Mechanisms and treatment of cardiovascular disease in Williams-Beuren syndrome von Pober, Barbara R, Johnson, Mark, Urban, Zsolt

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Williams syndrome von Kozel, Beth A., Barak, Boaz, Kim, Chong Ae, Mervis, Carolyn B., Osborne, Lucy R., Porter, Melanie, Pober, Barbara R.

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Diversity of Participants in Williams Syndrome Intervention Studies von Shin, Eva, Ravichandran, Caitlin, Renzi, Danielle, Pober, Barbara R., McDougle, Christopher J., Thom, Robyn P.

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Repetitive Thoughts and Repetitive Behaviors in Williams Syndrome von Huston, John C., Thom, Robyn P., Ravichandran, Caitlin T., Mullett, Jennifer E., Moran, Carly, Waxler, Jessica L., Pober, Barbara R., McDougle, Christopher J.

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Hypercalcemia in Patients with Williams-Beuren Syndrome von Sindhar, Sampat, BS, Lugo, Michael, BS, Levin, Mark D., MD, Danback, Joshua R., BS, Brink, Benjamin D., MS, Yu, Eric, BA, Dietzen, Dennis J., PhD, Clark, Amy L., DO, Purgert, Carolyn A., MD, PhD, Waxler, Jessica L., MS, Elder, Robert W., MD, Pober, Barbara R., MD, Kozel, Beth A., MD, PhD

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Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomes von Russell, Meaghan K, Longoni, Mauro, Wells, Julie, Maalouf, Faouzi I, Tracy, Adam A, Loscertales, Maria, Ackerman, Kate G, Pober, Barbara R, Lage, Kasper, Bult, Carol J, Donahoe, Patricia K

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Mutations in LRP2 , which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes von Noonan, Kristin M, MacLaughlin, David T, Loscertales, Maria, Robson, Caroline, Walsh, Christopher A, Al-Gazali, Lihadh, Hill, R Sean, Donnai, Dian, Russell, Meaghan K, Bieth, Eric, Devriendt, Koen, Liu, Tianming, Chassaing, Nicolas, Teebi, Ahmad, Pober, Barbara R, Black, Graeme C M, Lacombe, Didier, Donahoe, Patricia K, Kantarci, Sibel

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Glucose and lipid metabolism, bone density, and body composition in individuals with Williams syndrome von Shaikh, Sofia, Waxler, Jessica L., Lee, Hang, Grinke, Kathy, Garry, Jamie, Pober, Barbara R., Stanley, Takara L.

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Molecular pathogenesis of congenital diaphragmatic hernia revealed by exome sequencing, developmental data, and bioinformatics von Longoni, Mauro, High, Frances A., Russell, Meaghan K., Kashani, Alireza, Tracy, Adam A., Coletti, Caroline M., Hila, Regis, Shamia, Ahmed, Wells, Julie, Ackerman, Kate G., Wilson, Jay M., Bult, Carol J., Lee, Charles, Lage, Kasper, Pober, Barbara R., Donahoe, Patricia K.

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PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects von Petit, Florence, Longoni, Mauro, Wells, Julie, Maser, Richard S., Bogenschutz, Eric L., Dysart, Matthew J., Contreras, Hannah T.M., Frénois, Frederic, Pober, Barbara R., Clark, Robin D., Giampietro, Philip F., Ropers, Hilger H., Hu, Hao, Loscertales, Maria, Wagner, Richard, Ai, Xingbin, Brand, Harrison, Jourdain, Anne-Sophie, Delrue, Marie-Ange, Gilbert-Dussardier, Brigitte, Devisme, Louise, Keren, Boris, McCulley, David J., Qiao, Lu, Hernan, Rebecca, Wynn, Julia, Scott, Tiana M., Calame, Daniel G., Coban-Akdemir, Zeynep, Hernandez, Patricia, Hernandez-Garcia, Andres, Yonath, Hagith, Lupski, James R., Shen, Yufeng, Chung, Wendy K., Scott, Daryl A., Bult, Carol J., Donahoe, Patricia K., High, Frances A.

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Buspirone for the Treatment of Generalized Anxiety Disorder in Williams Syndrome: A Case Series von Thom, Robyn P., Keary, Christopher J., Waxler, Jessica L., Pober, Barbara R., McDougle, Christopher J.

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Body mass index variation in adults with Williams syndrome: associations with predicted dietary intake and food behaviors von Renzi, Danielle, Stanley, Takara, Waxler, Jessica, Lee, Hang, Pober, Barbara, Nordstrom, Marianne

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Williams Syndrome Predisposes to Vascular Stiffness Modified by Antihypertensive Use and Copy Number Changes in NCF1 von Kozel, Beth A, Danback, Joshua R, Waxler, Jessica L, Knutsen, Russell H, de las Fuentes, Lisa, Reusz, Gyorgy S, Kis, Eva, Bhatt, Ami B, Pober, Barbara R

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Frequency of QTc Interval Prolongation in Children and Adults with Williams Syndrome von Brink, Benjamin D., Feinn, Richard, Kozel, Beth A., Billington, Charles J., Liu, Delong, Yu, Eric, Sindhar, Sampat, He, Julie, Rouse, Charles, Lampert, Rachel, Pober, Barbara R., Elder, Robert W.

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The proceedings of the 15th professional conference on Williams Syndrome von Walton, Jennifer R., Martens, Marilee A., Pober, Barbara R.

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Social, neurodevelopmental, endocrine, and head size differences associated with atypical deletions in Williams–Beuren syndrome von Lugo, Michael, Wong, Zoë C., Billington, Charles J., Parrish, Phoebe C. R., Muldoon, Glennis, Liu, Delong, Pober, Barbara R., Kozel, Beth A.

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Mild macrocytosis in Williams-Beuren syndrome von Yu, Eric, Feinn, Richard, Bona, Robert, Brink, Benjamin, Sindhar, Sampat, Kozel, Beth A., Pober, Barbara R.

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Fog2 is required for normal diaphragm and lung development in mice and humans von Ackerman, Kate G, Herron, Bruce J, Vargas, Sara O, Huang, Hailu, Tevosian, Sergei G, Kochilas, Lazaros, Rao, Cherie, Pober, Barbara R, Babiuk, Randal P, Epstein, Jonathan A, Greer, John J, Beier, David R

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Rapamycin Inhibits Smooth Muscle Cell Proliferation and Obstructive Arteriopathy Attributable to Elastin Deficiency von Li, Wei, Li, Qingle, Qin, Lingfeng, Ali, Rahmat, Qyang, Yibing, Tassabehji, May, Pober, Barbara R, Sessa, William C, Giordano, Frank J, Tellides, George

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Brief Report: Major Depressive Disorder with Psychotic Features in Williams Syndrome: A Case Series von Valdes, Francisca, Keary, Christopher J., Mullett, Jennifer E., Palumbo, Michelle L., Waxler, Jessica L., Pober, Barbara R., McDougle, Christopher J.

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