Juvenile Huntington's Disease: and other trinucleotide repeat disorders - Oliver W J Quarrell - Grāmatas - Oxford University Press - 9780199236121 - 2009. gada 8. janvāris
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Oliver W J Quarrell
Juvenile Huntington's Disease: and other trinucleotide repeat disorders

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Huntington's disease (HD) is an inherited progressive neurodegenerative disorder. Although onset of HD usually occurs in adulthood, a small percentage of cases develop symptoms before 20 years of age (juvenile-onset Huntington's Disease or JHD). This book summarises, for the first time, the clinical and scientific knowledge available on JHD.

224 pages, 16 black and white line drawings and 10 photographs

Mediji Grāmatas     Hardcover Book   (Grāmata ar cieto muguriņu un vāku)
Izlaists 2009. gada 8. janvāris
ISBN13 9780199236121
Izdevēji Oxford University Press
Lapas 222
Izmēri 163 × 240 × 19 mm   ·   470 g
Valoda Angļu  
Redaktors Barker, Roger A. (Reader in Clinical Neuroscience and Honorary Consultant Neurologist, University of Cambridge and Addenbrooke's Hospital, UK)
Redaktors Brewer, Helen M. (Care Adviser - Juvenile Huntington's Disease, Huntington's Disease Association, England and Wales, UK)
Redaktors Landwehrmeyer, G. Bernhard (Professor of Neurology at the University of Ulm, Germany and Chief Executive of the European Huntington's Disease Network)
Redaktors Nance, Martha A. (Medical Director of the HDSA Center of Excellence, Hennepin County Medical Center, Minneapolis, USA and Adjunct Professor in the Department of Neurology at the University of Minnesota, USA)
Redaktors Quarrell, Oliver W.J. (Consultant in Clinical Genetics at Sheffield Children's Hospital, and Vice-Chair of the Huntington's Disease Association, UK)
Redaktors Squitieri, Ferdinando (, Director of the Neurogenetics Unit, IRCCS Neuromed and Centre for Rare diseases, Pozzilli, Italy)

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