Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease, Fifth Edition

Content: 
Front Matter, Pages i-iii
Copyright, Page iv
Dedications, Page v
Preface to the Fifth Edition, Pages xxxiii-xxxiv, Roger N. Rosenberg, Juan M. Pascual
Contributors, Pages xxxv-xxxix, Nicholas Ah Mew, Wado Akamatsu, Hasan Orhan Akman, Koji Aoyama, W. David Arnold, Rafael Artuch, Robert M. Bachoo, Sergio E. Baranzini, Michael Beck, Merrill D. Benson, Vladimir M. Berginer, Gerard T. Berry, Kevin M. Biglan, Thomas D. Bird, D. Montgomery Bissell, Michael H. Bloch, Aldobrando Broccolini, Robert H. Brown Jr., Allison Caban-Holt, Brenda Canine, C. Thomas Caskey,  et al.
Chapter 1 - Mendelian, Non-Mendelian, Multigenic Inheritance, and Epigenetics, Pages 3-27, Tamar Harel, Davut Pehlivan, C. Thomas Caskey, James R. Lupski
Chapter 2 - Genotype–Phenotype Correlations, Pages 29-38, Thomas D. Bird, Marie Y. Davis
Chapter 3 - Immunogenetics of Neurological Disease, Pages 39-50, Ramyiadarsini I. Elangovan, Sreeram V. Ramagopalan, David A. Dyment
Chapter 4 - Pharmacogenomic Approaches to the Treatment of Sporadic Alzheimer Disease using Cholinomimetic Agents, Pages 51-62, Judes Poirier, Justin Miron, Cynthia Picard
Chapter 5 - Application of Mouse Genetics to Human Disease: Generation and Analysis of Mouse Models, Pages 63-75, Teresa M. Gunn, Brenda Canine
Chapter 6 - DNA Sequencing and Other Methods of Exonic and Genomic Analyses, Pages 77-85, Jun Mitsui, Hiroyuki Ishiura, Shoji Tsuji
Chapter 7 - Association, Cause and Causal Association: Means, Methods and Measures, Pages 87-93, Walter A. Kukull
Chapter 8 - Gene Therapy for Neurological Disease, Pages 95-101, Theodore Friedmann
Chapter 9 - Direct Induction of Neural Stem Cells from Somatic Cells, Pages 103-106, Wado Akamatsu, Hideyuki Okano
Chapter 10 - Neuroimaging in Dementias, Pages 107-118, Prashanthi Vemuri, Melissa E. Murray, Clifford R. Jack Jr.
Chapter 11 - Cognitive Enhancers and Mental Impairment: Emerging Ethical Issues, Pages 119-126, Fabrice Jotterand, Jennifer L. McCurdy, Bernice Elger
Chapter 12 - Genetic Counseling, Pages 127-133, Wendy R. Uhlmann
Chapter 13 - Cerebral Malformations, Pages 137-150, William D. Graf, Shihui Yu
Chapter 14 - Global Developmental Delay and Intellectual Disability, Pages 151-161, Myriam Srour, Michael Shevell
Chapter 15 - Down Syndrome, Pages 163-170, Allison Caban-Holt, Elizabeth Head, Frederick Schmitt
Chapter 16 - An Overview of Rett Syndrome, Pages 171-182, Kristen L. Szabla, Lisa M. Monteggia
Chapter 17 - Fragile X-Associated Disorders, Pages 183-195, Reymundo Lozano, Emma B. Hare, Randi J. Hagerman
Chapter 18 - Autism Spectrum Disorders: Clinical Considerations, Pages 197-207, Patricia Evans, Sailaja Golla, Mary Ann Morris
Chapter 19 - Metabolic and Genetic Causes of Autism, Pages 209-217, Sailaja Golla, Patricia Evans
Chapter 20 - Angelman Syndrome, Pages 219-228, Charles A. Williams, Jennifer M. Mueller
Chapter 21 - Prion Diseases, Pages 229-254, James A. Mastrianni
