Visual and auditory event-related potentials in sporadic amyotrophic lateral sclerosis von Paulus, K.S, Magnano, I, Piras, M.R, Solinas, M.A, Solinas, G, Sau, G.F, Aiello, I

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Allocation of fault indicators in distribution feeders containing distributed generation von Sau, Rodrigo F.G., Dardengo, Victor P., de Almeida, Madson C.

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Identification and ranking of customers with energy theft using hypothesis tests von Sau, Rodrigo F.G., Garcia, Tailan R., Trindade, Fernanda C.L., de Almeida, Madson C., Venkatesh, Bala

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Influences of neck receptors on soleus motoneuron excitability in man von Traccis, S, Rosati, G, Patraskakis, S, Bissakou, M, Sau, G.F, Aiello, I

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Tonic neck reflexes on upper limb flexor tone in man von Aiello, I., Rosati, G., Sau, G.F., Patraskakis, S., Bissakou, M., Traccis, S.

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Pudendal nerve somatosensory evoked potentials in probable multiple sclerosis von Sau, G. F., Aiello, I., Siracusano, S., Belgrano, M., Pastorino, M., Balsamo, P., Magnano, I., Rosati, G.

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Modulation of soleus H reflex by lateral tilting in man von Aiello, I., Rosati, G., Sau, G. F., Cacciotto, R., Lentinu, M. E., Tidore, B., Traccis, S.

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Modulation of flexor carpi radialis H reflex by lateral tilts in man von Aiello, I., Rosati, G., Sau, G.F., Patraskakis, S., Bissakou, M., Traccis, S.

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Evoked potentials in patients with non-neurological Wilson's disease von AIELLO, I, SAU, G. F, CACCIOTTO, R, PULIGA, M. V, LENTINU, M. E, MUZZU, S, POSADINU, D, TRACCIS, S

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Long latency evoked potentials in a case of corpus callosum agenesia von Aiello, I., Sotgiu, S., Sau, G. F., Conti, M., Rosati, G.

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Active restoration accelerates the carbon recovery of human-modified tropical forests von Philipson, Christopher D., Cutler, Mark E. J., Brodrick, Philip G., Asner, Gregory P., Boyd, Doreen S., Moura Costa, Pedro, Fiddes, Joel, Foody, Giles M., van der Heijden, Geertje M. F., Ledo, Alicia, Lincoln, Philippa R., Margrove, James A., Martin, Roberta E., Milne, Sol, Pinard, Michelle A., Reynolds, Glen, Snoep, Martijn, Tangki, Hamzah, Sau Wai, Yap, Wheeler, Charlotte E., Burslem, David F. R. P.

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Foxp3+ follicular regulatory T cells control the germinal center response von Linterman, Michelle A, Pierson, Wim, Lee, Sau K, Kallies, Axel, Kawamoto, Shimpei, Rayner, Tim F, Srivastava, Monika, Divekar, Devina P, Beaton, Laura, Hogan, Jennifer J, Fagarasan, Sidonia, Liston, Adrian, Smith, Kenneth G C, Vinuesa, Carola G

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B cell priming for extrafollicular antibody responses requires Bcl-6 expression by T cells von Lee, Sau K, Rigby, Robert J, Zotos, Dimitra, Tsai, Louis M, Kawamoto, Shimpei, Marshall, Jennifer L, Ramiscal, Roybel R, Chan, Tyani D, Gatto, Dominique, Brink, Robert, Yu, Di, Fagarasan, Sidonia, Tarlinton, David M, Cunningham, Adam F, Vinuesa, Carola G

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Exome and genome sequencing of nasopharynx cancer identifies NF-[kappa]B pathway activating mutations von Li, Yvonne Y, Chung, Grace T Y, Lui, Vivian W Y, To, Ka-fai, Ma, Brigette B Y, Chow, Chit, Woo, John K S, Yip, Kevin Y, Seo, Jeongsun, Hui, Edwin P, Mak, Michael K F, Rusan, Maria, Chau, Nicole G, Or, Yvonne Y Y, Law, Marcus H N, Law, Peggy P Y, Liu, Zoey W Y, Ngan, Hoi-lam, Hau, Pok-man, Verhoeft, Krista R, Poon, Peony H Y, Yoo, Seong-keun, Shin, Jong-yeon, Lee, Sau-dan, Lun, Samantha W M, Jia, Lin, Chan, Anthony W H, Chan, Jason Y K, Lai, Paul B S, Fung, Choi-yi, Hung, Suet-ting, Wang, Lin, Chang, Ann Margaret V, Chiosea, Simion I, Hedberg, Matthew L, Tsao, Sai-wah, Van Hasselt, Andrew C, Chan, Anthony T C, Grandis, Jennifer R, Hammerman, Peter S, Lo, Kwok-wai

