Russell P Saneto

Summary

Affiliation: University of Washington
Country: USA

Publications

  1. ncbi request reprint A boy with muscle weakness, hypercarbia, and the mitochondrial DNA A3243G mutation
    Russell P Saneto
    Division of Pediatric Neurology, Children s Hospital and Regional Medical Center University of Washington, Seattle, USA
    J Child Neurol 21:77-9. 2006
  2. pmc Onset of action and seizure control in Lennox-Gaustaut syndrome: focus on rufinamide
    Russell P Saneto
    Division of Pediatric Neurology, Seattle Children s Hospital University of Washington, Seattle, Washington, USA
    Ther Clin Risk Manag 5:271-80. 2009
  3. pmc Mitochondrial disease in childhood: mtDNA encoded
    Russell P Saneto
    Division of Pediatric Neurology, Seattle Children s Hospital University of Washington, Seattle, WA 98105, USA
    Neurotherapeutics 10:199-211. 2013
  4. pmc Alpers-Huttenlocher syndrome
    Russell P Saneto
    Division of Pediatric Neurology and Neurology, Seattle Children s Hospital University of Washington, Seattle, WA 98105, USA
    Pediatr Neurol 48:167-78. 2013
  5. pmc Neuroimaging of mitochondrial disease
    Russell P Saneto
    Division of Pediatric Neurology, Children s Hospital and Regional Medical Center University of Washington, 4800 Sand Point Way NE, Seattle, WA 98105, USA
    Mitochondrion 8:396-413. 2008
  6. pmc Illness-induced exacerbation of Leigh syndrome in a patient with the MTATP6 mutation, m. 9185 T>C
    Russell P Saneto
    Division of Pediatric Neurology, Seattle Children s Hospital and University of Washington, Seattle, WA 98105, USA
    Mitochondrion 10:567-72. 2010
  7. doi request reprint Polymerase gamma disease through the ages
    Russell P Saneto
    Division of Pediatric Neurology, Seattle Children s Hospital University of Washington, 4800 Sand Point Way NE, Seattle, WA 98105, USA
    Dev Disabil Res Rev 16:163-74. 2010
  8. ncbi request reprint Persistence of suppression-bursts in a patient with Ohtahara syndrome
    Russell P Saneto
    Division of Pediatric Neurology, Children s Hospital and Regional Medical Center University of Washington, Seattle, Washington 98105, USA
    J Child Neurol 22:631-4. 2007
  9. ncbi request reprint Vagus nerve stimulation for intractable seizures in children
    Russell P Saneto
    Division of Pediatric Neurology, Children s Hospital and Regional Medical Center University of Washington, Seattle, WA 98105, USA
    Pediatr Neurol 35:323-6. 2006
  10. doi request reprint Tissue localization during resective epilepsy surgery
    Sandra L Poliachik
    Division of Pediatric Neurology, Seattle Children s Hospital, Seattle, WA 98105, USA
    Neurosurg Focus 34:E8. 2013

