Outcomes of Long-Term Anticoagulation in Frail Elderly Patients with Atrial Fibrillation von Goldenberg, Gregory M., Silverstone, Felix A., Rangu, Srinivas, Leventer, Susan L.

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Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease with α-Synuclein Pathology von Wilson, Gabrielle R., Sim, Joe C.H., McLean, Catriona, Giannandrea, Maila, Galea, Charles A., Riseley, Jessica R., Stephenson, Sarah E.M., Fitzpatrick, Elizabeth, Haas, Stefan A., Pope, Kate, Hogan, Kirk J., Gregg, Ronald G., Bromhead, Catherine J., Wargowski, David S., Lawrence, Christopher H., James, Paul A., Churchyard, Andrew, Gao, Yujing, Phelan, Dean G., Gillies, Greta, Salce, Nicholas, Stanford, Lynn, Marsh, Ashley P.L., Mignogna, Maria L., Hayflick, Susan J., Leventer, Richard J., Delatycki, Martin B., Mellick, George D., Kalscheuer, Vera M., D’Adamo, Patrizia, Bahlo, Melanie, Amor, David J., Lockhart, Paul J.

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The severe epilepsy syndromes of infancy: A population‐based study von Howell, Katherine B., Freeman, Jeremy L., Mackay, Mark T., Fahey, Michael C., Archer, John, Berkovic, Samuel F., Chan, Eunice, Dabscheck, Gabriel, Eggers, Stefanie, Hayman, Michael, Holberton, James, Hunt, Rodney W., Jacobs, Susan E., Kornberg, Andrew J., Leventer, Richard J., Mandelstam, Simone, McMahon, Jacinta M., Mefford, Heather C., Panetta, Julie, Riseley, Jessica, Rodriguez‐Casero, Victoria, Ryan, Monique M., Schneider, Amy L., Smith, Lindsay J., Stark, Zornitza, Wong, Flora, Yiu, Eppie M., Scheffer, Ingrid E., Harvey, A. Simon

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Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practice von Scheffer, Ingrid E., Bennett, Caitlin A., Gill, Deepak, Silva, Michelle G., Boggs, Kirsten, Marum, Justine, Baker, Naomi, Palmer, Elizabeth E., Howell, Katherine B., Andrews, Ian, Antony, Jayne, Ardern‐Holmes, Simone, Bye, Ann M, Cardamone, Michael, Chelakkadan, Shabeed, Clark, Damian, Curnow, Sarah R, Dabscheck, Gabriel, Fahey, Michael C, Freeman, Jeremy L, Gupta, Sachin, Harvey, A Simon, Hildebrand, Michael S, Inder, Marie, Kanhangad, Manoj, Kornberg, Andrew J, Kothur, Kavitha, Lawson, John A, Leventer, Richard J, Malone, Stephen, Menezes, Manoj P, Mohammad, Shekeeb, Nagarajan, Lakshmi, Pillai, Sekhar, Pridmore, Clair, Procopis, Peter G, Sampaio, Hugo, Silberstein, Jonathon, Sinclair, Adriane, Smith, Nicholas, Subramanian, Gopinath, Troedson, Christopher, Ware, Tyson, White, Susan M

