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Neurogenetics - 2 Parts

By: Geschwind, Daniel HContributor(s): Paulson, Henry L [editor] | Klein, Christine [editor] | Aminoff, Michael J. et. al [Series editors]Material type: TextTextSeries: Handbook of clinical neurology ; Vol.147, Part I | ; Vol.148, Part IIPublication details: Amsterdam Elsevier 27 cmDescription: xix, 391 p. 27 cm. Part I; xx, 395-826 p. 27 cm. Part IIISBN: 9780444632333Subject(s): Neurogenetics | Genetic Diseases, Inborn | Nervous System Diseases - geneticsDDC classification: WL340
Item type: Reference
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Reference Reference Library and Information Centre
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WL340-II GES (Browse shelf (Opens below)) Not for loan 29985
Reference Reference Library and Information Centre
Library and Information Centre
Reference
WL340-I GES (Browse shelf (Opens below)) Not for loan 29984

Section I.
Basic genetic concepts. Clinical approach to the patient with neurogenetic disease /​ Thomas Bird
Genetic and genomic testing for neurological disease in clinical practice /​ Brent L. Fogel and Daniel Geschwind
Ethical issues in neurogenetics /​ Wendy R. Uhlmann
Evolving views of human genetic variation and its relationship to neurologic and psychiatric disease /​ Daniel Geschwind
Epigenetic mechanisms underlying nervous system diseases /​ Mark F. Mehler and Irfan Qureshi
Pharmacogenetics /​ Jeffrey R. Bishop
Bioinformatics and genomic databases /​ Giovanni Coppola and Jason Chen
Towards precision medicine /​ Pedro Gonzalez-Alegre
Section II. Recurring biological themes in neurogenetics. Repeat expansion diseases /​ Henry Lauris Paulson
Mitochondrial diseases /​ Carolyn Sue
The CAG-polyglutamine repeat diseases: A clinical, molecular, genetic and pathophysiological nosology /​ Albert R. La Spada
Section III. Movement disorders. Autosomal dominant cerebellar ataxias /​ Vikram Shakkottai
Autosomal recessive cerebellar ataxias /​ Brent L. Fogel
Genetics of Parkinson disease /​ Aloysius Domingo and Christine Klein
Essential Tremor /​ Elan Louis and Lorraine Clark
Inherited dystonias: Clinical features and molecular pathways /​ Corinne Elise Weisheit, Samuel S. Pappas and William Dauer
Huntington's Disease /​ Sarah Tabrizi, Rhia Ghosh and Amanda Dolphin
Wilson Disease and related copper disorders /​ Matthew Lorincz
Neurodegeneration with brain iron accumulation (NBIA) /​ Susan Judith Hayflick and Penny Hogarth
Primary familial brain calcifications /​ Maria-Jesus Sobrido
Section IV. Neurodevelopmental disorders. Genetics of autism spectrum disorder /​ Daniel Geschwind
The emerging genetic landscape of cerebral palsy /​ Clare Louise van Eyk, Mark Corbett and Alastair MacLennan
Tourette disorder and other tic disorders /​ Thomas Fernandez, Matthew William State and Christopher Pittenger
Sex chromosome aneuploidies /​ David Skuse, Frida Printzlau and Jeanne Wolstencroft
Fragile X syndrome and fragile X-associated tremor ataxia syndrome /​ Deborah Ann Hall.

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