Change in approach and delivery of medical care in children with asthma: results from a multicenter emergency department educational asthma management program von Boychuk, Rodney B, Demesa, Charles J, Kiyabu, Kristi M, Yamamoto, Franklin, Yamamoto, Loren G, Sanderson, Ron, Gartner, Brenda, Donovan, Rebecca, Beckham, Sheila, Pang, Corilyn, Fanucchi, Rebecca, Chong, Valerie

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Therapy of highly active pediatric multiple sclerosis von Huppke, Peter, Huppke, Brenda, Ellenberger, David, Rostasy, Kevin, Hummel, Hannah, Stark, Wiebke, Brück, Wolfgang, Gärtner, Jutta

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Change in approach and delivery of medical care in children with asthma : Results from a multicenter emergency department educational asthma management program: Enhancing the role... von BOYCHUK, Rodney B, DEMESA, Charles J, FANUCCHI, Rebecca, CHONG, Valerie, KIYABU, Kristi M, YAMAMOTO, Franklin, YAMAMOTO, Loren G, SANDERSON, Ron, GARTNER, Brenda, DONOVAN, Rebecca, BECKHAM, Sheila, PANG, Corilyn

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Evaluation of secondhand smoking characteristics in asthmatic children presenting to four emergency departments on O'ahu, Hawai'i von Boychuk, Rodney B, Halm, Brunhild M, Garcia, Francisco, Yamamoto, Franklin Y, Sanderson, Ron R, Gartner, Brenda M, Beckham, Sheila, Fannucchi, Rebecca, Cadoy, Miguel, Day, Craig, Pang, Corilyn K S, Chong, Valerie, Kaahaaina, Darlene, Donavan, Rebecca, DeMesa, Charles J, Kiyabu, Kristi M

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Demographics and characteristics of wheezing/asthmatic children with repeat emergency department visits in O'ahu, Hawai'i von DeMesa, Charles J, Pang, Corilyn K S, Kiyabu, Kristi M, Yamamoto, Franklin Y, Sanderson, Ron R, Gartner, Brenda M, Beckham, Sheila, Asuncion, Daisy A, Nekoba, Ashlee C, Kitayama, Jonathan, Teruya, Brandon Y, Boychuk, Rodney B

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Acute disseminated encephalomyelitis followed by recurrent or monophasic optic neuritis in pediatric patients von Huppke, Peter, Rostasy, Kevin, Karenfort, Michael, Huppke, Brenda, Seidl, Rainer, Leiz, Steffen, Reindl, Markus, Gärtner, Jutta

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The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease von Ramoni, Rachel B., Mulvihill, John J., Adams, David R., Allard, Patrick, Ashley, Euan A., Gahl, William A., Loscalzo, Joseph, Adams, Christopher J., Alejandro, Mercedes E., Allard, Patrick, Ashley, Euan A., Azamian, Mashid S., Balasubramanyam, Ashok, Beggs, Alan H., Bellen, Hugo J., Bernstein, Jonathan A., Bick, David P., Birch, Camille L., Boone, Braden E., Briere, Lauren C., Brush, Matthew, Cogan, Joy D., Craigen, William J., Davids, Mariska, Dayal, Jyoti G., Dhar, Shweta U., Dipple, Katrina M., Dorrani, Naghmeh, Dorset, Daniel C., Eckstein, David J., Estwick, Tyra, Godfrey, Rena A., Goheen, Mitchell, Goldstein, David B., Gordon, Mary “Gracie” G., Gourdine, Jean-Philippe F., Haendel, Melissa, Hamid, Rizwan, Handley, Lori H., Hardee, Isabel, Holm, Ingrid A., Howerton, Ellen M., Jacob, Howard J., Jones, Angela L., Koehler, Alanna E., Kohler, Jennefer N., Krasnewich, Donna M., Kyle, Jennifer E., Latham, Lea, Lau, C. Christopher, Lazar, Jozef, Lee, Hane, Lee, Paul R., Levy, Shawn E., Levy, Denise J., Lewis, Richard A., Liebendorder, Adam P., Loomis, Carson R., Loscalzo, Joseph, Maas, Richard L., MacRae, Calum A., Manolio, Teri A., Markello, Thomas C., Mazur, Paul, McConkie-Rosell, Allyn, Metz, Thomas O., Might, Matthew, Moretti, Paolo M., Murphy, Jennifer L., Muzny, Donna M., Nehrebecky, Michele E., Nelson, Stan F., Newman, John H., Nicholas, Sarah K., Palmer, Christina G.S., Phillips, John A., Postlethwait, John H., Rosenfeld, Jill A., Schaffer, Katherine E., Schroeder, Molly C., Scott, Daryl A., Shashi, Vandana, Silverman, Edwin K., Sinsheimer, Janet S., Spillmann, Rebecca C., Stoler, Joan M., Stong, Nicholas, Sullivan, Jennifer A., Tolman, Nathanial J., Tran, Alyssa A., Valivullah, Zaheer M., Waggott, Daryl M., Walsh, Chris A., Wangler, Michael F., Warburton, Mike, Ward, Patricia A., Waters, Katrina M., Wheeler, Matthew T., Yu, Guoyun, Wise, Anastasia L.

