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DIANA GRINBERG, MD
MD
Emergency Medicine Physician
NPI: 1679769111IndividualAccepts Medicare
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
243218(NY)25MA08221300(NJ)
CMS Specialties
PrimaryEMERGENCY MEDICINE
Education
ALBERT EINSTEIN COLLEGE OF MEDICINE OF YESHIVA UNIVERSITY
Class of 2003
Research & Publications (20)
Polymorphisms and haplotypes across the osteoprotegerin gene associated with bone mineral density and osteoporotic fractures.
PMID 19436932·Osteoporos Int·2010
8-other
Identification and characterization of SMPD1 mutations causing Niemann-Pick types A and B in Spanish patients.
PMID 19405096·Hum Mutat·2009
8-other
An evolutionary and structure-based docking model for glucocerebrosidase-saposin C and glucocerebrosidase-substrate interactions - relevance for Gaucher disease.
PMID 17803231·Proteins·2008
8-other
SR proteins and the nonsense-mediated decay mechanism are involved in human GLB1 gene alternative splicing.
PMID 19114006·BMC Res Notes·2008
8-other
Haplotype analysis suggests a single Balkan origin for the Gaucher disease [D409H;H255Q] double mutant allele.
PMID 18429048·Hum Mutat·2008
8-other
A haplotype-based analysis of the LRP5 gene in relation to osteoporosis phenotypes in Spanish postmenopausal women.
PMID 18684085·J Bone Miner Res·2008
8-other
Recent patents relating to siRNAs and therapeutic strategies for genetic diseases.
PMID 19075944·Recent Pat DNA Gene Seq·2008
6-review
Double-dose external cardioversion for refractory unstable atrial fibrillation in the ED.
PMID 18358976·Am J Emerg Med·2008
5-case
Maroteaux-Lamy syndrome: functional characterization of pathogenic mutations and polymorphisms in the arylsulfatase B gene.
PMID 18406185·Mol Genet Metab·2008
7-preclinical
Identification of a novel pseudodeficiency allele in the GLB1 gene in a carrier of GM1 gangliosidosis.
PMID 17661814·Clin Genet·2007
7-preclinical
Expression and characterization of 14 GLB1 mutant alleles found in GM1-gangliosidosis and Morquio B patients.
PMID 17664528·J Lipid Res·2007
7-preclinical
Promoter 2 -1025 T/C polymorphism in the RUNX2 gene is associated with femoral neck bmd in Spanish postmenopausal women.
PMID 17878995·Calcif Tissue Int·2007
8-other
A CBS haplotype and a polymorphism at the MSR gene are associated with cardiovascular disease in a Spanish case-control study.
PMID 17553479·Clin Biochem·2007
8-other
Discrepancies in interpretation of ED body computed tomographic scans by radiology residents.
PMID 17157681·Am J Emerg Med·2007
8-other
Simvastatin and atorvastatin enhance gene expression of collagen type 1 and osteocalcin in primary human osteoblasts and MG-63 cultures.
PMID 17252541·J Cell Biochem·2007
8-other
Identification of 14 novel GLB1 mutations, including five deletions, in 19 patients with GM1 gangliosidosis from South America.
PMID 17309651·Clin Genet·2007
8-other
COL1A1, ESR1, VDR and TGFB1 polymorphisms and haplotypes in relation to BMD in Spanish postmenopausal women.
PMID 17021946·Osteoporos Int·2007
8-other
Polymorphisms in the interleukin-6 receptor gene are associated with bone mineral density and body mass index in Spanish postmenopausal women.
PMID 17984249·Eur J Endocrinol·2007
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 160 N MIDLAND AVE, ADULT HOSPITAL MEDICINE, NYACK HOSPITAL
NYACK, NY 10960 - Phone
- (845) 348-2000
Quick Facts
- NPI
- 1679769111
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 23
- Publications
- 20
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