Incident Vertebral Fractures and Risk Factors in the First Three Years Following Glucocorticoid Initiation Among Pediatric Patients With Rheumatic Disorders von LeBlanc, Claire MA, Ma, Jinhui, Taljaard, Monica, Roth, Johannes, Scuccimarri, Rosie, Miettunen, Paivi, Lang, Bianca, Huber, Adam M, Houghton, Kristin, Jaremko, Jacob L, Ho, Josephine, Shenouda, Nazih, Matzinger, Mary Ann, Lentle, Brian, Stein, Robert, Sbrocchi, Anne Marie, Oen, Kiem, Rodd, Celia, Jurencak, Roman, Cummings, Elizabeth A, Couch, Robert, Cabral, David A, Atkinson, Stephanie, Alos, Nathalie, Rauch, Frank, Siminoski, Kerry, Ward, Leanne M

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Résumés des communications von Andrew, Caroline, Bouchard, Lyne, Culligan, Denyse, Lemire, Denise, Beausoleil, Natalie, Gendron, Hélène, Merkle, Denise, Pharand, Gaëtane, Fournier, Danielle, Massicotte, Lucie, Gélinas, France, Carter, Mary, Dallaire, Hélène, Plante, Lucie, Prévost, Colette, LeBlanc, Lorraine, Lemonde, Manon, Mazerolle, Éva, Simard, Céline, Hodge, Anne, Dupont, Diane, Ngaba, Marie-Béatrice, Mboma, Anne-Marie, Côté, Denyse, Ladouceur, Lise, Bernier-Wilson, Michelle

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Risk of Falls and Motor Vehicle Collisions in Glaucoma von Haymes, Sharon A, LeBlanc, Raymond P, Nicolela, Marcelo T, Chiasson, Lorraine A, Chauhan, Balwantray C

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Metformin in women with type 2 diabetes in pregnancy (MiTy): a multicentre, international, randomised, placebo-controlled trial von Sanchez, J Johanna, Asztalos, Elizabeth, Armson, Anthony B, Barrett, Jon F R, Karanicolas, Paul J, Tian, Simon Yu, Murphy, Kellie E, Feig, Denice, Cleave, Barbara, Strom, Michele, Kamath, Aarthi, Godbout, Ariane, Mahone, Michele, Robinson, Melanie, Slater, Laurie, Oldford, Carolyn, Lodha, Abhay, Cooper, Stephanie, Gougeon, Claire, Zahedi, Afshan, Turner, Marci, Neculau, Madalena, Robb, Cathy, Szwiega, Krystyna, Lee, Grace, Perreault, Sophie, Coolen, Jillian, Slaunwhite, Janet, Fanning, Cora, Kader, Tina, Hirsimaki, Heidi, Chalifoux, Steve, McManus, Ruth, Watson, Margaret, Sultana, Munira, ArthurHayward, Vinolia, Marin, Mauricio, Cauchi, Lorraine, MacBean, Leila, Malcolm, Janine, Clark, Heather, Karovitch, Allan, Belanger, Heather, Champagne, Josee, Schutt, Kayla, Sloan, Jennifer, O'Shea, Elaine, McGuire, Debbie, St Omer, Dynika, Lee, Julie, Carr, Francina, Subrt, Peter, Smushkin, Galina, Phillips, Richard, Fergusson, Carol, Breen, Adriana, Ryan, Edmond A, Rylance, Heather, Khurana, Rshmi, McNab, Tammy, Beauchamp, Shirley, D'Amours, Martin, Julien, Valérie-Ève, Lambert, Camille, Bourbonniere, Marie-Claude, Rheaume, Louise, Bouchard, Myriam, Carson, George, Williams, Suzanne, Berger, Howard, Ray, Joel, De Souza, Leanne, Bastien, Louise, Segal, Shari, Orr, Christine, Galway, Brenda, Rideout, Krista, Rowe, Bernadette, Joyce, Carol, Newstead-Angel, Jill, Meier, Simona, Laurie, Josephine, Fox, Jane, Barrett, Helen, Nerdal-Bussell, Marnie, Nie, Wenjun, Cook, Anne, Rajagopal, Rohit, Vizza, Lisa, Bishop, Claudia, Hendon, Susan, Russell, Hamish, Zinman, Bernard, Fantus, George I, Lipscombe, Lorraine L, Barrett, Jon, Tomlinson, George, Karanicolas, Paul, Murphy, Helen, Sanchez, Johanna

