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CAMERON LEITCH, M.D.
M.D.
Diagnostic Radiology Physician
NPI: 1710327077IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
RL12841(ND)
Diagnostic Radiology PhysicianPrimary
Radiology — Diagnostic Radiology
Code: 2085R0202X
58387(MN)
CMS Specialties
PrimaryDIAGNOSTIC RADIOLOGY
Education
OTHER
Class of 2013
Research & Publications (20)
Genome-wide screen identifies drug-induced regulation of the gene giant axonal neuropathy (Gan) in a mouse model of antiretroviral-induced painful peripheral neuropathy.
PMID 19398414·Biol Res Nurs·2009
7-preclinical
Energy expenditure in extremely low birth weight infants near time of hospital discharge.
PMID 18657827·J Pediatr·2008
8-other
An essential role for DYF-11/MIP-T3 in assembling functional intraflagellar transport complexes.
PMID 18369462·PLoS Genet·2008
7-preclinical
Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome.
PMID 18327255·Nat Genet·2008
7-preclinical
Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response.
PMID 17906624·Nat Genet·2007
7-preclinical
Effect of late-onset sepsis on energy expenditure in extremely premature infants.
PMID 17413868·Pediatr Res·2007
8-other
Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome.
PMID 17160889·Am J Hum Genet·2007
7-preclinical
BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus.
PMID 16582908·Nat Genet·2006
8-other
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates.
PMID 16170314·Nat Genet·2005
7-preclinical
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2.
PMID 15731757·Nat Genet·2005
8-other
MKKS/BBS6, a divergent chaperonin-like protein linked to the obesity disorder Bardet-Biedl syndrome, is a novel centrosomal component required for cytokinesis.
PMID 15731008·J Cell Sci·2005
7-preclinical
Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse.
PMID 15322545·Nat Genet·2004
7-preclinical
Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene.
PMID 15137946·Cell·2004
4-observational
The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression.
PMID 15107855·Nat Genet·2004
7-preclinical
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome.
PMID 14520415·Nature·2003
7-preclinical
Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2.
PMID 12567324·Am J Hum Genet·2003
4-observational
Amino acids do not suppress proteolysis in premature neonates.
PMID 11500302·Am J Physiol Endocrinol Metab·2001
8-other
Large left-to-right shunts and congestive heart failure increase total energy expenditure in infants with ventricular septal defect.
PMID 11348620·Am J Cardiol·2001
8-other
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
- 1400 BELLINGER ST
EAU CLAIRE, WI 54703 - Phone
- (715) 838-3311
Quick Facts
- NPI
- 1710327077
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 2
- Years in Practice
- 13
- Publications
- 20
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