Geschwind, Daniel H.
Neurogenetics - 2 Parts - Amsterdam Elsevier 27 cm. - xix, 391 p. 27 cm. Part I xx, 395-826 p. 27 cm. Part II - Handbook of clinical neurology Vol.147, Part I Vol.148, Part II .
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.
9780444632333
Neurogenetics
Genetic Diseases, Inborn
Nervous System Diseases - genetics
WL340 / GES
Neurogenetics - 2 Parts - Amsterdam Elsevier 27 cm. - xix, 391 p. 27 cm. Part I xx, 395-826 p. 27 cm. Part II - Handbook of clinical neurology Vol.147, Part I Vol.148, Part II .
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.
9780444632333
Neurogenetics
Genetic Diseases, Inborn
Nervous System Diseases - genetics
WL340 / GES