.
Copyright Date
2010
Dewey Decimal
616.3995
Dewey Edition
22

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