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DAVID KOELLER, MD

MD

Clinical Biochemical Genetics Physician

NPI: 1629086145Individual

Specialties, Licenses & Credentials

Clinical Biochemical Genetics PhysicianPrimary

Medical Genetics — Clinical Biochemical Genetics

Code: 207SG0202X

MD22656(OR)
Pediatrics Physician

Pediatrics

Code: 208000000X

MD22656(OR)

Research & Publications (20)

Animal models for glutaryl-CoA dehydrogenase deficiency.
PMID 15505386·J Inherit Metab Dis·2004
7-preclinical
Biochemical, pathologic and behavioral analysis of a mouse model of glutaric acidemia type I.
PMID 11854167·Hum Mol Genet·2002
7-preclinical
Transport and distribution of 3-hydroxyglutaric acid before and during induced encephalopathic crises in a mouse model of glutaric aciduria type 1.
PMID 18348873·Biochim Biophys Acta·2008
7-preclinical
3-Hydroxyglutaric acid is transported via the sodium-dependent dicarboxylate transporter NaDC3.
PMID 17356845·J Mol Med (Berl)·2007
7-preclinical
Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I).
PMID 17203377·J Inherit Metab Dis·2007
6-review
Lysine intake and neurotoxicity in glutaric aciduria type I: towards a rationale for therapy?
PMID 16870879·Brain·2006
7-preclinical
Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiency.
PMID 16641220·Pediatr Res·2006
8-other
Intracerebral accumulation of glutaric and 3-hydroxyglutaric acids secondary to limited flux across the blood-brain barrier constitute a biochemical risk factor for neurodegeneration in glutaryl-CoA dehydrogenase deficiency.
PMID 16573641·J Neurochem·2006
4-observational
Save yourself! The importance of disaster recovery.
PMID 15754810·MGMA Connex·2005
8-other
Bioenergetics in glutaryl-coenzyme A dehydrogenase deficiency: a role for glutaryl-coenzyme A.
PMID 15840571·J Biol Chem·2005
7-preclinical
Excitotoxicity and bioenergetics in glutaryl-CoA dehydrogenase deficiency.
PMID 15505385·J Inherit Metab Dis·2004
6-review
Challenges for basic research in glutaryl-CoA dehydrogenase deficiency.
PMID 15505391·J Inherit Metab Dis·2004
6-review
Vascular dysfunction as an additional pathomechanism in glutaric aciduria type I.
PMID 15505389·J Inherit Metab Dis·2004
6-review
The mitochondrial ABC transporter Atm1p functions as a homodimer.
PMID 15225610·FEBS Lett·2004
8-other
Pathomechanisms of neurodegeneration in glutaryl-CoA dehydrogenase deficiency.
PMID 14705106·Ann Neurol·2004
6-review
Genomic organization of ATOX1, a human copper chaperone.
PMID 12594858·BMC Genet·2003
8-other
MDL1 is a high copy suppressor of ATM1: evidence for a role in resistance to oxidative stress.
PMID 12875842·J Mol Biol·2003
8-other
The role of the mitochondrion in cellular iron homeostasis.
PMID 16120268·Mitochondrion·2001
8-other
Apparent decreased energy requirements in children with organic acidemias: preliminary observations.
PMID 11019359·J Am Diet Assoc·2000
8-other
Analysis of the expression of murine glutaryl-CoA dehydrogenase: in vitro and in vivo studies.
PMID 10720438·Mol Genet Metab·2000
7-preclinical

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

Contact & Hours

Address
3181 SW SAM JACKSON PARK RD
PORTLAND, OR 97239

Location

Practice Location

3181 SW SAM JACKSON PARK RD, PORTLAND, OR
(503) 494-7859

Quick Facts

NPI
1629086145
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
2
Locations
1
Publications
20

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