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MARYBETH PARISI, M.D.
M.D.
Specialist
NPI: 1639158769IndividualAccepts Medicare
Specialties, Licenses & Credentials
SpecialistPrimary
Specialist
Code: 174400000X
216253-1(NY)
CMS Specialties
PrimaryDERMATOLOGY
Education
NEW YORK UNIVERSITY SCHOOL OF MEDICINE
Class of 1998
Research & Publications (20)
Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis).
PMID 19574260·J Med Genet·2010
5-case
Imaging after GliaSite brachytherapy: prognostic MRI indicators of disease control and recurrence.
PMID 19394153·Int J Radiat Oncol Biol Phys·2009
8-other
I219V polymorphism in hMLH1 gene in patients affected with ulcerative colitis.
PMID 19371218·Genet Test Mol Biomarkers·2009
8-other
[Diabetes immersion training as teaching method to medical practitioners].
PMID 19578598·Arq Bras Endocrinol Metabol·2009
8-other
MKS3-related ciliopathy with features of autosomal recessive polycystic kidney disease, nephronophthisis, and Joubert Syndrome.
PMID 19540516·J Pediatr·2009
5-case
F-type lectin from the sea bass (Dicentrarchus labrax): purification, cDNA cloning, tissue expression and localization, and opsonic activity.
PMID 19162197·Fish Shellfish Immunol·2009
7-preclinical
Gastric pneumatosis and portal venous gas: benign findings in hypertrophic pyloric stenosis.
PMID 19132358·Pediatr Radiol·2009
5-case
Calix[5]arene-based heteroditopic receptor for 2-phenylethylamine hydrochloride.
PMID 19419230·J Org Chem·2009
8-other
Polymorphism of mytilin B mRNA is not translated into mature peptide.
PMID 19054563·Mol Immunol·2009
7-preclinical
Congenital diaphragmatic hernia and microtia in a newborn with mycophenolate mofetil (MMF) exposure: phenocopy for Fryns syndrome or broad spectrum of teratogenic effects?
PMID 19449404·Am J Med Genet A·2009
5-case
Comparison of three systems of classification in predicting the outcome of diabetic foot ulcers in a Brazilian population.
PMID 18603574·Eur J Endocrinol·2008
4-observational
apoE isoform-specific disruption of amyloid beta peptide clearance from mouse brain.
PMID 19033669·J Clin Invest·2008
7-preclinical
Lysozyme gene expression and hemocyte behaviour in the Mediterranean mussel, Mytilus galloprovincialis, after injection of various bacteria or temperature stresses.
PMID 18495491·Fish Shellfish Immunol·2008
7-preclinical
Differential involvement of mussel hemocyte sub-populations in the clearance of bacteria.
PMID 18854215·Fish Shellfish Immunol·2008
7-preclinical
Procedure guideline for diuretic renography in children 3.0.
PMID 18765635·J Nucl Med Technol·2008
6-review
Self-assembly dynamics of modular homoditopic bis-calix[5]arenes and long-chain alpha,omega-alkanediyldiammonium components.
PMID 18698824·J Org Chem·2008
8-other
'Double trouble': incidental diagnosis of colonic duplication on spinal MRI.
PMID 18618104·Pediatr Radiol·2008
5-case
CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290.
PMID 18950740·Am J Hum Genet·2008
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
- 28 RYKOWSKI LN
MIDDLETOWN, NY 10941 - Phone
- (845) 692-3376
Quick Facts
- NPI
- 1639158769
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 28
- Publications
- 20
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