Variation in early number skills and mathematics achievement: Implications from cognitive profiles of children with or without Turner syndrome von Lukowski, Sarah L, Padrutt, Emily R, Sarafoglou, Kyriakie, Ross, Judith L, Law, Jennifer R, Olson, Rachel E, Mazzocco, Michèle M M

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Correction: Variation in early number skills and mathematics achievement: Implications from cognitive profiles of children with or without Turner syndrome von Lukowski, Sarah L, Padrutt, Emily R, Sarafoglou, Kyriakie, Ross, Judith L, Law, Jennifer R, Olson, Rachel E, Mazzocco, Michèle M M

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SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome von Shaw, Natalie D, Brand, Harrison, Kupchinsky, Zachary A, Bengani, Hemant, Plummer, Lacey, Jones, Takako I, Erdin, Serkan, Williamson, Kathleen A, Rainger, Joe, Stortchevoi, Alexei, Samocha, Kaitlin, Currall, Benjamin B, Dunican, Donncha S, Collins, Ryan L, Willer, Jason R, Lek, Angela, Lek, Monkol, Nassan, Malik, Pereira, Shahrin, Kammin, Tammy, Lucente, Diane, Silva, Alexandra, Seabra, Catarina M, Chiang, Colby, An, Yu, Ansari, Morad, Rainger, Jacqueline K, Joss, Shelagh, Smith, Jill Clayton, Lippincott, Margaret F, Singh, Sylvia S, Patel, Nirav, Jing, Jenny W, Law, Jennifer R, Ferraro, Nalton, Verloes, Alain, Rauch, Anita, Steindl, Katharina, Zweier, Markus, Scheer, Ianina, Sato, Daisuke, Okamoto, Nobuhiko, Jacobsen, Christina, Tryggestad, Jeanie, Chernausek, Steven, Schimmenti, Lisa A, Brasseur, Benjamin, Cesaretti, Claudia, García-Ortiz, Jose E, Buitrago, Tatiana Pineda, Silva, Orlando Perez, Hoffman, Jodi D, Mühlbauer, Wolfgang, Ruprecht, Klaus W, Loeys, Bart L, Shino, Masato, Kaindl, Angela M, Cho, Chie-Hee, Morton, Cynthia C, Meehan, Richard R, van Heyningen, Veronica, Liao, Eric C, Balasubramanian, Ravikumar, Hall, Janet E, Seminara, Stephanie B, Macarthur, Daniel, Moore, Steven A, Yoshiura, Koh-ichiro, Gusella, James F, Marsh, Joseph A, Graham, John M, Lin, Angela E, Katsanis, Nicholas, Jones, Peter L, Crowley, William F, Davis, Erica E, FitzPatrick, David R, Talkowski, Michael E

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Inspiring New Science to Guide Healthcare in Turner Syndrome: Rationale, design, and methods for the InsighTS Registry von Kanakatti Shankar, Roopa, Carl, Alexandra, Law, Jennifer R., Bamba, Vaneeta, Brickman, Wendy J., Prakash, Siddharth K., Dowlut McElroy, Tazim, Howell, Susan, Gutmark Little, Iris, Klein, Karen O., Pinnaro, Catherina T., Ranallo, Kelly, Good, Marybel, Davis, Shanlee M.

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Prevalence, diagnostic features, and medical outcomes of females with Turner syndrome with a trisomy X cell line (45,X/47,XXX): Results from the InsighTS Registry von Klamut, Natalia, Bothwell, Samantha, Carl, Alexandra E., Bamba, Vaneeta, Law, Jennifer R., Brickman, Wendy J., Klein, Karen O., Kanakatti Shankar, Roopa, Pinnaro, Catherina T., Fechner, Patricia Y., Prakash, Siddharth K., Gutmark‐Little, Iris, Howell, Susan, Tartaglia, Nicole, Good, Marybel, Ranallo, Kelly C., Davis, Shanlee M.

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Changes to care delivery at nine international pediatric diabetes clinics in response to the COVID‐19 global pandemic von Sarteau, Angelica Cristello, Souris, Katherine Janine, Wang, Jessica, Ramadan, Amira A., Addala, Ananta, Bowlby, Deborah, Corathers, Sarah, Forsander, Gun, King, Bruce, Law, Jennifer R., Liu, Wei, Malik, Faisal, Pihoker, Catherine, Seid, Michael, Smart, Carmel, Sundberg, Frida, Tandon, Nikhil, Yao, Michael, Headley, Terry, Mayer‐Davis, Elizabeth

