Danielle M Andrade

Summary

Publications

  1. doi request reprint Mutation of the CLN6 gene in teenage-onset progressive myoclonus epilepsy
    Danielle M Andrade
    Division of Neurology, Krembil Neuroscience Centre, University of Toronto, Toronto Western Hospital, 399 Bathurst Street, Toronto, Ontario, Canada
    Pediatr Neurol 47:205-8. 2012
  2. doi request reprint Dravet syndrome: seizure control and gait in adults with different SCN1A mutations
    Jennifer J Rilstone
    Program in Genetics and Genomic Biology, The Hospital for Sick Children, Toronto, Ontario, Canada
    Epilepsia 53:1421-8. 2012
  3. doi request reprint Treatment options for epileptic myoclonus and epilepsy syndromes associated with myoclonus
    Danielle M Andrade
    Division of Neurology, Krembil Neuroscience Centre, University of Toronto, Toronto Western Hospital, Toronto, Canada
    Expert Opin Pharmacother 10:1549-60. 2009
  4. doi request reprint Dravet syndrome and deep brain stimulation: seizure control after 10 years of treatment
    Danielle M Andrade
    Division of Neurology, Toronto Western Hospital, Krembil Neuroscience Centre, University of Toronto, Toronto, Ontario, Canada
    Epilepsia 51:1314-6. 2010
  5. doi request reprint Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome
    Evelyn Ning Man Cheung
    Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada
    Genet Med 16:40-4. 2014
  6. doi request reprint A comparison of antiepileptic drug therapy in patients with severe intellectual disability and patients with normal intellect
    Jonathan D Fridhandler
    Department of Medicine, University of Toronto, Canada
    Epilepsy Behav 25:196-9. 2012
  7. doi request reprint Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome)
    Miles D Thompson
    Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada
    Am J Med Genet A 158:553-8. 2012
  8. doi request reprint Genetic basis in epilepsies caused by malformations of cortical development and in those with structurally normal brain
    Danielle M Andrade
    Division of Neurology, Toronto Western Hospital, Krembil Neuroscience Centre, University of Toronto, 5W 445, 399 Bathurst St, Toronto M5T 2S8, Canada
    Hum Genet 126:173-93. 2009
  9. ncbi request reprint Mitochondrial Encephalopathy With Lactic Acidosis and Stroke-like Episodes (MELAS) May Respond to Adjunctive Ketogenic Diet
    Claude Steriade
    Division of Neurology, Department of Medicine, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada Electronic address
    Pediatr Neurol 50:498-502. 2014
  10. ncbi request reprint Hippocampal malrotation is associated with chromosome 22q11.2 microdeletion
    Danielle M Andrade
    Division of Neurology, University of Toronto
    Can J Neurol Sci 40:652-6. 2013

