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STUART MALCOLM, M.D.
M.D.
Internal Medicine Physician
NPI: 1124472055Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
A159926(CA)
Research & Publications (20)
Effects of atomoxetine on attention-deficit/hyperactivity disorder in clinical pediatric treatment settings: a naturalistic study.
PMID 18179733·Curr Med Res Opin·2008
8-other
In vitro and in vivo evaluation of O-alkyl derivatives of tramadol.
PMID 18242987·Bioorg Med Chem Lett·2008
7-preclinical
UMD-USHbases: a comprehensive set of databases to record and analyse pathogenic mutations and unclassified variants in seven Usher syndrome causing genes.
PMID 18484607·Hum Mutat·2008
8-other
Large genomic rearrangements within the PCDH15 gene are a significant cause of USH1F syndrome.
PMID 17277737·Mol Vis·2007
8-other
Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelination.
PMID 16969684·Neurogenetics·2007
5-case
Defining and detecting undesirable disturbance in the context of marine eutrophication.
PMID 17011591·Mar Pollut Bull·2007
6-review
Molecular and in silico analyses of the full-length isoform of usherin identify new pathogenic alleles in Usher type II patients.
PMID 17405132·Hum Mutat·2007
8-other
Assessing the impact of nutrient enrichment in estuaries: susceptibility to eutrophication.
PMID 17028037·Mar Pollut Bull·2007
8-other
Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1beta in persistent cloaca and associated kidney malformations.
PMID 17476318·J Pediatr Urol·2007
8-other
Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%.
PMID 16679490·J Med Genet·2006
8-other
Mutation analyses of Uroplakin II in children with renal tract malformations.
PMID 17012268·Nephrol Dial Transplant·2006
5-case
De novo Uroplakin IIIa heterozygous mutations cause human renal adysplasia leading to severe kidney failure.
PMID 15888565·J Am Soc Nephrol·2005
8-other
Small fiber diameter fibro-porous meshes: tissue response sensitivity to fiber spacing.
PMID 15657935·J Biomed Mater Res A·2005
8-other
Three or more copies of the proteolipid protein gene PLP1 cause severe Pelizaeus-Merzbacher disease.
PMID 15689360·Brain·2005
5-case
Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination.
PMID 16380909·Am J Hum Genet·2005
8-other
Mutation spectrum leading to an attenuated phenotype in dystrophinopathies.
PMID 16077730·Eur J Hum Genet·2005
5-case
Once-daily atomoxetine treatment for children with attention-deficit/hyperactivity disorder, including an assessment of evening and morning behavior: a double-blind, placebo-controlled trial.
PMID 15231966·Pediatrics·2004
3-trial
The role of muscle biopsy in analysis of the dystrophin gene in Duchenne muscular dystrophy: experience of a national referral centre.
PMID 15351422·Neuromuscul Disord·2004
4-observational
Density-dependent reduction and induction of milkweed cardenolides by a sucking insect herbivore.
PMID 15139307·J Chem Ecol·2004
4-observational
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
- 6036 SE 40TH AVE
PORTLAND, OR 97202 - Phone
- (770) 687-7654
Quick Facts
- NPI
- 1124472055
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 2
- Publications
- 20
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