Comparison of FilmArray Respiratory Panel and laboratory-developed real-time reverse transcription–polymerase chain reaction assays for respiratory virus detection von Renaud, Christian, Crowley, Janet, Jerome, Keith R, Kuypers, Jane

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Differential Expression of Cholesterol Hydroxylases in Alzheimer's Disease von Brown, 3rd, James, Theisler, Catherine, Silberman, Simone, Magnuson, Debra, Gottardi-Littell, Numa, Lee, John M, Yager, Debra, Crowley, Janet, Sambamurti, Kumar, Rahman, Mohammad M, Reiss, Allison B, Eckman, Christopher B, Wolozin, Benjamin

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Rule-Out Outbreak: 24-Hour Metagenomic Next-Generation Sequencing for Characterizing Respiratory Virus Source for Infection Prevention von Greninger, Alexander L., Waghmare, Alpana, Adler, Amanda, Qin, Xuan, Crowley, Janet L., Englund, Janet A., Kuypers, Jane M., Jerome, Keith R., Zerr, Danielle M.

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52; A Quality Improvement Initiative in the Stroke Rehabilitation Unit von Craven, Fiona, Noel, Suzanne, Doyle, Rachael, Bourke, Laura, McCaffrey, Kate, Crowley, Janet, Mullen, Eithne, Doyle, Siobhan

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52A Quality Improvement Initiative in the Stroke Rehabilitation Unit von Craven, Fiona, Noel, Suzanne, Doyle, Rachael, Bourke, Laura, McCaffrey, Kate, Crowley, Janet, Mullen, Eithne, Doyle, Siobhan

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Strategies to avoid the mis-identification of anatoxin-a using mass spectrometry in the forensic investigation of acute neurotoxic poisoning von Furey, Ambrose, Crowley, Janet, Hamilton, Brett, Lehane, Mary, James, Kevin J.

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Anatoxins and degradation products, determined using hybrid quadrupole time-of-flight and quadrupole ion-trap mass spectrometry: forensic investigations of cyanobacterial neurotoxi... von James, Kevin J., Crowley, Janet, Hamilton, Brett, Lehane, Mary, Skulberg, Olav, Furey, Ambrose

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Liquid chromatography with electrospray ion-trap mass spectrometry for the determination of anatoxins in cyanobacteria and drinking water von Furey, Ambrose, Crowley, Janet, Lehane, Mary, James, Kevin J.

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The first identification of the rare cyanobacterial toxin, homoanatoxin-a, in Ireland von Furey, Ambrose, Crowley, Janet, Shuilleabhain, Aine Ni, Skulberg, Olav M, James, Kevin J

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Oligogenic basis of isolated gonadotropin-releasing hormone deficiency von Sykiotis, Gerasimos P., Plummer, Lacey, Hughes, Virginia A., Au, Margaret, Durrani, Sadia, Nayak-Young, Sadhana, Dwyer, Andrew A., Quinton, Richard, Hall, Janet E., Gusella, James F., Seminara, Stephanie B., Crowley, William F., Pitteloud, Nelly, Donahoe, Patricia K.

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Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism von Miraoui, Hichem, Dwyer, Andrew A., Sykiotis, Gerasimos P., Plummer, Lacey, Chung, Wilson, Feng, Bihua, Beenken, Andrew, Clarke, Jeff, Pers, Tune H., Dworzynski, Piotr, Keefe, Kimberley, Niedziela, Marek, Raivio, Taneli, Crowley, William F., Seminara, Stephanie B., Quinton, Richard, Hughes, Virginia A., Kumanov, Philip, Young, Jacques, Yialamas, Maria A., Hall, Janet E., Van Vliet, Guy, Chanoine, Jean-Pierre, Rubenstein, John, Mohammadi, Moosa, Tsai, Pei-San, Sidis, Yisrael, Lage, Kasper, Pitteloud, Nelly

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Mutations in Fibroblast Growth Factor Receptor 1 Cause Both Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism von Pitteloud, Nelly, Acierno, James S., Meysing, Astrid, Eliseenkova, Anna V., Ma, Jinghong, Ibrahimi, Omar A., Metzger, Daniel L., Hayes, Frances J., Dwyer, Andrew A., Hughes, Virginia A., Yialamas, Maria, Hall, Janet E., Grant, Ellen, Mohammadi, Moosa, Crowley, William F.

