Neurogenetics - 2 Parts
Material type:
TextSeries: 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
Reference
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Library and Information Centre | Library and Information Centre Reference | WL340-II GES (Browse shelf (Opens below)) | Not for loan | 29985 | |
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Library and Information Centre | Library and Information Centre Reference | WL340-I GES (Browse shelf (Opens below)) | Not for loan | 29984 |
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| WL340-II ASB Peripheral nerve disorders 2 | WL340-II CHA Gale encyclopedia of neurological disorders | WL340-II CHA The Gale encyclopaedia of neurological disorders | WL340-II GES Neurogenetics - 2 Parts | WL340-II MAT Recent advances in clinical neurology | WL340-II MUR Reviews in neurology | WL340-II NOS Neurological therapeutics |
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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