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De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome von Chen, Yuyang, Kim, Hyung Chul, Ljungdahl, Alicia, Stenton, Sarah L., Lord, Jenny, Lemire, Gabrielle, Martin-Geary, Alexandra C., Ganesh, Vijay S., Ma, Jialan, Ellingford, Jamie M., Delage, Erwan, D’Souza, Elston N., Dong, Shan, Adams, David R., Allan, Kirsten, Bakshi, Madhura, Baldwin, Erin E., Berger, Seth I., Brown, Natasha J., Burrage, Lindsay C., Chapman, Kimberly, Coman, David J., Compton, Alison G., Cunningham, Chloe A., D’Souza, Precilla, Danecek, Petr, Délot, Emmanuèle C., Dias, Kerith-Rae, Elias, Ellen R., Elmslie, Frances, Evans, Care-Anne, Ezell, Kimberly, Fraser, Jamie L., Gallacher, Lyndon, Genetti, Casie A., Grant, Christina L., Haack, Tobias, Higgs, Jenny E., Hinch, Anjali G., Hurles, Matthew E., Kuechler, Alma, Lecoquierre, François, Fevre, Anna Le, Leventer, Richard J., Liebelt, Jan E., Lindsay, Sarah, Lockhart, Paul J., Ma, Alan S., Macnamara, Ellen F., Mendez, Hector R., Metcalfe, Kay, Montgomery, Stephen B., Moosajee, Mariya, Nassogne, Marie-Cécile, Neumann, Serena, O’Donoghue, Michael, O’Leary, Melanie, Palmer, Elizabeth E., Pattani, Nikhil, Pitsava, Georgia, Pysar, Ryan, Rehm, Heidi L., Reuter, Chloe M., Revencu, Nicole, Riess, Angelika, Rodan, Lance, Roscioli, Tony, Rosenfeld, Jill A., Sachdev, Rani, Shaw-Smith, Charles J., Simons, Cas, Sisodiya, Sanjay M., Snell, Penny, St Clair, Laura, Stewart, Helen S., Tan, Natalie B., Temple, Suzanna E. L., Thorburn, David R., Tifft, Cynthia J., VanNoy, Grace E., Vilain, Eric, Viskochil, David H., Wedd, Laura, Wheeler, Matthew T., White, Susan M., Wojcik, Monica, Wolfe, Lynne A., Wolfenson, Zoe, Wright, Caroline F., Xiao, Changrui, Zocche, David, Rubenstein, John L., Markenscoff-Papadimitriou, Eirene, Fica, Sebastian M., Baralle, Diana, Depienne, Christel, MacArthur, Daniel G., Sanders, Stephan J., O’Donnell-Luria, Anne, Whiffin, Nicola

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Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2 von Dobyns, William B., Mirzaa, Ghayda, Christian, Susan L., Petras, Kristin, Roseberry, Jessica, Clark, Gary D., Curry, Cynthia J.R., McDonald-McGinn, Donna, Medne, Livija, Zackai, Elaine, Parsons, Julie, Zand, Dina J., Hisama, Fuki M., Walsh, Christopher A., Leventer, Richard J., Martin, Christa L., Gajecka, Marzena, Shaffer, Lisa G.

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A novel AMPD2 mutation outside the AMP deaminase domain causes pontocerebellar hypoplasia type 9 von Marsh, Ashley P. L., Yap, Patrick, Tan, Tiong, Pope, Kate, White, Susan M., Chong, Belinda, Mcgillivray, George, Boys, Amber, Stephenson, Sarah E. M., Leventer, Richard J., Stark, Zornitza, Lockhart, Paul J.

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Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease with [alpha]-Synuclein Pathology von Wilson, Gabrielle R, Sim, Joe CH, McLean, Catriona, Giannandrea, Maila, Galea, Charles A, Riseley, Jessica R, Stephenson, Sarah EM, Fitzpatrick, Elizabeth, Haas, Stefan A, Pope, Kate, Hogan, Kirk J, Gregg, Ronald G, Bromhead, Catherine J, Wargowski, David S, Lawrence, Christopher H, James, Paul A, Churchyard, Andrew, Gao, Yujing, Phelan, Dean G, Gillies, Greta, Salce, Nicholas, Stanford, Lynn, Marsh, Ashley PL, Mignogna, Maria L, Hayflick, Susan J, Leventer, Richard J, Delatycki, Martin B, Mellick, George D, Kalscheuer, Vera M, D'Adamo, Patrizia, Bahlo, Melanie, Amor, David J, Lockhart, Paul J

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Consistent Chromosome Abnormalities Identify Novel Polymicrogyria Loci in lp36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2 von DOBYNS, William B, MIRZAA, Ghayda, PARSONS, Julie, ZAND, Dina J, HISAMA, Fuki M, WALSH, Christopher A, LEVENTER, Richard J, MARTIN, Christa L, GAJECKA, Marzena, SHAFFER, Lisa G, CHRISTIAN, Susan L, PETRAS, Kristin, ROSEBERRY, Jessica, CLARK, Gary D, CURRY, Cynthia J. R, MCDONALD-MCGINN, Donna, MEDNE, Livija, ZACKAI, Elaine

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A novel AMPD2 mutation outside the AMP deaminase domain causes pontocerebellar hypoplasia type 9 von Marsh, Ashley P L, Yap, Patrick, Tan, Tiong, Pope, Kate, White, Susan M, Chong, Belinda, Mcgillivray, George, Boys, Amber, Stephenson, Sarah E M, Leventer, Richard J, Stark, Zornitza, Lockhart, Paul J

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