Treffer 1 - 7 von 7 für Suche 'Weis, Megan E', Suchdauer: 0,86s Treffer weiter einschränken
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    Twelve‐month psychosocial outcomes of continuous glucose monitoring with behavioural support in parents of young children with type 1 diabetes von Commissariat, Persis V., DiMeglio, Linda A., Kanapka, Lauren G., Laffel, Lori M., Miller, Kellee M., Anderson, Barbara J., Hilliard, Marisa E., DiMeglio, Linda A., Woerner, Stephanie, Laffel, Lori M., Harrington, Kara, Anderson, Barbara J., Hilliard, Marisa E., DeSalvo, Daniel, Tamborlane, William, Van Name, Michelle, Miller, Kellee M., Laffel, Lori, Harrington, Kara, Hanono, Anat, Naik, Nisha, Ambler‐Osborn, Louise, Schultz, Alan, DiMeglio, Linda, Woerner, Stephanie, Jolivette, Heather, Ismail, Heba, Tebbe, Megan, Newnum, America, Legge, Megan, Tamborlane, William, Van Name, Michelle, Weyman, Kate, Finnegan, Jennifer, Steffen, Amy, Zgorski, Melinda, DeSalvo, Daniel, Hilliard, Marisa, Anderson, Barbara, DeLaO, Kylie, Xie, Cicilyn, Levy, Wendy, Wadwa, R. Paul, Forlenza, Greg, Majidi, Shideh, Alonso, Guy, Weber, Isabel, Clay, Michelle, Simmons, Emily, Nathan, Brandon, Sunni, Muna, Sweet, Jessica, Pappenfus, Beth, Kogler, Anne, Ludwig, Marrissa, Nelson, Brittney, Street, Anne, Weingartner, Darcy, Albanese‐O’Neill, Anastasia, Haller, Michael, Adams, Janey, Cintron, Miriam, Thomas, Nicole, Kelley, Jennifer, Simmons, Jill, William, George, Brendle, Faith, Goland, Robin, Williams, Kristen, Gandica, Rachelle, Pollak, Sarah, Casciano, Emily, Robinson, Elizabeth, Willi, Steven, Minnock, Pantea, Olivos, Diana, Carchidi, Cathy, Grant, Brian, Wong, Jenise C., Adi, Saleh, Corathers, Sarah, Sheanon, Nicole, Fox, Cathy, Weis, Tammy, MacLeish, Sarah, Wood, Jamie, Casey, Terri, Campbell, Wendy, McGuigan, Paul, Wintergerst, Kupper, Watson, Sara, Kingery, Suzanne, Pierce, Gwen, Ruch, Heather, Rayborn, Lauren, Rodriguez‐Luna, Manuel, Deuser, Amy

    Veröffentlicht in Diabetic medicine

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    Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities von Cali, Elisa, Suri, Mohnish, Scala, Marcello, Ferla, Matteo P., Alavi, Shahryar, Faqeih, Eissa Ali, Bijlsma, Emilia K., Wigby, Kristen M., Baralle, Diana, Mehrjardi, Mohammad Y.V., Schwab, Jennifer, Platzer, Konrad, Steindl, Katharina, Hashem, Mais, Jones, Marilyn, Niyazov, Dmitriy M., Jacober, Jennifer, Littlejohn, Rebecca Okashah, Weis, Denisa, Zadeh, Neda, Rodan, Lance, Goldenberg, Alice, Lecoquierre, François, Dutra-Clarke, Marina, Horvath, Gabriella, Young, Dana, Orenstein, Naama, Bawazeer, Shahad, Vulto-van Silfhout, Anneke T., Herenger, Yvan, Dehghani, Mohammadreza, Seyedhassani, Seyed Mohammad, Bahreini, Amir, Nasab, Mahya E., Ercan-Sencicek, A. Gulhan, Firoozfar, Zahra, Movahedinia, Mojtaba, Efthymiou, Stephanie, Striano, Pasquale, Karimiani, Ehsan Ghayoor, Salpietro, Vincenzo, Taylor, Jenny C., Redman, Melody, Stegmann, Alexander P.A., Laner, Andreas, Abdel-Salam, Ghada, Li, Megan, Bengala, Mario, Müller, Amelie Johanna, Digilio, Maria C., Rauch, Anita, Gunel, Murat, Titheradge, Hannah, Schweitzer, Daniela N., Kraus, Alison, Valenzuela, Irene, McLean, Scott D., Phornphutkul, Chanika, Salih, Mustafa, Begtrup, Amber, Schnur, Rhonda E., Torti, Erin, Haack, Tobias B., Prada, Carlos E., Alkuraya, Fowzan S., Houlden, Henry, Maroofian, Reza

    Veröffentlicht in Genetics in medicine

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