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GARY RUDOLPH, MD
MD
Emergency Medicine Physician
NPI: 1164595476Individual
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
150496(NY)
Research & Publications (20)
Influence of dominant bile duct stenoses and biliary infections on outcome in primary sclerosing cholangitis.
PMID 19410324·J Hepatol·2009
8-other
Optical inline measurement procedures for counting and sizing cells in bioprocess technology.
PMID 19609497·Adv Biochem Eng Biotechnol·2009
6-review
Mitochondrial 12S rRNA susceptibility mutations in aminoglycoside-associated and idiopathic bilateral vestibulopathy.
PMID 18851951·Biochem Biophys Res Commun·2008
8-other
Online monitoring of microcarrier based fibroblast cultivations with in situ microscopy.
PMID 17546690·Biotechnol Bioeng·2008
7-preclinical
Visual loss as a first sign of adult-type chronic myeloid leukemia in a child.
PMID 16226538·Am J Ophthalmol·2005
5-case
Phenotypic variability in three carriers from a family with choroideremia and a frameshift mutation 1388delCCinsG in the REP-1 gene.
PMID 14566650·Ophthalmic Genet·2003
5-case
Spondylo-ocular syndrome: a new entity with crystalline lens malformation, cataract, retinal detachment, osteoporosis, and platyspondyly.
PMID 12719077·Am J Ophthalmol·2003
8-other
Scanning laser ophthalmoscope-evoked multifocal ERG (SLO-mfERG) in patients with macular holes and normal individuals.
PMID 14528241·Eye (Lond)·2003
8-other
Intestinal absorption and biliary secretion of ursodeoxycholic acid and its taurine conjugate.
PMID 12190957·Eur J Clin Invest·2002
3-trial
Hemifacial atrophy (Parry-Romberg syndrome, #141300) with papillitis, retinal alterations, and restriction of motility.
PMID 11997811·J AAPOS·2002
5-case
[Mutations in the ABCA4 gene in a family with Stargardt's disease and retinitis pigmentosa (STGD1/RP19)].
PMID 12353176·Klin Monbl Augenheilkd·2002
5-case
X-linked ocular albinism (Nettleship-Falls): a novel 29-bp deletion in exon 1. Carrier detection by ophthalmic examination and DNA analysis.
PMID 11405065·Graefes Arch Clin Exp Ophthalmol·2001
8-other
A review of non-invasive optical-based image analysis systems for continuous bioprocess monitoring.
PMID 19396466·Bioprocess Biosyst Eng·2010
6-review
[Retinal detachment in pediatrics : Etiology and risk factors].
PMID 19609777·Ophthalmologe·2010
8-other
ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies.
PMID 18285826·Eur J Hum Genet·2008
8-other
Outcome of patients who present to the emergency department with an elevated international normalized ratio.
PMID 18380679·J Am Geriatr Soc·2008
4-observational
Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2.
PMID 18235024·Invest Ophthalmol Vis Sci·2008
8-other
The incidence of cholangiocarcinoma in primary sclerosing cholangitis after long-time treatment with ursodeoxycholic acid.
PMID 17489059·Eur J Gastroenterol Hepatol·2007
8-other
Case-control genetic association study of fibulin-6 (FBLN6 or HMCN1) variants in age-related macular degeneration (AMD).
PMID 17216616·Hum Mutat·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
- NSUH DEPT OF EMERGENCY MEDICINE, 300 COMMUNITY DRIVE
MANHASSET, NY 11030 - Phone
- (516) 562-3090
Quick Facts
- NPI
- 1164595476
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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