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URIAN KIM, MD

MD

Pediatrics Physician

NPI: 1851487292Individual

Specialties, Licenses & Credentials

Pediatrics PhysicianPrimary

Pediatrics

Code: 208000000X

25MA07864200(NJ)ME125625(FL)

Research & Publications (20)

A novel frameshift mutation in the EYA1 gene in a Korean family with branchio-oto-renal syndrome.
PMID 19667416·Ann Clin Lab Sci·2009
5-case
Elastic properties and apparent density of human edentulous maxilla and mandible.
PMID 19647417·Int J Oral Maxillofac Surg·2009
8-other
Simultaneous sorting of multiple bacterial targets using integrated dielectrophoretic-magnetic activated cell sorter.
PMID 19636461·Lab Chip·2009
8-other
Two-year outcomes of the sirolimus-eluting stent according to unprotected left main lesion.
PMID 19569064·Clin Cardiol·2009
8-other
A case of myotonic dystrophy with pigmentary retinal changes.
PMID 19568364·Korean J Ophthalmol·2009
5-case
Thin film transistors using preferentially grown semiconducting single-walled carbon nanotube networks by water-assisted plasma-enhanced chemical vapor deposition.
PMID 19567966·Nanotechnology·2009
8-other
A Family of H723R Mutation for SLC26A4 Associated with Enlarged Vestibular Aqueduct Syndrome.
PMID 19565036·Clin Exp Otorhinolaryngol·2009
8-other
Pharmacokinetic, tolerability, and bioequivalence comparison of three different intravenous formulations of recombinant human erythropoietin in healthy Korean adult male volunteers: an open-label, randomized-sequence, three-treatment, three-way crossover study.
PMID 19539105·Clin Ther·2009
4-observational
Advances in the diagnosis and management of persistent pulmonary hypertension of the newborn.
PMID 19501693·Pediatr Clin North Am·2009
6-review
[Primary carcinoid tumor of the testis metastatic to the para-aortic lymph nodes in six years after the first operation: a case report].
PMID 19462831·Hinyokika Kiyo·2009
5-case
Role of calcium/calmodulin signaling pathway in Vibrio vulnificus cytolysin-induced hyperpermeability.
PMID 19447166·Microb Pathog·2009
7-preclinical
Novel POU3F4 mutations and clinical features of DFN3 patients with cochlear implants.
PMID 19438930·Clin Genet·2009
8-other
Construction of a DNA chip for screening of genetic hearing loss.
PMID 19434291·Clin Exp Otorhinolaryngol·2009
8-other
Gastrointestinal 18F-FDG accumulation on PET without a corresponding CT abnormality is not an early indicator of cancer development.
PMID 19415294·Eur Radiol·2009
8-other
Correlations between physical properties of jawbone and dental implant initial stability.
PMID 19410065·J Prosthet Dent·2009
8-other
Different functional consequences of two missense mutations in the GJB2 gene associated with non-syndromic hearing loss.
PMID 19384972·Hum Mutat·2009
8-other
In vitro evaluation of bacterial leakage resistance of an ultrasonically placed mineral trioxide aggregate orthograde apical plug in teeth with wide open apexes: a preliminary study.
PMID 19327633·Oral Surg Oral Med Oral Pathol Oral Radiol Endod·2009
8-other
Intermediate to long-term outcomes of endoluminal stent-graft repair in patients with chronic type B aortic dissection.
PMID 19281291·J Endovasc Ther·2009
8-other
Identification of novel variants in the COL4A4 gene in Korean patients with thin basement membrane nephropathy.
PMID 19675380·Indian J Med Res·2009
8-other
Clinical and molecular characterizations of novel POU3F4 mutations reveal that DFN3 is due to null function of POU3F4 protein.
PMID 19671658·Physiol Genomics·2009
7-preclinical

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

Contact & Hours

Address
1100 SAWGRASS VILLAGE DR STE 100
PONTE VEDRA, FL 32082

Location

Practice Location

1100 SAWGRASS VILLAGE DR STE 100, PONTE VEDRA, FL
(904) 285-9355

Quick Facts

NPI
1851487292
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
2
Locations
1
Publications
20

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