检索结果 - Stamou, Maria
- Showing 1 - 14 results of 14
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Tumor lysis-like syndrome in a child during treatment for visceral leishmaniasis 由 Tragiannidis, Athanasios, Papageorgiou, Maria, Stamou, Maria, Hatzipantelis, Emmanuel, Papageorgiou, Theodotis, Giannopoulos, Andreas, Damianidou, Lamprini, Pappa, Anna, Pappa, Stiliani, Hatzistilianou, Maria
出版 2016Text -
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Newly diagnosed diabetes vs. pre-existing diabetes upon admission for COVID-19: Associated factors, short-term outcomes, and long-term glycemic phenotypes 由 Cromer, Sara J., Colling, Caitlin, Schatoff, Daria, Leary, Michael, Stamou, Maria I., Selen, Daryl J., Putman, Melissa S., Wexler, Deborah J.
出版 2022Text -
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Integrating partner notification and contact tracing services across Europe: findings from the Integrate project 由 Glaspy, Shannon, Cosmaro, Lella, Botsi, Chryssoula, Stamou, Maria, Giannopoulou, Maria, Isari, Aikaterini M., Downey, Cheyenne, Hugh, Tina Mc, Avramovic, Gordana, Lambert, John S.
出版 2021Text -
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Prevalence and Phenotypic Effects of Copy Number Variants in Isolated Hypogonadotropic Hypogonadism 由 Stamou, Maria I, Brand, Harrison, Wang, Mei, Wong, Isaac, Lippincott, Margaret F, Plummer, Lacey, Crowley, William F, Talkowski, Michael, Seminara, Stephanie, Balasubramanian, Ravikumar
出版 2022Text -
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A Balanced Translocation in Kallmann Syndrome Implicates a Long Noncoding RNA, RMST, as a GnRH Neuronal Regulator 由 Stamou, Maria, Ng, Shi-Yan, Brand, Harrison, Wang, Harold, Plummer, Lacey, Best, Lyle, Havlicek, Steven, Hibberd, Martin, Khor, Chiea Chuen, Gusella, James, Balasubramanian, Ravikumar, Talkowski, Michael, Stanton, Lawrence W, Crowley, William F
出版 2019Text -
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Phenotypic continuum between Waardenburg syndrome and Idiopathic Hypogonadotropic Hypogonadism in humans with SOX10 mutations 由 Rojas, Rebecca A., Kutateladze, Anna A., Plummer, Lacey, Stamou, Maria, Keefe, David L., Salnikov, Kathyrn B., Delaney, Angela, Hall, Janet E., Sadreyev, Ruslan, Ji, Fei, Fliers, Eric, Gambosova, Katarina, Quinton, Richard, Merino, Paulina M, Mericq, Veronica, Seminara, Stephanie B, Crowley, William F., Balasubramanian, Ravikumar
出版 2021Text -
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Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations 由 Ge, Tian, Irvin, Marguerite R., Patki, Amit, Srinivasasainagendra, Vinodh, Lin, Yen-Feng, Tiwari, Hemant K., Armstrong, Nicole D., Benoit, Barbara, Chen, Chia-Yen, Choi, Karmel W., Cimino, James J., Davis, Brittney H., Dikilitas, Ozan, Etheridge, Bethany, Feng, Yen-Chen Anne, Gainer, Vivian, Huang, Hailiang, Jarvik, Gail P., Kachulis, Christopher, Kenny, Eimear E., Khan, Atlas, Kiryluk, Krzysztof, Kottyan, Leah, Kullo, Iftikhar J., Lange, Christoph, Lennon, Niall, Leong, Aaron, Malolepsza, Edyta, Miles, Ayme D., Murphy, Shawn, Namjou, Bahram, Narayan, Renuka, O’Connor, Mark J., Pacheco, Jennifer A., Perez, Emma, Rasmussen-Torvik, Laura J., Rosenthal, Elisabeth A., Schaid, Daniel, Stamou, Maria, Udler, Miriam S., Wei, Wei-Qi, Weiss, Scott T., Ng, Maggie C. Y., Smoller, Jordan W., Lebo, Matthew S., Meigs, James B., Limdi, Nita A., Karlson, Elizabeth W.
出版 2022Text