Neurology of Hereditary Metabolic Diseases of Children: Third Edition

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9780071445085: Neurology of Hereditary Metabolic Diseases of Children: Third Edition

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
  • Treatment for disorders that previously had no known treatment options
  • Thorough discussion of new molecular, biochemical, and brain imaging tests - and how to select the one most likely to reveal a particular disease
  • Case examples with clinical pearls
  • Web sites and contact information for patient support groups
  • "synopsis" may belong to another edition of this title.

    Review:

    "...this is a significant addition to the various books on hereditary neurologic diseases."
    -- European Journal of Paediatric Neurology, May 2008

    About the Author:

    Gilles Lyon, MD is Adjunct Professor, Department of Neurology, New York University School of Medicine.

    Edwin H. Kolodny, MD, is Vice-Chairman of the Executive Committee of the Medical Board of the Tisch Hospital and C-Chairman of the Executive Advisory Committee of the General Clinical Research Center.

    Gregory M. Pastores, MD, Assistant Professor of Neurology and Pediatrics, Member of the New York University Neurology Associates and New York University Neurogenetics Lab.

    "About this title" may belong to another edition of this title.

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    Book Description McGraw-Hill Education - Europe, United States, 2011. Hardback. Book Condition: New. 3rd Revised edition. 239 x 188 mm. Language: English . Brand New Book. 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: Coverage of newly discovered disorders - complete with differential diagnosis, diagnosis, and treatment; Tables categorizing diseases by mechanisms; Treatment for disorders that previously had no known treatment options; Thorough discussion of new molecular, biochemical, and brain imaging tests - and how to select the one most likely to reveal a particular disease; Case examples with clinical pearls; and, Web sites and contact information for patient support groups. Bookseller Inventory # AA39780071445085

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