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CLEMENS BERGWITZ, MD
MD
Endocrinology, Diabetes & Metabolism Physician
NPI: 1518957067IndividualAccepts Medicare
Specialties, Licenses & Credentials
Endocrinology, Diabetes & Metabolism PhysicianPrimary
Internal Medicine — Endocrinology, Diabetes & Metabolism
Code: 207RE0101X
52826(CT)
CMS Specialties
PrimaryENDOCRINOLOGY
Education
OTHER
Class of 1993
Research & Publications (15)
Hypophosphatemic rickets with hypercalciuria due to mutation in SLC34A3/NaPi-IIc can be masked by vitamin D deficiency and can be associated with renal calcifications.
PMID 18523928·Exp Clin Endocrinol Diabetes·2009
5-case
A patient with hypophosphatemia, a femoral fracture, and recurrent kidney stones: report of a novel mutation in SLC34A3.
PMID 18996815·Endocr Pract·2008
5-case
Cellular mechanism of decreased bone in Brtl mouse model of OI: imbalance of decreased osteoblast function and increased osteoclasts and their precursors.
PMID 18684089·J Bone Miner Res·2008
7-preclinical
A novel missense mutation in SLC34A3 that causes hereditary hypophosphatemic rickets with hypercalciuria in humans identifies threonine 137 as an important determinant of sodium-phosphate cotransport in NaPi-IIc.
PMID 18480181·Am J Physiol Renal Physiol·2008
7-preclinical
Genetic evidence of serum phosphate-independent functions of FGF-23 on bone.
PMID 18688277·PLoS Genet·2008
7-preclinical
NHERF1 mutations and responsiveness of renal parathyroid hormone.
PMID 19073985·N Engl J Med·2008
8-other
SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis.
PMID 16358214·Am J Hum Genet·2006
8-other
Brittle IV mouse model for osteogenesis imperfecta IV demonstrates postpubertal adaptations to improve whole bone strength.
PMID 15005849·J Bone Miner Res·2004
7-preclinical
A patient with autoimmune hepatitis type I, Addison's disease, atrophic thyroiditis, atrophic gastritis, exocrine pancreatic insufficiency, and heterozygous alpha1-antitrypsin deficiency.
PMID 12003388·Am J Gastroenterol·2002
5-case
Cyclic-adenosine 3',5'-monophosphate-stimulated c-fos gene transcription involves distinct calcium pathways in single beta-cells.
PMID 11850128·Mol Cell Endocrinol·2002
8-other
Identification of novel CBFA1/RUNX2 mutations causing cleidocranial dysplasia.
PMID 11768584·J Inherit Metab Dis·2001
8-other
Familial isolated parathyroid adenoma in a consanguineous family.
PMID 11407655·J Endocrinol Invest·2001
5-case
Wnts differentially regulate colony growth and differentiation of chondrogenic rat calvaria cells.
PMID 11336784·Biochim Biophys Acta·2001
4-observational
A versatile chondrogenic rat calvaria cell line R-tTA-24 that permits tetracycline-regulated gene expression.
PMID 10766267·Histochem Cell Biol·2000
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 35 PARK ST, YALE NEW HAVEN HOSPITAL, SMILOW CANCER CENTER
NEW HAVEN, CT 06519 - Phone
- (203) 200-3636
Quick Facts
- NPI
- 1518957067
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 33
- Publications
- 15
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