Annals of Neurology

© 2013 American Neurological Association

Cover image for Annals of Neurology

Supplement: Pediatric Neurotransmitter Diseases

2003

Volume 54, Issue S6

Pages S1–S109

  1. Foreword

    1. Top of page
    2. Foreword
    3. Articles
    1. Foreword (pages S1–S2)

      Darryl C. De Vivo and Michael V. Johnston

      Article first published online: 25 JUL 2003 | DOI: 10.1002/ana.10703

  2. Articles

    1. Top of page
    2. Foreword
    3. Articles
    1. GABA, γ-hydroxybutyric acid, and neurological disease (pages S3–S12)

      C. Guin Ting Wong, Teodoro Bottiglieri and O. Carter Snead III

      Article first published online: 25 JUL 2003 | DOI: 10.1002/ana.10696

    2. The lumbar puncture for diagnosis of pediatric neurotransmitter diseases (pages S13–S17)

      Keith Hyland

      Article first published online: 25 JUL 2003 | DOI: 10.1002/ana.10627

    3. Approach to the diagnosis of neurotransmitter diseases exemplified by the differential diagnosis of childhood-onset dystonia (pages S18–S24)

      Birgit Assmann, Robert Surtees and Georg F. Hoffmann

      Article first published online: 25 JUL 2003 | DOI: 10.1002/ana.10628

    4. Magnetic resonance spectroscopy of neurotransmitters in human brain (pages S25–S31)

      Edward J. Novotny Jr., Robert K. Fulbright, Phillip L. Pearl, K. Michael Gibson and Douglas L. Rothman

      Article first published online: 25 JUL 2003 | DOI: 10.1002/ana.10697

    5. Autosomal dominant guanosine triphosphate cyclohydrolase I deficiency (Segawa disease) (pages S32–S45)

      Masaya Segawa, Yoshiko Nomura and Nobuyoshi Nishiyama

      Article first published online: 25 JUL 2003 | DOI: 10.1002/ana.10630

    6. The hph-1 mouse: A model for dominantly inherited GTP-cyclohydrolase deficiency (pages S46–S48)

      Keith Hyland, Richard S. Gunasekara, Tracy L. Munk-Martin, Lauren A. Arnold and Todd Engle

      Article first published online: 25 JUL 2003 | DOI: 10.1002/ana.10695

    7. Aromatic L-amino acid decarboxylase deficiency: Overview of clinical features and outcomes (pages S49–S55)

      Kathryn J. Swoboda, J. Philip Saul, Catherine E. McKenna, Nancy B. Speller and Keith Hyland

      Article first published online: 25 JUL 2003 | DOI: 10.1002/ana.10631

    8. Tyrosine hydroxylase deficiency causes progressive encephalopathy and dopa-nonresponsive dystonia (pages S56–S65)

      Georg F. Hoffmann, Birgit Assmann, Christa Bräutigam, Carlo Dionisi-Vici, Martin Häussler, Johannes B. C. De Klerk, Markus Naumann, Gerry C. H. Steenbergen-Spanjers, Hans-Michael Strassburg and Ron A. Wevers

      Article first published online: 25 JUL 2003 | DOI: 10.1002/ana.10632

    9. Vigabatrin and newer interventions in succinic semialdehyde dehydrogenase deficiency (pages S66–S72)

      Andrea Gropman

      Article first published online: 25 JUL 2003 | DOI: 10.1002/ana.10626

    10. Succinic semialdehyde dehydrogenase deficiency in children and adults (pages S73–S80)

      Phillip L. Pearl, Edward J. Novotny, Maria T. Acosta, Cornelis Jakobs and K. Michael Gibson

      Article first published online: 25 JUL 2003 | DOI: 10.1002/ana.10629

    11. Murine succinate semialdehyde dehydrogenase deficiency (pages S81–S90)

      Maneesh Gupta, Boris M. Hogema, Markus Grompe, Teodoro G. Bottiglieri, Alessandra Concas, Giovanni Biggio, Cristiana Sogliano, Antonello E. Rigamonti, Phillip L. Pearl, O. Carter Snead III, Cornelis Jakobs and K. Michael Gibson

      Article first published online: 25 JUL 2003 | DOI: 10.1002/ana.10625

    12. Transgenic mouse models of dopamine deficiency (pages S91–S102)

      Linan Chen and Xiaoxi Zhuang

      Article first published online: 25 JUL 2003 | DOI: 10.1002/ana.10655

    13. Potential of gene therapy for pediatric neurotransmitter diseases: Lessons from Parkinson's disease (pages S103–S109)

      Un Jung Kang and Ken Nakamura

      Article first published online: 25 JUL 2003 | DOI: 10.1002/ana.10654

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