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Vertebral Body Reshaping after Fractures: An Important Index of Recovery in Glucocorticoid-Treated Children von Ma, Jinhui, Siminoski, Kerry, Jaremko, Jacob L, Koujok, Khaldoun, Matzinger, Mary Ann, Shenouda, Nazih, Wilson, Nagwa, Cheng, Megan, Alos, Nathalie, Atkinson, Stephanie, Cummings, Elizabeth A, Ho, Josephine, Rodd, Celia, Sbrocchi, Anne Marie, Stein, Robert, Barr, Ronald, Cairney, Elizabeth, Dix, David B, Fernandez, Conrad V, Grant, Ronald, Halton, Jacqueline, Israels, Sara, Laverdière, Caroline, Lewis, Victor A, Cabral, David A, Huber, Adam, Houghton, Kristin, Jurencak, Roman, Lang, Bianca, Larché, Maggie, LeBlanc, Claire M A, Miettunen, Paivi, Roth, Johannes, Scuccimarri, Rosie, Bell, Lorraine, Blydt-Hansen, Tom, Filler, Guido, Feber, Janusz, Phan, Véronique, Smit, Kevin, Rauch, Frank, Ward, Leanne M

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Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts von Frésard, Laure, Smail, Craig, Ferraro, Nicole M., Teran, Nicole A., Li, Xin, Smith, Kevin S., Bonner, Devon, Kernohan, Kristin D., Marwaha, Shruti, Zappala, Zachary, Balliu, Brunilda, Davis, Joe R., Liu, Boxiang, Prybol, Cameron J., Kohler, Jennefer N., Zastrow, Diane B., Reuter, Chloe M., Fisk, Dianna G., Grove, Megan E., Davidson, Jean M., Hartley, Taila, Joshi, Ruchi, Strober, Benjamin J., Utiramerur, Sowmithri, Lind, Lars, Ingelsson, Erik, Battle, Alexis, Bejerano, Gill, Bernstein, Jonathan A., Ashley, Euan A., Boycott, Kym M., Merker, Jason D., Wheeler, Matthew T., Montgomery, Stephen B.

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Glaucoma and On-Road Driving Performance von Haymes, Sharon A, LeBlanc, Raymond P, Nicolela, Marcelo T, Chiasson, Lorraine A, Chauhan, Balwantray C

