Endocrine Associates, Massachusetts General Hospital
Endocrinology
Dr. Clemens Bergwitz, MD
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Dr. Clemens Bergwitz is an expert in the field of Endocrinology. He went to Hannover Medical School. Clemens Bergwitz is also a published doctor. He has 38 publication published. The most recent publication is: Identification, functional characterization, and developmental expression of two nonallelic parathyroid hormone (PTH)/PTH-related peptide receptor isoforms in Xenopus ... He accepts all Medicare patients.
Publications
- Genetic determinants of phosphate response in Drosophila.
- Fanconi-Bickel Syndrome and Autosomal Recessive Proximal Tubulopathy With Hypercalciuria (ARPTH) Are Allelic Variants Caused by GLUT2 Mutations.
- Novel NaPi-IIc mutations causing HHRH and idiopathic hypercalciuria in several unrelated families: Long-term follow-up in one kindred.
- Identification of novel CBFA1/RUNX2 mutations causing cleidocranial dysplasia.
- Familial isolated Parathyroid adenoma in a consanguineous family.
- Wnts differentially regulate colony growth and differentiation of chondrogenic rat calvaria cells.
- A versatile chondrogenic rat calvaria cell line R-tTA-24 that permits tetracycline-regulated gene expression.
- A G protein-coupled receptor from zebrafish is activated by human Parathyroid hormone and not by human or teleost Parathyroid hormone-related peptide. Implications for...
- The cadherin-catenin system: implications for growth and differentiation of endocrine tissues.
- Identification, functional characterization, and developmental expression of two nonallelic Parathyroid hormone (PTH)/PTH-related peptide receptor isoforms in Xenopus ...
- Residues in the membrane-spanning and extracellular loop regions of the Parathyroid hormone (PTH)-2 receptor determine signaling selectivity for PTH and PTH-related pe...
- Cloning and characterization of the Vitamin D receptor from Xenopus laevis.
- Full activation of chimeric receptors by hybrids between Parathyroid hormone and calcitonin. Evidence for a common pattern of ligand-receptor interaction.
- Rapid desensitization of Parathyroid hormone dependent adenylate cyclase in perifused human osteosarcoma cells (SaOS-2).
- Polymorphism in exon M7 of the PTHR gene.
- Pseudohypoparathyroidism Type Ib is not caused by mutations in the coding exons of the human parathyroid hormone (PTH)/PTH-related peptide receptor gene.
- Specific, high-affinity binding sites for angiotensin II on Mycoplasma hyorhinis.
- 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.
- A patient with autoimmune hepatitis type I, Addison's disease, atrophic thyroiditis, atrophic gastritis, exocrine pancreatic Insufficiency, and heterozygous alpha1-ant...
- Cyclic-adenosine 3'',5''-monophosphate-stimulated c-fos gene transcription involves distinct calcium pathways in single beta-cells.
- A novel missense mutation in SLC34A3 that causes hereditary hypophosphatemic rickets With hypercalciuria in humans identifies threonine 137 as an important determinant...
- SLC34A3 mutations in patients With hereditary hypophosphatemic rickets With hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in mainta...
- Brittle IV mouse model for osteogenesis imperfecta IV demonstrates postpubertal adaptations to improve whole bone strength.
- Roles of major facilitator superfamily transporters in phosphate response in Drosophila.
- Case records of the Massachusetts General Hospital. Case 33-2011. A 56-year-old man With hypophosphatemia.
- An integrative approach to ortholog prediction for Disease-focused and other functional studies.
- Phosphate sensing.
- Hereditary hypophosphatemic rickets With hypercalciuria and nephrolithiasis-identification of a novel SLC34A3/NaPi-IIc mutation.
- Autoimmune hypocalciuric hypercalcemia unresponsive to glucocorticoid therapy in a patient With blocking autoantibodies against the calcium-sensing receptor.
- Acute down-regulation of sodium-dependent phosphate transporter NPT2a involves predominantly the cAMP/PKA pathway as revealed by signaling-selective Parathyroid hormon...
- Regulation of phosphate homeostasis by PTH, Vitamin D, and FGF23.
- Defective O-glycosylation due to a novel homozygous S129P mutation is associated With lack of fibroblast growth factor 23 secretion and tumoral calcinosis.
- Disorders of phosphate homeostasis and tissue mineralisation.
- NHERF1 mutations and responsiveness of Renal parathyroid hormone.
- A patient With hypophosphatemia, a femoral fracture, and recurrent kidney stones: report of a novel mutation in SLC34A3.
- Genetic evidence of serum phosphate-independent functions of FGF-23 on bone.
- Cellular mechanism of decreased bone in Brtl mouse model of OI: imbalance of decreased osteoblast function and increased osteoclasts and their precursors.
Conditions Treated
- AdRenal Insufficiency
- Diabetes Insipidus
- Diabetes Type 2
- Diabetes With Renal Manifestations
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Doctors Specialties
- Endocrinology
Accepted Insurances
Education
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Massachusetts General Hospital -
Hannover Medical School
Hospital
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Massachusetts General Hospital
Drug Facts
| NPI NUMBER | 1518957067 | |
| NPPES Provider LastName | BERGWITZ | |
| NPPES Provider FirstName | CLEMENS | |
| NPPES Provider ZIPCode | 021142621 | |
| NPPES Provider State | MA | |
| Specialty Description | Internal Medicine | |
| Total Claim Count | 146.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1518957067 |
| Last Name Of The Provider | BERGWITZ |
| First Name Of The Provider | CLEMENS |
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