Kolodny edwin h (9 Ergebnisse)

Zustand: Fine. 2nd. Used book that is in almost brand-new condition. May contain a remainder mark. Better World Books: Buy Books. Do Good.

Zustand: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.

Zustand: New. pp. xvi + 313 Illus.

Zustand: Used. pp. xvi + 313.

Taschenbuch. Zustand: Neu. Bioimaging in Neurodegeneration | Patricia A. Broderick (u. a.) | Taschenbuch | Contemporary Neuroscience | xvi | Englisch | 2014 | Humana | EAN 9781627038119 | Verantwortliche Person für die EU: Humana Press in Springer Science + Business Media, Heidelberger Platz 3, 14197 Berlin, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu. …

Zustand: New. In English.

Zustand: New. Editor(s): Broderick, Patricia A.; Rahni, David N.; Kolodny, Edwin H. Series: Contemporary Neuroscience. Num Pages: 330 pages, biography. BIC Classification: PSAN. Category: (G) General (US: Trade). Dimension: 279 x 210 x 18. Weight in Grams: 820. . 2014. Paperback. . . . . Books ship from the US and Ireland.…

Gebunden. Zustand: New. Offers a clinical step-by-step approach to treating the complex and often baffling neurogenetic diseases found in children. Conveniently organized by age groups, this title includes chapters that begins by describing symptoms, and then guides you through co.

Buch. Zustand: Neu. Neuware - The expert, up-to-date guidance you need to identify, understand, and treat neurogenetic disorders in childrenWritten 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 treatmentTables categorizing diseases by mechanismsTreatment for disorders that previously had no known treatment optionsThorough discussion of new molecular, biochemical, and brain imaging tests - and how to select the one most likely to reveal a particular diseaseCase examples with clinical pearlsWeb sites and contact information for patient support groups.…