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Advanced chronic kidney disease populations have elevated trimethylamine N-oxide levels associated with increased cardiovascular events von Kim, Richard B., Morse, Bridget L., Djurdjev, Ognjenka, Tang, Mila, Barrett, Brendan, Holmes, Daniel T., Madore, Francois, Rigatto, Claudio, Agharazii, Mohsen, Blouin, Joanne, Samson, France, Akbarii, Ayub, Cheesman, Judy, Courtney, Jennilea, Hamer, Sabrina, Delic, Edita, Cronin, Valerie, Barré, Paul, Golden, Jeffrey, Barrett, Brendan, Langille, Elizabeth, Adams, Sandra, Morgan, Janet, Clase, Catherine, Moreau, Cathy, Cooper, Susan, Forzley, Brian, Caron, Susan, Valley, Susan, Sather, Helen, Cournoyer, Serge, Roy, Michèle, Skidmore, Hélène, Beaudry, Dolores, Sahraei, Valla, Donnelly, Sandra, Dacouris, Niki, Marticorena, Rosa, Hemmelgarn, Brenda, Gulewich, Sharon, Hamilton, Troy, Keown, Paul, Zalunardo, Nadia, Rogers, Daniel, Tut, Reena, Paquette, Matthew, Yung, Rossitta, Levin, Adeera, Ferguson, Nancy, Tang, Mila, Chiu, Helen, Carlson, Kathleen, Sioson, Lina, Perry, Taylor, Sheriff, Zainab, Rozen, Naama, Lok, Charmaine, Cross, Michelle, Forrester, Cathy, Madore, François, Moist, Louise, Gallo, Kerri, Langford, Sarah, Slamen, Leah, Cram, Danielle, Muirhead, Norman, Edgar, Mary Jeanne, Edgar, Cameron, Groeneweg, Karen, McKinnon, Eileen, Blackie, Kyla, Nathoo, Bharat, Lau, Kimmy, Parmar, Malvinder, Gelinas, Sylvie, Leblanc, Martine, Lépine, Lucie, Rigatto, Claudio, Friesen, Dolores, Soroka, Steven, Fleet, Susan, Squires, Jeanette, Thanamayooran, Siva, Binder, Michael, Hines, Christine, McNeil, Brenda, McDougall, Patrice, Howard, Joy, Hines, Kathleen, Tobe, Sheldon, Chessman, Mary, Perkins, Nancy, Agelopoulos, Martha, Knox, Stacey, Richards, Tiffany, Tonelli, Marcello, Szigety, Susan, Opgenorth, Dawn, Yeates, Karen, Mahoney, Karen

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Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal Acidification von Becerril, Alissa, Larson, Austin, Zerfas, Patricia M., Acosta, Maria T., Agrawal, Pankaj, Alejandro, Mercedes E., Andrews, Ashley, Bacino, Carlos A., Bademci, Guney, Baker, Eva, Baldridge, Dustin, Bale, Jim, Barbouth, Deborah, Batzli, Gabriel F., Bayrak-Toydemir, Pinar, Bernstein, Jonathan A., Birch, Camille L., Bivona, Stephanie, Bohnsack, John, Bonnenmann, Carsten, Bostwick, Bret L., Brokamp, Elly, Burrage, Lindsay C., Carey, John, Clark, Gary D., Cope, Heidi, Dasari, Surendra, Dayal, Jyoti G., Dorset, Daniel C., Eng, Christine M., Esteves, Cecilia, Fresard, Laure, Goldman, Alica M., Goldstein, David B., Groden, Catherine A., Haendel, Melissa, Hayes, Nichole, Holm, Ingrid A., Jiang, Yong-hui, Johnston, Jean M., Jones, Angela L., Kohane, Isaac S., Krakow, Deborah, Krasnewich, Donna M., Korrick, Susan, Krier, Joel B., Lalani, Seema R., Lam, Byron, Lazar, Jozef, Levy, Shawn E., Liu, Xue Zhong, Malicdan, May Christine V., Mamounas, Laura A., Markello, Thomas C., Marom, Ronit, Martínez-Agosto, Julian A., McCormack, Colleen E., McCray, Alexa T., Might, Matthew, Morava-Kozicz, Eva, Murdock, David R., Nath, Avi, Nelson, Stan F., Newman, John H., Orengo, James P., Pace, Laura, Papp, Jeanette C., Parker, Neil H., Potocki, Lorraine, Raja, Archana N., Reuter, Chloe M., Rives, Lynette, Rowley, Robb K., Sampson, Jacinda B., Saporta, Mario, Schedl, Timothy, Shields, Kathleen, Signer, Rebecca, Sillari, Catherine H., Sisco, Kathy, Spillmann, Rebecca C., Stoler, Joan M., Stong, Nicholas, Sullivan, Jennifer A., Tekin, Mustafa, Thorson, Willa, Tran, Alyssa A., Wahl, Colleen E., Wan, Jijun, Wang, Lee-kai, Wangler, Michael F., Westerfield, Monte, Wheeler, Matthew T., Wolfe, Lynne A., Woods, Jeremy D., Worthey, Elizabeth A., Yamamoto, Shinya, Zuchner, Stephan, Day-Salvatore, Debra L., Mindell, Joseph A.

