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CAROLINA BRUNO MD
MD
Endocrinology, Diabetes & Metabolism Physician
NPI: 1417110362Individual
Specialties, Licenses & Credentials
Endocrinology, Diabetes & Metabolism PhysicianPrimary
Internal Medicine — Endocrinology, Diabetes & Metabolism
Code: 207RE0101X
01067041(IN)
Research & Publications (20)
Electrochemical and theoretical investigation of corannulene reduction processes.
PMID 19173564·J Phys Chem B·2009
8-other
Gray-scale ultrasonography in the evaluation of bone callus in distraction osteogenesis of the mandible: initial findings.
PMID 18224324·Eur Radiol·2008
8-other
Plasma ICAM-1 and VCAM-1 levels in type 2 diabetic patients with and without microalbuminuria.
PMID 18299691·Minerva Med·2008
8-other
Clinical and genetic characterization of Chanarin-Dorfman syndrome.
PMID 18339307·Biochem Biophys Res Commun·2008
8-other
Growth of p- and n-dopable films from electrochemically generated C60 cations.
PMID 18314972·J Am Chem Soc·2008
8-other
Non-parametric smoothing of multivariate genetic distances in the analysis of spatial population structure at fine scale.
PMID 18592207·Theor Appl Genet·2008
7-preclinical
Neuromuscular forms of glycogen branching enzyme deficiency.
PMID 17915577·Acta Myol·2007
7-preclinical
Adverse health effects of fluoro-edenitic fibers: epidemiological evidence and public health priorities.
PMID 17119254·Ann N Y Acad Sci·2006
8-other
McArdle disease: the mutation spectrum of PYGM in a large Italian cohort.
PMID 16786513·Hum Mutat·2006
8-other
Chronic anaemia and adhesion molecules in patients with liver cirrhosis. A preliminary report.
PMID 15990708·Minerva Gastroenterol Dietol·2005
8-other
Circulating adhesion molecules in patients with virus-related chronic diseases of the liver.
PMID 16052689·World J Gastroenterol·2005
8-other
Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV).
PMID 15452297·Neurology·2004
5-case
Clinical and molecular findings in patients with giant axonal neuropathy (GAN).
PMID 14718689·Neurology·2004
5-case
Plasma erythropoietin levels in anaemic and non-anaemic patients with chronic liver diseases.
PMID 15112358·World J Gastroenterol·2004
8-other
Mitochondrial myopathy and respiratory failure associated with a new mutation in the mitochondrial transfer ribonucleic acid glutamic acid gene.
PMID 12760436·J Child Neurol·2003
5-case
Progressive exercise intolerance associated with a new muscle-restricted nonsense mutation (G142X) in the mitochondrial cytochrome b gene.
PMID 14506725·Muscle Nerve·2003
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 550 UNIVERSITY BLVD
INDIANAPOLIS, IN 46202 - Phone
- (317) 944-8660
Quick Facts
- NPI
- 1417110362
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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