Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jamie Streit"'
Autor:
Iris R. Hartley, Kelly L. Roszko, Xiaobai Li, Karen Pozo, Jamie Streit, Jaydira delRivero, M. Teresa Magone, Michaele R. Smith, Roo Vold, Carl L. Dambkowski, Michael T. Collins, Rachel I. Gafni
Publikováno v:
JBMR Plus, Vol 6, Iss 8, Pp n/a-n/a (2022)
ABSTRACT Tumor‐induced osteomalacia (TIO) is a rare paraneoplastic syndrome caused by ectopic production of fibroblast growth factor 23 (FGF23) by phosphaturic mesenchymal tumors (PMTs). Acting on renal tubule cells, excess FGF23 decreases phosphat
Externí odkaz:
https://doaj.org/article/71b3882bac484d0c8a46a775d681c4d2
Autor:
Kelly L Roszko, Rachel I Gafni, Susan Moran, Iris R Hartley, Roo Vold, Mike Arango, Edmond J. FitzGibbon, Jaydira Del Rivero, Jamie Streit, M. Teresa Magone, Rachel Bishop, Michael T. Collins, Karen A Pozo
Publikováno v:
Ophthalmology. 128:624-626
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1ff1e4711abb597750823a883fea482
https://doi.org/10.1016/j.ophtha.2020.08.026
https://doi.org/10.1016/j.ophtha.2020.08.026
Autor:
M. Teresa Magone, Iris R. Hartley, Edmond FitzGibbon, Rachel Bishop, Mike Arango, Susan Moran, Roo Vold, Jaydira del Rivero, Karen Pozo, Jamie Streit, Kelly L. Roszko, Michael T. Collins, Rachel I. Gafni
Publikováno v:
Ophthalmology. 128:e44-e45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac0a27623c54cd1c0270fddce2959cb4
https://doi.org/10.1016/j.ophtha.2021.05.015
https://doi.org/10.1016/j.ophtha.2021.05.015
Autor:
Edward F. Nemeth, Martin Schepelmann, Sarah C. Brennan, Daniela Riccardi, Mohd Ezuan Bin Khayat, Jamie Streit, Jeff Gelb, David Gash, Michael T. Collins, Beth A Brillante, Ralf Rosskamp, Eva Krusinska, Lori C. Guthrie, Donald T. Ward, Rachel I Gafni, Mary Scott Roberts
Publikováno v:
Ward, D 2019, ' Treatment of Autosomal Dominant Hypocalcemia Type 1 with the Calcilytic NPSP795 (SHP635). ', Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research . https://doi.org/10.1002/jbmr.3747
J Bone Miner Res
J Bone Miner Res
Autosomal dominant hypocalcemia type 1 (ADH1) is a rare form of hypoparathyroidism caused by heterozygous, gain-of-function mutations of the calcium-sensing receptor gene (CAR). Individuals are hypocalcemic with inappropriately low parathyroid hormon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc1fd563ea9b5eb45560eb4f5adf46fe
https://www.research.manchester.ac.uk/portal/en/publications/treatment-of-autosomal-dominant-hypocalcemia-type-1-with-the-calcilytic-npsp795-shp635(7c119083-254a-4840-ac56-5b5cfe3d19ab).html
https://www.research.manchester.ac.uk/portal/en/publications/treatment-of-autosomal-dominant-hypocalcemia-type-1-with-the-calcilytic-npsp795-shp635(7c119083-254a-4840-ac56-5b5cfe3d19ab).html
