Why is something as important as screening for MRSA so difficult to achieve? von Clark, Beverley, Fryer, Jill, Emslie, Angela, Bhan, Angela, Barnass, Stella, Roberts, Honor

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The prevalence of neurodevelopmental disorders in children prenatally exposed to antiepileptic drugs von Bromley, Rebecca Louise, Mawer, George E, Briggs, Maria, Cheyne, Christopher, Clayton-Smith, Jill, García-Fiñana, Marta, Kneen, Rachel, Lucas, Sam B, Shallcross, Rebekah, Baker, Gus A

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Clinical and genetic aspects of KBG syndrome von Low, Karen, Ashraf, Tazeen, Canham, Natalie, Clayton-Smith, Jill, Deshpande, Charu, Donaldson, Alan, Fisher, Richard, Flinter, Frances, Foulds, Nicola, Fryer, Alan, Gibson, Kate, Hayes, Ian, Hills, Alison, Holder, Susan, Irving, Melita, Joss, Shelagh, Kivuva, Emma, Lachlan, Kathryn, Magee, Alex, McConnell, Vivienne, McEntagart, Meriel, Metcalfe, Kay, Montgomery, Tara, Newbury-Ecob, Ruth, Stewart, Fiona, Turnpenny, Peter, Vogt, Julie, Fitzpatrick, David, Williams, Maggie, Smithson, Sarah

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Memantine for dementia in adults older than 40 years with Down's syndrome (MEADOWS): a randomised, double-blind, placebo-controlled trial von Hanney, Marisa, PhD, Prasher, Vee, MD, Williams, Nicola, MSc, Jones, Emma L, DPhil, Aarsland, Dag, Prof, Corbett, Anne, PhD, Lawrence, Dale, MRCPsych, Yu, Ly-Mee, PhD, Tyrer, Stephen, FRCPsych, Francis, Paul T, Prof, Johnson, Tony, PhD, Bullock, Roger, MRCPsych, Ballard, Clive, Prof

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IQ at 6 years after in utero exposure to antiepileptic drugs: A controlled cohort study von Baker, Gus A, Bromley, Rebecca L, Briggs, Maria, Cheyne, Christopher P, Cohen, Morris J, García-Fiñana, Marta, Gummery, Alison, Kneen, Rachel, Loring, David W, Mawer, George, Meador, Kimford J, Shallcross, Rebekah, Clayton-Smith, Jill

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Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6 von Ratbi, Ilham, Falkenberg, Kim D., Sommen, Manou, Al-Sheqaih, Nada, Guaoua, Soukaina, Vandeweyer, Geert, Urquhart, Jill E., Chandler, Kate E., Williams, Simon G., Roberts, Neil A., El Alloussi, Mustapha, Black, Graeme C., Ferdinandusse, Sacha, Ramdi, Hind, Heimler, Audrey, Fryer, Alan, Lynch, Sally-Ann, Cooper, Nicola, Ong, Kai Ren, Smith, Claire E.L., Inglehearn, Christopher F., Mighell, Alan J., Elcock, Claire, Poulter, James A., Tischkowitz, Marc, Davies, Sally J., Sefiani, Abdelaziz, Mironov, Aleksandr A., Newman, William G., Waterham, Hans R., Van Camp, Guy

