Web-Based Mindfulness-Based Interventions for Well-being: Randomized Comparative Effectiveness Trial
Sylvia, Louisa G, Lunn, Mitchell R, Obedin-Maliver, Juno, McBurney, Robert N, Nowell, W Benjamin, Nosheny, Rachel L, Mularski, Richard A, Long, Millie D, Merkel, Peter A, Pletcher, Mark J, Tovey, Roberta E, Scalchunes, Christopher, Sutphen, Rebecca, Martin, Ann S, Horn, Elizabeth J, O'Boyle, Megan, Pitch, Lisa, Seid, Michael, Redline, Susan, Greenebaum, Sophie, George, Nevita, French, Noah J, Faria, Caylin M, Puvanich, Nicha, Rabideau, Dustin J, Selvaggi, Caitlin A, Yu, Chu, Faraone, Stephen V, Venkatachalam, Shilpa, McCall, Debbe, Terry, Sharon F, Deckersbach, Thilo, Nierenberg, Andrew A
Published in Journal of medical Internet research (12.09.2022)
Published in Journal of medical Internet research (12.09.2022)
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The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations
Bladen, Catherine L., Salgado, David, Monges, Soledad, Foncuberta, Maria E., Kekou, Kyriaki, Kosma, Konstantina, Dawkins, Hugh, Lamont, Leanne, Roy, Anna J., Chamova, Teodora, Guergueltcheva, Velina, Chan, Sophelia, Korngut, Lawrence, Campbell, Craig, Dai, Yi, Wang, Jen, Barišić, Nina, Brabec, Petr, Lahdetie, Jaana, Walter, Maggie C., Schreiber-Katz, Olivia, Karcagi, Veronika, Garami, Marta, Viswanathan, Venkatarman, Bayat, Farhad, Buccella, Filippo, Kimura, En, Koeks, Zaïda, van den Bergen, Janneke C., Rodrigues, Miriam, Roxburgh, Richard, Lusakowska, Anna, Kostera-Pruszczyk, Anna, Zimowski, Janusz, Santos, Rosário, Neagu, Elena, Artemieva, Svetlana, Rasic, Vedrana Milic, Vojinovic, Dina, Posada, Manuel, Bloetzer, Clemens, Jeannet, Pierre-Yves, Joncourt, Franziska, Díaz-Manera, Jordi, Gallardo, Eduard, Karaduman, A. Ayşe, Topaloğlu, Haluk, El Sherif, Rasha, Stringer, Angela, Shatillo, Andriy V., Martin, Ann S., Peay, Holly L., Bellgard, Matthew I., Kirschner, Jan, Flanigan, Kevin M., Straub, Volker, Bushby, Kate, Verschuuren, Jan, Aartsma-Rus, Annemieke, Béroud, Christophe, Lochmüller, Hanns
Published in Human mutation (01.04.2015)
Published in Human mutation (01.04.2015)
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Delays in diagnosis of Duchenne muscular dystrophy: An evaluation of genotypic and sociodemographic factors
Counterman, Kevin J., Furlong, Pat, Wang, Richard T., Martin, Ann S.
Published in Muscle & nerve (01.01.2020)
Published in Muscle & nerve (01.01.2020)
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DMD genotype correlations from the Duchenne Registry: Endogenous exon skipping is a factor in prolonged ambulation for individuals with a defined mutation subtype
Wang, Richard T., Barthelemy, Florian, Martin, Ann S., Douine, Emilie D., Eskin, Ascia, Lucas, Ann, Lavigne, Jenifer, Peay, Holly, Khanlou, Negar, Sweeney, Lee, Cantor, Rita M., Miceli, M. Carrie, Nelson, Stanley F.