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Co-Creation of Knowledge Mobilization Strategies: Findings from a Collaborative Symposium von Terry, Amanda, Nicholson, Kathryn, Brown, Judith, Mathews, Maria, Menear, Matthew, Bayliss, Lorraine, Ramsden, Vivian, LeBlanc, Annie, Breton, Mylaine, Ashcroft, Rachelle, Pinto, Andrew, Ganann, Rebecca, Fortin, Martin, Donnelly, Catherine, Reid, Graham, Poitras, Marie-Eve, Sasseville, Maxime, Stewart, Moira, Wilson, Erin, Ryan, Bridget

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De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation von Mao, Dongxue, Reuter, Chloe M., Farrow, Emily G., Rosenfeld, Jill A., Mackenzie, Katherine M., Küry, Sébastien, Genetti, Casie A., Alejandro, Mercedes, Agrawal, Pankaj B., Alvey, Justin, Ashley, Euan A., Balasubramanyam, Ashok, Beck, Anita, Bellen, Hugo J., Berg-Rood, Beverly, Bernier, Raphael, Bivona, Stephanie, Bohnsack, John, Briere, Lauren C., Burke, Elizabeth A., Butte, Manish J., Carrasquillo, Olveen, Cogan, Joy D., Cole, F. Sessions, Colley, Heather A., Cooper, Cynthia M., Craigen, William J., Cunningham, Michael, Dasari, Surendra, Dayal, Jyoti G., Dhar, Shweta U., Emrick, Lisa T., Estwick, Tyra, Ferreira, Carlos, Fieg, Elizabeth L., Fogel, Brent L., Forghani, Irman, Gahl, William A., Godfrey, Rena A., Goldman, Alica M., Hahn, Sihoun, Hanchard, Neil A., Hing, Anne, Holm, Ingrid A., Huang, Yong, Jamal, Fariha, Jayadev, Suman, Karaviti, Lefkothea, Kelley, Emily G., Kohane, Isaac S., Kohler, Jennefer N., Krakow, Deborah, Korrick, Susan, Koziura, Mary, Krier, Joel B., Lam, Byron, Lanpher, Brendan C., Lanza, Ian R., Lee, Brendan H., Lewis, Richard A., Loo, Sandra K., Majcherska, Marta M., Malicdan, May Christine V., Mamounas, Laura A., Markello, Thomas C., Martin, Martin G., Martínez-Agosto, Julian A., McCormack, Colleen E., Merritt, J. Lawrence, Moretti, Paolo M., Mulvihill, John J., Murdock, David R., Nickerson, Deborah, Pallais, J. Carl, Posey, Jennifer E., Potocki, Lorraine, Raja, Archana N., Renteria, Genecee, Rosenfeld, Jill A., Samson, Susan L., Schedl, Timothy, Shakachite, Lisa, Signer, Rebecca, Silverman, Edwin K., Sybert, Virginia, Tekin, Mustafa, Thorson, Willa, Tran, Alyssa A., Urv, Tiina K., Wahl, Colleen E., Wegner, Daniel, Wheeler, Matthew T., Yamamoto, Shinya, Yang, John, Yoon, Amanda J., Yu, Guoyun, Zastrow, Diane B., Zhao, Chunli, Bernstein, Jonathan A., Chao, Hsiao-Tuan

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SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia von Srivastava, Siddharth, Shaked, Hagar Mor, Gable, Kenneth, Gupta, Sita D, Pan, Xueyang, Somashekarappa, Niranjanakumari, Han, Gongshe, Mohassel, Payam, Gotkine, Marc, Doney, Elizabeth, Goldenberg, Paula, Tan, Queenie K G, Gong, Yi, Kleinstiver, Benjamin, Wishart, Brian, Cope, Heidi, Pires, Claudia Brito, Stutzman, Hannah, Spillmann, Rebecca C, Sadjadi, Reza, Elpeleg, Orly, Lee, Chia-Hsueh, Bellen, Hugo J, Edvardson, Simon, Eichler, Florian, Dunn, Teresa M