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Insight Into the Ontogeny of GnRH Neurons From Patients Born Without a Nose von Delaney, Angela, Volochayev, Rita, Meader, Brooke, Lee, Janice, Almpani, Konstantinia, Noukelak, Germaine Y, Henkind, Jennifer, Chalmers, Laura, Law, Jennifer R, Williamson, Kathleen A, Jacobsen, Christina M, Buitrago, Tatiana Pineda, Perez, Orlando, Cho, Chie-Hee, Kaindl, Angela, Rauch, Anita, Steindl, Katharina, Garcia, Jose Elias, Russell, Bianca E, Prasad, Rameshwar, Mondal, Uttam K, Reigstad, Hallvard M, Clements, Scott, Kim, Susan, Inoue, Kaoru, Arora, Gazal, Salnikov, Kathryn B, DiOrio, Nicole P, Prada, Rolando, Capri, Yline, Morioka, Kosuke, Mizota, Michiyo, Zechi-Ceide, Roseli M, Kokitsu-Nakata, Nancy M, Tonello, Cristiano, Vendramini-Pittoli, Siulan, da Silva Dalben, Gisele, Balasubramanian, Ravikumar, Dwyer, Andrew A, Seminara, Stephanie B, Crowley, William F, Plummer, Lacey, Hall, Janet E, Graham, John M, Lin, Angela E, Shaw, Natalie D

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EndoBridge 2023: highlights and pearls von Yildiz, Bulent Okan, Boguszewski, Cesar Luiz, da Silva Boguszewski, Margaret Cristina, Busetto, Luca, Celik, Ozlem, Fuleihan, Ghada El-Hajj, Goulis, Dimitrios G., Hammer, Gary D., Haymart, Megan R., Kaltsas, Gregory, Law, Jennifer R., Lim, Amanda Yuan Ling, Luger, Anton, Macut, Djuro, McGowan, Barbara, McClung, Michael, Miras, Alexander Dimitri, Patti, Mary Elizabeth, Peeters, Robin P., Pignatelli, Duarte, Saeed, Hamayle, Sipos, Jennifer, Stratakis, Constantine A., Tsoli, Marina, van der Lely, A. J., Witchel, Selma F., Yazici, Dilek

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Alcohol consumption patterns in young adults with type 1 diabetes: The SEARCH for diabetes in youth study von Roberts, Alissa J., Law, Jennifer R., Suerken, Cynthia K., Reboussin, Beth A., Lawrence, Jean M., Taplin, Craig E., Mayer-Davis, Elizabeth J., Pihoker, Catherine

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Understanding antagonism and synergism: A qualitative assessment of weight management in youth with Type 1 diabetes mellitus von Kahkoska, Anna R., Watts, Madison E., Driscoll, Kimberly A., Bishop, Franziska K., Mihas, Paul, Thomas, Joan, Law, Jennifer R., Jain, Nina, Mayer-Davis, Elizabeth J.

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Hepatocellular Carcinoma, Virilization, and Hilus Cell Hyperplasia in a Girl With Turner Syndrome von Law, Jennifer R, Lee, Sang, Sasatomi, Eizaburo, Bookhout, Christine E, Blatt, Julie

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Association of parental history of diabetes with cardiovascular disease risk factors in children with type 2 diabetes von Law, Jennifer R, Stafford, Jeanette M, D'Agostino, Ralph B, Badaru, Angela, Crume, Tessa L, Dabelea, Dana, Dolan, Lawrence M, Lawrence, Jean M, Pettitt, David J, Mayer-Davis, Elizabeth J

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Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner Syndrome Meeting von Gravholt, Claus H, Andersen, Niels H, Conway, Gerard S, Dekkers, Olaf M, Geffner, Mitchell E, Klein, Karen O, Lin, Angela E, Mauras, Nelly, Quigley, Charmian A, Rubin, Karen, Sandberg, David E, Sas, Theo C J, Silberbach, Michael, Söderström-Anttila, Viveca, Stochholm, Kirstine, van Alfen-van derVelden, Janielle A, Woelfle, Joachim, Backeljauw, Philippe F

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The influence of exposure to maternal diabetes in utero on the rate of decline in β-cell function among youth with diabetes von Crume, Tessa L, Andrews, Jeanette S, D'Agostino, Jr, Ralph B, Pettitt, David J, Mayer-Davis, Elizabeth J, Law, Jennifer R, Dolan, Lawrence, Lawrence, Jean M, Saydah, Sharon, Greenbaum, Carla, Rodriguez, Beatriz L, Dabelea, Dana

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TURNER SYNDROME: UNDERSTANDING INDIVIDUALIZED MEDICAL RISKS DETERMINED BY KARYOTYPE SUBGROUP von Purusothaman, Vaishnavi, Fitz, Victoria W., Law, Jennifer R., Rosen, Emma M., Peavey, Mary

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Evaluating Substance Use and Insulin Misuse in Adolescents With Type 1 Diabetes von Snyder, Lydia L., Truong, Young Kinh-Nhue, Law, Jennifer R.

