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MICHAEL SHY, MD

MD

Neuromuscular Medicine (Psychiatry & Neurology) Physician

NPI: 1982642617IndividualAccepts Medicare

Specialties, Licenses & Credentials

Neurology Physician

Psychiatry & Neurology — Neurology

Code: 2084N0400X

4301064663(MI)MD-40090(IA)
Neuromuscular Medicine (Psychiatry & Neurology) PhysicianPrimary

Psychiatry & Neurology — Neuromuscular Medicine

Code: 2084N0008X

MD-40090(IA)

CMS Specialties

PrimaryNEUROLOGY

Education

ALBANY MEDICAL COLLEGE OF UNION UNIVERSITY

Class of 1979

Research & Publications (20)

PMP22 expression in dermal nerve myelin from patients with CMT1A.
PMID 19447823·Brain·2009
8-other
Ascorbic acid for treatment of CMT1A: the jury is still out.
PMID 19427270·Lancet Neurol·2009
8-other
Association of monoamine oxidase A (MAOA) polymorphisms and clinical subgroups of major depressive disorders in the Han Chinese population.
PMID 19224413·World J Biol Psychiatry·2009
8-other
Brain-derived neurotrophic factor Val66Met polymorphism: association with psychopathological symptoms of schizophrenia?
PMID 19359449·J Neuropsychiatry Clin Neurosci·2009
8-other
X-linked distal hereditary motor neuropathy maps to the DSMAX locus on chromosome Xq13.1-q21.
PMID 19153371·Neurology·2009
8-other
Persistent CNS dysfunction in a boy with CMT1X.
PMID 19193385·J Neurol Sci·2009
5-case
Charcot-Marie-Tooth neuropathies: diagnosis and management.
PMID 18351520·Semin Neurol·2008
6-review
Neither single-marker nor haplotype analyses support an association between monoamine oxidase A gene and bipolar disorder.
PMID 18437281·Eur Arch Psychiatry Clin Neurosci·2008
8-other
Mutation of FIG4 causes a rapidly progressive, asymmetric neuronal degeneration.
PMID 18556664·Brain·2008
5-case
Obstructive sleep apnoea and CMT1A: answers and more questions.
PMID 18559457·J Neurol Neurosurg Psychiatry·2008
8-other
Norepinephrine transporter polymorphisms T-182C and G1287A are not associated with alcohol dependence and its clinical subgroups.
PMID 17630229·Drug Alcohol Depend·2008
8-other
Different clinical and magnetic resonance imaging features between Charcot-Marie-Tooth disease type 1A and 2A.
PMID 18602827·Neuromuscul Disord·2008
8-other
Hereditary motor neuropathy and heat shock proteins: a shocking transformation.
PMID 19015482·Neurology·2008
8-other
Correlation between clinical/neurophysiological findings and quality of life in Charcot-Marie-Tooth type 1A.
PMID 18346232·J Peripher Nerv Syst·2008
4-observational
Neuropathy progression in Charcot-Marie-Tooth disease type 1A.
PMID 18227419·Neurology·2008
8-other
Different cellular and molecular mechanisms for early and late-onset myelin protein zero mutations.
PMID 18337304·Hum Mol Genet·2008
7-preclinical
Diabetes mellitus exacerbates motor and sensory impairment in CMT1A.
PMID 19192070·J Peripher Nerv Syst·2008
8-other
Plasticity of adenylyl cyclase-related signaling sequelae after long-term morphine treatment.
PMID 18045853·Mol Pharmacol·2008
4-observational
Mutations in PRPS1, which encodes the phosphoribosyl pyrophosphate synthetase enzyme critical for nucleotide biosynthesis, cause hereditary peripheral neuropathy with hearing loss and optic neuropathy (cmtx5).
PMID 17701900·Am J Hum Genet·2007
8-other
Stoichiometric alteration of PMP22 protein determines the phenotype of hereditary neuropathy with liability to pressure palsies.
PMID 17620487·Arch Neurol·2007
8-other

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
200 HAWKINS DR
IOWA CITY, IA 52242

Location

Practice Location

200 HAWKINS DR, IOWA CITY, IA
(319) 356-8753

Quick Facts

NPI
1982642617
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
3
Locations
1
Years in Practice
47
Publications
20

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