Michael Mannstadt Endocrine Unit, Massachusetts General Hospital Harvard Medical School Biography Publications Institution JoVE Articles Michael Mannstadt has not added a biography. If you are Michael Mannstadt and would like to personalize this page please email our Author Liaison for assistance. Publications Knockin Mouse with Mutant Gα11 Mimics Human Inherited Hypocalcemia and is Rescued by Pharmacologic Inhibitors JCI Insight. Feb, 2017 | Pubmed ID: 28194446 Parathyroid Hormone Directs Bone Marrow Mesenchymal Cell Fate Cell Metabolism. Mar, 2017 | Pubmed ID: 28162969 Effects of Parathyroid Hormone RhPTH(1-84) on Phosphate Homeostasis and Vitamin D Metabolism in Hypoparathyroidism: REPLACE Phase 3 Study Endocrine. Jan, 2017 | Pubmed ID: 27734257 Autosomal Dominant Hypocalcemia (Hypoparathyroidism) Types 1 and 2 Frontiers in Physiology. 2016 | Pubmed ID: 27803672 Total Synthesis and Structure-activity Relationship Studies of a Series of Selective G Protein Inhibitors Nature Chemistry. Nov, 2016 | Pubmed ID: 27768111 Epidemiology and Diagnosis of Hypoparathyroidism The Journal of Clinical Endocrinology and Metabolism. Jun, 2016 | Pubmed ID: 26943720 Management of Hypoparathyroidism: Present and Future The Journal of Clinical Endocrinology and Metabolism. Jun, 2016 | Pubmed ID: 26938200 Diphtheria Toxin- and GFP-Based Mouse Models of Acquired Hypoparathyroidism and Treatment With a Long-Acting Parathyroid Hormone Analog Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research. May, 2016 | Pubmed ID: 26678919 A Homozygous [Cys25]PTH(1-84) Mutation That Impairs PTH/PTHrP Receptor Activation Defines a Novel Form of Hypoparathyroidism Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research. Oct, 2015 | Pubmed ID: 25891861 Hypoparathyroidism - disease Update and Emerging Treatments Annales D'endocrinologie. May, 2015 | Pubmed ID: 25882889 Hypoparathyroidism and Central Diabetes Insipidus: in Search of the Link European Journal of Pediatrics. Dec, 2014 | Pubmed ID: 25367057 Case Records of the Massachusetts General Hospital. Case 24-2014. A 27-year-old Man with Severe Osteoporosis and Multiple Bone Fractures The New England Journal of Medicine. Jul, 2014 | Pubmed ID: 25075839 Efficacy and Safety of Recombinant Human Parathyroid Hormone (1-84) in Hypoparathyroidism (REPLACE): a Double-blind, Placebo-controlled, Randomised, Phase 3 Study The Lancet. Diabetes & Endocrinology. Dec, 2013 | Pubmed ID: 24622413 Germline Mutations Affecting Gα11 in Hypoparathyroidism The New England Journal of Medicine. Jun, 2013 | Pubmed ID: 23802536 Long-term Follow-up of Patients with Hypoparathyroidism The Journal of Clinical Endocrinology and Metabolism. Dec, 2012 | Pubmed ID: 23043192 Fanconi-Bickel Syndrome and Autosomal Recessive Proximal Tubulopathy with Hypercalciuria (ARPTH) Are Allelic Variants Caused by GLUT2 Mutations The Journal of Clinical Endocrinology and Metabolism. Oct, 2012 | Pubmed ID: 22865906 Effects of Phosphate Binders in Moderate CKD Journal of the American Society of Nephrology : JASN. Aug, 2012 | Pubmed ID: 22822075 Identification and Characterization of C106R, a Novel Mutation in the DNA-binding Domain of GCMB, in a Family with Autosomal-dominant Hypoparathyroidism Clinical Endocrinology. May, 2012 | Pubmed ID: 22066718 Mutational Analysis of GCMB, a Parathyroid-specific Transcription Factor, in Parathyroid Adenoma of Primary Hyperparathyroidism The Journal of Endocrinology. Aug, 2011 | Pubmed ID: 21642377 Fibroblast Growth Factor 23 and Mortality Among Patients Undergoing Hemodialysis The New England Journal of Medicine. Aug, 2008 | Pubmed ID: 18687639 Rapid Detection of Intact FGF-23 in Tumor Tissue from Patients with Oncogenic Osteomalacia Clinical Chemistry. Jul, 2008 | Pubmed ID: 18593970 Dominant-negative GCMB Mutations Cause an Autosomal Dominant Form of Hypoparathyroidism The Journal of Clinical Endocrinology and Metabolism. Sep, 2008 | Pubmed ID: 18583467 Case Records of the Massachusetts General Hospital. Case 7-2007. A 59-year-old Woman with Diabetic Renal Disease and Nonhealing Skin Ulcers The New England Journal of Medicine. Mar, 2007 | Pubmed ID: 17347459 اثنين من التقنيات لخلق الفئران قصور الدريقات: استئصال جارات الدرق عن طريق GFP الغدد والخناق-السمية بوساطة الغدة الدرقية تذرية Ruiye Bi1,2, Yi Fan2,3, En Luo2,4, Quan Yuan2,4, Michael Mannstadt1 1Endocrine Unit, Massachusetts General Hospital, Harvard Medical School, 2West China School of Stomatology, Sichuan University, 3Department of Oral Medicine, Infection and Immunity, Harvard School of Dental Medicine, 4State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University Medicine
اثنين من التقنيات لخلق الفئران قصور الدريقات: استئصال جارات الدرق عن طريق GFP الغدد والخناق-السمية بوساطة الغدة الدرقية تذرية Ruiye Bi1,2, Yi Fan2,3, En Luo2,4, Quan Yuan2,4, Michael Mannstadt1 1Endocrine Unit, Massachusetts General Hospital, Harvard Medical School, 2West China School of Stomatology, Sichuan University, 3Department of Oral Medicine, Infection and Immunity, Harvard School of Dental Medicine, 4State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University Medicine
