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MIHIR UPADHYAYA, MD
MD
Psychiatry Physician
NPI: 1366963308IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
A165031(CA)
CMS Specialties
PrimaryPSYCHIATRY
Education
OTHER
Class of 2010
Research & Publications (20)
Long-term results of central venous access devices in children with haemophilia.
PMID 19455342·Pediatr Surg Int·2009
8-other
The spectrum of somatic and germline NF1 mutations in NF1 patients with spinal neurofibromas.
PMID 19221814·Neurogenetics·2009
8-other
Germline and somatic NF1 gene mutation spectrum in NF1-associated malignant peripheral nerve sheath tumors (MPNSTs).
PMID 17960768·Hum Mutat·2008
8-other
Germline and somatic NF1 gene mutations in plexiform neurofibromas.
PMID 18484666·Hum Mutat·2008
8-other
An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation.
PMID 17160901·Am J Hum Genet·2007
8-other
The heterogeneous nature of germline mutations in NF1 patients with malignant peripheral serve sheath tumours (MPNSTs).
PMID 16786508·Hum Mutat·2006
8-other
Neurofibromatosis type 1: a common familial cancer syndrome.
PMID 14733318·Methods Mol Med·2004
8-other
Characterization of the somatic mutational spectrum of the neurofibromatosis type 1 (NF1) gene in neurofibromatosis patients with benign and malignant tumors.
PMID 14722917·Hum Mutat·2004
4-observational
Recurrent immature mediastinal teratoma with life-threatening respiratory distress in a neonate.
PMID 14743329·Eur J Pediatr Surg·2003
5-case
Three different pathological lesions in the NF1 gene originating de novo in a family with neurofibromatosis type 1.
PMID 12483293·Hum Genet·2003
5-case
Detection of NF1 mutations utilizing the protein truncation test (PTT).
PMID 12491944·Methods Mol Biol·2003
8-other
Life-threatening respiratory distress in a neonate with a pericardial cyst.
PMID 14600770·Pediatr Surg Int·2003
8-other
Molecular diagnosis of facioscapulohumeral muscular dystrophy.
PMID 11962336·Expert Rev Mol Diagn·2002
6-review
Achalasia of the cardia: experience with hydrostatic balloon dilatation in children.
PMID 12029340·Pediatr Radiol·2002
8-other
Management of traumatic urethral disruption in children: Oman experience, 1988-2000.
PMID 12378452·J Pediatr Surg·2002
8-other
Intraductal papillary mucinous neoplasms of the pancreas: correlation of helical CT features with pathologic findings.
PMID 19586733·Eur J Radiol·2010
8-other
Therapeutic endoscopy of localized gastric varices: pretherapy screening and posttreatment evaluation with MDCT portography.
PMID 19030919·Abdom Imaging·2010
8-other
SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype.
PMID 19443465·J Med Genet·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
- 5060 SHOREHAM PL STE 100
SAN DIEGO, CA 92122 - Phone
- (858) 427-5060
Quick Facts
- NPI
- 1366963308
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 16
- Publications
- 20
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