Seminars in Neurology
Issue 03 · July 2014
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Introduction to the Guest Editor
235
Greer, David M.:
Ali Fatemi, MD
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Preface
237
Fatemi, Ali:
Neurogenetics
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239
Poretti, Andrea; Boltshauser, Eugen; Huisman, Thierry A.G.M.:
Congenital Brain Abnormalities: An Update on Malformations of Cortical Development and Infratentorial Malformations
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249
Weissman, Jacqueline; Naidu, Sakkubai; Bjornsson, Hans T.:
Abnormalities of the DNA Methylation Mark and Its Machinery: An Emerging Cause of Neurologic Dysfunction
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258
Yu, Timothy W.; Berry-Kravis, Elizabeth:
Autism and Fragile X Syndrome
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266
Olson, Heather E.; Poduri, Annapurna; Pearl, Phillip L.:
Genetic Forms of Epilepsies and Other Paroxysmal Disorders
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280
Storey, Elsdon:
Genetic Cerebellar Ataxias
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293
Fink, John K.:
Hereditary Spastic Paraplegia: Clinical Principles and Genetic Advances
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306
Segawa, Masaya; Nomura, Yoshiko:
Genetics and Pathophysiology of Primary Dystonia with Special Emphasis on DYT1 and DYT5
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312
Gordon, Hannah B.; Letsou, Anthea; Bonkowsky, Joshua L.:
The Leukodystrophies
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321
Haas, R.H.; Zolkipli, Z.:
Mitochondrial Disorders Affecting the Nervous System
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341
Helman, Guy; Pacheco-Colón, Ileana; Gropman, Andrea L.:
The Urea Cycle Disorders
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350
Stockler-Ipsiroglu, Sylvia; van Karnebeek, Clara D.M.:
Cerebral Creatine Deficiencies: A Group of Treatable Intellectual Developmental Disorders
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357
Barone, Rita; Fiumara, Agata; Jaeken, Jaak:
Congenital Disorders of Glycosylation with Emphasis on Cerebellar Involvement
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