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Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate–binding region von Kelly, McKenna, Park, Meredith, Mihalek, Ivana, Pérez‐Palma, Eduardo, Anselm, Irina, Briere, Lauren C., High, Frances A., Sweetser, David A., Allard, Patrick, Ashley, Euan A., Bacino, Carlos A., Baker, Eva, Barseghyan, Hayk, Batzli, Gabriel F., Behnam, Babak, Bellen, Hugo J., Bernstein, Jonathan A., Bican, Anna, Bostwick, Bret L., Brush, Matthew, Burke, Elizabeth A., Burrage, Lindsay C., Butte, Manish J., Clark, Gary D., Colley, Heather A., Cooper, Cynthia M., Davids, Mariska, Dell’Angelica, Esteban C., Dorrani, Naghmeh, Douine, Emilie D., Emrick, Lisa T., Fairbrother, Laura, Fernandez, Liliana, Ferreira, Carlos, Fieg, Elizabeth L., Fisher, Paul G., Friedman, Noah D., Gahl, William A., Gourdine, Jean‐Philippe F., Groden, Catherine A., Gropman, Andrea L., Haendel, Melissa, Hom, Jason, Howerton, Ellen M., Jamal, Fariha, Jiang, Yong‐hui, Johnston, Jean M., Jones, Angela L., Karaviti, Lefkothea, Koeller, David M., Kohane, Isaac S., Koziura, Mary, Lalani, Seema R., Lazar, Jozef, Levy, Shawn E., Lincoln, Sharyn A., Maas, Richard L., Macnamara, Ellen F., MacRae, Calum A., Maduro, Valerie V., Majcherska, Marta M., Malicdan, May Christine V., Mamounas, Laura A., Manolio, Teri A., Markello, Thomas C., Marom, Ronit, Martínez‐Agosto, Julian A., May, Thomas, Morimoto, Marie, Mulvihill, John J., Murphy, Jennifer L., Nelson, Stan F., Newman, John H., Novacic, Donna, Orange, Jordan S., Potocki, Lorraine, Reuter, Chloe M., Rives, Lynette, Robertson, Amy K., Rodan, Lance H., Sampson, Jacinda B., Samson, Susan L., Schoch, Kelly, Silverman, Edwin K., Sinsheimer, Janet S., Smith, Kevin S., Spillmann, Rebecca C., Stong, Nicholas, Sullivan, Jennifer A., Waggott, Daryl M., Walsh, Chris A., Wangler, Michael F., Ward, Patricia A., Waters, Katrina M., Westerfield, Monte, Wheeler, Matthew T., Wise, Anastasia L., Worthey, Elizabeth A., Yoon, Amanda J., Zastrow, Diane B.

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Cigarette Purchasing Patterns, Readiness to Quit, and Quit Attempts Among Homeless Smokers von Wrighting, Quentaxia, Businelle, Michael S., Kendzor, Darla E., LeBlanc, Hannah, Reitzel, Lorraine R.

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Participation in a national diagnostic research study: assessing the patient experience von Rosenfeld, Lindsay E, LeBlanc, Kimberly, Nagy, Anna, Ego, Braeden K, McCray, Alexa T