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Trial of Fingolimod versus Interferon Beta-1a in Pediatric Multiple Sclerosis von Chitnis, Tanuja, Arnold, Douglas L, Banwell, Brenda, Brück, Wolfgang, Ghezzi, Angelo, Giovannoni, Gavin, Greenberg, Benjamin, Krupp, Lauren, Rostásy, Kevin, Tardieu, Marc, Waubant, Emmanuelle, Wolinsky, Jerry S, Bar-Or, Amit, Stites, Tracy, Chen, Yu, Putzki, Norman, Merschhemke, Martin, Gärtner, Jutta

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Standards for the care of people with cystic fibrosis; establishing and maintaining health von Southern, Kevin W, Addy, Charlotte, Bell, Scott C, Bevan, Amanda, Borawska, Urzula, Brown, Catherine, Burgel, Pierre-Régis, Button, Brenda, Castellani, Carlo, Chansard, Audrey, Chilvers, Mark A, Davies, Gwyneth, Davies, Jane C, De Boeck, Kris, Declercq, Dimitri, Doumit, Michael, Drevinek, Pavel, Fajac, Isabelle, Gartner, Silvia, Georgiopoulos, Anna M, Gursli, Sandra, Gramegna, Andrea, Hansen, Carina ME, Hug, Martin J, Lammertyn, Elise, Landau, Edwina (Eddie) C., Langley, Ross, Mayer-Hamblett, Nicole, Middleton, Anna, Middleton, Peter G, Mielus, Monika, Morrison, Lisa, Munck, Anne, Plant, Barry, Ploeger, Maarten, Bertrand, Dominique Pougheon, Pressler, Tacjana, Quon, Bradley S, Radtke, Thomas, Saynor, Zoe L, Shufer, Ilan, Smyth, Alan R, Smith, Chris, van Koningsbruggen-Rietschel, Silke

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Dossier: Gartner Inc von Duvall, Mel

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Mutations in TAF8 cause a neurodegenerative disorder von Wong, Keit Men, Jepsen, Wayne M, Efthymiou, Stephanie, Salpietro, Vincenzo, Sanchez-Castillo, Meredith, Yip, Janice, Kriouile, Yamna, Diegmann, Susann, Dreha-Kulaczewski, Steffi, Altmüller, Janine, Thiele, Holger, Nürnberg, Peter, Toosi, Mehran Beiraghi, Akhondian, Javad, Ghayoor Karimiani, Ehsan, Hummel-Abmeier, Hannah, Huppke, Brenda, Houlden, Henry, Gärtner, Jutta, Maroofian, Reza, Huppke, Peter

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Association of Obesity With Multiple Sclerosis Risk and Response to First-line Disease Modifying Drugs in Children von Huppke, Brenda, Ellenberger, David, Hummel, Hannah, Stark, Wiebke, Röbl, Markus, Gärtner, Jutta, Huppke, Peter

