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CHRISTIAN MOYA, M.D.
M.D.
Surgical Critical Care Physician
NPI: 1417260845Individual
Specialties, Licenses & Credentials
Surgery Physician
Surgery
Code: 208600000X
254031(NY)
Surgical Critical Care PhysicianPrimary
Surgery — Surgical Critical Care
Code: 2086S0102X
254031(NY)
General Practice Physician
General Practice
Code: 208D00000X
254031(NY)
Research & Publications (20)
NMDA receptors mediate an early up-regulation of brain-derived neurotrophic factor expression in substantia nigra in a rat model of presymptomatic Parkinson's disease.
PMID 19326433·J Neurosci Res·2009
7-preclinical
WNT/beta-catenin increases the production of incretins by entero-endocrine cells.
PMID 19582394·Diabetologia·2009
7-preclinical
Tumor vasculature-targeted delivery of tumor necrosis factor-alpha.
PMID 19090007·Cancer·2009
7-preclinical
Use of a low dose of equine purified FSH to induce multiple ovulations in mares.
PMID 18673335·Reprod Domest Anim·2009
7-preclinical
Synthesis and an evaluation of the bioactivity of the C-glycoside of pseudopterosin A methyl ether.
PMID 18710290·J Org Chem·2008
7-preclinical
Association study of 69 genes in the ret pathway identifies low-penetrance loci in sporadic medullary thyroid carcinoma.
PMID 17909067·Cancer Res·2007
8-other
Effect of uncoupling protein-1 expression on 3T3-L1 adipocyte gene expression.
PMID 18061577·FEBS Lett·2007
7-preclinical
Studies in animal model on the thrombogenicity of a new prothrombin complex concentrate from Argentina.
PMID 17903146·Transfus Med·2007
7-preclinical
Pseudopterosin A inhibits phagocytosis and alters intracellular calcium turnover in a pertussis toxin sensitive site in Tetrahymena thermophila.
PMID 16759914·Comp Biochem Physiol C Toxicol Pharmacol·2006
7-preclinical
A hybrid vector for ligand-directed tumor targeting and molecular imaging.
PMID 16630824·Cell·2006
7-preclinical
Functional study of a novel single deletion in the TITF1/NKX2.1 homeobox gene that produces congenital hypothyroidism and benign chorea but not pulmonary distress.
PMID 16507635·J Clin Endocrinol Metab·2006
5-case
Ligand-directed surface profiling of human cancer cells with combinatorial peptide libraries.
PMID 16397212·Cancer Res·2006
8-other
[The thyroid as a model for molecular mechanisms in genetic diseases].
PMID 16042141·Medicina (B Aires)·2005
6-review
A new case of congenital goiter with hypothyroidism caused by a homozygous p.R277X mutation in the exon 7 of the thyroglobulin gene: a mutational hot spot could explain the recurrence of this mutation.
PMID 15769978·J Clin Endocrinol Metab·2005
5-case
[Gender sensitivity in the formulation of Spanish health plans: what it could have been but wasn't].
PMID 15171843·Gac Sanit·2004
6-review
Two distinct compound heterozygous constellations (R277X/IVS34-1G>C and R277X/R1511X) in the thyroglobulin (TG) gene in affected individuals of a Brazilian kindred with congenital goiter and defective TG synthesis.
PMID 14764776·J Clin Endocrinol Metab·2004
5-case
Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defect.
PMID 12938097·Hum Mutat·2003
8-other
Compound heterozygous mutations in the thyroglobulin gene (1143delC and 6725G-->A [R2223H]) resulting in fetal goitrous hypothyroidism.
PMID 12915634·J Clin Endocrinol Metab·2003
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
- 95 GRASSLANDS RD # 616
VALHALLA, NY 10595 - Phone
- (914) 437-9334
Quick Facts
- NPI
- 1417260845
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 1
- Publications
- 20
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