Mutational analysis of GCMB, a parathyroid-specific transcription factor, in parathyroid adenoma of primary hyperparathyroidism

Por Mannstadt, Michael, Holick, Emily, Zhao, Wenping, Jüppner, Harald
Publicado em 2011

Autosomal Dominant Hypocalcemia (Hypoparathyroidism) Types 1 and 2

Por Roszko, Kelly L., Bi, Ruiye D., Mannstadt, Michael
Publicado no Front Physiol (2016)

Effects of parathyroid hormone rhPTH(1–84) on phosphate homeostasis and vitamin D metabolism in hypoparathyroidism: REPLACE phase 3 study

Por Clarke, Bart L., Vokes, Tamara J., Bilezikian, John P., Shoback, Dolores M., Lagast, Hjalmar, Mannstadt, Michael
Publicado no Endocrine (2016)

Diphtheria Toxin- and GFP-based mouse models of acquired hypoparathyroidism and treatment with a long-acting parathyroid hormone analog

Por Bi, Ruiye, Fan, Yi, Lauter, Kelly, Hu, Jing, Watanabe, Tomoyuki, Cradock, Jim, Yuan, Quan, Gardella, Thomas, Mannstadt, Michael
Publicado no J Bone Miner Res (2016)

Dominant-Negative GCMB Mutations Cause an Autosomal Dominant Form of Hypoparathyroidism

Por Mannstadt, Michael, Bertrand, Guylène, Muresan, Mihaela, Weryha, Georges, Leheup, Bruno, Pulusani, Sirish R., Grandchamp, Bernard, Jüppner, Harald, Silve, Caroline
Publicado em 2008

Identification and characterization of C106R, a novel mutation in the DNA-binding domain of GCMB, in a family with autosomal-dominant hypoparathyroidism

Por Yi, Hyon-Seung, Eom, Young Sil, Park, Ie Byung, Lee, Sangho, Hong, Suntaek, Jüppner, Harald, Mannstadt, Michael, Lee, Sihoon
Publicado em 2012

Hypoparathyroidism and central diabetes insipidus: in search of the link

Por Eyal, Ori, Oren, Asaf, Jüppner, Harald, Somech, Raz, De Bellis, Annamaria, Mannstadt, Michael, Szalat, Auryan, Bleiberg, Margalit, Weisman, Yosef, Weintrob, Naomi
Publicado no Eur J Pediatr (2014)

A Homozygous [Cys25]PTH(1-84) Mutation That Impairs PTH/PTHrP Receptor Activation Defines a Novel Form of Hypoparathyroidism

Por Lee, Sihoon, Mannstadt, Michael, Guo, Jun, Kim, Seul Min, Yi, Hyon-Seung, Khatri, Ashok, Dean, Thomas, Okazaki, Makoto, Gardella, Thomas J, Jüppner, Harald
Publicado no J Bone Miner Res (2015)

Fanconi-Bickel Syndrome and Autosomal Recessive Proximal Tubulopathy with Hypercalciuria (ARPTH) Are Allelic Variants Caused by GLUT2 Mutations

Por Mannstadt, Michael, Magen, Daniella, Segawa, Hiroko, Stanley, Takara, Sharma, Amita, Sasaki, Shohei, Bergwitz, Clemens, Mounien, Lourdes, Boepple, Paul, Thorens, Bernhard, Zelikovic, Israel, Jüppner, Harald
Publicado em 2012

Long-Term Follow-Up of Patients with Hypoparathyroidism

Por Mitchell, Deborah M., Regan, Susan, Cooley, Michael R., Lauter, Kelly B., Vrla, Michael C., Becker, Carolyn B., Burnett-Bowie, Sherri-Ann M., Mannstadt, Michael
Publicado em 2012

Germline Mutations Affecting Gα(11) in Hypoparathyroidism

Por Mannstadt, Michael, Harris, Mark, Bravenboer, Bert, Chitturi, Sridhar, Dreijerink, Koen M.A., Lambright, David G., Lim, Elaine T., Daly, Mark J., Gabriel, Stacey, Jüppner, Harald
Publicado em 2013

Fibroblast Growth Factor 23 and Mortality among Patients Undergoing Hemodialysis

Por Gutiérrez, Orlando M., Mannstadt, Michael, Isakova, Tamara, Rauh-Hain, Jose Alejandro, Tamez, Hector, Shah, Anand, Smith, Kelsey, Lee, Hang, Thadhani, Ravi, Jüppner, Harald, Wolf, Myles
Publicado em 2008

Knockin mouse with mutant Gα(11) mimics human inherited hypocalcemia and is rescued by pharmacologic inhibitors

Por Roszko, Kelly L., Bi, Ruiye, Gorvin, Caroline M., Bräuner-Osborne, Hans, Xiong, Xiao-Feng, Inoue, Asuka, Thakker, Rajesh V., Strømgaard, Kristian, Gardella, Thomas, Mannstadt, Michael
Publicado no JCI Insight (2017)

Management of Hypoparathyroidism: Present and Future

Por Bilezikian, John P., Brandi, Maria Luisa, Cusano, Natalie E., Mannstadt, Michael, Rejnmark, Lars, Rizzoli, René, Rubin, Mishaela R., Winer, Karen K., Liberman, Uri A., Potts, John T.
Publicado no J Clin Endocrinol Metab (2016)

Epidemiology and Diagnosis of Hypoparathyroidism

Por Clarke, Bart L., Brown, Edward M., Collins, Michael T., Jüppner, Harald, Lakatos, Peter, Levine, Michael A., Mannstadt, Michael M., Bilezikian, John P., Romanischen, Anatoly F., Thakker, Rajesh V.
Publicado no J Clin Endocrinol Metab (2016)

Effects of Phosphate Binders in Moderate CKD

Por Block, Geoffrey A., Wheeler, David C., Persky, Martha S., Kestenbaum, Bryan, Ketteler, Markus, Spiegel, David M., Allison, Matthew A., Asplin, John, Smits, Gerard, Hoofnagle, Andrew N., Kooienga, Laura, Thadhani, Ravi, Mannstadt, Michael, Wolf, Myles, Chertow, Glenn M.
Publicado em 2012

Parathyroid Hormone Directs Bone Marrow Mesenchymal Cell Fate

Por Fan, Yi, Hanai, Jun-ichi, Le, Phuong T., Bi, Ruiye, Maridas, David, DeMambro, Victoria, Figueroa, Carolina A., Kir, Serkan, Zhou, Xuedong, Mannstadt, Michael, Baron, Roland, Bronson, Roderick T., Horowitz, Mark C., Wu, Joy Y., Bilezikian, John P., Dempster, David W., Rosen, Clifford J., Lanske, Beate
Publicado no Cell Metab (2017)