Mutations in the thyroid transcription factor gene NKX2-1 result in decreased expression of SFTPB and SFTPC von Attarian, Stephanie J, Leibel, Sandra L, Yang, Ping, Alfano, Danielle N, Hackett, Brian P, Cole, F Sessions, Hamvas, Aaron

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Minoxidil‐Associated Anorexia in an Infant with Refractory Hypertension von Vesoulis, Zachary A., Attarian, Stephanie J., Zeller, Brandy, Cole, Francis Sessions

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The neurodevelopmental impact of neonatal morphine administration von Attarian, Stephanie, Tran, Lan Chi, Moore, Aimee, Stanton, George, Meyer, Eric, Moore, Robert P

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Improving Postpartum Breast Pumping in Mothers of Babies in the NICU von Kaur, Karampreet, Zuckerwise, Lisa, Attarian, Stephanie, Dye, Mary

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Minoxidil-Associated Anorexia in an Infant with Refractory Hypertension von Vesoulis, Zachary A., Attarian, Stephanie J., Zeller, Brandy, Cole, Francis Sessions

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MUSK, a new target for mutations causing congenital myasthenic syndrome von Chevessier, Frédéric, Faraut, Brice, Ravel-Chapuis, Aymeric, Richard, Pascale, Gaudon, Karen, Bauché, Stéphanie, Prioleau, Cassandra, Herbst, Ruth, Goillot, Evelyne, Ioos, Christine, Azulay, Jean-Philippe, Attarian, Shahram, Leroy, Jean-Paul, Fournier, Emmanuel, Legay, Claire, Schaeffer, Laurent, Koenig, Jeanine, Fardeau, Michel, Eymard, Bruno, Pouget, Jean, Hantaï, Daniel

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Safety and efficacy of cipaglucosidase alfa plus miglustat versus alglucosidase alfa plus placebo in late-onset Pompe disease (PROPEL): an international, randomised, double-blind,... von Schoser, Benedikt, Roberts, Mark, Byrne, Barry J, Sitaraman, Sheela, Jiang, Hai, Laforêt, Pascal, Toscano, Antonio, Castelli, Jeff, Díaz-Manera, Jordi, Goldman, Mitchell, van der Ploeg, Ans T, Bratkovic, Drago, Kuchipudi, Srilakshmi, Mozaffar, Tahseen, Kishnani, Priya S, Sebok, Agnes, Pestronk, Alan, Dominovic-Kovacevic, Aleksandra, Khan, Aneal, Koritnik, Blaž, Tard, Celine, Lindberg, Christopher, Quinn, Colin, Eldridge, Crystal, Bodkin, Cynthia, Reyes-Leiva, David, Hughes, Derralynn, Stefanescu, Ela, SALORT-CAMPANA, Emmanuelle, Butler, Ernest, Bouhour, Francoise, Kim, Gee, Konstantinos Papadimas, George, Parenti, Giancarlo, Bartosik-Psujek, Halina, Kushlaf, Hani, Akihiro, Hashiguchi, Lau, Heather, Pedro, Helio, Andersen, Henning, Amartino, Hernan, Shiraishi, Hideaki, Kobayashi, Hiroshi, Tarnev, Ivaylo, Vengoechea, Jaime, Avelar, Jennifer, Shin, Jin-Hong, Cauci, Jonathan, Alonso-Pérez, Jorge, Janszky, Jozsef, Berthy, Julie, Cornelia, Kornblum, Gutschmidt, Kristina, Claeys, Kristl, Judit Molnar, Maria, Wencel, Marie, Tarnopolsky, Mark, Dimachkie, Mazen, Tchan, Michel, Freimer, Miriam, Longo, Nicola, Vidal-Fernandez, Nuria, Musumeci, Olimpia, Goker-Alpan, Ozlem, Deegan, Patrick, Clemens, Paula R., Roxburgh, Richard, Henderson, Robert, Hopkin, Robert, Sacconi, Sabrina, Fecarotta, Simona, Attarian, Shahram, Wenninger, Stephan, Dearmey, Stephanie, Hiwot, Tarekegn, Burrow, Thomas, Ruck, Tobias, Sawada, Tomo, Laszlo, Vescei, Löscher, Wolfgang, Chien, Yin-Hsiu

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0046 Is Eating Close to the Dim Light Melatonin Onset Associated with Body Mass Index? von Culnan, Elizabeth, Zee, Phyllis C, Attarian, Hrayr, Crowley, Stephanie J, Baron, Kelly G

