Robert Surtees

Summary

Affiliation: University College London
Country: UK

Publications

  1. ncbi request reprint Demyelination and single-carbon transfer pathway metabolites during the treatment of acute lymphoblastic leukemia: CSF studies
    R Surtees
    Institute of Child Health, University College London Medical School, Department of Haematology and Oncology, Great Ormond Street Hospital for Children National Health Service Trust, United Kingdom
    J Clin Oncol 16:1505-11. 1998
  2. pmc Influenza virus associated encephalopathy
    R Surtees
    UCL Institute of Child Health, London, UK
    Arch Dis Child 91:455-6. 2006
  3. pmc Treatable neonatal epilepsy
    Robert Surtees
    Neurosciences Unit, UCL Institute of Child Health, London, UK
    Arch Dis Child 92:659-61. 2007
  4. ncbi request reprint Inherited ion channel disorders
    R Surtees
    Institute of Child Health UCLMS, London, UK
    Eur J Pediatr 159:S199-203. 2000
  5. ncbi request reprint The neurochemistry of phenylketonuria
    R Surtees
    Institute of Child Health UCLMS, London, UK
    Eur J Pediatr 159:S109-13. 2000
  6. ncbi request reprint Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelination
    Nicole I Wolf
    Clinical and Molecular Genetics Unit, Institute of Child Health, London, UK
    Neurogenetics 8:39-44. 2007
  7. ncbi request reprint Complex chromosomal rearrangement and associated counseling issues in a family with Pelizaeus-Merzbacher disease
    Karen Woodward
    Clinical and Molecular Genetics Unit, Institute of Child Health, London, United Kingdom
    Am J Med Genet A 118:15-24. 2003
  8. ncbi request reprint Longitudinal study evaluating a seating system using a sacral pad and kneeblock for children with cerebral palsy
    Rachael L McDonald
    UCL Institute of Child Health, The Wolfson Centre, London, UK
    Disabil Rehabil 29:1041-7. 2007
  9. ncbi request reprint Three or more copies of the proteolipid protein gene PLP1 cause severe Pelizaeus-Merzbacher disease
    Nicole I Wolf
    Clinical and Molecular Genetics, Institute of Child Health, London, UK
    Brain 128:743-51. 2005
  10. ncbi request reprint Idiopathic catastrophic epileptic encephalopathy presenting with acute onset intractable status
    Peter Baxter
    Childrens Hospital, Sheffield, UK
    Seizure 12:379-87. 2003

Collaborators

Detail Information

Publications11

  1. ncbi request reprint Demyelination and single-carbon transfer pathway metabolites during the treatment of acute lymphoblastic leukemia: CSF studies
    R Surtees
    Institute of Child Health, University College London Medical School, Department of Haematology and Oncology, Great Ormond Street Hospital for Children National Health Service Trust, United Kingdom
    J Clin Oncol 16:1505-11. 1998
    ..To investigate the hypothesis that methotrexate causes demyelination due to a deficiency in S-adenosylmethionine (SAM) during the treatment of acute lymphoblastic leukemia (ALL)...
  2. pmc Influenza virus associated encephalopathy
    R Surtees
    UCL Institute of Child Health, London, UK
    Arch Dis Child 91:455-6. 2006
  3. pmc Treatable neonatal epilepsy
    Robert Surtees
    Neurosciences Unit, UCL Institute of Child Health, London, UK
    Arch Dis Child 92:659-61. 2007
  4. ncbi request reprint Inherited ion channel disorders
    R Surtees
    Institute of Child Health UCLMS, London, UK
    Eur J Pediatr 159:S199-203. 2000
    ..Finally, neuronal calcium channelopathies can cause episodic ataxia type 2, familial hemiplegic migraine and spinocerebellar ataxia type 6...
  5. ncbi request reprint The neurochemistry of phenylketonuria
    R Surtees
    Institute of Child Health UCLMS, London, UK
    Eur J Pediatr 159:S109-13. 2000
    ..Similar mechanisms appear to be operating when blood phenylalanine concentrations are in the range expected for early continuously treated phenylketonuria...
  6. ncbi request reprint Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelination
    Nicole I Wolf
    Clinical and Molecular Genetics Unit, Institute of Child Health, London, UK
    Neurogenetics 8:39-44. 2007
    ..In children with nystagmus, ataxia and dysmyelination, mutation analysis of GJA12 should be considered early, especially if inheritance is autosomal recessive...
  7. ncbi request reprint Complex chromosomal rearrangement and associated counseling issues in a family with Pelizaeus-Merzbacher disease
    Karen Woodward
    Clinical and Molecular Genetics Unit, Institute of Child Health, London, United Kingdom
    Am J Med Genet A 118:15-24. 2003
    ..Prenatal diagnosis was carried out in a recent pregnancy and the complex counseling issues associated with these chromosomal rearrangements are discussed...
  8. ncbi request reprint Longitudinal study evaluating a seating system using a sacral pad and kneeblock for children with cerebral palsy
    Rachael L McDonald
    UCL Institute of Child Health, The Wolfson Centre, London, UK
    Disabil Rehabil 29:1041-7. 2007
    ..We sought to evaluate how effective these systems are for a group of children with cerebral palsy...
  9. ncbi request reprint Three or more copies of the proteolipid protein gene PLP1 cause severe Pelizaeus-Merzbacher disease
    Nicole I Wolf
    Clinical and Molecular Genetics, Institute of Child Health, London, UK
    Brain 128:743-51. 2005
    ..It highlights the significance of PLP1 dosage in CNS myelinogenesis as well as the importance of accurate determination of PLP1 gene copy number in the diagnosis of PMD and carrier detection...
  10. ncbi request reprint Idiopathic catastrophic epileptic encephalopathy presenting with acute onset intractable status
    Peter Baxter
    Childrens Hospital, Sheffield, UK
    Seizure 12:379-87. 2003
    ..To delineate a catastrophic childhood epileptic syndrome of unknown cause presenting with persistent intractable multifocal status...
  11. ncbi request reprint Epilepsy in inborn errors of metabolism
    Nicole I Wolf
    Department of Paediatric Neurology, University Children s Hospital Heidelberg, Germany
    Epileptic Disord 7:67-81. 2005
    ..We also discuss vitamin-responsive epilepsies and a number of other metabolic disorders focusing on possible pathogenetic mechanisms and their implication for diagnosis and treatment...