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SAMUEL JACOBSON, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1255912002Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Abnormally high levels of virus-infected IFN-gamma+ CCR4+ CD4+ CD25+ T cells in a retrovirus-associated neuroinflammatory disorder.
PMID 19654865·PLoS One·2009
8-other
Higher infant blood lead levels with longer duration of breastfeeding.
PMID 19595371·J Pediatr·2009
4-observational
Iron deficiency anemia in infancy and reach and grasp development.
PMID 19592115·Infant Behav Dev·2009
8-other
Thyroid hormone levels of pregnant inuit women and their infants exposed to environmental contaminants.
PMID 19590699·Environ Health Perspect·2009
8-other
Human RPE65 gene therapy for Leber congenital amaurosis: persistence of early visual improvements and safety at 1 year.
PMID 19583479·Hum Gene Ther·2009
3-trial
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy.
PMID 19578027·Invest Ophthalmol Vis Sci·2009
8-other
The relation of lead neurotoxicity to the event-related potential P3b component in Inuit children from arctic Québec.
PMID 19576242·Neurotoxicology·2009
8-other
Effect of (r)-9-[4-hydroxy-2-(hydroxymethyl)butyl]guanine (H2G) and AZT-lipid-PFA on human herpesvirus-6B infected cells.
PMID 19524486·J Clin Virol·2009
8-other
Prenatal alcohol exposure and interhemispheric transfer of tactile information: Detroit and Cape Town findings.
PMID 19519722·Alcohol Clin Exp Res·2009
8-other
Detection of human herpesvirus-6 variants in pediatric brain tumors: association of viral antigen in low grade gliomas.
PMID 19505845·J Clin Virol·2009
8-other
Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: retained photoreceptors adjacent to retinal disorganization.
PMID 19503738·Mol Vis·2009
8-other
Histological biocompatibility of a stainless steel miniature glaucoma drainage device in humans: a case report.
PMID 19458389·Toxicol Pathol·2009
5-case
Idiopathic suppurative pylephlebitis: interventional radiological diagnosis and management.
PMID 19449066·Cardiovasc Intervent Radiol·2009
5-case
Prescription of antihypertensive agents to haemodialysis patients: time trends and associations with patient characteristics, country and survival in the DOPPS.
PMID 19443648·Nephrol Dial Transplant·2009
4-observational
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies.
PMID 19430481·Nat Genet·2009
7-preclinical
Mathematical modeling and mechanical and histopathological testing of porous prosthetic pylon for direct skeletal attachment.
PMID 19675985·J Rehabil Res Dev·2009
7-preclinical
Vision 1 year after gene therapy for Leber's congenital amaurosis.
PMID 19675341·N Engl J Med·2009
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
- 710 W 168TH ST
NEW YORK, NY 10032 - Phone
- (212) 305-2500
Quick Facts
- NPI
- 1255912002
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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