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Seminars in Pediatric Neurology|December 19, 2012
Neurologic disorders due to mitochondrial DNA mutationsSuzanne Debrosse, Sumit ParikhDevelopmental Disabilities Research Reviews|September 7, 2010
The neurologic manifestations of mitochondrial diseaseSumit ParikhDisability and Health Journal|November 15, 2020
Kleefstra syndrome: Impact on parentsAlexandria Haseley, Kimberly Wallis, Suzanne DeBrosseSeminars in Pediatric Neurology|March 8, 2013
Autonomic dysfunction in epilepsy and mitochondrial diseasesSumit Parikh, Ajay GuptaPediatric Neurology|March 23, 2004
Misplaced peripherally inserted central catheter: an unusual cause of strokeSumit Parikh, Vinodh NarayananHeadache|January 22, 2016
Migraine Variants or Episodic Syndromes That May Be Associated With Migraine and Other Unusual Pediatric Headache SyndromesA David Rothner, Sumit ParikhPediatric Clinics of North America|March 6, 2018
Inborn Errors of Metabolism with Movement Disorders: Defects in Metal Transport and Neurotransmitter MetabolismTrishna Kantamneni, Lileth Mondok, Sumit ParikhJIMD Reports|September 13, 2023
Understanding the impact of pediatric single large-scale mtDNA deletion syndromes on caregivers: Burdens and challengesMcKenzie Chappell, Sumit Parikh, Elizabeth ReynoldsJournal of Primary Care & Community Health|August 30, 2023
Navigating Life With Primary Mitochondrial Myopathies: The Importance of the Patient Voice and Implications for Clinical PracticeMargaret Moore, Philip Yeske, Sumit ParikhJournal of Child Neurology|September 24, 2011
Late infantile neuronal ceroid lipofuscinosis and dopamine deficiencyNgoc Minh D Le, Sumit ParikhPageof 10