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RICHARD SANTAMARIA, M.D.
M.D.
Internal Medicine Physician
NPI: 1568488468IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
25MA07041700(NJ)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
HAHNEMANN UNIVERSITY COLLEGE OF MEDICINE
Class of 1997
Research & Publications (20)
Ovariectomy and estrogen treatment modulate iron metabolism in rat adipose tissue.
PMID 19501056·Biochem Pharmacol·2009
7-preclinical
Acid loading in vivo and low pH in culture increase angiotensin receptor expression: enhanced ammoniagenic response to angiotensin II.
PMID 18945827·Am J Physiol Renal Physiol·2008
7-preclinical
Haplotype analysis suggests a single Balkan origin for the Gaucher disease [D409H;H255Q] double mutant allele.
PMID 18429048·Hum Mutat·2008
8-other
Pressure and size effects in endohedrally confined hydrogen clusters.
PMID 18282047·J Chem Phys·2008
8-other
The rap GTPases regulate B cell morphology, immune-synapse formation, and signaling by particulate B cell receptor ligands.
PMID 18191594·Immunity·2008
7-preclinical
Expression of iron-related proteins during infection by bovine herpes virus type-1.
PMID 17990282·J Cell Biochem·2008
7-preclinical
Serial magnetic resonance imaging and neurophysiological studies in multiple sulphatase deficiency.
PMID 17881260·Eur J Paediatr Neurol·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
Expression and characterization of 14 GLB1 mutant alleles found in GM1-gangliosidosis and Morquio B patients.
PMID 17664528·J Lipid Res·2007
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
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
Oxalomalate affects the inducible nitric oxide synthase expression and activity.
PMID 17257628·Life Sci·2007
7-preclinical
SSR180711, a novel selective alpha7 nicotinic receptor partial agonist: (1) binding and functional profile.
PMID 17019409·Neuropsychopharmacology·2007
7-preclinical
Homozygosity for the double D409H+H255Q allele in type II Gaucher disease.
PMID 16830265·J Inherit Metab Dis·2006
8-other
Twenty-one novel mutations in the GLB1 gene identified in a large group of GM1-gangliosidosis and Morquio B patients: possible common origin for the prevalent p.R59H mutation among gypsies.
PMID 16941474·Hum Mutat·2006
8-other
Induction of H-ferritin synthesis by oxalomalate is regulated at both the transcriptional and post-transcriptional levels.
PMID 16828896·Biochim Biophys Acta·2006
7-preclinical
Selectivity of a model zeolite ring over hydrocarbons with different symmetry, travelling with different orientations and speeds.
PMID 16866430·J Phys Chem B·2005
8-other
Divergent modulation of iron regulatory proteins and ferritin biosynthesis by hypoxia/reoxygenation in neurones and glial cells.
PMID 16135072·J Neurochem·2005
4-observational
A mutation within the saposin D domain in a Gaucher disease patient with normal glucocerebrosidase activity.
PMID 15856305·Hum Genet·2005
5-case
Six novel alleles identified in Italian hereditary fructose intolerance patients enlarge the mutation spectrum of the aldolase B gene.
PMID 15532022·Hum Mutat·2004
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3829 CHURCH RD STE 100
MOUNT LAUREL, NJ 08054 - Phone
- (856) 536-1515
Quick Facts
- NPI
- 1568488468
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 29
- Publications
- 20
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