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ANDREA CHAKRAPANI, M.D.
M.D.
Dermatopathology (Pathology) Physician
NPI: 1659514958IndividualAccepts Medicare
Specialties, Licenses & Credentials
Anatomic Pathology & Clinical Pathology Physician
Pathology — Anatomic Pathology & Clinical Pathology
Code: 207ZP0102X
MD160746(OR)
Dermatopathology (Pathology) PhysicianPrimary
Pathology — Dermatopathology
Code: 207ZD0900X
MD160746(OR)
Education
OREGON HEALTH SCIENCES UNIVERSITY SCHOOL OF MEDICINE
Class of 2009
Research & Publications (20)
Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) as a cause of liver disease in infants in the UK.
PMID 19517266·J Inherit Metab Dis·2009
5-case
Severe HDL deficiency due to novel defects in the ABCA1 transporter.
PMID 19019193·J Intern Med·2009
8-other
Novel microcatheters for selective intra-arterial injection of fluid in the rat brain.
PMID 19357381·AJNR Am J Neuroradiol·2009
7-preclinical
Does maternal knowledge and parent education affect blood phenylalanine control in phenylketonuria?
PMID 18721402·J Hum Nutr Diet·2008
8-other
Prospective treatment of cerebrotendinous xanthomatosis with cholic acid therapy.
PMID 19125350·J Inherit Metab Dis·2008
5-case
Long-term compliance with a novel vitamin and mineral supplement in older people with PKU.
PMID 18941921·J Inherit Metab Dis·2008
4-observational
Late presentation of medium-chain acyl-CoA dehydrogenase deficiency.
PMID 17143576·J Inherit Metab Dis·2007
5-case
Prospective treatment in carnitine-acylcarnitine translocase deficiency.
PMID 17508264·J Inherit Metab Dis·2007
5-case
Nanoparticles and microparticles as vaccine-delivery systems.
PMID 17931159·Expert Rev Vaccines·2007
6-review
Efficacy of sapropterin dihydrochloride (tetrahydrobiopterin, 6R-BH4) for reduction of phenylalanine concentration in patients with phenylketonuria: a phase III randomised placebo-controlled study.
PMID 17693179·Lancet·2007
3-trial
A case of acute papillary muscle rupture in a child with campylobacter enteritis and citrullinaemia.
PMID 17952406·Intensive Care Med·2007
5-case
'Ready to drink' protein substitute is easier is for people with phenylketonuria.
PMID 16736099·J Inherit Metab Dis·2006
2-rct
Fumarase deficiency caused by homozygous P131R mutation and paternal partial isodisomy of chromosome 1.
PMID 16575891·Am J Med Genet A·2006
5-case
Successful treatment of pyridoxine-unresponsive homocystinuria with betaine in pregnancy.
PMID 16972179·J Inherit Metab Dis·2006
5-case
Protein substitute dosage in PKU: how much do young patients need?
PMID 16547085·Arch Dis Child·2006
2-rct
Home delivery of dietary products in inherited metabolic disorders reduces prescription and dispensing errors.
PMID 16961684·J Hum Nutr Diet·2006
2-rct
Case 36-2005: a woman with seizure, disturbed gait, and altered mental status.
PMID 16525154·N Engl J Med·2006
8-other
Successful pregnancy in a treated patient with biotinidase deficiency.
PMID 16151912·J Inherit Metab Dis·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
- Address
- 12254 SW GARDEN PL
TIGARD, OR 97223 - Phone
- (503) 906-7300
Quick Facts
- NPI
- 1659514958
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 17
- Publications
- 20
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