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

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    Greer, David M.:

    Ali Fatemi, MD

    • Preface

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    Fatemi, Ali:

    Neurogenetics

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    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

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    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

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    Haas, R.H.; Zolkipli, Z.:

    Mitochondrial Disorders Affecting the Nervous System

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    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

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    Barone, Rita; Fiumara, Agata; Jaeken, Jaak:

    Congenital Disorders of Glycosylation with Emphasis on Cerebellar Involvement