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804-P: Alcohol Consumption Patterns among Young Adults with Type 1 Diabetes von ROBERTS, ALISSA J., LAW, JENNIFER R., SUERKEN, CYNTHIA, REBOUSSIN, BETH A., LAWRENCE, JEAN M., TAPLIN, CRAIG, MAYER-DAVIS, ELIZABETH, PIHOKER, CATHERINE

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Insight Into the ontogeny of GnRH neurons from patients born without a nose von Delaney, Angela, Volochayev, Rita, Meader, Brooke, Lee, Janice, Almpani, Konstantinia, Noukelak, Germaine Y, Henkind, Jennifer, Chalmers, Laura, Law, Jennifer R, Williamson, Kathleen A, Jacobsen, Christina M, Buitrago, Tatiana Pineda, Perez, Orlando, Cho, Chie-Hee, Kaindl, Angela, Rauch, Anita, Steindl, Katharina, Garcia, Jose Elias, Russell, Bianca E, Prasad, Rameshwar, Mondal, Uttam K, Reigstad, Hallvard M, Clements, Scott, Kim, Susan, Inoue, Kaoru, Arora, Gazal, Salnikov, Kathryn B, DiOrio, Nicole P, Prada, Rolando, Capri, Yline

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Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome von Shaw, Natalie D, Brand, Harrison, Kupchinsky, Zachary A, Bengani, Hemant, Plummer, Lacey, Jones, Takako I, Erdin, Serkan, Williamson, Kathleen A, Rainger, Joe, Stortchevoi, Alexei, Samocha, Kaitlin, Currall, Benjamin B, Dunican, Donncha S, Collins, Ryan L, Willer, Jason R, Lek, Angela, Lek, Monkol, Nassan, Malik, Pereira, Shahrin, Kammin, Tammy, Lucente, Diane, Silva, Alexandra, Seabra, Catarina M, Chiang, Colby, An, Yu, Ansari, Morad, Rainger, Jacqueline K, Joss, Shelagh, Smith, Jill Clayton, Lippincott, Margaret F, Singh, Sylvia S, Patel, Nirav, Jing, Jenny W, Law, Jennifer R, Ferraro, Nalton, Verloes, Alain, Rauch, Anita, Steindl, Katharina, Zweier, Markus, Scheer, Ianina, Sato, Daisuke, Okamoto, Nobuhiko, Jacobsen, Christina, Tryggestad, Jeanie, Chernausek, Steven, Schimmenti, Lisa A, Brasseur, Benjamin, Cesaretti, Claudia, García-Ortiz, Jose E, Buitrago, Tatiana Pineda, Silva, Orlando Perez, Hoffman, Jodi D, Mühlbauer, Wolfgang, Ruprecht, Klaus W, Loeys, Bart L, Shino, Masato, Kaindl, Angela M, Cho, Chie-Hee, Morton, Cynthia C, Meehan, Richard R, van Heyningen, Veronica, Liao, Eric C, Balasubramanian, Ravikumar, Hall, Janet E, Seminara, Stephanie B, Macarthur, Daniel, Moore, Steven A, Yoshiura, Koh-Ichiro, Gusella, James F, Marsh, Joseph A, Graham, Jr, John M, Lin, Angela E, Katsanis, Nicholas, Jones, Peter L, Crowley, Jr, William F, Davis, Erica E, FitzPatrick, David R, Talkowski, Michael E

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Correction: Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome von Shaw, Natalie D, Brand, Harrison, Kupchinsky, Zachary A, Bengani, Hemant, Plummer, Lacey, Jones, Takako I, Erdin, Serkan, Williamson, Kathleen A, Rainger, Joe, Stortchevoi, Alexei, Samocha, Kaitlin, Currall, Benjamin B, Dunican, Donncha S, Collins, Ryan L, Willer, Jason R, Lek, Angela, Lek, Monkol, Nassan, Malik, Pereira, Shahrin, Kammin, Tammy, Lucente, Diane, Silva, Alexandra, Seabra, Catarina M, Chiang, Colby, An, Yu, Ansari, Morad, Rainger, Jacqueline K, Joss, Shelagh, Smith, Jill Clayton, Lippincott, Margaret F, Singh, Sylvia S, Patel, Nirav, Jing, Jenny W, Law, Jennifer R, Ferraro, Nalton, Verloes, Alain, Rauch, Anita, Steindl, Katharina, Zweier, Markus, Scheer, Ianina, Sato, Daisuke, Okamoto, Nobuhiko, Jacobsen, Christina, Tryggestad, Jeanie, Chernausek, Steven, Schimmenti, Lisa A, Brasseur, Benjamin, Cesaretti, Claudia, García-Ortiz, Jose E, Buitrago, Tatiana Pineda, Silva, Orlando Perez, Hoffman, Jodi D, Mühlbauer, Wolfgang, Ruprecht, Klaus W, Loeys, Bart L, Shino, Masato, Kaindl, Angela M, Cho, Chie-Hee, Morton, Cynthia C, Meehan, Richard R, van Heyningen, Veronica, Liao, Eric C, Balasubramanian, Ravikumar, Hall, Janet E, Seminara, Stephanie B, Macarthur, Daniel, Moore, Steven A, Yoshiura, Koh-ichiro, Gusella, James F, Marsh, Joseph A, Graham, John M, Lin, Angela E, Katsanis, Nicholas, Jones, Peter L, Crowley, William F, Davis, Erica E, FitzPatrick, David R, Talkowski, Michael E

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