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OLAF BODAMER, MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1487958146IndividualAccepts Medicare
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
261496(MA)
CMS Specialties
PrimaryMEDICAL GENETICS AND GENOMICS
Education
OTHER
Class of 1989
Research & Publications (20)
Variant Gaucher disease characterized by dysmorphic features, absence of cardiovascular involvement, laryngospasm, and compound heterozygosity for a novel mutation (D409H/C16S).
PMID 11992489·Am J Med Genet·2002
5-case
Use of denaturing HPLC to provide efficient detection of mutations causing familial hypercholesterolemia.
PMID 12406975·Clin Chem·2002
8-other
Multiple fractures in a 3-month-old infant with severe infantile osteopetrosis.
PMID 11885723·J Paediatr Child Health·2001
5-case
Uses of stable isotopes in clinical diagnosis and research in the paediatric population.
PMID 11316697·Arch Dis Child·2001
6-review
Analysis of guanidinoacetate and creatine by isotope dilution electrospray tandem mass spectrometry.
PMID 11412830·Clin Chim Acta·2001
4-observational
Adult-onset combined methylmalonic aciduria and homocystinuria (cblC).
PMID 11320193·Neurology·2001
5-case
Protein, glucose and energy metabolism in Gaucher disease type I.
PMID 10682313·J Inherit Metab Dis·2000
5-case
The effects of l-alanine supplementation in late-onset glycogen storage disease type II.
PMID 10980742·Neurology·2000
8-other
Screening for X-linked creatine transporter (SLC6A8) deficiency via simultaneous determination of urinary creatine to creatinine ratio by tandem mass-spectrometry.
PMID 19188083·Mol Genet Metab·2009
8-other
Low creatinine: the diagnostic clue for a treatable neurologic disorder.
PMID 19255414·Neurology·2009
5-case
Danon disease: case report and detection of new mutation.
PMID 19588270·J Inherit Metab Dis·2009
5-case
Development and evaluation of quality control dried blood spot materials in newborn screening for lysosomal storage disorders.
PMID 18988750·Clin Chem·2009
8-other
Prediction of outcome in isolated methylmalonic acidurias: combined use of clinical and biochemical parameters.
PMID 19642010·J Inherit Metab Dis·2009
4-observational
Introduction of a novel prototype bioartificial liver support system utilizing small human hepatocytes in rotary culture.
PMID 18847359·Tissue Eng Part A·2009
8-other
Newborn screening in Fabry disease: what can be achieved with early diagnosis?
PMID 18395134·Clin Ther·2008
8-other
Heparin cofactor II-thrombin complex: a biomarker of MPS disease.
PMID 18511319·Mol Genet Metab·2008
4-observational
Diagnostic work-up and management of patients with isolated methylmalonic acidurias in European metabolic centres.
PMID 18563634·J Inherit Metab Dis·2008
8-other
Newborn screening for Pompe disease by measuring acid alpha-glucosidase activity using tandem mass spectrometry.
PMID 18703766·Clin Chem·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 300 LONGWOOD AVE
BOSTON, MA 02115 - Phone
- (617) 355-6000
Quick Facts
- NPI
- 1487958146
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 2
- Years in Practice
- 37
- Publications
- 20
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