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MARGUERITE PARISI, MD
MD
Pediatric Radiology Physician
NPI: 1801950084IndividualAccepts Medicare
Specialties, Licenses & Credentials
Pediatric Radiology PhysicianPrimary
Radiology — Pediatric Radiology
Code: 2085P0229X
MD00040576(WA)
CMS Specialties
PrimaryDIAGNOSTIC RADIOLOGY
Education
STATE UNIVERSITY OF NEW YORK DOWNSTATE MEDICAL CENTER
Class of 1977
Research & Publications (20)
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
A Gender Assessment Team: experience with 250 patients over a period of 25 years.
PMID 17575501·Genet Med·2007
4-observational
Differentiated pediatric thyroid cancer: correlates with adult disease, controversies in treatment.
PMID 17707241·Semin Nucl Med·2007
6-review
AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndrome.
PMID 16155189·J Med Genet·2006
8-other
Evaluation of Hox11L1 in the fmc/fmc rat model of chronic intestinal pseudo-obstruction.
PMID 16291166·J Pediatr Surg·2005
7-preclinical
The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndrome.
PMID 15138899·Am J Hum Genet·2004
8-other
Cerebral and cerebellar motor activation abnormalities in a subject with Joubert syndrome: functional magnetic resonance imaging (MRI) study.
PMID 15119482·J Child Neurol·2004
5-case
Genetic background modifies intestinal pseudo-obstruction and the expression of a reporter gene in Hox11L1-/- mice.
PMID 14598259·Gastroenterology·2003
7-preclinical
Micropenis with testicular regression, low LH levels, and poor androgen and HCG responses: a distinct syndrome?
PMID 11992480·Am J Med Genet·2002
5-case
Hydrocephalus and intestinal aganglionosis: is L1CAM a modifier gene in Hirschsprung disease?
PMID 11857550·Am J Med Genet·2002
8-other
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
Calix[5]arene-based heteroditopic receptor for 2-phenylethylamine hydrochloride.
PMID 19419230·J Org Chem·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
Imaging after GliaSite brachytherapy: prognostic MRI indicators of disease control and recurrence.
PMID 19394153·Int J Radiat Oncol Biol Phys·2009
8-other
[Diabetes immersion training as teaching method to medical practitioners].
PMID 19578598·Arq Bras Endocrinol Metabol·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
- 4800 SAND POINT WAY NE
SEATTLE, WA 98105 - Phone
- (206) 987-2133
Quick Facts
- NPI
- 1801950084
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 49
- Publications
- 20
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