Published in Human mutation (01.09.2018)
Published in Human mutation (01.09.2018)
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Evaluating Implementation of the Updated Care Considerations for Duchenne Muscular Dystrophy
Ong, Katherine S, Kinnett, Kathi, Soelaeman, Rieza, Webb, Lauren, Bain, Jennifer S, Martin, Ann S, Westfield, Christina, Bolen, Julie, Street, Natalie
Published in Pediatrics (Evanston) (01.10.2018)
Published in Pediatrics (Evanston) (01.10.2018)
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Journal Article
Genetic counseling for the dystrophinopathies-Practice resource of the National Society of Genetic Counselors
Pickart, Angela M, Martin, Ann S, Gross, Brianna N, Dellefave-Castillo, Lisa M, McCallen, Leslie M, Nagaraj, Chinmayee B, Rippert, Alyssa L, Schultz, Catherine P, Ulm, Elizabeth A, Armstrong, Niki
Published in Journal of genetic counseling (29.04.2024)
Published in Journal of genetic counseling (29.04.2024)
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Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database
Koeks, Zaïda, Bladen, Catherine L., Salgado, David, van Zwet, Erik, Pogoryelova, Oksana, McMacken, Grace, Monges, Soledad, Foncuberta, Maria E., Kekou, Kyriaki, Kosma, Konstantina, Dawkins, Hugh, Lamont, Leanne, Bellgard, Matthew I., Roy, Anna J., Chamova, Teodora, Guergueltcheva, Velina, Chan, Sophelia, Korngut, Lawrence, Campbell, Craig, Dai, Yi, Wang, Jen, Barišić, Nina, Brabec, Petr, Lähdetie, Jaana, Walter, Maggie C., Schreiber-Katz, Olivia, Karcagi, Veronika, Garami, Marta, Herczegfalvi, Agnes, Viswanathan, Venkatarman, Bayat, Farhad, Buccella, Filippo, Ferlini, Alessandra, Kimura, En, van den Bergen, Janneke C., Rodrigues, Miriam, Roxburgh, Richard, Lusakowska, Anna, Kostera-Pruszczyk, Anna, Santos, Rosário, Neagu, Elena, Artemieva, Svetlana, Rasic, Vedrana Milic, Vojinovic, Dina, Posada, Manuel, Bloetzer, Clemens, Klein, Andrea, Díaz-Manera, Jordi, Gallardo, Eduard, Karaduman, A. Ayşe, Oznur, Tunca, Topaloğlu, Haluk, El Sherif, Rasha, Stringer, Angela, Shatillo, Andriy V., Martin, Ann S., Peay, Holly L., Kirschner, Jan, Flanigan, Kevin M., Straub, Volker, Bushby, Kate, Béroud, Christophe, Verschuuren, Jan J., Lochmüller, Hanns
Published in Journal of neuromuscular diseases (21.11.2017)
Published in Journal of neuromuscular diseases (21.11.2017)
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The TREAT-NMD Duchenne Muscular Dystrophy Registries: Conception, Design, and Utilization by Industry and Academia
Bladen, Catherine L., Rafferty, Karen, Straub, Volker, Monges, Soledad, Moresco, Angélica, Dawkins, Hugh, Roy, Anna, Chamova, Teodora, Guergueltcheva, Velina, Korngut, Lawrence, Campbell, Craig, Dai, Yi, Barišić, Nina, Kos, Tea, Brabec, Petr, Rahbek, Jes, Lahdetie, Jaana, Tuffery-Giraud, Sylvie, Claustres, Mireille, Leturcq, France, Ben Yaou, Rabah, Walter, Maggie C., Schreiber, Olivia, Karcagi, Veronika, Herczegfalvi, Agnes, Viswanathan, Venkatarman, Bayat, Farhad, de la caridad Guerrero Sarmiento, Isis, Ambrosini, Anna, Ceradini, Francesca, Kimura, En, van den Bergen, Janneke C., Rodrigues, Miriam, Roxburgh, Richard, Lusakowska, Anna, Oliveira, Jorge, Santos, Rosário, Neagu, Elena, Butoianu, Niculina, Artemieva, Svetlana, Rasic, Vedrana Milic, Posada, Manuel, Palau, Francesc, Lindvall, Björn, Bloetzer, Clemens, Karaduman, Ayşe, Topaloğlu, Haluk, Inal, Serap, Oflazer, Piraye, Stringer, Angela, Shatillo, Andriy V., Martin, Ann S., Peay, Holly, Flanigan, Kevin M., Salgado, David, von Rekowski, Brigitta, Lynn, Stephen, Heslop, Emma, Gainotti, Sabina, Taruscio, Domenica, Kirschner, Jan, Verschuuren, Jan, Bushby, Kate, Béroud, Christophe, Lochmüller, Hanns
Published in Human mutation (01.11.2013)
Published in Human mutation (01.11.2013)
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Evidence-Based Consensus and Systematic Review on Reducing the Time to Diagnosis of Duchenne Muscular Dystrophy
Aartsma-Rus, Annemieke, Hegde, Madhuri, Ben-Omran, Tawfeg, Buccella, Filippo, Ferlini, Alessandra, Gallano, Pia, Howell, R. Rodney, Leturcq, France, Martin, Ann S., Potulska-Chromik, Anna, Saute, Jonas A., Schmidt, Wolfgang M., Sejersen, Thomas, Tuffery-Giraud, Sylvie, Uyguner, Zehra Oya, Witcomb, Luci A., Yau, Shu, Nelson, Stanley F.
