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The Journal of Endocrinology|June 7, 2011
Mutational analysis of GCMB, a parathyroid-specific transcription factor, in parathyroid adenoma of primary hyperparathyroidismMichael Mannstadt, Emily Holick, Wenping Zhao, et al.
JCEM Case Reports|November 1, 2023
Bartter Syndrome Type 1 Due to Novel SLC12A1 Mutations Associated With Pseudohypoparathyroidism Type IIZentaro Kiuchi, Kandai Nozu, Kunimasa Yan, et al.
Annals of the New York Academy of Sciences|July 13, 2006
Autosomal-dominant pseudohypoparathyroidism type Ib is caused by different microdeletions within or upstream of the GNAS locusHarald Jüppner, Agnès Linglart, Leopold F Fröhlich, et al.
American Journal of Physiology. Endocrinology and Metabolism|August 27, 2009
TIP39/parathyroid hormone type 2 receptor signaling is a potent inhibitor of chondrocyte proliferation and differentiationDibiyendu Panda, David Goltzman, Harald Jüppner, et al.
JCEM Case Reports|August 28, 2024
Growth Hormone Deficiency in an Adolescent With Pseudohypoparathyroidism Type 1BSabitha Sasidharan Pillai, Monica Reyes, Harald Jüppner, et al.
Frontiers in Endocrinology|September 4, 2025
Human diseases caused by homozygous PTH1R mutationsIgnacio Portales-Castillo, Jakob Höppner, Harald Jüppner, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
FGF23 Is Not Associated With Age-Related Changes in Phosphate, but Enhances Renal Calcium Reabsorption in GirlsDeborah M Mitchell, Harald Jüppner, Sherri-Ann M Burnett-Bowie
The Journal of Clinical Endocrinology and Metabolism|February 9, 2013
Oncogenic osteomalacia due to FGF23-expressing colon adenocarcinomaDavid E Leaf, Renata C Pereira, Hasan Bazari, et al.
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