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De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia von Kanca, Oguz, Andrews, Jonathan C., Patel, Chirag, Slavotinek, Anne M., Williams, Judy, Indaram, Maanasa, Lau, C. Christopher, Adams, David R., Agrawal, Pankaj, Bademci, Guney, Baker, Eva, Baldridge, Dustin, Bale, Jim, Batzli, Gabriel F., Bayrak-Toydemir, Pinar, Bernstein, Jonathan A., Bick, David P., Bohnsack, John, Briere, Lauren C., Carey, John, Cogan, Joy D., Cole, F. Sessions, D'Souza, Precilla, Dayal, Jyoti G., Dorset, Daniel C., Douine, Emilie D., Draper, David D., Duncan, Laura, Fieg, Elizabeth L., Forghani, Irman, Fresard, Laure, Godfrey, Rena A., Goldman, Alica M., Groden, Catherine A., Haendel, Melissa, Hayes, Nichole, Huang, Alden, Huang, Yong, Jones, Angela L., Krasnewich, Donna M., Kyle, Jennifer E., Lalani, Seema R., Lau, C. Christopher, Levy, Shawn E., Liu, Xue Zhong, Loo, Sandra K., Loscalzo, Joseph, Markello, Thomas C., Marth, Gabor, McConkie-Rosell, Allyn, Might, Matthew, Morimoto, Marie, Nelson, Stan F., Newberry, J. Scott, Newman, John H., Orengo, James P., Pak, Stephen, Pallais, J. Carl, Palmer, Christina G.S., Papp, Jeanette C., Parker, Neil H., Pusey, Barbara N., Quinlan, Aaron, Raja, Archana N., Rosenfeld, Jill A., Ruzhnikov, Maura, Samson, Susan L., Schaechter, Judy, Schedl, Timothy, Schoch, Kelly, Shakachite, Lisa, Sharma, Prashant, Shashi, Vandana, Shields, Kathleen, Sillari, Catherine H., Sinsheimer, Janet S., Smith, Kevin S., Solnica-Krezel, Lilianna, Spillmann, Rebecca C., Stong, Nicholas, Sweetser, David A., Tekin, Mustafa, Telischi, Fred, Tran, Alyssa A., Urv, Tiina K., Vogel, Tiphanie P., Wahl, Colleen E., Walley, Nicole M., Wang, Lee-kai, Wangler, Michael F., Wegner, Daniel, Wolfe, Lynne A., Worthey, Elizabeth A., Yu, Guoyun, Zhao, Chunli, Chung, Wendy K., Dobyns, William B., Adams, David R., Gahl, William A., Malicdan, May Christine V.

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An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids von Ruiter, Jos P.N., van Lint, Alida E.M., Pras-Raves, Mia, Wever, Eric, Guillen Sacoto, Maria J., Begtrup, Amber, Tarnopolsky, Mark, Sell, Susan L., Nowak, Catherine B., Douglas, Jessica, Perlman, Seth, Martin, Nicole, Brault, Jennifer, Gahl, William A., Alejandro, Mercedes E., Dai, Hongzheng, Dhar, Shweta U., Hanchard, Neil A., Lee, Brendan H., Moretti, Paolo M., Murdock, David R., Nicholas, Sarah K., Potocki, Lorraine, Scott, Daryl A., Eng, Christine M., Deardorff, Matthew, Hassey, Kelly, Sullivan, Kathleen, Tan, Queenie K.-G., Beggs, Alan H., Berry, Gerard T., Cooper, Cynthia M., Pallais, J. Carl, Rodan, Lance H., Kelley, Emily G., Morava, Eva, Forghani, Irman, Lam, Byron, Levitt, Roy, Liu, Xue Zhong, McCauley, Jacob, Tekin, Mustafa, Thorson, Willa, Findley, Laurie C., Krasnewich, Donna M., Manolio, Teri A., Goldrich, Madison P., Draper, David D., Nath, Avi, Pusey, Barbara N., Toro, Camilo, Baker, Eva, Gochuico, Bernadette, Mosbrook-Davis, Deborah, Rossignol, Francis, Adam, Margaret, Amendola, Laura, Cunningham, Michael, Jarvik, Gail P., Jarvik, Jeffrey, Lam, Christina, Raskind, Wendy, Sybert, Virginia, Ashley, Euan A., Coakley, Terra R., Hom, Jason, Majcherska, Marta M., Martin, Beth A., Marwaha, Shruti, Ruzhnikov, Maura, Tabor, Holly K., Tucker, Brianna M., Zastrow, Diane B., Byrd, William E., Dell’Angelica, Esteban C., Douine, Emilie D., Mak, Bryan C., Martin, Martin G., Martínez-Agosto, Julian A., McGee, Elisabeth, Nelson, Stanley F., Parker, Neil H., Sinsheimer, Janet S., Wang, Lee-kai, Perry, Katherine Wesseling, Woods, Jeremy D., Pace, Laura, Marth, Gabor, Viskochil, Dave, Bayrak-Toydemir, Pinar, Duncan, Laura, Robertson, Amy K., Solem, Emily, Schedl, Timothy, Shin, Jimann, Solnica-Krezel, Lilianna, Waisfisz, Quinten, Zwijnenburg, Petra J.G., Wanders, Ronald J.A., Vaz, Frédéric M.

