Michael Evett Shy MD

Neurology•Iowa City, IA

Neuromuscular Medicine

Professor, Neurology, University of Iowa College of Medicine

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200 Hawkins DrIowa City, IA 52242
Phone+1 319-356-8753
Fax+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

NY State Medical License 1982 - Present
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
Recruiting
Genetics of Charcot Marie Tooth (CMT) - Modifiers of CMT1A, New Causes of CMT2 Start of enrollment: 2010 May 01
Recruiting
Development of Charcot Marie Tooth Disease (CMT) Pediatric Scale for Children With CMT Start of enrollment: 2010 Apr 01
Recruiting
Disability Severity Scale (DSI) and Hereditary Motor and Sensory Neuropathy Overall Disability Scale (HMSN-R-ODS) Start of enrollment: 2014 Apr 01
Completed
Patient Reported Outcomes Measures (PROM) in Carpal Tunnel Therapies in Patients With Inherited Neuropathies Start of enrollment: 2016 Jun 01
Completed
Pharmacodynamic EffIcacy and Clinical Benefit of AT 007 in Patients With Sorbitol Dehydrogenase (SORD) Deficiency Start of enrollment: 2022 Jan 01
Active, not recruiting
Phase 2, Phase 3
Roles: Contact, Study Chair
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Publications & Presentations

PubMed

Generation of two induced pluripotent stem cell lines from Charcot-Marie-Tooth type 1B patients harboring autosomal dominant mutations in myelin protein zero gene.
Jingting Zhu, Gongbo Guo, Fatemeh Mehryab, Mary Kate McCulloch, Wilson Marques Junior
Stem Cell Research. 2025-04-01
The Spastic Paraplegia-Centers of Excellence Research Network (SP-CERN): Clinical Trial Readiness for Hereditary Spastic Paraplegia.
Luca Schierbaum, Vicente Quiroz, Kathryn Yang, Joshua Rong, Nicole Battaglia
Neurology. Genetics. 2025-04-01
Heterozygous loss-of-function variants in SPTAN1 cause an early childhood onset distal myopathy.
Jonathan De Winter, Liedewei Van de Vondel, Biljana Ermanoska, Alice Monticelli, Arnaud Isapof
Genetics in Medicine. 2025-02-26

Journal Articles

Development and Validation of the Charcot-Marie-Tooth Disease Infant Scale
Michael 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 DiseaseUNIVERSITY OF MIAMI SCHOOL OF MEDICINE2019–2025
The Inherited Neuropathy Consortium (INC) RDCRC- OverallUNIVERSITY OF IOWA2009–2025
The Inherited Neuropathy Consortium (INC) RDCRC- OverallUNIVERSITY OF IOWA2009–2025
The Inherited Neuropathy Consortium (INC) RDCRC- OverallUNIVERSITY OF IOWA2009–2025
Genomic Studies In Charcot-Marie-Tooth DiseaseNational Institute Of Neurological Disorders And Stroke2012
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