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Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients von Santen, Gijs W.E., Aten, Emmelien, Vulto-van Silfhout, Anneke T., Pottinger, Caroline, van Bon, Bregje W.M., van Minderhout, Ivonne J.H.M., Snowdowne, Ronelle, van der Lans, Christian A.C., Boogaard, Merel, Linssen, Margot M.L., Vijfhuizen, Linda, van der Wielen, Michiel J.R., Vollebregt, M.J. (Ellen), Breuning, Martijn H., Kriek, Marjolein, van Haeringen, Arie, den Dunnen, Johan T., Hoischen, Alexander, Clayton-Smith, Jill, de Vries, Bert B.A., Hennekam, Raoul C.M., van Belzen, Martine J., Almureikhi, Mariam, Baban, Anwar, Barbosa, Mafalda, Ben-Omran, Tawfeg, Berry, Katherine, Bigoni, Stefania, Boute, Odile, Brueton, Louise, van der Burgt, Ineke, Canham, Natalie, Chandler, Kate E., Chrzanowska, Krystyna, Collins, Amanda L., de Toni, Teresa, Dean, John, den Hollander, Nicolette S., Flore, Leigh Anne, Fryer, Alan, Gardham, Alice, Graham Jr, John M., Harrison, Victoria, Horn, Denise, Jongmans, Marjolijn C., Josifova, Dragana, Kant, Sarina G., Kapoor, Seema, Kingston, Helen, Kini, Usha, Kleefstra, Tjitske, Krajewska-Walasek, Małgorzata, Kramer, Nancy, Maas, Saskia M., Maciel, Patricia, Mancini, Grazia M.S., Maystadt, Isabelle, McKee, Shane, Milunsky, Jeff M., Nampoothiri, Sheela, Newbury-Ecob, Ruth, Nikkel, Sarah M., Parker, Michael J., Pérez-Jurado, Luis A., Robertson, Stephen P., Rooryck, Caroline, Shears, Debbie, Silengo, Margherita, Singh, Ankur, Smigiel, Robert, Soares, Gabriela, Splitt, Miranda, Stewart, Helen, Sweeney, Elizabeth, Tassabehji, May, Tuysuz, Beyhan, van Eerde, Albertien M., Vincent-Delorme, Catherine, Wilson, Louise C., Yesil, Gozde

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Mutations in LZTR1 add to the complex heterogeneity of schwannomatosis von Smith, Miriam J, Isidor, Bertand, Beetz, Christian, Williams, Simon G, Bhaskar, Sanjeev S, Richer, Wilfrid, OʼSullivan, James, Anderson, Beverly, Daly, Sarah B, Urquhart, Jill E, Fryer, Alan, Rustad, Cecilie F, Mills, Samantha J, Samii, Amir, du Plessis, Daniel, Halliday, Dorothy, Barbarot, Sebastien, Bourdeaut, Franck, Newman, William G, Evans, D Gareth

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AUTISM SPECTRUM DISORDERS FOLLOWING IN UTERO EXPOSURE TO ANTIEPILEPTIC DRUGS von BROMLEY, R. L, MAWER, G, CLAYTON-SMITH, J, BAKER, G. A

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Early cognitive development in children born to women with epilepsy: A prospective report von Bromley, Rebecca L., Mawer, George, Love, Jenna, Kelly, James, Purdy, Laura, McEwan, Lauren, Briggs, Maria, Smith, Jill Clayton, Sin, Xin, Baker, Gus A

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Mutations in CKAP2L, the Human Homolog of the Mouse Radmis Gene, Cause Filippi Syndrome von Hussain, Muhammad Sajid, Battaglia, Agatino, Szczepanski, Sandra, Kaygusuz, Emrah, Toliat, Mohammad Reza, Sakakibara, Shin-ichi, Altmüller, Janine, Thiele, Holger, Nürnberg, Gudrun, Moosa, Shahida, Yigit, Gökhan, Beleggia, Filippo, Tinschert, Sigrid, Clayton-Smith, Jill, Vasudevan, Pradeep, Urquhart, Jill E., Donnai, Dian, Fryer, Alan, Percin, Ferda, Brancati, Francesco, Dobbie, Angus, Śmigiel, Robert, Gillessen-Kaesbach, Gabriele, Wollnik, Bernd, Noegel, Angelika Anna, Newman, William G., Nürnberg, Peter

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Physical Rehabilitation in Critically Ill Children: A Multicenter Point Prevalence Study in the United States von Kudchadkar, Sapna R., Nelliot, Archana, Awojoodu, Ronke, Vaidya, Dhananjay, Traube, Chani, Walker, Tracie, Needham, Dale M.

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Whole-Exome-Sequencing Identifies Mutations in Histone Acetyltransferase Gene KAT6B in Individuals with the Say-Barber-Biesecker Variant of Ohdo Syndrome von Clayton-Smith, Jill, O'Sullivan, James, Daly, Sarah, Bhaskar, Sanjeev, Day, Ruth, Anderson, Beverley, Voss, Anne K., Thomas, Tim, Biesecker, Leslie G., Smith, Philip, Fryer, Alan, Chandler, Kate E., Kerr, Bronwyn, Tassabehji, May, Lynch, Sally-Ann, Krajewska-Walasek, Malgorzata, McKee, Shane, Smith, Janine, Sweeney, Elizabeth, Mansour, Sahar, Mohammed, Shehla, Donnai, Dian, Black, Graeme

