Back to Search
PATRICK RICHARD, M.D./M.P.H.
M.D./M.P.H.
Radiation Oncology Physician
NPI: 1134418890IndividualAccepts Medicare
Specialties, Licenses & Credentials
Radiation Oncology PhysicianPrimary
Radiology — Radiation Oncology
Code: 2085R0001X
DR.0057119(CO)ML 60285285(WA)
Education
UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE
Class of 2016
Research & Publications (20)
Competition between antiferromagnetism and superconductivity in the electron-doped cuprates triggered by oxygen reduction.
PMID 17995205·Phys Rev Lett·2007
8-other
Effect of the anisotropy of the cells on the topological properties of two- and three-dimensional froths.
PMID 11415150·Phys Rev E Stat Nonlin Soft Matter Phys·2001
8-other
Wildfire responses to abrupt climate change in North America.
PMID 19190185·Proc Natl Acad Sci U S A·2009
8-other
Safety of short-term discontinuation of antiplatelet therapy in patients with drug-eluting stents.
PMID 19289638·Circulation·2009
6-review
delta(15)N and delta(13)C in the Mondego estuary food web: seasonal variation in producers and consumers.
PMID 19111337·Mar Environ Res·2009
7-preclinical
D-galacturonic acid catabolism in microorganisms and its biotechnological relevance.
PMID 19159926·Appl Microbiol Biotechnol·2009
6-review
Angle-resolved photoemission spectroscopy of the Fe-Based Ba0.6K0.4Fe2As2 high temperature superconductor: evidence for an orbital selective electron-mode coupling.
PMID 19257465·Phys Rev Lett·2009
8-other
Novel epsilon subunit mutation of the muscle acetylcholine receptor causing a slow-channel congenital myasthenic syndrome.
PMID 19289485·J Neurol Neurosurg Psychiatry·2009
5-case
A mutation in the SEPN1 selenocysteine redefinition element (SRE) reduces selenocysteine incorporation and leads to SEPN1-related myopathy.
PMID 19067361·Hum Mutat·2009
8-other
Germinal mosaicism for LMNA mimics autosomal recessive congenital muscular dystrophy.
PMID 19084400·Neuromuscul Disord·2009
8-other
Striking phenotypic variability in two familial cases of myosin storage myopathy with a MYH7 Leu1793pro mutation.
PMID 19138847·Neuromuscul Disord·2009
5-case
Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study.
PMID 19151983·Acta Neuropathol·2009
8-other
Safety of Tdap-IPV given one month after Td-IPV booster in healthy young adults: a placebo-controlled trial.
PMID 19011374·Hum Vaccin·2009
4-observational
Symmetric heteropolynuclear Ti(IV)/Cu(I) complexes exhibiting stepwise electrochemical reductions to Ti(III) species.
PMID 19254008·Inorg Chem·2009
8-other
Usher syndrome type 1: early detection of electroretinographic changes.
PMID 19006676·Eur J Paediatr Neurol·2009
8-other
A cardio-neurological form of laminopathy: dilated cardiomyopathy with permanent partial atrial standstill and axonal neuropathy.
PMID 19272076·Pacing Clin Electrophysiol·2009
5-case
Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescue.
PMID 19015158·Brain·2009
8-other
Prospective observational study of low thresholds for platelet transfusion in adult dengue patients.
PMID 19320862·Transfusion·2009
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 4715 ARAPAHOE AVE
BOULDER, CO 80303 - Phone
- (303) 285-2000
Quick Facts
- NPI
- 1134418890
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 10
- Publications
- 20
Are you this provider?
Claim Your Profile