Chapter 22 - The Mitochondrial Genome, Pages 259-269, Eric A. Schon
Chapter 23 - Mitochondrial Disorders Due to Mutations in the Mitochondrial Genome, Pages 271-281, Salvatore DiMauro, Carmen Paradas
Chapter 24 - Mitochondrial Disorders Due to Mutations in the Nuclear Genome, Pages 283-290, Patrick F. Chinnery
Chapter 25 - Pyruvate Dehydrogenase, Pyruvate Carboxylase, Krebs Cycle and Mitochondrial Transport Disorders, Pages 291-297, Mireia Tondo, Isaac Marin-Valencia, Qian Ma, Juan M. Pascual
Chapter 26 - Gaucher Disease: Neuronopathic Forms, Pages 301-311, Raphael Schiffmann
Chapter 27 - The Niemann–Pick Diseases, Pages 313-320, Edward H. Schuchman, Robert J. Desnick
Chapter 28 - GM2-Gangliosidoses, Pages 321-330, Gregory M. Pastores, Gustavo H.B. Maegawa
Chapter 29 - Metachromatic Leukodystrophy and Multiple Sulfatase Deficiency, Pages 331-336, Florian S. Eichler
Chapter 30 - Krabbe Disease: Globoid Cell Leukodystrophy, Pages 337-346, David A. Wenger, Paola Luzi
Chapter 31 - The Mucopolysaccharidoses, Pages 347-363, Reuben Matalon, Kimberlee Michals Matalon, Geetha L. Radhakrishnan
Chapter 32 - The Mucolipidoses, Pages 365-368, Reuben Matalon, Kimberlee Michals Matalon
Chapter 33 - Disorders of Glycoprotein Degradation: Sialidosis, Fucosidosis, α-Mannosidosis, β-Mannosidosis, and Aspartylglycosaminuria, Pages 369-383, William G. Johnson
Chapter 34 - β-Galactosidase Deficiency: GM1 Gangliosidosis, Morquio B Disease, and Galactosialidosis, Pages 385-394, William G. Johnson
Chapter 35 - Acid Ceramidase Deficiency: Farber Lipogranulomatosis and Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy, Pages 395-402, Michael Beck, Hugo W. Moser, Konrad Sandhoff
Chapter 36 - Wolman Disease, Pages 403-409, Isaac Marin-Valencia, Juan M. Pascual
Chapter 37 - Lysosomal Membrane Disorders: LAMP-2 Deficiency, Pages 411-417, Kazuma Sugie, Ichizo Nishino
Chapter 38 - Fabry Disease: α-Galactosidase A Deficiency, Pages 419-430, Robert J. Desnick
Chapter 39 - Schindler Disease: Deficient- N-Acetylgalactosaminidase Activity, Pages 431-439, Detlev Schindler, Robert J. Desnick
Chapter 40 - Wilson Disease, Pages 443-453, Golder N. Wilson
Chapter 41 - Menkes Disease and Other ATP7A Disorders, Pages 455-462, Juan M. Pascual, John H. Menkes
Chapter 42 - Neurodegeneration with Brain Iron Accumulation, Pages 463-472, Susanne A. Schneider
Chapter 43 - Pantothenate Kinase-Associated Neurodegeneration, Pages 473-481, Michael C. Kruer
Chapter 44 - Disorders of Manganese Transport, Pages 483-493, Isaac Marin-Valencia
Chapter 45 - Aceruloplasminemia, Pages 495-506, Satoshi Kono, Hiroaki Miyajima
Chapter 46 - Genetic and Dietary Influences on Lifespan, Pages 509-520, Yian Gu, Nicole Schupf, Richard Mayeux
Chapter 47 - Vitamins: Cobalamin and Folate, Pages 521-529, David Watkins, Charles P. Venditti, David S. Rosenblatt
Chapter 48 - Disorders of Biotin Metabolism, Pages 531-539, Sara Elrefai, Barry Wolf
Chapter 49 - Disorders of Pyridoxine Metabolism, Pages 541-555, Clara van Karnebeek, Sidney M. Gospe Jr.
