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SONIA PHADKE, MD
MD
Diagnostic Radiology Physician
NPI: 1851823157IndividualAccepts Medicare
Specialties, Licenses & Credentials
Diagnostic Radiology PhysicianPrimary
Radiology — Diagnostic Radiology
Code: 2085R0202X
10123(GA)DR.0070853(CO)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
CMS Specialties
PrimaryDIAGNOSTIC RADIOLOGY
Education
INDIANA UNIVERSITY SCHOOL OF MEDICINE
Class of 2017
Research & Publications (20)
Milder form of pachydermoperiostosis: a report of four cases.
PMID 19305192·Clin Dysmorphol·2009
5-case
Genetic analysis of the SRD5A2 gene in Indian patients with 5alpha-reductase deficiency.
PMID 19492581·J Pediatr Endocrinol Metab·2009
5-case
Mutation analysis in Indian children with achondroplasia - utility of molecular diagnosis.
PMID 19330302·Indian J Pediatr·2009
8-other
A report of a patient with interstitial deletion of 15q22: further delineation of a new micro deletion syndrome.
PMID 18627036·Am J Med Genet A·2008
5-case
Challenges in identifying genetic risk factors for common multifactorial disorders.
PMID 18403786·Indian J Med Res·2008
8-other
Post-mortem examination of prenatally diagnosed fatal renal malformation.
PMID 18596710·J Perinatol·2008
8-other
Long-term efficacy of oral deferiprone in management of iron overload in beta thalassemia major.
PMID 18616872·Hematology·2008
8-other
Spondylothoracic dysplasia: prenatal diagnosis and the problems of nosologic overlap.
PMID 17366581·Am J Med Genet A·2007
5-case
Torg-Winchester syndrome: lack of efficacy of pamidronate therapy.
PMID 17351352·Clin Dysmorphol·2007
5-case
Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences.
PMID 18072967·BMC Med Genet·2007
8-other
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders.
PMID 17564967·Am J Hum Genet·2007
8-other
Pericentric inversion causing duplication and deletion of chromosome region 13q22 --> qter in the offspring.
PMID 17163534·Am J Med Genet A·2007
5-case
Short stature, ulnar deviation of hands with absent carpals and joint contractures: a new syndrome.
PMID 17159517·Clin Dysmorphol·2007
5-case
Uptake of invasive prenatal diagnostic tests in women after detection of soft markers for chromosomal abnormality on ultrasonographic evaluation.
PMID 17611609·J Perinatol·2007
4-observational
Morphometric analysis of face in dysmorphology.
PMID 17118483·Comput Methods Programs Biomed·2007
8-other
Basal ganglia changes: a diagnostic clue to Sandhoff disease.
PMID 17079839·Indian Pediatr·2006
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
- 10240 PARK MEADOWS DR
LONE TREE, CO 80124 - Phone
- (303) 338-4545
Quick Facts
- NPI
- 1851823157
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 1
- Years in Practice
- 9
- Publications
- 20
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