Collaborators

Detail Information

Publications25

  1. ncbi request reprint A boy with muscle weakness, hypercarbia, and the mitochondrial DNA A3243G mutation
    Russell P Saneto
    Division of Pediatric Neurology, Children s Hospital and Regional Medical Center University of Washington, Seattle, USA
    J Child Neurol 21:77-9. 2006
    ..This case demonstrates that isolated muscle weakness in the context of other organ system abnormalities should make the investigator consider MELAS. (J Child Neurol 2006;21:77-79)...
  2. pmc Onset of action and seizure control in Lennox-Gaustaut syndrome: focus on rufinamide
    Russell P Saneto
    Division of Pediatric Neurology, Seattle Children s Hospital University of Washington, Seattle, Washington, USA
    Ther Clin Risk Manag 5:271-80. 2009
    ..Our focus will be on the role of the new medication rufinamide in seizure reduction in patients with Lennox-Gaustaut syndrome...
  3. pmc Mitochondrial disease in childhood: mtDNA encoded
    Russell P Saneto
    Division of Pediatric Neurology, Seattle Children s Hospital University of Washington, Seattle, WA 98105, USA
    Neurotherapeutics 10:199-211. 2013
    ..We hope that as we unfold this fascinating part of clinical medicine, the reader will see how alterations in the tapestry of mitochondrial biochemistry and genetics can give rise to human illness...
  4. pmc Alpers-Huttenlocher syndrome
    Russell P Saneto
    Division of Pediatric Neurology and Neurology, Seattle Children s Hospital University of Washington, Seattle, WA 98105, USA
    Pediatr Neurol 48:167-78. 2013
    ..Diagnosis involves the constellation of organ involvement, not the sequence of signs. This disorder is relentlessly progressive and ultimately fatal...
  5. pmc Neuroimaging of mitochondrial disease
    Russell P Saneto
    Division of Pediatric Neurology, Children s Hospital and Regional Medical Center University of Washington, 4800 Sand Point Way NE, Seattle, WA 98105, USA
    Mitochondrion 8:396-413. 2008
    ..Once a diagnosis has been established, these non-invasive tools can also aid in following disease progression and evaluate the effects of therapeutic interventions...
  6. pmc Illness-induced exacerbation of Leigh syndrome in a patient with the MTATP6 mutation, m. 9185 T>C
    Russell P Saneto
    Division of Pediatric Neurology, Seattle Children s Hospital and University of Washington, Seattle, WA 98105, USA
    Mitochondrion 10:567-72. 2010
    ..This case demonstrates an episodic pattern of febrile illness-induced disease exacerbation with corresponding MRI changes...
  7. doi request reprint Polymerase gamma disease through the ages
    Russell P Saneto
    Division of Pediatric Neurology, Seattle Children s Hospital University of Washington, 4800 Sand Point Way NE, Seattle, WA 98105, USA
    Dev Disabil Res Rev 16:163-74. 2010
    ..When possible, we also identify genotype-phenotype relationships, give clues for diagnosis, and summarize the major clinical phenotypes in the spectrum of POLG disease presenting from birth to old age...
  8. ncbi request reprint Persistence of suppression-bursts in a patient with Ohtahara syndrome
    Russell P Saneto
    Division of Pediatric Neurology, Children s Hospital and Regional Medical Center University of Washington, Seattle, Washington 98105, USA
    J Child Neurol 22:631-4. 2007
    ..Over her lifetime, neither hypsarrhythmia nor diffuse slow spike-wave pattern were seen. This suggests that in Ohtahara syndrome, a suppression-burst pattern can persist over a long period of time...
  9. ncbi request reprint Vagus nerve stimulation for intractable seizures in children
    Russell P Saneto
    Division of Pediatric Neurology, Children s Hospital and Regional Medical Center University of Washington, Seattle, WA 98105, USA
    Pediatr Neurol 35:323-6. 2006
    ..Thirty-seven percent had at least 90% reduction. Vagus nerve stimulation was effective in children with generalized, mixed, and partial medically refractory seizures...
  10. doi request reprint Tissue localization during resective epilepsy surgery
    Sandra L Poliachik
    Division of Pediatric Neurology, Seattle Children s Hospital, Seattle, WA 98105, USA
    Neurosurg Focus 34:E8. 2013
    ..Tracking tissue in this fashion allows for better correlation of patient outcome to clinical factors, functional neuroimaging findings, and pathological characteristics and molecular studies of resected tissue...
  11. doi request reprint Is postresective intraoperative electrocorticography predictive of seizure outcomes in children?
    Carter D Wray
    Department of Neurology, University of Washington, Seattle, WA, USA
    J Neurosurg Pediatr 9:546-51. 2012
    ..The predictive value of postresective discharges in pediatric epilepsy surgery has not been extensively studied...
  12. pmc POLG DNA testing as an emerging standard of care before instituting valproic acid therapy for pediatric seizure disorders
    Russell P Saneto
    Division of Pediatric Neurology, Seattle Children s Hospital University of Washington, Seattle, WA 98105, USA
    Seizure 19:140-6. 2010
    ..To review our clinical experience and determine if there are appropriate signs and symptoms to consider POLG sequencing prior to valproic acid (VPA) dosing in patients with seizures...
  13. doi request reprint The use of neuroimaging in the diagnosis of mitochondrial disease
    Seth D Friedman
    Division of Radiology, Seattle Children s Hospital University of Washington, 4800 Sand Point Way NE, Seattle, WA 98105, USA
    Dev Disabil Res Rev 16:129-35. 2010
    ..The present review summarizes the role of neuroimaging in the diagnosis and characterization of patients with suspected mitochondrial disease...
  14. ncbi request reprint Vagus nerve stimulation in children with mitochondrial electron transport chain deficiencies
