Dr. Shy is on Doximity
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Office
200 Hawkins Dr
Iowa City, IA 52242Phone+1 319-356-8753Fax+1 319-384-7199
Education & Training
New York Presbyterian Hospital (Columbia Campus)Residency, Neurology, 1981 - 1982
Albany Medical CenterInternship, Internal Medicine, 1979 - 1980
Albany Medical CollegeClass of 1979
Certifications & Licensure
IA State Medical License 2012 - 2025
MI State Medical License 1994 - 2013
PA State Medical License 1986 - 1994- American Board of Psychiatry and Neurology Neurology
Clinical Trials
- Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and Others Start of enrollment: 2010 Apr 01
- Genetics of Charcot Marie Tooth (CMT) - Modifiers of CMT1A, New Causes of CMT2 Start of enrollment: 2010 May 01
- Development of Charcot Marie Tooth Disease (CMT) Pediatric Scale for Children With CMT Start of enrollment: 2010 Apr 01
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Publications & Presentations
PubMed
- 11 citationsRydel-Seiffer fork revisited: Beyond a simple case of black and whiteFrancis B. Panosyan, Joan M. Mountain, Mary M. Reilly, Michael E. Shy, David N. Herrmann
Neurology. 2016-08-16 - 132 citationsMissense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy.Marina L. Kennerson, Garth A. Nicholson, Stephen G. Kaler, Bartosz Kowalski, Julian F.B. Mercer
American Journal of Human Genetics. 2010-03-12 - 101 citationsA novel mutation in VCP causes Charcot–Marie–Tooth Type 2 diseaseMichael A. Gonzalez, Shawna M. E. Feely, Fiorella Speziani, Alleene V. Strickland, Matt C. Danzi
Brain. 2014-11-01
Journal Articles
- Development and Validation of the Charcot-Marie-Tooth Disease Infant ScaleMichael E Shy, Rosemary Shy, Gyula Acsadi, Brain
Press Mentions
Investigational Treatment Promising for SORD DeficiencyJuly 5th, 2024
Grant Support
- Genomic Studies In Charcot-Marie-Tooth DiseaseNational Institute Of Neurological Disorders And Stroke2012
- TrainingNational Institute Of Neurological Disorders And Stroke2009–2011
- Natural HistoryNational Institute Of Neurological Disorders And Stroke2009–2011
- Inherited Neurophathies Consortium (RDCRC)National Institute Of Neurological Disorders And Stroke2009–2011
- Early And LATE Onset CMT1BNational Institute Of Neurological Disorders And Stroke2006–2010
- Genotype Phenotype Correlation In CMTXNational Institute Of Neurological Disorders And Stroke2003–2006
- Adhesion And Gene Expression In CMT1BNational Institute Of Neurological Disorders And Stroke2001–2004
- Third International Research Symposium On CMT DisordersNational Institute Of Neurological Disorders And Stroke1998
- Antibodies To Gangliosides GM1 And GD1BNational Institute Of Neurological Disorders And Stroke1989–1992
- Antibodies To Gangliosides GM1 &Gd1b &Their EffectsNational Institute Of Neurological Disorders And Stroke1988
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