SumitParikhMD(He/Him)
[Pronunciation: sue-meet]
Child Neurology • Cleveland, OHAssociate Professor, Neurology, Case Western Reserve University School of Medicine
Dr. Parikh is on Doximity
As a Doximity member you'll join over two million verified healthcare professionals in a private, secure network.
- Gain access to free telehealth tools, such as our “call shielding” and one-way patient texting.
- Connect with colleagues in the same hospital or clinic.
- Read the latest clinical news, personalized to your specialty.
Office
9500 Euclid Ave, S60
Cleveland, OH 44195Phone+1 216-444-1994
Summary
- Child Neurologist specializing in Neurogenetic/Neurometabolic Disorders, especially Mitochondrial Disease
See additional information at bit.ly/parikhbio
Education & Training
Cleveland Clinic FoundationFellowship, Endocrinology, Diabetes, and Metabolism, 2004 - 2006
UPMC Medical EducationFellowship, Child Neurology, 2001 - 2004- UPMC Medical EducationResidency, Pediatrics, 1998 - 2001
Case Western Reserve University School of MedicineClass of 1998
Certifications & Licensure
OH State Medical License 2003 - 2026
CA State Medical License 2010 - 2022
PA State Medical License 1999 - 2004- American Board of Psychiatry and Neurology Neurology with Special Qualification in Child Neurology
Awards, Honors, & Recognition
- CMS Meaningful Use Stage 1 Certification EpicCare Ambulatory EMR, Epic Systems Corporation, 2011, 2013
Clinical Trials
- North American Mitochondrial Disease Consortium Patient Registry and Biorepository (NAMDC) Start of enrollment: 2010 Dec 01
- Phase 2 Study of EPI-743 in Children With Pearson Syndrome Start of enrollment: 2014 Aug 31
- Survey on Supplement Use in Mitochondrial Disease Start of enrollment: 2014 Sep 01
- Join now to see all
Publications & Presentations
PubMed
- 404 citationsPhenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number VariantsSanthosh Girirajan, Jill A. Rosenfeld, Bradley P. Coe, Sumit Parikh, Neil R. Friedman
The New England Journal of Medicine. 2012-10-03 - 42 citationsRecurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats.Pawel Stankiewicz, Shashikant Kulkarni, Avinash V. Dharmadhikari, Srirangan Sampath, Samarth Bhatt
Human Mutation. 2012-01-01 - 181 citationsMitochondrial disease: a practical approach for primary care physicians.Richard H. Haas, Sumit Parikh, Marni J. Falk, Russell P. Saneto, Nicole I. Wolf
Pediatrics. 2007-12-01
Press Mentions
Understanding Genetics of Common, Rare Disorders Advance Treatment in Pediatric NeurologyAugust 31st, 2020
Why Having Healthy Mitochondria Matters—and How to Power Yours UpApril 24th, 2018
Mitochondrial Organizations Cooperate to Launch Pilot Phase of the Mitochondrial Care NetworkJanuary 8th, 2018- Join now to see all
Professional Memberships
- Member
Viewing the full profile is available to verified healthcare professionals only.
Find your profile and take control of your online presence:
