DOI: 10.1055/s-00000071

Seminars in Neurology

Issue 03 · Volume 34 · July 2014 DOI: 10.1055/s-004-27616 Neurogenetics Guest Editor, Ali Fatemi, MD

Introduction to the Guest Editor

235
Greer, David M.: Ali Fatemi, MD

Preface

237
Fatemi, Ali: Neurogenetics

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