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Assessing the upper motor neuron in amyotrophic lateral sclerosis using the triple stimulation technique: A multicenter prospective study von Grapperon, Aude-Marie, Verschueren, Annie, Jouve, Elisabeth, Morizot-Koutlidis, Régine, Lenglet, Timothée, Pradat, Pierre-François, Salachas, François, Bernard, Emilien, Delstanche, Stéphanie, Maertens de Noordhout, Alain, Guy, Nathalie, Danel, Véronique, Delval, Arnaud, Delmont, Emilien, Rolland, Anne-Sophie, PULSE Study Group, Jomir, Laurent, Devos, David, Wang, François, Attarian, Shahram

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104-week efficacy and safety of cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a phase III open-label extension study (ATB200-07) von Schoser, Benedikt, Kishnani, Priya S., Bratkovic, Drago, Byrne, Barry J., Claeys, Kristl G., Díaz-Manera, Jordi, Laforêt, Pascal, Roberts, Mark, Toscano, Antonio, van der Ploeg, Ans T., Castelli, Jeff, Goldman, Mitchell, Holdbrook, Fred, Sitaraman Das, Sheela, Wasfi, Yasmine, Mozaffar, Tahseen

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Switching treatment to cipaglucosidase alfa plus miglustat positively affects patient-reported outcome measures in patients with late-onset Pompe disease von Kishnani, Priya S., Byrne, Barry J., Claeys, Kristl G., Díaz-Manera, Jordi, Dimachkie, Mazen M., Kushlaf, Hani, Mozaffar, Tahseen, Roberts, Mark, Schoser, Benedikt, Hummel, Noemi, Kopiec, Agnieszka, Holdbrook, Fred, Shohet, Simon, Toscano, Antonio

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MUSK, a new target for mutations causing congenital myasthenic syndrome von Chevessier, Frédéric, Faraut, Brice, Ravel-Chapuis, Aymeric, Richard, Pascale, Gaudon, Karen, Bauché, Stéphanie, Prioleau, Cassandra, Herbst, Ruth, Goillot, Evelyne, Ioos, Christine, Azulay, Jean-Philippe, Attarian, Shahram, Leroy, Jean-Paul, Fournier, Emmanuel, Legay, Claire, Schaeffer, Laurent, Koenig, Jeanine, Fardeau, Michel, Eymard, Bruno, Pouget, Jean, Hantaï, Daniel

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Mutations in MUSK cause congenital myasthenic syndrome von Chevessier, Frédéric, Faraut, Brice, Ravel-Chapuis, Aymeric, Richard, Pascale, Gaudon, Karen, Bauché, Stéphanie, Prioleau, Cassandra, Herbst, Ruth, Goillot, Evelyne, Ioos, Christine, Azulay, Jean-Philippe, Attarian, Shahram, Leroy, Jean-Paul, Fournier, Emmanuel, Legay, Claire, Schaeffer, Laurent, Koenig, Jeanine, Fardeau, Michel, Eymard, Bruno, Pouget, Jean, Hantaï, Daniel

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Pathophysiological characterization of congenital myasthenic syndromes: the example of mutations in the MUSK gene von Chevessier, Frédéric, Faraut, Brice, Ravel-Chapuis, Aymeric, Richard, Pascale, Gaudon, Karen, Bauché, Stéphanie, Prioleau, Cassandra, Herbst, Ruth, Goillot, Evelyne, Ioos, Christine, Azulay, Jean-Philippe, Attarian, Shahram, Leroy, Jean-Paul, Fournier, Emmanuel, Legay, Claire, Schaeffer, Laurent, Koenig, Jeanine, Fardeau, Michel, Eymard, Bruno, Pouget, Jean, Hantaï, Daniel

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Caractérisation physiopathologique des syndromes myasthéniques congénitaux : l'exemple de mutations dans le gène MUSK von Chevessier, Frédéric, Faraut, Brice, Ravel-Chapuis, Aymeric, Richard, Pascale, Gaudon, Karen, Bauché, Stéphanie, Prioleau, Cassandra, Herbst, Ruth, Goillot, Evelyne, Ioos, Christine, Azulay, Jean-Philippe, Attarian, Shahram, Leroy, Jean-Paul, Fournier, Emmanuel, Legay, Claire, Schaeffer, Laurent, Koenig, Jeanine, Fardeau, Michel, Eymard, Bruno, Pouget, Jean, Hantaï, Daniel

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Caractérisation physiopathologique des syndromes myasthéniques congénitaux : l'exemple de mutations dans le gène MUSK von Chevessier, Frédéric, Faraut, Brice, Ravel-Chapuis, Aymeric, Richard, Pascale, Gaudon, Karen, Bauché, Stéphanie, Prioleau, Cassandra, Herbst, Ruth, Goillot, Evelyne, Ioos, Christine, Azulay, Jean-Philippe, Attarian, Shahram, Leroy, Jean-Paul, Fournier, Emmanuel, Legay, Claire, Schaeffer, Laurent, Koenig, Jeanine, Fardeau, Michel, Eymard, Bruno, Pouget, Jean, Hantaï, Daniel

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