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SHIRLEY MALCOLM, DO
DO
Family Medicine Physician
NPI: 1316951510Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
DO17513(OR)
Research & Publications (20)
An examination of HIV/AIDS patients who have excellent adherence to HAART.
PMID 12856346·AIDS Care·2003
8-other
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
In vitro and in vivo evaluation of O-alkyl derivatives of tramadol.
PMID 18242987·Bioorg Med Chem Lett·2008
7-preclinical
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
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
Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelination.
PMID 16969684·Neurogenetics·2007
5-case
Large genomic rearrangements within the PCDH15 gene are a significant cause of USH1F syndrome.
PMID 17277737·Mol Vis·2007
8-other
Assessing the impact of nutrient enrichment in estuaries: susceptibility to eutrophication.
PMID 17028037·Mar Pollut Bull·2007
8-other
Defining and detecting undesirable disturbance in the context of marine eutrophication.
PMID 17011591·Mar Pollut Bull·2007
6-review
Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1beta in persistent cloaca and associated kidney malformations.
PMID 17476318·J Pediatr Urol·2007
8-other
Mutation analyses of Uroplakin II in children with renal tract malformations.
PMID 17012268·Nephrol Dial Transplant·2006
5-case
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
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
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
De novo Uroplakin IIIa heterozygous mutations cause human renal adysplasia leading to severe kidney failure.
PMID 15888565·J Am Soc Nephrol·2005
8-other
Intrinsic Klebsiella pneumoniae contamination of liquid germicidal hand soap containing chlorhexidine.
PMID 15518034·Infect Control Hosp Epidemiol·2004
8-other
OFD1 is a centrosomal/basal body protein expressed during mesenchymal-epithelial transition in human nephrogenesis.
PMID 15466260·J Am Soc Nephrol·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
- Address
- 70 BOWER DR
MEDFORD, OR 97501 - Phone
- (541) 734-3430
Quick Facts
- NPI
- 1316951510
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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