Výsledky vyhledávání - Lines, Kate E
- Zobrazuji výsledky 1 - 16 z 16
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Pasireotide Therapy of Multiple Endocrine Neoplasia Type 1–Associated Neuroendocrine Tumors in Female Mice Deleted for an Men1 Allele Improves Survival and Reduces Tumor Progressio... Autor Walls, Gerard V., Stevenson, Mark, Soukup, Benjamin S., Lines, Kate E., Grossman, Ashley B., Schmid, Herbert A., Thakker, Rajesh V.
Vydáno 2016Text -
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The Bartter-Gitelman Spectrum: 50-Year Follow-up With Revision of Diagnosis After Whole-Genome Sequencing Autor Stevenson, Mark, Pagnamenta, Alistair T, Mack, Heather G, Savige, Judith, Giacopuzzi, Edoardo, Lines, Kate E, Taylor, Jenny C, Thakker, Rajesh V
Vydáno 2022Text -
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Whole genome sequence analysis identifies a PAX2 mutation to establish a correct diagnosis for a syndromic form of hyperuricemia Autor Stevenson, Mark, Pagnamenta, Alistair T., Reichart, Silvia, Philpott, Charlotte, Lines, Kate E., Gorvin, Caroline M., Lhotta, Karl, Taylor, Jenny C., Thakker, Rajesh V.
Vydáno 2020Text -
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Multiple Endocrine Neoplasia Type 1 (MEN1) Phenocopy Due to a Cell Cycle Division 73 (CDC73) Variant Autor Lines, Kate E, Nachtigall, Lisa B, Dichtel, Laura E, Cranston, Treena, Boon, Hannah, Zhang, Xun, Kooblall, Kreepa G, Stevenson, Mark, Thakker, Rajesh V
Vydáno 2020Text -
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TWO SYNCHRONOUS PITUITARY ADENOMAS CAUSING CUSHING DISEASE AND ACROMEGALY Autor Schorr, Melanie, Zhang, Xun, Zhao, Wenxiu, Abedi, Parisa, Lines, Kate E., Hedley-Whyte, E. Tessa, Swearingen, Brooke, Klibanski, Anne, Miller, Karen K., Thakker, Rajesh V., Nachtigall, Lisa B.
Vydáno 2019Text -
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Activating Mutations of the G-protein Subunit α (11) Interdomain Interface Cause Autosomal Dominant Hypocalcemia Type 2 Autor Gorvin, Caroline M, Stokes, Victoria J, Boon, Hannah, Cranston, Treena, Glück, Anna K, Bahl, Shailini, Homfray, Tessa, Aung, Theingi, Shine, Brian, Lines, Kate E, Hannan, Fadil M, Thakker, Rajesh V
Vydáno 2019Text -
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Clinical MEN-1 Among a Large Cohort of Patients With Acromegaly Autor Nachtigall, Lisa B, Guarda, Francisco J, Lines, Kate E, Ghajar, Alireza, Dichtel, Laura, Mumbach, Giselle, Zhao, Wenxiu, Zhang, Xun, Tritos, Nicholas A, Swearingen, Brooke, Miller, Karen K, Thakker, Rajesh V
Vydáno 2020Text -
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PTH infusion ameliorates seizures in autosomal dominant hypocalcemia type 1 Autor Sastre, Ana, Valentino, Kevin, Hannan, Fadil M., Lines, Kate E., Gluck, Anna K., Stevenson, Mark, Ryalls, Michael, Pullen, Debbie, Buck, Jackie, Sankar, Sailesh, Allgrove, Jeremy, Thakker, Rajesh V., Gevers, Evelien F.
Vydáno 2021Text -
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Genetic background influences tumour development in heterozygous Men1 knockout mice Autor Lines, Kate E, Javid, Mahsa, Reed, Anita A C, Walls, Gerard V, Stevenson, Mark, Simon, Michelle, Kooblall, Kreepa G, Piret, Sian E, Christie, Paul T, Newey, Paul J, Mallon, Ann-Marie, Thakker, Rajesh V
Vydáno 2020Text -
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Association of prolactin receptor (PRLR) variants with prolactinomas Autor Gorvin, Caroline M, Newey, Paul J, Rogers, Angela, Stokes, Victoria, Neville, Matt J, Lines, Kate E, Ntali, Georgia, Lees, Peter, Morrison, Patrick J, Singhellakis, Panagiotis N, Malandrinou, Fotini Ch, Karavitaki, Niki, Grossman, Ashley B, Karpe, Fredrik, Thakker, Rajesh V
Vydáno 2019Text -
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Somatic mutations of GNA11 and GNAQ in CTNNB1-mutant aldosterone-producing adenomas presenting in puberty, pregnancy or menopause Autor Zhou, Junhua, Azizan, Elena A. B., Cabrera, Claudia P., Fernandes-Rosa, Fabio L., Boulkroun, Sheerazed, Argentesi, Giulia, Cottrell, Emily, Amar, Laurence, Wu, Xilin, O’Toole, Sam, Goodchild, Emily, Marker, Alison, Senanayake, Russell, Garg, Sumedha, Åkerström, Tobias, Backman, Samuel, Jordan, Suzanne, Polubothu, Satyamaanasa, Berney, Daniel M., Gluck, Anna, Lines, Kate E., Thakker, Rajesh V., Tuthill, Antoinette, Joyce, Caroline, Kaski, Juan Pablo, Frankl, Fiona E. Karet, Metherell, Lou A., Teo, Ada E. D., Gurnell, Mark, Parvanta, Laila, Drake, William M., Wozniak, Eva, Klinzing, David, Kuan, Jyn Ling, Tiang, Zenia, Gomez Sanchez, Celso E., Hellman, Per, Foo, Roger S. Y., Mein, Charles A., Kinsler, Veronica A., Björklund, Peyman, Storr, Helen L., Zennaro, Maria-Christina, Brown, Morris J.
Vydáno 2021Text