    Todd M Arthur
    Division of Pediatric Neurology, Children s Hospital and Regional Medical Center University of Washington, B 5552, 4800 Sand Point Way NE, Seattle, WA 98105, USA
    Mitochondrion 7:279-83. 2007
    ..All five children did not have significant reduction in seizure frequency with VNS. VNS may not be an effective method to control myoclonic seizures in children with electron transport chain disorders...
  15. ncbi request reprint Apnea caused by mesial temporal lobe mass lesions in infants: report of 3 cases
    Tadashi Miyagawa
    Department of Neurological Surgery, University of Washington School of Medicine, Children s Hospital and Regional Medical Center, Seattle, Washington 98105, USA
    J Child Neurol 22:1079-83. 2007
    ..Magnetic resonance imaging showed an inferior mesial temporal lobe mass lesion in all infants. All patients underwent lesion removal, and they are seizure free with normal psychomotor development...
  16. doi request reprint Dravet syndrome: patients with co-morbid SCN1A gene mutations and mitochondrial electron transport chain defects
    Alexa K Craig
    Division of Pediatric Neurology, Seattle Children s Hospital University of Washington, 4800 Sand Point Way NE, Seattle, WA 98105, United States
    Seizure 21:17-20. 2012
    ..To review our cohort of patients with Dravet syndrome and determine if patients with SCN1A mutations can also express mitochondrial disease due to electron transport chain dysfunction...
  17. doi request reprint Sensory ataxic neuropathy with dysarthria and ophthalmoparesis (SANDO) in late life due to compound heterozygous POLG mutations
    Michael D Weiss
    Department of Neurology, University of Washington Medical Center, Box 356115, 1959 NE Pacific Street, Seattle, Washington 98195, USA
    Muscle Nerve 41:882-5. 2010
    ..To our knowledge, none of these mutations have been demonstrated previously in SANDO. This patient's late presentation illustrates that a mitochondrial disorder should be considered regardless of age if the clinical symptoms warrant...
  18. doi request reprint Localization of extratemporal seizure with noninvasive dense-array EEG. Comparison with intracranial recordings
    Mark D Holmes
    Department of Neurology, University of Washington, Seattle, WA 98105, USA
    Pediatr Neurosurg 44:474-9. 2008
    ..Noninvasive dense-array EEG, used in conjunction with realistic source analysis methods, may have the potential to assist in localizing seizure onsets when standard methods fail...
  19. doi request reprint Epilepsy surgery after treatment of pediatric malignant brain tumors
    Jeffrey G Ojemann
    Department of Neurological Surgery, University of Washington, USA
    Seizure 21:624-30. 2012
    ..Aggressive surgical management of intractable epilepsy can be considered in survivors of malignant brain tumors...
  20. doi request reprint Mitochondrial electron transport chain deficiency, cardiomyopathy, and long-term cardiac transplant outcome
    Alana S Golden
    Division of Pediatric Neurology, Seattle Children s Hospital and University of Washington, Seattle, WA 98105, USA
    Pediatr Transplant 16:265-8. 2012
    ..Our results suggest that with proper patient selection in this population, cardiac transplantation is feasible and can have good outcomes...
  21. doi request reprint Next-generation sequencing for mitochondrial diseases: a wide diagnostic spectrum
    Valeria Vasta
    University of Washington School of Medicine, Seattle Children s Research Institute, C9S, 1900 9th Avenue, Seattle, WA 98101, USA
    Pediatr Int 54:585-601. 2012
    ..Clinical sequencing tests are available only for a limited number of genes. Recently, massively parallel sequencing has become a powerful tool for testing genetically heterogeneous conditions such as mitochondrial disorders...
  22. doi request reprint Current oral and non-oral routes of antiepileptic drug delivery
    Gail D Anderson
    Department of Pharmacy, University of Washington, Seattle, Washington, USA
    Adv Drug Deliv Rev 64:911-8. 2012
    ..There is a significant need for new non-oral formulations of the antiepileptic drugs when oral administration is not possible...
  23. doi request reprint Functional magnetic resonance imaging for presurgical evaluation of very young pediatric patients with epilepsy
    Hillary Shurtleff
    Department of Neurology, Seattle Children s Hospital, Seattle, Washington, USA
    J Neurosurg Pediatr 5:500-6. 2010
    ..Most fMR imaging clinical work has been done in adults, and although children as young as 8 years of age have been included in larger clinical series, cases in younger children are rarely reported...
  24. pmc The in-depth evaluation of suspected mitochondrial disease
    Richard H Haas
    Department of Neurosciences, University of California San Diego, La Jolla, CA and Rady Children s Hospital San Diego, San Diego, CA, United States
    Mol Genet Metab 94:16-37. 2008
    ..The aim of this work is to facilitate the diagnosis of mitochondrial disease by geneticists, neurologists, and other metabolic specialists who face the challenge of evaluating patients of all ages with suspected mitochondrial disease...
  25. ncbi request reprint Outcome following surgery for temporal lobe epilepsy with hippocampal involvement in preadolescent children: emphasis on mesial temporal sclerosis
    Matthew D Smyth
    Department of Neurosurgery, Washington University, St Louis Children s Hospital, St Louis, Missouri 63110 1077, USA
    J Neurosurg 106:205-10. 2007
    ..The authors conducted a multiinstitutional, retrospective analysis to better define outcome and prognostic indicators for temporal lobe epilepsy surgery for suspected mesial temporal sclerosis (MTS) in young children...