Back to Search
RAHUL THAKKER, MD
MD
Emergency Medicine Physician
NPI: 1538664354Individual
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
315141(NY)
Research & Publications (20)
OCRL1 mutations in Dent 2 patients suggest a mechanism for phenotypic variability.
PMID 19390221·Nephron Physiol·2009
4-observational
Mutational analysis of CLC-5, cofilin and CLC-4 in patients with Dent's disease.
PMID 19546591·Nephron Physiol·2009
8-other
A prospective randomized, controlled study comparing low pressure versus high pressure pneumoperitoneum during laparoscopic cholecystectomy.
PMID 19542853·Surg Laparosc Endosc Percutan Tech·2009
4-observational
Uromodulin mutations causing familial juvenile hyperuricaemic nephropathy lead to protein maturation defects and retention in the endoplasmic reticulum.
PMID 19465746·Hum Mol Genet·2009
8-other
Genetic background influences embryonic lethality and the occurrence of neural tube defects in Men1 null mice: relevance to genetic modifiers.
PMID 19587266·J Endocrinol·2009
7-preclinical
Asymptomatic children with multiple endocrine neoplasia type 1 mutations may harbor nonfunctioning pancreatic neuroendocrine tumors.
PMID 19622622·J Clin Endocrinol Metab·2009
5-case
Characterization of Dent's disease mutations of CLC-5 reveals a correlation between functional and cell biological consequences and protein structure.
PMID 19019917·Am J Physiol Renal Physiol·2009
8-other
Multiple endocrine neoplasia type 1 knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemia.
PMID 19620250·Endocr Relat Cancer·2009
7-preclinical
Parafibromin, a component of the human PAF complex, regulates growth factors and is required for embryonic development and survival in adult mice.
PMID 18212049·Mol Cell Biol·2008
7-preclinical
Oncogenic hypophosphataemic osteomalacia: biomarker roles of fibroblast growth factor 23, 1,25-dihydroxyvitamin D3 and lymphatic vessel endothelial hyaluronan receptor 1.
PMID 18230836·Eur J Endocrinol·2008
5-case
Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene.
PMID 18084346·Nat Clin Pract Endocrinol Metab·2008
5-case
Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene.
PMID 17879353·Hum Mutat·2008
6-review
A novel MEN1 intronic mutation associated with multiple endocrine neoplasia type 1.
PMID 17388795·Clin Endocrinol (Oxf)·2007
8-other
Cox-2 promotes chromogranin A expression and bioactivity: evidence for a prostaglandin E2-dependent mechanism and the involvement of a proximal cyclic adenosine 5'-monophosphate-responsive element.
PMID 17540723·Endocrinology·2007
7-preclinical
Lymphatic vessels are present in phosphaturic mesenchymal tumours.
PMID 17674036·Virchows Arch·2007
6-review
Genetics of hypercalciuric nephrolithiasis: renal stone disease.
PMID 17872384·Ann N Y Acad Sci·2007
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 1 GUSTAVE L LEVY PL # 1149
NEW YORK, NY 10029 - Phone
- (212) 824-8069
Quick Facts
- NPI
- 1538664354
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 2
- Publications
- 20
Are you this provider?
Claim Your Profile