Chapter 50 - Disorders of Lipid Metabolism, Pages 559-576, Stefano Di Donato, Franco Taroni
Chapter 51 - Lipoprotein Disorders, Pages 577-588, Mary J. Malloy, John P. Kane
Chapter 52 - Cerebrotendinous Xanthomatosis, Pages 589-598, Vladimir M. Berginer, Gerald Salen, Shailendra B. Patel
Chapter 53 - Organic Acid Disorders, Pages 601-606, Margretta Reed Seashore
Chapter 54 - Glycogen Storage Diseases, Pages 607-614, Salvatore DiMauro, Hasan Orhan Akman
Chapter 55 - Disorders of Galactose Metabolism, Pages 615-626, Gerard T. Berry
Chapter 56 - Inborn Errors of Amino Acid Metabolism, Pages 627-632, William L. Nyhan, Richard Haas
Chapter 57 - Urea Cycle Disorders, Pages 633-647, Nicholas Ah Mew, Maria Belen Pappa, Andrea L. Gropman
Chapter 58 - Glucose Transporter Type I Deficiency and Other Glucose Flux Disorders, Pages 649-662, Juan M. Pascual, Dong Wang, Darryl C. De Vivo
Chapter 59 - Maple Syrup Urine Disease: Clinical and Therapeutic Considerations, Pages 663-672, David T. Chuang, R. Max Wynn, Rody P. Cox, Jacinta L. Chuang
Chapter 60 - Congenital Disorders of N-linked Glycosylation, Pages 673-686, Marc C. Patterson
Chapter 61 - Disorders of Glutathione Metabolism, Pages 687-694, Koji Aoyama, Toshio Nakaki
Chapter 62 - Canavan Disease, Pages 695-701, Reuben Matalon, Kimberlee Michals Matalon
Chapter 63 - Neurotransmitter Disorders, Pages 703-712, Àngels García-Cazorla, Rafael Artuch
Chapter 64 - Peroxisomal Disorders, Pages 713-724, Gerald V. Raymond
Chapter 65 - Disorders of Purine Metabolism, Pages 725-730, William L. Nyhan
Chapter 66 - The Porphyrias, Pages 731-749, D. Montgomery Bissell
Chapter 67 - Alzheimer Disease, Pages 753-768, Dennis J. Selkoe
Chapter 68 - Genetics of Parkinson Disease and Related Diseases, Pages 769-778, Jill S. Goldman, Stanley Fahn
Chapter 69 - Frontotemporal Dementia, Pages 779-791, Shunichiro Shinagawa, Bruce L. Miller
Chapter 70 - The Neuronal Ceroid-Lipofuscinoses (Batten Disease), Pages 793-808, Sara E. Mole, Matti Haltia
Chapter 71 - The Inherited Ataxias, Pages 811-832, Roger N. Rosenberg, Pravin Khemani
Chapter 72 - Friedreich Ataxia, Pages 833-843, Massimo Pandolfo
Chapter 73 - Ataxia-Telangiectasia, Pages 845-848, Shuki Mizutani
Chapter 74 - Dystonia, Pages 849-860, Katja Lohmann, Christine Klein
Chapter 75 - Huntington Disease, Pages 861-868, Andrew J. McGarry, Kevin Biglan, Frederick Marshall
Chapter 76 - Non-Parkinsonian Movement Disorders, Pages 869-890, Stanley Fahn, Jill S. Goldman
Chapter 77 - Hereditary Spastic Paraplegia, Pages 891-906, John K. Fink
Chapter 78 - Glioblastoma, Pages 909-917, Elizabeth A. Maher, Robert M. Bachoo
Chapter 79 - Neurofibromatoses, Pages 921-933, Adam P. Ostendorf, David H. Gutmann
Chapter 80 - Tuberous Sclerosis Complex, Pages 935-943, Monica P. Islam, E. Steve Roach
Chapter 81 - Sturge–Weber Syndrome, Pages 945-953, Anne M. Comi, Douglas A. Marchuk, Jonathan Pevsner
Chapter 82 - Hemangioblastomas of the Central Nervous System, Pages 955-961, Ana Metelo, Othon Iliopoulos
Chapter 83 - Incontinentia Pigmenti, Pages 963-969, A. Yasmine Kirkorian, Bernard Cohen
Chapter 84 - The Genetic Epilepsies, Pages 973-998, Robert L. Macdonald, Martin J. Gallagher
Chapter 85 - Multiple Sclerosis, Pages 1001-1014, Stephen L. Hauser, Jorge R. Oksenberg, Sergio E. Baranzini
Chapter 86 - Vanishing White Matter Disease, Pages 1015-1030, Orna Elroy-Stein, Raphael Schiffmann
Chapter 87 - Amyotrophic Lateral Sclerosis, Pages 1033-1050, Jemeen Sreedharan, Robert H. Brown Jr.
