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CRISTINA SHAW, PHD, MSW
PHD, MSW
Clinical Social Worker
NPI: 1912129545Individual
Specialties, Licenses & Credentials
Clinical Social WorkerPrimary
Social Worker — Clinical
Code: 1041C0700X
2363-C(AR)
Research & Publications (20)
Consensus review of discordant findings maximizes cancer detection rate in double-reader screening mammography: Irish National Breast Screening Program experience.
PMID 19188311·Radiology·2009
8-other
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6.
PMID 19251628·Science·2009
7-preclinical
Do European hospitals have quality and safety governance systems and structures in place?
PMID 19188462·Qual Saf Health Care·2009
8-other
Neurodegenerative diseases: neurotoxins as sufficient etiologic agents?
PMID 17985252·Neuromolecular Med·2008
6-review
Deregulation of PKN1 activity disrupts neurofilament organisation and axonal transport.
PMID 18519042·FEBS Lett·2008
7-preclinical
Photosystem II herbicide pollution in Hong Kong and its potential photosynthetic effects on corals.
PMID 18486951·Mar Pollut Bull·2008
7-preclinical
Familial amyotrophic lateral sclerosis-linked SOD1 mutants perturb fast axonal transport to reduce axonal mitochondria content.
PMID 17725983·Hum Mol Genet·2007
7-preclinical
Intravenous immunoglobulins and haematopoietic growth factors in the prevention and treatment of neonatal sepsis: ground reality or glorified myths?
PMID 17313617·Int J Clin Pract·2007
6-review
Non-recurrent 17p11.2 deletions are generated by homologous and non-homologous mechanisms.
PMID 15526218·Hum Genet·2005
8-other
Xerophthalmia: a study among malnourished children of West Mednipur District.
PMID 16173295·J Indian Med Assoc·2005
8-other
Nitric oxide and the resolution of inflammation: implications for atherosclerosis.
PMID 15962101·Mem Inst Oswaldo Cruz·2005
6-review
Spontaneous rupture of the liver following a normal pregnancy and delivery.
PMID 15782733·Ir Med J·2005
5-case
A girl with duplication 17p10-p12 associated with a dicentric chromosome.
PMID 14699617·Am J Med Genet A·2004
5-case
Uncommon deletions of the Smith-Magenis syndrome region can be recurrent when alternate low-copy repeats act as homologous recombination substrates.
PMID 15148657·Am J Hum Genet·2004
4-observational
Validity and reliability of a questionnaire to measure the impact of lower urinary tract symptoms on quality of life: the Leicester Impact Scale.
PMID 15098218·Neurourol Urodyn·2004
3-trial
Small marker chromosomes in two patients with segmental aneusomy for proximal 17p.
PMID 15098121·Hum Genet·2004
5-case
Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease.
PMID 14764619·Hum Mol Genet·2004
6-review
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
- 3050 BROADWAY ST
BOULDER, CO 80304 - Phone
- (303) 775-7221
Quick Facts
- NPI
- 1912129545
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 2
- Publications
- 20
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