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KIRTI KALIDAS, M.D.
M.D.
Internal Medicine Physician
NPI: 1407016876Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
50026(FL)
Research & Publications (15)
Inherited metabolic disorders and cerebral infarction.
PMID 18986243·Expert Rev Neurother·2008
6-review
Homozygous mutation of desmocollin-2 in arrhythmogenic right ventricular cardiomyopathy with mild palmoplantar keratoderma and woolly hair.
PMID 18957847·Cardiology·2009
5-case
Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the Amish.
PMID 18467358·Heart·2008
8-other
The natural history of Noonan syndrome: a long-term follow-up study.
PMID 16990350·Arch Dis Child·2007
8-other
Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11.
PMID 15690106·J Hum Genet·2005
5-case
CD14 C(-260)T promoter polymorphism and prevalence of acute coronary syndromes.
PMID 15686783·Int J Cardiol·2005
8-other
Association of the -159C/T polymorphism of the endotoxin receptor (CD14) with carotid artery disease and cardiovascular mortality in dialysis patients.
PMID 15640605·Blood Purif·2005
8-other
A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1-12q14.
PMID 15635080·J Med Genet·2005
8-other
Paternal germline origin and sex-ratio distortion in transmission of PTPN11 mutations in Noonan syndrome.
PMID 15248152·Am J Hum Genet·2004
8-other
Association of interleukin-6 -174G/C promoter polymorphism with hypertension and left ventricular hypertrophy in dialysis patients.
PMID 12846758·Kidney Int·2003
8-other
Different mutations in the NF1 gene are associated with Neurofibromatosis-Noonan syndrome (NFNS).
PMID 12707950·Am J Med Genet A·2003
5-case
Polymorphism of renin-angiotensin system genes in dialysis patients--association with cerebrovascular disease.
PMID 12454231·Nephrol Dial Transplant·2002
8-other
Absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome.
PMID 12384786·Hum Genet·2002
6-review
PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity.
PMID 11992261·Am J Hum Genet·2002
8-other
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome.
PMID 11704759·Nat Genet·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
- Address
- 6651 VINELAND RD, SUITE 150
ORLANDO, FL 32819 - Phone
- (407) 355-9246
Quick Facts
- NPI
- 1407016876
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 15
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