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Child development following in utero exposure: Levetiracetam vs sodium valproate von SHALLCROSS, R, BROMLEY, R. L, IRWIN, B, BONNETT, L. J, MORROW, J, BAKER, G. A

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Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals von Kharbanda, Mira, Pilz, Daniela T, Tomkins, Susan, Chandler, Kate, Saggar, Anand, Fryer, Alan, McKay, Victoria, Louro, Pedro, Smith, Jill Clayton, Burn, John, Kini, Usha, De Burca, Anna, FitzPatrick, David R, Kinning, Esther

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Clinical and molecular consequences of disease-associated de novo mutations in SATB2 von Bengani, Hemant, Handley, Mark, Alvi, Mohsan, Ibitoye, Rita, Lees, Melissa, Lynch, Sally Ann, Lam, Wayne, Fannemel, Madeleine, Nordgren, Ann, Malmgren, H., Kvarnung, M., Mehta, Sarju, McKee, Shane, Whiteford, Margo, Stewart, Fiona, Connell, Fiona, Clayton-Smith, Jill, Mansour, Sahar, Mohammed, Shehla, Fryer, Alan, Morton, Jenny, Grozeva, Detelina, Asam, Tara, Moore, David, Sifrim, Alejandro, McRae, Jeremy, Hurles, Matthew E., Firth, Helen V., Raymond, F. Lucy, Kini, Usha, Nellåker, Christoffer, DDD study, FitzPatrick, David R.

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Pharmacological modulation of TSPO in microglia/macrophages and neurons in a chronic neurodegenerative model of prion disease von Vicente-Rodríguez, Marta, Mancuso, Renzo, Peris-Yague, Alba, Simmons, Camilla, Gómez-Nicola, Diego, Perry, V Hugh, Turkheimer, Federico, Lovestone, Simon, Parker, Christine A, Cash, Diana

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Clinical and molecular consequences of disease-associated de novo mutations in SATB2 von Bengani, Hemant, Handley, Mark, Alvi, Mohsan, Ibitoye, Rita, Lees, Melissa, Lynch, Sally Ann, Lam, Wayne, Fannemel, Madeleine, Nordgren, Ann, Malmgren, H., Kvarnung, M., Mehta, Sarju, McKee, Shane, Whiteford, Margo, Stewart, Fiona, Connell, Fiona, Clayton-Smith, Jill, Mansour, Sahar, Mohammed, Shehla, Fryer, Alan, Morton, Jenny, Grozeva, Detelina, Asam, Tara, Moore, David, Sifrim, Alejandro, McRae, Jeremy, Hurles, Matthew E., Firth, Helen V., Raymond, F. Lucy, Kini, Usha, Nellåker, Christoffer, FitzPatrick, David R.

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Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis von DE MUNNIK, Sonja A, BICKNELL, Louise S, HAGEN, Johanna M.van, HENNEKAM, Raoul C, JANSWEIJER, Maaike Ce, JOHNSON, Diana, KANT, Sarina G, OPITZ, John M, RADHA RAMADEVI, A, REARDON, Willie, ROSS, Alison, SARDA, Pierre, AFTIMOS, Salim, SCHRANDER-STUMPEL, Constance Trm, SCHOOTS, Jeroen, KAREN TEMPLE, I, TERHAL, Paulien A, TOUTAIN, Annick, WISE, Carol A, WRIGHT, Michael, SKIDMORE, David L, ESAMUELS, Mark, HHOEFSLOOT, Lies, AL-AAMA, Jumana Y, VAMKNOERS, Nine, BRUNNER, Han G, JACKSON, Andrew P, BONGERS, Ernie Mhf, BEVER, Yolande Van, BOBER, Michael B, CLAYTON-SMITH, Jill, EDREES, Alaa Y, FEINGOLD, Murray, FRYER, Alan

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Pregnancy with epilepsy: Obstetric and neonatal outcome of a controlled study von Mawer, G, Briggs, M, Baker, G.A, Bromley, R, Coyle, H, Eatock, J, Kerr, L, Kini, U, Kuzmyshcheva, L, Lucas, S.B, Wyatt, L, Clayton-Smith, J

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