Walker phd ruth (28 Ergebnisse)

Hardcover. Zustand: Fine.

Hardcover. Zustand: New.

Hardcover. Zustand: New. Brand new hardback; never opened; pristine.

Zustand: Good. This is an ex-library book and may have the usual library/used-book markings inside.This book has hardback covers. In good all round condition. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,850grams, ISBN:9780195393514.

Zustand: New. pp. xxi + 452 Illus.

Zustand: New. pp. xxi + 452.

Zustand: Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.

Zustand: New. pp. xxi + 452.

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. Brand New Original US Edition. Customer service! Satisfaction Guaranteed.

Zustand: Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.

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. Brand New! Fast Delivery This is an International Edition and ship within 24-48 hours. Deliver by FedEx and Dhl, & Aramex, UPS, & USPS and we do accept APO and PO BOX Addresses. Order can be delivered worldwide within 6-10 days and we do have flat rate for up to 2LB. Extra shipping charges will be requested if the Book weight is more than 5 LB. This Item May be shipped from India, United states & United Kingdom. Depending on your location and availability.…

Rilegato in Tela. Zustand: fine. Oxford, 2010; clothbound, pp. 480, cm 16x23. Libro.

Zustand: New.

Zustand: As New. Unread book in perfect condition.

Zustand: New.

Zustand: New. Editor(s): Walker, Ruth, PhD. Num Pages: 480 pages, 41 illustrations. BIC Classification: MJN. Category: (P) Professional & Vocational. Dimension: 242 x 160 x 28. Weight in Grams: 786. . 2010. Illustrated. hardcover. . . . .

Zustand: As New. Unread book in perfect condition.

Hardback. Zustand: New. The involuntary movement disorder known as chorea can be due to a wide variety of neurological conditions, both genetic and acquired. This volume provides a comprehensive account of these conditions. While Huntington's disease is the prototypic inherited chorea, with the development of the genetic test for this disorder it has become apparent that a small but significant proportion of patients with this phenotype do not have this diagnosis. Although less common than Huntington's disease, it is vital to correctly diagnose these patients. Advances in molecular medicine have resulted in the identification of new genetic causes of chorea and expanded the phenotype of disorders not typically thought to cause this movement disorder. Non-genetic etiologies are discussed, including medications, structural lesions, psychogenic causes, and metabolic abnormalities. This book describes in detail the latest clinical and etiological information regarding the causes of chorea. Psychopathology, management, and pathophysiology of chorea, are also addressed. Many chapters are contributed by authors working at the forefront of research in the specific disorders, and provide the latest basic and clinical research, some from their own laboratories.…

Zustand: New. Editor(s): Walker, Ruth, PhD. Num Pages: 480 pages, 41 illustrations. BIC Classification: MJN. Category: (P) Professional & Vocational. Dimension: 242 x 160 x 28. Weight in Grams: 786. . 2010. Illustrated. hardcover. . . . . Books ship from the US and Ireland.

Hardback. Zustand: New. The involuntary movement disorder known as chorea can be due to a wide variety of neurological conditions, both genetic and acquired. This volume provides a comprehensive account of these conditions. While Huntington's disease is the prototypic inherited chorea, with the development of the genetic test for this disorder it has become apparent that a small but significant proportion of patients with this phenotype do not have this diagnosis. Although less common than Huntington's disease, it is vital to correctly diagnose these patients. Advances in molecular medicine have resulted in the identification of new genetic causes of chorea and expanded the phenotype of disorders not typically thought to cause this movement disorder. Non-genetic etiologies are discussed, including medications, structural lesions, psychogenic causes, and metabolic abnormalities. This book describes in detail the latest clinical and etiological information regarding the causes of chorea. Psychopathology, management, and pathophysiology of chorea, are also addressed. Many chapters are contributed by authors working at the forefront of research in the specific disorders, and provide the latest basic and clinical research, some from their own laboratories.…

Zustand: new. Questo è un articolo print on demand.

HRD. Zustand: New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

HRD. Zustand: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

Hardcover. Zustand: new. Hardcover. The involuntary movement disorder known as chorea can be due to a wide variety of neurological conditions, both genetic and acquired. This volume provides a comprehensive account of these conditions. While Huntington's disease is the prototypic inherited chorea, with the development of the genetic test for this disorder it has become apparent that a small but significant proportion of patients with this phenotype do not have this diagnosis. Although less common thanHuntington's disease, it is vital to correctly diagnose these patients with advances in molecular medicine, it is now easier to identify new genetic causes of chorea and expand the phenotype ofdisorders not typically thought to cause this movement disorder. Non-genetic etiologies are also discussed, including medications, structural lesions, psychogenic causes, and metabolic abnormalities.This book describes in detail the latest clinical and etiological information regarding the causes of chorea. Psychopathology, management, and pathophysiology of chorea, are also addressed.Many chapters are contributed by authors working at the forefront ofresearch in the specific disorders, and provide the latest basic and clinical research, some from their own laboratories. Chorea can be the manifestation of a wide variety of neurological conditions, both genetic and acquired. Advances in genetics have demonstrated that chorea can be due to a large number of inherited disorders. This volume provides a comprehensive account of the causes of chorea, in addition to pathophysiology and management. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability. …

Buch. Zustand: Neu. Differential Diagnosis of Chorea | Ruth H. Walker | Buch | Gebunden | Englisch | 2010 | OUP US | EAN 9780195393514 | Verantwortliche Person für die EU: Libri GmbH, Europaallee 1, 36244 Bad Hersfeld, gpsr[at]libri[dot]de | Anbieter: preigu Print on Demand.

Buch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - The involuntary movement disorder known as chorea can be due to a wide variety of neurological conditions, both genetic and acquired. This volume provides a comprehensive account of these conditions. While Huntington's disease is the prototypic inherited chorea, with the development of the genetic test for this disorder it has become apparent that a small but significant proportion of patients with this phenotype do not have this diagnosis. Although less common than Huntington's disease, it is vital to correctly diagnose these patients. Advances in molecular medicine have resulted in the identification of new genetic causes of chorea and expanded the phenotype of disorders not typically thought to cause this movement disorder. Non-genetic etiologies are discussed, including medications, structural lesions, psychogenic causes, and metabolic abnormalities. This book describes in detail the latest clinical and etiological information regarding the causes of chorea. Psychopathology, management, and pathophysiology of chorea, are also addressed. Many chapters are contributed by authors working at the forefront of research in the specific disorders, and provide the latest basic and clinical research, some from their own laboratories.…