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FRANK BAUMEISTER, M.D.
M.D.
Specialist
NPI: 1194779645Individual
Specialties, Licenses & Credentials
SpecialistPrimary
Specialist
Code: 174400000X
MD7679(OR)
Research & Publications (20)
A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice.
PMID 18713754·Hum Mol Genet·2008
7-preclinical
Allelic and non-allelic heterogeneities in pyridoxine dependent seizures revealed by ALDH7A1 mutational analysis.
PMID 17433748·Mol Genet Metab·2007
5-case
Biochemical and molecular characterization of 18 patients with pyridoxine-dependent epilepsy and mutations of the antiquitin (ALDH7A1) gene.
PMID 17068770·Hum Mutat·2007
8-other
Monitoring of ketogenic diet for carnitine metabolites by subcutaneous microdialysis.
PMID 16690958·Pediatr Res·2006
3-trial
Subcutaneous microdialysis for children - safe biochemical tissue monitoring based on a minimal traumatizing no touch insertion technique.
PMID 16287603·Eur J Med Res·2005
8-other
The eye-of-the-tiger sign is not a reliable disease marker for Hallervorden-Spatz syndrome.
PMID 15944911·Neuropediatrics·2005
5-case
Pipecolic acid as a diagnostic marker of pyridoxine-dependent epilepsy.
PMID 15944906·Neuropediatrics·2005
8-other
Fatal propofol infusion syndrome in association with ketogenic diet.
PMID 15328567·Neuropediatrics·2004
5-case
Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome.
PMID 15305058·Cytogenet Genome Res·2004
8-other
[Onset of bilateral blindness in the first year of life. Alström syndrome].
PMID 15004717·Ophthalmologe·2004
5-case
Diagnosis of Ambras syndrome: comments on complex cytogenetic rearrangement of chromosome 8q in a case of Ambras syndrome.
PMID 11932999·Am J Med Genet·2002
8-other
Glucose monitoring with long-term subcutaneous microdialysis in neonates.
PMID 11694701·Pediatrics·2001
8-other
Determination of amino acid tissue concentrations by microdialysis: method evaluation and relation to plasma values.
PMID 11665809·Amino Acids·2001
8-other
Griscelli syndrome: report of the first peripheral blood stem cell transplant and the role of mutations in the RAB27A gene as an indication for BMT.
PMID 11571516·Bone Marrow Transplant·2001
5-case
Lymphoproliferative syndrome in an infant after stem cell transplantation: successful therapy with T-lymphocytes and anti-CD20 monoclonal antibodies.
PMID 11070486·Med Pediatr Oncol·2000
5-case
Cerebellar hemorrhage in preterm infants with intraventricular hemorrhage: a missed diagnosis? A patient report.
PMID 11063043·Clin Pediatr (Phila)·2000
8-other
Thrombosis of the deep cerebral veins with excessive bilateral infarction in a premature infant with the thrombogenic 4G/4G genotype of the plasminogen activator inhibitor-1.
PMID 10789926·Eur J Pediatr·2000
5-case
Differentiation of Ambras syndrome from Hypertrichosis Universalis.
PMID 10735640·Clin Genet·2000
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
- 1130 NW 22ND AVE, SUITE 410
PORTLAND, OR 97210 - Phone
- (503) 229-7137
Quick Facts
- NPI
- 1194779645
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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