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JAMES CHRISTODOULOU, MD
MD
Cardiovascular Disease Physician
NPI: 1265592653Individual
Specialties, Licenses & Credentials
Cardiovascular Disease PhysicianPrimary
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
099508(NY)
Research & Publications (20)
Myelodysplastic syndrome (RARS) with +i(12p) abnormality in a patient 10 months after diagnosis and successful treatment of a mediastinal germ cell tumor (MGCT).
PMID 14615911·Ann Hematol·2004
5-case
Structure, dynamics and folding of an immunoglobulin domain of the gelation factor (ABP-120) from Dictyostelium discoideum.
PMID 19281823·J Mol Biol·2009
7-preclinical
Congenital disorder of glycosylation type Ia: heterogeneity in the clinical presentation from multivisceral failure to hyperinsulinaemic hypoglycaemia as leading symptoms in three infants with phosphomannomutase deficiency.
PMID 19396570·J Inherit Metab Dis·2009
5-case
1H, 15N and 13C assignments of domain 5 of Dictyostelium discoideum gelation factor (ABP-120) in its native and 8M urea-denatured states.
PMID 19636940·Biomol NMR Assign·2009
8-other
Probing side-chain dynamics of a ribosome-bound nascent chain using methyl NMR spectroscopy.
PMID 19492839·J Am Chem Soc·2009
7-preclinical
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome.
PMID 19349604·Neurology·2009
8-other
Expanded newborn screening: outcome in screened and unscreened patients at age 6 years.
PMID 19620191·Pediatrics·2009
8-other
On the mechanism of nonspecific inhibitors of protein aggregation: dissecting the interactions of alpha-synuclein with Congo red and lacmoid.
PMID 19645507·Biochemistry·2009
8-other
Inherited surfactant deficiency caused by uniparental disomy of rare mutations in the surfactant protein-B and ATP binding cassette, subfamily a, member 3 genes.
PMID 19647838·J Pediatr·2009
5-case
Molecular determinants of the aggregation behavior of alpha- and beta-synuclein.
PMID 18436957·Protein Sci·2008
4-observational
Glutaric aciduria type I: outcome following detection by newborn screening.
PMID 18683078·J Inherit Metab Dis·2008
8-other
Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease.
PMID 18940309·Am J Hum Genet·2008
5-case
Costeff optic atrophy syndrome: new clinical case and novel molecular findings.
PMID 18985435·J Inherit Metab Dis·2008
5-case
A coupled equilibrium shift mechanism in calmodulin-mediated signal transduction.
PMID 18462678·Structure·2008
8-other
Immunological features of alpha-synuclein in Parkinson's disease.
PMID 18671754·J Cell Mol Med·2008
6-review
Environmental enrichment ameliorates a motor coordination deficit in a mouse model of Rett syndrome--Mecp2 gene dosage effects and BDNF expression.
PMID 18557922·Eur J Neurosci·2008
7-preclinical
MECP2 genomic structure and function: insights from ENCODE.
PMID 18820302·Nucleic Acids Res·2008
6-review
The extremely slow-exchanging core and acid-denatured state of green fluorescent protein.
PMID 19436495·HFSP J·2008
8-other
Engineering a camelid antibody fragment that binds to the active site of human lysozyme and inhibits its conversion into amyloid fibrils.
PMID 18816062·Biochemistry·2008
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
- 625 PARK AVE
NEW YORK, NY 10065 - Phone
- (212) 744-1118
Quick Facts
- NPI
- 1265592653
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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