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Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability von Dutta, Debdeep, Kanca, Oguz, Shridharan, Rishi V, Marcogliese, Paul C, Steger, Benjamin, Morimoto, Marie, Frost, F Graeme, Macnamara, Ellen, Wangler, Michael F, Yamamoto, Shinya, Jenny, Andreas, Adams, David, Malicdan, May C, Bellen, Hugo J

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Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations von Kurata, Harley T., Jamra, Rami Abou, Alkelai, Anna, Antonarakis, Stylianos E., Bolkier, Yoav, Dickson, Patricia, Donald, Kirsten A., Eliyahu, Aviva, Emrick, Lisa, Odent, Sylvie, Ortiz-Gonzalez, Xilma, Rosenfeld, Jill A., Skraban, Cara, Alejandro, Mercedes E., Azamian, Mahshid S., Chao, Hsiao-Tuan, Dai, Hongzheng, Dhar, Shweta U., Karaviti, Lefkothea, Lee, Brendan H., Rosenfeld, Jill A., Scott, Daryl A., Wangler, Michael F., Eng, Christine M., Sullivan, Kathleen, Goldstein, David B., McConkie-Rosell, Allyn, Schoch, Kelly, Shashi, Vandana, Beggs, Alan H., Cobban, Laurel A., Cooper, Cynthia M., Fieg, Elizabeth L., Korrick, Susan, Loscalzo, Joseph, Maas, Richard L., MacRae, Calum A., Stoler, Joan M., Nagy, Anna, Dasari, Surendra, Lanpher, Brendan C., Bivona, Stephanie, Isasi, Rosario, Levitt, Roy, Tekin, Mustafa, Thorson, Willa, Eckstein, David J., Mamounas, Laura A., D’Souza, Precilla, Ferreira, Carlos, Godfrey, Rena A., Groden, Catherine A., Macnamara, Ellen F., Maduro, Valerie V., Nath, Avi, Baker, Eva, Power, Bradley, Mosbrook-Davis, Deborah, Rossignol, Francis, Yousef, Muhammad, Amendola, Laura, Bamshad, Michael, Beck, Anita, Bennett, Jimmy, Blue, Elizabeth, Chanprasert, Sirisak, Glass, Ian, Jarvik, Gail P., Jarvik, Jeffrey, Mefford, Heather, Merritt, J. Lawrence, Raskind, Wendy, Sybert, Virginia, Wener, Mark, Wenger, Tara, Fisher, Paul G., Reuter, Chloe M., Smith, Kevin S., Zastrow, Diane B., Nakano-Okuno, Mariko, Whitlock, Jordan, Butte, Manish J., Fogel, Brent L., Krakow, Deborah, Lee, Hane, Palmer, Christina G.S., Papp, Jeanette C., Woods, Jeremy D., Andrews, Ashley, Pace, Laura, Viskochil, Dave, Bican, Anna, Kennedy, Jennifer, Cogan, Joy D., Cole, F. Sessions, Kiley, Dana, Sisco, Kathy, Schedl, Timothy, Solnica-Krezel, Lilianna, Pitt, Geoffrey S.

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Black breast cancer survivors experience greater upper extremity disability von Dean, Lorraine T., DeMichele, Angela, LeBlanc, Mously, Stephens-Shields, Alisa, Li, Susan Q., Colameco, Chris, Coursey, Morgan, Mao, Jun J.

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