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MARYBETH PARISI, M.D.
M.D.
Specialist
NPI: 1639158769IndividualAccepts Medicare
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
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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