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CHRISTINA BRUNO, MD
MD
Ophthalmology Physician
NPI: 1760490486IndividualAccepts Medicare
Specialties, Licenses & Credentials
Glaucoma Specialist (Ophthalmology) Physician
Ophthalmology — Glaucoma Specialist
Code: 207WX0009X
0101241201(VA)
Ophthalmology PhysicianPrimary
Ophthalmology
Code: 207W00000X
0101241201(VA)
Education
PENNSYLVANIA STATE UNIVERSITY COLLEGE OF MEDICINE
Class of 1996
Research & Publications (20)
The association between maternal body mass index and severity of neonatal illness in very low birth weight infants.
PMID 19488942·J Matern Fetal Neonatal Med·2009
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
Clinical and genetic characterization of Chanarin-Dorfman syndrome.
PMID 18339307·Biochem Biophys Res Commun·2008
8-other
Neuromuscular forms of glycogen branching enzyme deficiency.
PMID 17915577·Acta Myol·2007
7-preclinical
McArdle disease: the mutation spectrum of PYGM in a large Italian cohort.
PMID 16786513·Hum Mutat·2006
8-other
Clinical and molecular findings in patients with giant axonal neuropathy (GAN).
PMID 14718689·Neurology·2004
5-case
Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV).
PMID 15452297·Neurology·2004
5-case
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
A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency.
PMID 12026244·J Child Neurol·2002
5-case
Two new mutations in the myophosphorylase gene in Italian patients with McArdle's disease.
PMID 12031624·Neuromuscul Disord·2002
5-case
Novel mutation in the CPT II gene in a child with periodic febrile myalgia and myoglobinuria.
PMID 10868782·J Child Neurol·2000
5-case
SMN transcript levels in leukocytes of SMA patients determined by absolute real-time PCR.
PMID 19603064·Eur J Hum Genet·2010
8-other
Synthesis and in vitro sodium channel blocking activity evaluation of novel homochiral mexiletine analogs.
PMID 19544349·Chirality·2010
7-preclinical
Caveolinopathies: from the biology of caveolin-3 to human diseases.
PMID 19584897·Eur J Hum Genet·2010
6-review
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study.
PMID 19299310·Neurology·2009
4-observational
Synthesis, photophysical, electrochemical, and electrochemiluminescent properties of 5,15-bis(9-anthracenyl)porphyrin derivatives.
PMID 19462051·Org Biomol Chem·2009
8-other
Electrochemical and theoretical investigation of corannulene reduction processes.
PMID 19173564·J Phys Chem B·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
- 6231 LEESBURG PIKE, SUITE 608
FALLS CHURCH, VA 22044 - Phone
- (703) 534-3137
Quick Facts
- NPI
- 1760490486
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 30
- Publications
- 20
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