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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
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
- 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
- A recurrent missense variant in ITPR3 causes demyelinating Charcot-Marie-Tooth with variable severity.Danique Beijer, Maike F Dohrn, Adriana Rebelo, Matt C Danzi, Bianca Rose Grosz
Brain. 2025-01-07 - 1 citationsTRPV4 neuromuscular disease registry highlights bulbar, skeletal and proximal limb manifestations.Gage P Kosmanopoulos, Jack K Donohue, Maya Hoke, Simone Thomas, Margo A Peyton
Brain. 2025-01-07 - Disrupting the transmembrane domain interface between PMP22 and MPZ causes peripheral neuropathy.Natalya Pashkova, Tabitha A Peterson, Christopher P Ptak, Stanley C Winistorfer, Debbie Guerrero-Given
Iscience. 2024-11-15
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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