Published in The Journal of pediatrics (01.01.2019)
Published in The Journal of pediatrics (01.01.2019)
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Draft Guidance for Industry Duchenne Muscular Dystrophy, Becker Muscular Dystrophy, and Related Dystrophinopathies – Developing Potential Treatments for the Entire Spectrum of Disease
McDonald, Craig, Camino, Eric, Escandon, Rafael, Finkel, Richard S., Fischer, Ryan, Flanigan, Kevin, Furlong, Pat, Juhasz, Rose, Martin, Ann S., Villa, Chet, Sweeney, H. Lee
Published in Journal of neuromuscular diseases (05.03.2024)
Published in Journal of neuromuscular diseases (05.03.2024)
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Associations Between Self-Reported Behavioral and Learning Concerns and DMD Isoforms in Duchenne Muscular Dystrophy
Counterman, Kevin J., Fatovic, Kathy, Good, Daniel C., Martin, Ann S., Dasgupta, Sonali, Anziska, Yaacov
Published in Journal of neuromuscular diseases (01.01.2022)
Published in Journal of neuromuscular diseases (01.01.2022)
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Clinical Phenotypes of DMD Exon 51 Skip Equivalent Deletions: A Systematic Review
Waldrop, Megan A., Yaou, Rabah Ben, Lucas, Karin K., Martin, Ann S., O’Rourke, Erin, Ferlini, Alessandra, Muntoni, Francesco, Leturcq, France, Tuffery-Giraud, Sylvie, Weiss, Robert B., Flanigan, Kevin M.
Published in Journal of neuromuscular diseases (01.01.2020)
Published in Journal of neuromuscular diseases (01.01.2020)
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Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats
Stankiewicz, Paweł, Kulkarni, Shashikant, Dharmadhikari, Avinash V., Sampath, Srirangan, Bhatt, Samarth S., Shaikh, Tamim H., Xia, Zhilian, Pursley, Amber N., Cooper, M. Lance, Shinawi, Marwan, Paciorkowski, Alex R., Grange, Dorothy K., Noetzel, Michael J., Saunders, Scott, Simons, Paul, Summar, Marshall, Lee, Brendan, Scaglia, Fernando, Fellmann, Florence, Martinet, Danielle, Beckmann, Jacques S., Asamoah, Alexander, Platky, Kathryn, Sparks, Susan, Martin, Ann S., Madan-Khetarpal, Suneeta, Hoover, Jacqueline, Medne, Livija, Bonnemann, Carsten G., Moeschler, John B., Vallee, Stephanie E., Parikh, Sumit, Irwin, Polly, Dalzell, Victoria P., Smith, Wendy E., Banks, Valerie C., Flannery, David B., Lovell, Carolyn M., Bellus, Gary A., Golden-Grant, Kathryn, Gorski, Jerome L., Kussmann, Jennifer L., McGregor, Tracy L., Hamid, Rizwan, Pfotenhauer, Jean, Ballif, Blake C., Shaw, Chad A., Kang, Sung-Hae L., Bacino, Carlos A., Patel, Ankita, Rosenfeld, Jill A., Cheung, Sau Wai, Shaffer, Lisa G.
Published in Human mutation (01.01.2012)
Published in Human mutation (01.01.2012)
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Prevalence, Clinical Profile and Risk Factors of Cefepime Induced Neurotoxicity among Chronic Kidney Disease Patients in a Tertiary Hospital in Southern Philippines: PUB367
Serenina-Martin, Ann Kristine S., Querequincia, Karen Ann
Published in Journal of the American Society of Nephrology (01.11.2023)
Published in Journal of the American Society of Nephrology (01.11.2023)
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Cover Image, Volume 39, Issue 9
Wang, Richard T., Barthelemy, Florian, Martin, Ann S., Douine, Emilie D., Eskin, Ascia, Lucas, Ann, Lavigne, Jenifer, Peay, Holly, Khanlou, Negar, Sweeney, Lee, Cantor, Rita M., Miceli, M. Carrie, Nelson, Stanley F.
Published in Human mutation (01.09.2018)
Published in Human mutation (01.09.2018)
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Knowledge of carrier status and barriers to testing among mothers of sons with duchenne or becker muscular dystrophy
Bogue, Lauren, MS, Peay, Holly, PhD, Martin, Ann, MS, Lucas, Ann, MS, Ramchandren, Sindhu, MD, MS
Published in Neuromuscular disorders : NMD (01.12.2016)
Published in Neuromuscular disorders : NMD (01.12.2016)
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Journal Article
Online Self-Report Data for Duchenne Muscular Dystrophy confirms natural history and can be used to assess for therapeutic benefits
Wang, Richard T, Silverstein Fadlon, Cheri A, Ulm, J Wes, Jankovic, Ivana, Eskin, Ascia, Lu, Ake, Miller, Vanessa, Cantor, Rita M, Li, Ning, Elashoff, Robert, Martin, Ann S, Peay, Holly, Nelson, Stanley F
Published in bioRxiv (08.12.2014)
Published in bioRxiv (08.12.2014)
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