Chapter 88 - Peripheral Neuropathies, Pages 1051-1074, Steven S. Scherer, Kleopas A. Kleopa, Merrill D. Benson
Chapter 89 - Spinal Muscular Atrophy, Pages 1075-1088, Bakri H. Elsheikh, W. David Arnold, John T. Kissel
Chapter 90 - Pain Genetics, Pages 1089-1100, William Renthal
Chapter 91 - Dystrophinopathies, Pages 1103-1111, Eric P. Hoffman
Chapter 92 - Limb-Girdle Muscular Dystrophy, Pages 1113-1120, Wen-Chen Liang, Ichizo Nishino
Chapter 93 - The Congenital Myopathies, Pages 1121-1129, Heinz Jungbluth, Caroline Sewry, Francesco Muntoni
Chapter 94 - The Distal Myopathies, Pages 1131-1143, Ami Mankodi, Bjarne Udd, Robert C. Griggs
Chapter 95 - Hereditary Inclusion-Body Myopathies, Pages 1145-1152, Aldobrando Broccolini, Massimiliano Mirabella
Chapter 96 - The Myotonic Dystrophies, Pages 1153-1168, Richard T. Moxley III, James E. Hilbert, Giovanni Meola
Chapter 97 - Facioscapulohumeral Dystrophy, Pages 1169-1176, Rabi Tawil
Chapter 98 - Muscle Channelopathies: Periodic Paralyses and Nondystrophic Myotonias, Pages 1177-1189, Jeffrey Ralph, Louis Ptáček
Chapter 99 - Congenital Myasthenic Syndromes, Pages 1191-1208, Andrew G. Engel
Chapter 100 - Cerebral Vasculopathies, Pages 1211-1222, Michael M. Dowling
Chapter 101 - Coagulopathies, Pages 1223-1235, Fenella J. Kirkham
Chapter 102 - Sickle Cell Disease, Pages 1237-1249, Fenella J. Kirkham
Chapter 103 - Depression, Pages 1253-1274, Steven T. Szabo, Charles B. Nemeroff
Chapter 104 - Bipolar Disorder, Pages 1275-1291, Scott C. Fears, Victor I. Reus
Chapter 105 - Schizophrenia, Pages 1293-1299, David W. Volk, David A. Lewis
Chapter 106 - Obsessive–Compulsive Disorder, Pages 1301-1310, Michael H. Bloch, Jessica B. Lennington, Gabor Szuhay, Paul J. Lombroso
Chapter 107 - Tourette Syndrome, Pages 1311-1320, Jessica B. Lennington, Michael H. Bloch, Lawrence D. Scahill, Gabor Szuhay, Paul J. Lombroso, Flora M. Vaccarino
Chapter 108 - Addiction, Pages 1321-1329, Scott D. Philibin, John C. Crabbe
Chapter 109 - A Neurologic Gene Map, Pages 1333-1400, Saima N. Kayani, Kathleen S. Wilson, Roger N. Rosenberg
Index, Pages 1401-1424