Back to Search

VIRGINIA KIMONIS, MD

MD

Clinical Genetics (M.D.) Physician

NPI: 1912964925IndividualAccepts Medicare

Specialties, Licenses & Credentials

Clinical Genetics (M.D.) PhysicianPrimary

Medical Genetics — Clinical Genetics (M.D.)

Code: 207SG0201X

156969(MA)C52311(CA)
Clinical Biochemical Genetics Physician

Medical Genetics — Clinical Biochemical Genetics

Code: 207SG0202X

156969(MA)
Pediatrics Physician

Pediatrics

Code: 208000000X

156969(MA)

CMS Specialties

PrimaryPEDIATRIC MEDICINE

Education

OTHER

Class of 1976

Research & Publications (20)

VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: review of a unique disorder.
PMID 18845250·Biochim Biophys Acta·2008
6-review
Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia.
PMID 18260132·Am J Med Genet A·2008
5-case
Genetics of craniosynostosis.
PMID 17980312·Semin Pediatr Neurol·2007
6-review
Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): a possible locus for Fryns syndrome.
PMID 16333846·Am J Med Genet A·2006
5-case
Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome.
PMID 19563863·Neurosci Lett·2011
4-observational
Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia.
PMID 19380227·Neuromuscul Disord·2009
6-review
Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD).
PMID 19593370·PLoS Genet·2009
7-preclinical
NR2F1 deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafness.
PMID 19353646·Am J Med Genet A·2009
5-case
TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia.
PMID 18796596·J Neurol Neurosurg Psychiatry·2008
8-other
Subglossopalatal synechia in association with cardiac and digital anomalies.
PMID 18333647·Cleft Palate Craniofac J·2008
5-case
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome.
PMID 18642388·Hum Mutat·2008
8-other
Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.
PMID 17935506·Clin Genet·2007
5-case
Encephalocraniocutaneous lipomatosis accompanied by the formation of bone cysts: Harboring clues to pathogenesis?
PMID 18000896·Am J Med Genet A·2007
5-case
Diagnostic utility of array-based comparative genomic hybridization in a clinical setting.
PMID 17910064·Am J Med Genet A·2007
4-observational
Nuclear localization of valosin-containing protein in normal muscle and muscle affected by inclusion-body myositis.
PMID 17626287·Muscle Nerve·2007
8-other
APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD).
PMID 17224685·Genet Med·2007
8-other
TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations.
PMID 17279000·J Neuropathol Exp Neurol·2007
8-other
Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations.
PMID 17522620·Eur J Hum Genet·2007
5-case
Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literature.
PMID 18000976·Am J Med Genet A·2007
8-other
Pathological consequences of VCP mutations on human striated muscle.
PMID 16984901·Brain·2007
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
101 THE CITY DR S # ZC4482, DIVISION OF GENETICS AND METABOLISM
ORANGE, CA 92868

Location

Practice Location

101 THE CITY DR S # ZC4482, ORANGE, CA
(714) 456-5792

Quick Facts

NPI
1912964925
Entity Type
Individual
Gender
Female
Medicare
Accepted
Specialties
4
Locations
1
Years in Practice
50
Publications
20

Are you this provider?

Claim Your Profile