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ROBERT CASPARI, MD
MD
Internal Medicine Physician
NPI: 1205340676Individual
Specialties, Licenses & Credentials
Research & Publications (20)
MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype.
PMID 16557584·Int J Cancer·2006
8-other
New reconstruction of Krapina 5, a male Neandertal cranial vault from Krapina, Croatia.
PMID 16395724·Am J Phys Anthropol·2006
7-preclinical
Is human longevity a consequence of cultural change or modern biology?
PMID 16342259·Am J Phys Anthropol·2006
7-preclinical
Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis.
PMID 15689459·J Med Genet·2005
8-other
Comparison of capsule endoscopy and magnetic resonance imaging for the detection of polyps of the small intestine in patients with familial adenomatous polyposis or with Peutz-Jeghers' syndrome.
PMID 15578294·Endoscopy·2004
3-trial
Familial adenomatous polyposis: aberrant splicing due to missense or silent mutations in the APC gene.
PMID 15459959·Hum Mutat·2004
8-other
Older age becomes common late in human evolution.
PMID 15252198·Proc Natl Acad Sci U S A·2004
7-preclinical
E-cadherin expression is homogeneously reduced in adenoma from patients with familial adenomatous polyposis: an immunohistochemical study of E-cadherin, beta-catenin and cyclooxygenase-2 expression.
PMID 14986031·Int J Colorectal Dis·2004
4-observational
Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis.
PMID 14523376·Eur J Hum Genet·2004
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
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Contact & Hours
- Address
- 2465 CANA CT
LAFAYETTE, CO 80026 - Phone
- (303) 442-2519
Quick Facts
- NPI
- 1205340676
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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