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Standards for the care of people with cystic fibrosis; establishing and maintaining health von Southern, Kevin W, Addy, Charlotte, Bell, Scott C, Bevan, Amanda, Borawska, Urzula, Brown, Catherine, Burgel, Pierre-Régis, Button, Brenda, Castellani, Carlo, Chansard, Audrey, Chilvers, Mark, Davies, Gwyneth, Davies, Jane C, De Boeck, Kris, Declercq, Dimitri, Doumit, Michael, Drevinek, Pavel, Fajac, Isabelle, Gartner, Silvia, Georgiopoulos, Anna M, Gursli, Sandra, Gramegna, Andrea, Hansen, Carina M E, Hug, Martin J, Lammertyn, Elise, Landau, Edwina (Eddie) C, Langley, Ross, Mayer-Hamblett, Nicole, Middleton, Anna, Middleton, Peter G, Radtke, Thomas

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Activating de novo mutations in NFE2L2 encoding NRF2 cause a multisystem disorder von Huppke, Peter, Weissbach, Susann, Church, Joseph A., Schnur, Rhonda, Krusen, Martina, Dreha-Kulaczewski, Steffi, Kühn-Velten, W. Nikolaus, Wolf, Annika, Huppke, Brenda, Millan, Francisca, Begtrup, Amber, Almusafri, Fatima, Thiele, Holger, Altmüller, Janine, Nürnberg, Peter, Müller, Michael, Gärtner, Jutta

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Pretreatment Neurofilament Light Chain Serum Levels, Early Disease Severity, and Treatment Response in Pediatric Multiple Sclerosis von Huppke, Brenda, Reinert, Marie-Christine, Hummel-Abmeier, Hannah, Stark, Wiebke, Gärtner, Jutta, Huppke, Peter

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Evaluation of Novel Enhancer Compounds in Gentamicin-Mediated Readthrough of Nonsense Mutations in Rett Syndrome von Wong, Keit Men, Wegener, Eike, Baradaran-Heravi, Alireza, Huppke, Brenda, Gärtner, Jutta, Huppke, Peter

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Phase II safety, tolerability, and dose selection study of isradipine as a potential disease-modifying intervention in early Parkinson's disease (STEADY-PD) von Parkinson Study Group

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Temporal profile of lymphocyte counts and relationship with infections with fingolimod therapy in paediatric patients with multiple sclerosis: Results from the PARADIGMS study von Chitnis, Tanuja, Banwell, Brenda, Krupp, Lauren, Arnold, Douglas L, Bar-Or, Amit, Brück, Wolfgang, Giovannoni, Gavin, Greenberg, Benjamin, Ghezzi, Angelo, Waubant, Emmanuelle, Rostasy, Kevin, Deiva, Kumaran, Huppke, Peter, Wolinsky, Jerry S, Zhang, Ying, Azmon, Amin, K-Laflamme, Annik, Karan, Rajesh, Gärtner, Jutta

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A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy von Brodehl, Andreas, Weiss, Jürgen, Debus, Jana Davina, Stanasiuk, Caroline, Klauke, Bärbel, Deutsch, Marcus André, Fox, Henrik, Bax, Jördis, Ebbinghaus, Hans, Gärtner, Anna, Tiesmeier, Jens, Laser, Thorsten, Peterschröder, Andreas, Gerull, Brenda, Gummert, Jan, Paluszkiewicz, Lech, Milting, Hendrik

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Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset von Brodehl, Andreas, Meshkov, Alexey, Myasnikov, Roman, Kiseleva, Anna, Kulikova, Olga, Klauke, Bärbel, Sotnikova, Evgeniia, Stanasiuk, Caroline, Divashuk, Mikhail, Pohl, Greta Marie, Kudryavtseva, Maria, Klingel, Karin, Gerull, Brenda, Zharikova, Anastasia, Gummert, Jan, Koretskiy, Sergey, Schubert, Stephan, Mershina, Elena, Gärtner, Anna, Pilus, Polina, Laser, Kai Thorsten, Sinitsyn, Valentin, Boytsov, Sergey, Drapkina, Oxana, Milting, Hendrik

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