Barbara Plecko

Summary

Country: Austria

Publications

  1. doi request reprint Pyridoxine and pyridoxalphosphate-dependent epilepsies
    Barbara Plecko
    Department of Pediatrics, University of Zurich, Zurich, Switzerland Electronic address
    Handb Clin Neurol 113:1811-7. 2013
  2. pmc Pyridoxine responsiveness in novel mutations of the PNPO gene
    Barbara Plecko
    From the Department of Pediatrics B P, L A, Division of Child Neurology, University Hospital Zurich, Switzerland the Department of Pediatrics B P, Division of Neurology and Inborn Errors of Metabolism, Medical University Graz, Austria radiz Rare Disease Initiative Zurich, Clinical Research Priority Program for Rare Diseases University of Zurich B P, L A CRC Clinical Research Center B P, University Childrens Hospital Zurich, Switzerland the Laboratory of Metabolic Diseases K P, E P, D H, Department of Pediatrics, University Hospital Graz, Austria UCL Institute of Child Health P M, P C, Clinical and Molecular Genetics Unit, London, UK Childrens Hospital St Gallen O M, O H, Switzerland the Department of Pediatrics G H, Klinikum Esslingen the Department of Pediatrics S K, St Marien Hospital, Landshut, Germany the Division of Child Neurology M C and Division of Biochemical Diseases S S, Department of Pediatrics, University of British Columbia, Vancouver, Canada the Department of Pediatrics, Division of Child Neurology N W, VU University Medical Center and Neuroscience Campus Amsterdam and the Department of Clinical Chemistry E S, Vrije Universiteit Amsterdam, The Netherlands
    Neurology 82:1425-33. 2014

Collaborators

Detail Information

Publications2

  1. doi request reprint Pyridoxine and pyridoxalphosphate-dependent epilepsies
    Barbara Plecko
    Department of Pediatrics, University of Zurich, Zurich, Switzerland Electronic address
    Handb Clin Neurol 113:1811-7. 2013
    ..Patients and parents have to be informed about the lifelong dependency and recurrence risks in forthcoming pregnancies...
  2. pmc Pyridoxine responsiveness in novel mutations of the PNPO gene
    Barbara Plecko
    From the Department of Pediatrics B P, L A, Division of Child Neurology, University Hospital Zurich, Switzerland the Department of Pediatrics B P, Division of Neurology and Inborn Errors of Metabolism, Medical University Graz, Austria radiz Rare Disease Initiative Zurich, Clinical Research Priority Program for Rare Diseases University of Zurich B P, L A CRC Clinical Research Center B P, University Childrens Hospital Zurich, Switzerland the Laboratory of Metabolic Diseases K P, E P, D H, Department of Pediatrics, University Hospital Graz, Austria UCL Institute of Child Health P M, P C, Clinical and Molecular Genetics Unit, London, UK Childrens Hospital St Gallen O M, O H, Switzerland the Department of Pediatrics G H, Klinikum Esslingen the Department of Pediatrics S K, St Marien Hospital, Landshut, Germany the Division of Child Neurology M C and Division of Biochemical Diseases S S, Department of Pediatrics, University of British Columbia, Vancouver, Canada the Department of Pediatrics, Division of Child Neurology N W, VU University Medical Center and Neuroscience Campus Amsterdam and the Department of Clinical Chemistry E S, Vrije Universiteit Amsterdam, The Netherlands
    Neurology 82:1425-33. 2014
    ..To determine whether patients with pyridoxine-responsive seizures but normal biomarkers for antiquitin deficiency and normal sequencing of the ALDH7A1 gene may have PNPO mutations...