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HEIDI ARCHER, MD

MD

Physical Medicine & Rehabilitation Physician

NPI: 1902890536Individual

Specialties, Licenses & Credentials

Physical Medicine & Rehabilitation PhysicianPrimary

Physical Medicine & Rehabilitation

Code: 208100000X

0101050030(VA)

Research & Publications (20)

Microglial activation and amyloid deposition in mild cognitive impairment: a PET study.
PMID 19122031·Neurology·2009
8-other
Strategies for the generation of parametric images of [11C]PIB with plasma input functions considering discriminations and reproducibility.
PMID 19591948·Neuroimage·2009
8-other
Conversion of amyloid positive and negative MCI to AD over 3 years: an 11C-PIB PET study.
PMID 19587325·Neurology·2009
4-observational
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
CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients.
PMID 16611748·J Med Genet·2006
8-other
People with MECP2 mutation-positive Rett disorder who converse.
PMID 16629931·J Intellect Disabil Res·2006
8-other
Amyloid load and cerebral atrophy in Alzheimer's disease: an 11C-PIB positron emission tomography study.
PMID 16802294·Ann Neurol·2006
8-other
Germline mosaicism for a MECP2 mutation in a man with two Rett daughters.
PMID 16965328·Clin Genet·2006
5-case
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
NTNG1 mutations are a rare cause of Rett syndrome.
PMID 16502428·Am J Med Genet A·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
A mouse model of hereditary pancreatitis generated by transgenic expression of R122H trypsinogen.
PMID 17087933·Gastroenterology·2006
7-preclinical
Oedema with proteinuria in Gambian children--a descriptive study.
PMID 16404628·Pediatr Nephrol·2006
8-other
p.R270X MECP2 mutation and mortality in Rett syndrome.
PMID 16077729·Eur J Hum Genet·2005
8-other
Dimensional phenotypic analysis and functional categorisation of mutations reveal novel genotype-phenotype associations in Rett syndrome.
PMID 16077736·Eur J Hum Genet·2005
8-other
Improving nitrogen reduction in waste stabilisation ponds.
PMID 16114675·Water Sci Technol·2005
4-observational

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
46165 WESTLAKE DR, SUITE 100
STERLING, VA 20165

Location

Practice Location

46165 WESTLAKE DR, STERLING, VA
(703) 433-1700

Quick Facts

NPI
1902890536
Entity Type
Individual
Gender
Female
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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