Back to Search
MICHAEL SHY, M.D. PH.D.
M.D. PH.D.
Urology Physician
NPI: 1396067609IndividualAccepts Medicare
Specialties, Licenses & Credentials
Urology PhysicianPrimary
Urology
Code: 208800000X
278900(NY)
CMS Specialties
PrimaryUROLOGY
Education
STATE UNIVERSITY OF NEW YORK DOWNSTATE MEDICAL CENTER
Class of 2009
Research & Publications (20)
Plasticity of adenylyl cyclase-related signaling sequelae after long-term morphine treatment.
PMID 18045853·Mol Pharmacol·2008
4-observational
X-linked distal hereditary motor neuropathy maps to the DSMAX locus on chromosome Xq13.1-q21.
PMID 19153371·Neurology·2009
8-other
Brain-derived neurotrophic factor Val66Met polymorphism: association with psychopathological symptoms of schizophrenia?
PMID 19359449·J Neuropsychiatry Clin Neurosci·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
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
Different clinical and magnetic resonance imaging features between Charcot-Marie-Tooth disease type 1A and 2A.
PMID 18602827·Neuromuscul Disord·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
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
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
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
- 92-29 QUEENS BLVD., SUITE 2B
REGO PARK, NY 11374 - Phone
- (718) 606-6912
Quick Facts
- NPI
- 1396067609
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 17
- Publications
- 20
Are you this provider?
Claim Your Profile