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ROSEMARY POMPONIO, M.D.
M.D.
Family Medicine Physician
NPI: 1215058367Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
55752(MA)
Research & Publications (20)
Microemulsion electrokinetic chromatography of corticosteroids. Effect of surfactants and cyclodextrins on the separation selectivity.
PMID 16013593·J Chromatogr A·2005
8-other
Photostability studies on nicardipine-cyclodextrin complexes by capillary electrophoresis.
PMID 15063461·J Pharm Biomed Anal·2004
8-other
Analysis of catechins in extracts of Cistus species by microemulsion electrokinetic chromatography.
PMID 12685600·J Chromatogr A·2003
8-other
Microemulsion electrokinetic chromatography for the analysis of green tea catechins: effect of the cosurfactant on the separation selectivity.
PMID 12761797·Electrophoresis·2003
8-other
Analysis of phenolic acids by micellar electrokinetic chromatography: application to Echinacea purpurea plant extracts.
PMID 11860138·J Chromatogr A·2002
8-other
Evidences of cyclodextrin-mediated enantioselective photodegradation of rac-nicardipine by capillary electrophoresis.
PMID 11589286·Electrophoresis·2001
8-other
Novel mutations cause biotinidase deficiency in Turkish children.
PMID 10801053·J Inherit Metab Dis·2000
3-trial
Novel mutations in children with profound biotinidase deficiency from Saudi Arabia.
PMID 10801060·J Inherit Metab Dis·2000
3-trial
Pompe disease in a Brazilian series: clinical and molecular analyses with identification of nine new mutations.
PMID 19588081·J Neurol·2009
8-other
Update of the Pompe disease mutation database with 107 sequence variants and a format for severity rating.
PMID 18425781·Hum Mutat·2008
7-preclinical
p.[G576S; E689K]: pathogenic combination or polymorphism in Pompe disease?
PMID 18301443·Eur J Hum Genet·2008
5-case
Rapid diagnosis of late-onset Pompe disease by fluorometric assay of alpha-glucosidase activities in dried blood spots.
PMID 17270480·Mol Genet Metab·2007
8-other
Pompe disease (glycogen storage disease type II) in Argentineans: clinical manifestations and identification of 9 novel mutations.
PMID 17056254·Neuromuscul Disord·2007
8-other
Broad spectrum of Pompe disease in patients with the same c.-32-13T->G haplotype.
PMID 17210890·Neurology·2007
8-other
Precision study on capillary electrophoresis methods for metacycline.
PMID 16718715·Electrophoresis·2006
4-observational
Two clinical forms of glycogen-storage disease type II in two generations of the same family.
PMID 16433701·Clin Genet·2006
5-case
A comparison of the phenotype and genotype in adenomatous polyposis patients with and without a family history.
PMID 15951963·Fam Cancer·2005
4-observational
Gaucher disease in Colombia: mutation identification and comparison to other Hispanic populations.
PMID 16185907·Mol Genet Metab·2005
4-observational
Study of donepezil binding to serum albumin by capillary electrophoresis and circular dichroism.
PMID 12955395·Anal Bioanal Chem·2003
8-other
Analysis of amphetamine and congeners in illicit samples by liquid chromatography and capillary electrophoresis.
PMID 11300514·J Anal Toxicol·2001
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 376 ARSENAL ST
WATERTOWN, MA 02472 - Phone
- (617) 953-5817
Quick Facts
- NPI
- 1215058367
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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