Muscle function in A canine model of X-linked myotubular myopathy von Grange, Robert W., Doering, Jon, Mitchell, Erin, Holder, Melanie N., Guan, Xuan, Goddard, Melissa, Tegeler, Christopher, Beggs, Alan H., Childers, Martin K.

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Major publications in the critical care pharmacotherapy literature: 2019 von Condeni, Melanie Smith, Basting, Alyson T., Costello, Patrick G., DePriest, Ashley, Eriksson, Evert A., Evans, Heather, Hertel, Kristie, Holder, Andre L., Kester, Alyssa N., Kowalski, Kinsey R., Bell, Carolyn Magee, McLean, Barbara, Reichert, Michael, Santibañez, Melissa, Wieruszewski, Patrick M., Newsome, Andrea Sikora

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Persistent Short Sleep Duration From Pregnancy to 2 to 7 Years After Delivery and Metabolic Health von Kim, Minjee, Wiener, Laura Elizabeth, Gilbert, Jace, McNeil, Rebecca B, Reid, Kathryn J, Grobman, William A, Facco, Francesca, Haas, David M, Silver, Robert M, Greenland, Philip, Yee, Lynn M, Zee, Phyllis C

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SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile von Al-Jawahiri, Reem, Foroutan, Aidin, McConkey, Haley, Levy, Michael, Haghshenas, Sadegheh, Rooney, Kathleen, Turner, Jasmin, Shears, Debbie, Holder, Muriel, Lefroy, Henrietta, Castle, Bruce, Reis, Linda M., Semina, Elena V., Nickerson, Deborah, Bamshad, Michael, Leal, Suzanne, Lachlan, Katherine, Chandler, Kate, Clayton-Smith, Jill, Hug, Franziska Phan, Pitteloud, Nelly, Bartoloni, Lucia, Hoffjan, Sabine, Park, Soo-Mi, Thankamony, Ajay, Lees, Melissa, Wakeling, Emma, Naik, Swati, Hanker, Britta, Girisha, Katta M., Agolini, Emanuele, Giuseppe, Zampino, Alban, Ziegler, Tessarech, Marine, Keren, Boris, Afenjar, Alexandra, Zweier, Christiane, Smol, Thomas, Nobuhiko, Okamoto, Sekiguchi, Futoshi, Tsuchida, Naomi, Matsumoto, Naomichi, Kou, Ikuyo, Yonezawa, Yoshiro, Ikegawa, Shiro, Callewaert, Bert, Ambrose, John C., Arumugam, Prabhu, Bleda, Marta, Boardman-Pretty, Freya, Boustred, Christopher R., Brittain, Helen, Caulfield, Mark J., Chan, Georgia C., Fowler, Tom, Giess, Adam, Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J.P., Jones, Louise J., Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Leigh, Sarah E.A., Leong, Ivonne U.S., Lopez, Javier F., FionaMaleady-Crowe, McEntagart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C., Odhams, Chris A., Patch, Christine, Perez-Gil, Daniel, Pullinger, John, Rendon, Augusto, TimRogers, Savage, Kevin, Sawant, Kushmita, Scott, Richard H., Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C., Sosinsky, Alona, Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R.A., Thompson, Simon R., Tucci, Arianna, Williams, Eleanor, Kleinendorst, Lotte, Donaldson, Alan, Alders, Marielle, De Paepe, Anne, Sadikovic, Bekim, McNeill, Alisdair

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Chronic administration of a leupeptin-derived calpain inhibitor fails to ameliorate severe muscle pathology in a canine model of duchenne muscular dystrophy von Childers, Martin K, Bogan, Janet R, Bogan, Daniel J, Greiner, Hansel, Holder, Melanie, Grange, Robert W, Kornegay, Joe N

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The Phenotype of Leber Congenital Amaurosis in Patients With AIPL1 Mutations von Dharmaraj, Sharola, Leroy, Bart P, Sohocki, Melanie M, Koenekoop, Robert K, Perrault, Isabelle, Anwar, Khalid, Khaliq, Shagufta, Devi, R. Summathi, Birch, David G, De Pool, Elaine, Izquierdo, Natalio, Van Maldergem, Lionel, Ismail, Mohammad, Payne, Annette M, Holder, Graham E, Bhattacharya, Shomi S, Bird, Alan C, Kaplan, Josseline, Maumenee, Irene H

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