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HARRY ARCHER MD
MD
General Practice Physician
NPI: 1407906076IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
ACN234(FL)
General Practice PhysicianPrimary
General Practice
Code: 208D00000X
ACN234(FL)
Education
OTHER
Class of 1983
Research & Publications (20)
Conversion of amyloid positive and negative MCI to AD over 3 years: an 11C-PIB PET study.
PMID 19587325·Neurology·2009
4-observational
Strategies for the generation of parametric images of [11C]PIB with plasma input functions considering discriminations and reproducibility.
PMID 19591948·Neuroimage·2009
8-other
Microglial activation and amyloid deposition in mild cognitive impairment: a PET study.
PMID 19122031·Neurology·2009
8-other
Structural and biochemical characterization of the therapeutic Anabaena variabilis phenylalanine ammonia lyase.
PMID 18556022·J Mol Biol·2008
7-preclinical
Microglia, amyloid, and cognition in Alzheimer's disease: An [11C](R)PK11195-PET and [11C]PIB-PET study.
PMID 18786637·Neurobiol Dis·2008
8-other
Two sisters with Rett syndrome and non-identical paternally-derived microdeletions in the MECP2 gene.
PMID 18810657·Genomic Med·2008
8-other
Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation.
PMID 16905679·J Med Genet·2007
4-observational
Amyloid, hypometabolism, and cognition in Alzheimer disease: an [11C]PIB and [18F]FDG PET study.
PMID 17065593·Neurology·2007
8-other
Germline mosaicism for a MECP2 mutation in a man with two Rett daughters.
PMID 16965328·Clin Genet·2006
5-case
Amyloid load and cerebral atrophy in Alzheimer's disease: an 11C-PIB positron emission tomography study.
PMID 16802294·Ann Neurol·2006
8-other
Do symptoms of memory impairment correspond to cognitive impairment: a cross sectional study of a clinical cohort.
PMID 16977678·Int J Geriatr Psychiatry·2006
8-other
Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patients.
PMID 16183801·J Med Genet·2006
8-other
CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients.
PMID 16611748·J Med Genet·2006
8-other
A mouse model of hereditary pancreatitis generated by transgenic expression of R122H trypsinogen.
PMID 17087933·Gastroenterology·2006
7-preclinical
People with MECP2 mutation-positive Rett disorder who converse.
PMID 16629931·J Intellect Disabil Res·2006
8-other
Oedema with proteinuria in Gambian children--a descriptive study.
PMID 16404628·Pediatr Nephrol·2006
8-other
Variation in exon 1 coding region and promoter of MECP2 in Rett syndrome and controls.
PMID 15367913·Eur J Hum Genet·2005
4-observational
Improving nitrogen reduction in waste stabilisation ponds.
PMID 16114675·Water Sci Technol·2005
4-observational
Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter.
PMID 15937949·Am J Med Genet A·2005
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via BORINQUEN HEALTH CARE CENTER, INC. · 2 locations total
- Address
- 7801 NE 2ND AVE
MIAMI, FL 33138 - Phone
- (305) 576-6611
Quick Facts
- NPI
- 1407906076
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 2
- Years in Practice
- 43
- Publications
- 20
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