Collaborators

Detail Information

Publications13

  1. doi request reprint Mutation of the CLN6 gene in teenage-onset progressive myoclonus epilepsy
    Danielle M Andrade
    Division of Neurology, Krembil Neuroscience Centre, University of Toronto, Toronto Western Hospital, 399 Bathurst Street, Toronto, Ontario, Canada
    Pediatr Neurol 47:205-8. 2012
    ..This work also exemplifies the potentiality of next-generation sequencing in the genetic identification and diagnosis of patients with neurologic diseases of unknown cause...
  2. doi request reprint Dravet syndrome: seizure control and gait in adults with different SCN1A mutations
    Jennifer J Rilstone
    Program in Genetics and Genomic Biology, The Hospital for Sick Children, Toronto, Ontario, Canada
    Epilepsia 53:1421-8. 2012
    ..The purpose of this study is to correlate different types of SCN1A mutations and (1) seizure control, (2) occurrence of convulsive status epilepticus (cSE), and (3) the presence of crouch gait in adult patients...
  3. doi request reprint Treatment options for epileptic myoclonus and epilepsy syndromes associated with myoclonus
    Danielle M Andrade
    Division of Neurology, Krembil Neuroscience Centre, University of Toronto, Toronto Western Hospital, Toronto, Canada
    Expert Opin Pharmacother 10:1549-60. 2009
    ..Myoclonus is a brief shock-like movement that has many different etiologies. The degree to which it disturbs quality of life is extremely variable, as is its response to treatment...
  4. doi request reprint Dravet syndrome and deep brain stimulation: seizure control after 10 years of treatment
    Danielle M Andrade
    Division of Neurology, Toronto Western Hospital, Krembil Neuroscience Centre, University of Toronto, Toronto, Ontario, Canada
    Epilepsia 51:1314-6. 2010
    ..We speculate that the results of DBS for epilepsy in patients with Dravet syndrome may be related to age at initiation of DBS treatment and seizure type...
  5. doi request reprint Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome
    Evelyn Ning Man Cheung
    Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada
    Genet Med 16:40-4. 2014
    ..2 deletion syndrome. Neonatal hypocalcemia may affect neurodevelopment. We hypothesized that neonatal hypocalcemia would be associated with rare, more severe forms of intellectual disability in 22q11.2 deletion syndrome...
  6. doi request reprint A comparison of antiepileptic drug therapy in patients with severe intellectual disability and patients with normal intellect
    Jonathan D Fridhandler
    Department of Medicine, University of Toronto, Canada
    Epilepsy Behav 25:196-9. 2012
    ..This difference is likely related to greater seizure frequency and co-morbid behavioral disturbance in the ID group as no bias was identified against utilization of the newer AEDs in patients with ID...
  7. doi request reprint Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome)
    Miles D Thompson
    Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada
    Am J Med Genet A 158:553-8. 2012
    ..2010] have PIGV mutations, we suggest that other genes critical to GPI anchor biosynthesis are likely to be disrupted in some patients...
  8. doi request reprint Genetic basis in epilepsies caused by malformations of cortical development and in those with structurally normal brain
    Danielle M Andrade
    Division of Neurology, Toronto Western Hospital, Krembil Neuroscience Centre, University of Toronto, 5W 445, 399 Bathurst St, Toronto M5T 2S8, Canada
    Hum Genet 126:173-93. 2009
    ..Juvenile myoclonic epilepsy, childhood absence epilepsy, some familial forms of focal epilepsy and epilepsies associated with febrile seizures are discussed as examples of epileptic conditions in (apparently) structurally normal brains...
  9. ncbi request reprint Mitochondrial Encephalopathy With Lactic Acidosis and Stroke-like Episodes (MELAS) May Respond to Adjunctive Ketogenic Diet
    Claude Steriade
    Division of Neurology, Department of Medicine, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada Electronic address
    Pediatr Neurol 50:498-502. 2014
    ..Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome can present management challenges. Refractory seizures and stroke-like episodes leading to disability are common...
  10. ncbi request reprint Hippocampal malrotation is associated with chromosome 22q11.2 microdeletion
    Danielle M Andrade
    Division of Neurology, University of Toronto
    Can J Neurol Sci 40:652-6. 2013
    ..In this study we used a dedicated seizure imaging protocol to look for additional structural abnormalities in these individuals that may explain the elevated risk of seizure disorder in this patient group...
  11. doi request reprint Chromosome 1p36 in migraine with aura: association study of the 5HT(1D) locus
    Miles D Thompson
    Department of Laboratory Medicine and Pathobiology, London Health Sciences Centre, Toronto, Ontario, Canada
    Neuroreport 23:45-8. 2012
    ..Further work using a genome-wide association study approach in familial typical migraine, consisting of those affected by MO or MA, will serve to further distinguish how and why MA differs from MO...
  12. ncbi request reprint Genetics of epilepsies
    Danielle M Andrade
    University of Toronto, Division of Neurology, Krembil Neuroscience Centre, Toronto Western Hospital, Toronto, Canada
    Expert Rev Neurother 7:727-34. 2007
    ..This review will focus on the monogenic familial epilepsies and the clinical and molecular aspects of these diseases...
  13. ncbi request reprint Protein therapy for Unverricht-Lundborg disease using cystatin B transduction by TAT-PTD. Is it that simple?
    Danielle M Andrade
    Department of Molecular and Medical Genetics, University of Toronto, Canada
    Epilepsy Res 72:75-9. 2006
    ..Importantly, we discuss precautions to avoid false-positive results when working with TAT-PTD for protein therapy of neurological diseases...