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555 S 18th StColumbus, OH 43205
Phone+1 614-722-6200
Fax+1 614-722-3273
Dr. Sahenk is on Doximity
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Education & Training
Ohio State University HospitalResidency, Neurology, 1975 - 1978- Ohio State University HospitalResidency, Internal Medicine, 1974 - 1975
- Ohio State University HospitalResidency, Physical Medicine and Rehabilitation, 1972 - 1974
Hacettepe University FOMClass of 1972
Certifications & Licensure
OH State Medical License 1978 - 2026
IL State Medical License 1977 - 1984
American Board of Psychiatry and Neurology Neurology
Awards, Honors, & Recognition
- Regional Top Doctor Castle Connolly, 2014
Clinical Trials
- Phase I/IIa Trial of scAAV1.tMCK.NTF3 for Treatment of CMT1A
- NT-3 Levels and Function in Individuals With CMT Start of enrollment: 2027 Nov 13
Publications & Presentations
PubMed
- Validity and Reliability of Clinical and Patient-Reported Outcomes in Multisystem Proteinopathy 1.Lindsay N Alfano, Megan A Iammarino, Natalie F Reash, Linda P Lowes, Lindsay Pietruszewski
Annals of Clinical and Translational Neurology. 2025-07-01 - 1 citationsAAV1.NT3 gene therapy mitigates the severity of autoimmune encephalomyelitis in the mouse model for multiple sclerosis.Lingying Tong, Burcak Ozes, Kyle Moss, Morgan Myers, Zayed Attia
Gene Therapy. 2025-07-01 - Like father, like son: RNA-sequencing from a 30-year-old muscle biopsy identifies a novel splice variant in ACTA1 as the cause of an attenuated nemaline myopathy pheno...Alayne P Meyer, Sana Yousfi, Stefan Nicolau, Afrooz Rashnonejad, Jingting Zhu
Neuromuscular Disorders. 2025-07-01
Journal Articles
- Assessment of Systemic Delivery of rAAVrh74.MHCK7.micro-dystrophin in Children with Duchenne Muscular DystrophyJerry R Mendell, Zarife Sahenk, Samiah Al-Zaidy, Richard Shell, JAMA Neurology
Authored Content
- Assessment of Systemic Delivery of rAAVrh74.MHCK7.micro-dystrophin in Children with Duchenne Muscular DystrophyJune 2020
Press Mentions
Sarepta Therapeutics Executes Licensing Agreement for Gene Therapy Program from Nationwide Children’s Hospital to Treat Limb-Girdle Muscular Dystrophy Type 2ASeptember 3rd, 2021- First Global CMT Research Convention Planned for SeptemberJune 16th, 2021
Sarepta Announces Agreement with Nationwide Children’s Hospital for Rights to Its Gene Therapy Program to Treat Limb-Girdle Muscular Dystrophy Type 2A, the Most Common Form of Limb-Girdle Muscular DystrophyMay 8th, 2019- Join now to see all
Grant Support
- NT-3 Gene Therapy To Improve Peripheral Nerve Function Induced By Genetic DefectNational Institute Of Neurological Disorders And Stroke2010–2011
- Histopathology CoreEunice Kennedy Shriver National Institute Of Child Health &Human Development2010–2011
- Histopathology CoreNational Institute Of Neurological Disorders And Stroke2007–2010
Professional Memberships
- Member
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