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Juvenile Huntington's Disease
Huntington's disease (HD) is an inherited progressive neurodegenerative disorder. Although onset of Huntington's Disease usually occurs in adulthood, the age of onset of the condition is extremely variable with approximately 5-10% of cases having an onset of less than 20 years, or Juvenile Huntington's Disease (JHD). While JHD shares many of the clinical features of adult HD (e.g., chorea and personality disorders), patients with JHD often experience additional problems including seizures, dystonia and Parkinsonism. Diagnosis in patients with JHD is often delayed because of the failure of clinicians to recognise the characteristic features of the condition. While several textbooks have been ...
Juvenile Huntington's Disease
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.
Bibliographia Karaitica
Winner of the Association for Jewish Libraries 2012 Judaica Bibliography Award! This is the first comprehensive bibliography on the Karaites and Karaism. Including over 8,000 items in twenty languages, this bibliography, with its extensive annotations, thoroughly documents the present state of Karaite Studies and provides a solid foundation for future research. Special attention has been given to the organizational structure of the bibliography. A detailed table of contents and a complete set of indices enable the reader to easily navigate through the material. Translations of items from non-Western languages increase the bibliography’s utility for the English-speaking reader. Especially n...
Huntington's Disease
Huntingtons disease, or Huntingtons chorea, is a progressive genetic disease marked by death of brain cells coupled with loss of muscular control and coordination, declining mental abilities, and erratic behavior. Currently, this form of dementia has no cure. "Huntingtons Disease" offers introduces this disease, detailing its history and progression, and discusses the search for the gene that causes it and the development of genetic tests for the gene. This title also addresses the ethical questions of testing people for a disease whose symptoms typically develop later in life.
