- We will send in 10–14 business days.
/images/books/2799432/9780071445085.jpg)
- Author: Gilles Lyon
- Publisher: McGraw Hill / Medical
- ISBN-10: 0071445080
- ISBN-13: 9780071445085
- Format: 19.8 x 24.4 x 3.6 cm, kieti viršeliai
- Language: English
- SAVE -10% with code: EXTRA
Neurology of Hereditary Metabolic Diseases of Children: Third Edition (e-book) (used book) | bookbook.eu
Reviews
Description
Publisher's Note: Products purchased from Third Party sellers are not guaranteed by the publisher for quality, authenticity, or access to any online entitlements included with the product.
The expert, up-to-date guidance you need to identify, understand, and treat neurogenetic disorders in children
Written in a readily-accessible, highly-readable style, this unique reference offers a sound starting point and clinical step-by-step approach to treating the complex and often baffling neurogenetic diseases found in children. Conveniently organized by age groups from prenatal diagnosis to neonate to childhood, each chapter begins by describing symptoms (similar to the way a patient would present), and then guides you through confirming the diagnosis and choosing the appropriate course of therapy.
Completely updated to reflect the significant advances made following the discovery of the DNA sequence on the human genome, the Third Edition of Neurology of Hereditary Metabolic Diseases of Children clarifies the complicated genetics and biochemistry of these illnesses and will prove to be invaluable to the non-specialist and specialist alike.
New to the Third Edition:
Tables categorizing diseases by mechanismsEXTRA 10 % discount with code: EXTRA
The promotion ends in 21d.09:04:16
The discount code is valid when purchasing from 10 €. Discounts do not stack.
- Author: Gilles Lyon
- Publisher: McGraw Hill / Medical
- ISBN-10: 0071445080
- ISBN-13: 9780071445085
- Format: 19.8 x 24.4 x 3.6 cm, kieti viršeliai
- Language: English English
Publisher's Note: Products purchased from Third Party sellers are not guaranteed by the publisher for quality, authenticity, or access to any online entitlements included with the product.
The expert, up-to-date guidance you need to identify, understand, and treat neurogenetic disorders in children
Written in a readily-accessible, highly-readable style, this unique reference offers a sound starting point and clinical step-by-step approach to treating the complex and often baffling neurogenetic diseases found in children. Conveniently organized by age groups from prenatal diagnosis to neonate to childhood, each chapter begins by describing symptoms (similar to the way a patient would present), and then guides you through confirming the diagnosis and choosing the appropriate course of therapy.
Completely updated to reflect the significant advances made following the discovery of the DNA sequence on the human genome, the Third Edition of Neurology of Hereditary Metabolic Diseases of Children clarifies the complicated genetics and biochemistry of these illnesses and will prove to be invaluable to the non-specialist and specialist alike.
New to the Third Edition:
Tables categorizing diseases by mechanisms
Reviews