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Prioritizing Genetic Testing in Patients With Kallmann Syndrome Using Clinical Phenotypes von Costa-Barbosa, Flavia Amanda, Balasubramanian, Ravikumar, Keefe, Kimberly W, Shaw, Natalie D, Al-Tassan, Nada, Plummer, Lacey, Dwyer, Andrew A, Buck, Cassandra L, Choi, Jin-Ho, Seminara, Stephanie B, Quinton, Richard, Monies, Dorota, Meyer, Brian, Hall, Janet E, Pitteloud, Nelly, Crowley, William F

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Service user involvement in preregistration general nurse education: a systematic review von Scammell, Janet, Heaslip, Vanessa, Crowley, Emma

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A Genetic Basis for Functional Hypothalamic Amenorrhea von Caronia, Lisa M, Martin, Kathryn A, Martin, Cecilia, Welt, Corrine K, Sykiotis, Gerasimos P, Quinton, Richard, Thambundit, Apisadaporn, Avbelj, Magdalena, Dhruvakumar, Sadhana, Plummer, Lacey, Hughes, Virginia A, Seminara, Stephanie B, Boepple, Paul A, Sidis, Yisrael, Crowley, William F, Hall, Janet E, Pitteloud, Nelly

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Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism von Tornberg, Janne, Sykiotis, Gerasimos P, Keefe, Kimberly, Plummer, Lacey, Hoang, Xuan, Hall, Janet E, Quinton, Richard, Seminara, Stephanie B, Hughes, Virginia, Van Vliet, Guy, Van Uum, Stan, Crowley, William F, Habuchi, Hiroko, Kimata, Koji, Pitteloud, Nelly, Bülow, Hannes E

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Phenotypic continuum between Waardenburg syndrome and idiopathic hypogonadotropic hypogonadism in humans with SOX10 variants von Rojas, Rebecca A., Kutateladze, Anna A., Plummer, Lacey, Stamou, Maria, Keefe, David L., Salnikov, Kathryn B., Delaney, Angela, Hall, Janet E., Sadreyev, Ruslan, Ji, Fei, Fliers, Eric, Gambosova, Katarina, Quinton, Richard, Merino, Paulina M., Mericq, Veronica, Seminara, Stephanie B., Crowley, William F., Balasubramanian, Ravikumar

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Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism von Pitteloud, Nelly, Quinton, Richard, Pearce, Simon, Raivio, Taneli, Acierno, James, Dwyer, Andrew, Plummer, Lacey, Hughes, Virginia, Seminara, Stephanie, Cheng, Yu-Zhu, Li, Wei-Ping, Maccoll, Gavin, Eliseenkova, Anna V, Olsen, Shaun K, Ibrahimi, Omar A, Hayes, Frances J, Boepple, Paul, Hall, Janet E, Bouloux, Pierre, Mohammadi, Moosa, Crowley, William

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Longitudinal Evaluation of Reproductive Endocrine Function in Men with ACTH-Dependent Cushing Syndrome von Shekhar, Skand, McGlotten, Raven N, Cutler, Jr, Gordon B, Crowley, Matthew J, Pieper, Carl F, Nieman, Lynnette K, Hall, Janet E

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Expanding the Spectrum of Founder Mutations Causing Isolated Gonadotropin-Releasing Hormone Deficiency von Choi, Jin-Ho, Balasubramanian, Ravikumar, Lee, Phil H, Shaw, Natalie D, Hall, Janet E, Plummer, Lacey, Buck, Cassandra L, Kottler, Marie-Laure, Jarzabek, Katarzyna, Wołczynski, Sławomir, Quinton, Richard, Latronico, Ana Claudia, Dode, Catherine, Ogata, Tsutomu, Kim, Hyung-Goo, Layman, Lawrence C, Gusella, James F, Crowley, William F

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