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Uncertainties in projected impacts of climate change on European agriculture and terrestrial ecosystems based on scenarios from regional climate models von Olesen, J. E, Carter, T. R, Díaz-Ambrona, C. H, Fronzek, S, Heidmann, T, Hickler, T, Holt, T, Minguez, M. I, Morales, P, Palutikof, J. P, Quemada, M, Ruiz-Ramos, M, Rubæk, G. H, Sau, F, Smith, B, Sykes, M. T

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Mortality rates, life expectancy, and causes of death in people with hemophilia A or B in the United Kingdom who were not infected with HIV von Darby, Sarah C., Kan, Sau Wan, Spooner, Rosemary J., Giangrande, Paul L.F., Hill, Frank G.H., Hay, Charles R.M., Lee, Christine A., Ludlam, Christopher A., Williams, Michael

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De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations von Reijnders, Margot R.F., Zachariadis, Vasilios, Latour, Brooke, Jolly, Lachlan, Mancini, Grazia M., Pfundt, Rolph, Wu, Ka Man, van Ravenswaaij-Arts, Conny M.A., Veenstra-Knol, Hermine E., Anderlid, Britt-Marie M., Wood, Stephen A., Cheung, Sau Wai, Barnicoat, Angela, Probst, Frank, Magoulas, Pilar, Brooks, Alice S., Malmgren, Helena, Harila-Saari, Arja, Marcelis, Carlo M., Vreeburg, Maaike, Hobson, Emma, Sutton, V. Reid, Stark, Zornitza, Vogt, Julie, Cooper, Nicola, Lim, Jiin Ying, Price, Sue, Lai, Angeline Hwei Meeng, Domingo, Deepti, Reversade, Bruno, Gecz, Jozef, Gilissen, Christian, Brunner, Han G., Kini, Usha, Roepman, Ronald, Nordgren, Ann, Kleefstra, Tjitske

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Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size von Shinawi, Marwan, Liu, Pengfei, Kang, Sung-Hae L, Shen, Joseph, Belmont, John W, Scott, Daryl A, Probst, Frank J, Craigen, William J, Graham, Brett H, Pursley, Amber, Clark, Gary, Lee, Jennifer, Proud, Monica, Stocco, Amber, Rodriguez, Diana L, Kozel, Beth A, Sparagana, Steven, Roeder, Elizabeth R, McGrew, Susan G, Kurczynski, Thaddeus W, Allison, Leslie J, Amato, Stephen, Savage, Sarah, Patel, Ankita, Stankiewicz, Pawel, Beaudet, Arthur L, Cheung, Sau Wai, Lupski, James R

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Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36 von Zaveri, Hitisha P, Beck, Tyler F, Hernández-García, Andrés, Shelly, Katharine E, Montgomery, Tara, van Haeringen, Arie, Anderlid, Britt-Marie, Patel, Chirag, Goel, Himanshu, Houge, Gunnar, Morrow, Bernice E, Cheung, Sau Wai, Lalani, Seema R, Scott, Daryl A

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TBX6 Null Variants and a Common Hypomorphic Allele in Congenital Scoliosis von Wu, Nan, Ming, Xuan, Xiao, Jianqiu, Wu, Zhihong, Chen, Xiaoli, Shinawi, Marwan, Shen, Yiping, Yu, Guangju, Liu, Jiaqi, Xie, Hua, Gucev, Zoran S, Liu, Sen, Yang, Nan, Al-Kateb, Hussam, Chen, Jun, Zhang, Jian, Hauser, Natalie, Zhang, Ting, Tasic, Velibor, Liu, Pengfei, Su, Xinlin, Pan, Xuedong, Liu, Chunyu, Wang, Liwen, Shen, Joseph, Shen, Jianxiong, Chen, Yulin, Zhang, Ting, Zhang, Jianguo, Choy, Kwong Wai, Wang, Jun, Wang, Qiqi, Li, Shugang, Zhou, Weichen, Guo, Jin, Wang, Yipeng, Zhang, Cheng, Zhao, Hong, An, Yu, Zhao, Yu, Wang, Jiucun, Liu, Zhenlei, Zuo, Yuzhi, Tian, Ye, Weng, Xisheng, Sutton, V. Reid, Wang, Hongyan, Ming, Yue, Kulkarni, Shashikant, Zhong, Tao P, Giampietro, Philip F, Dunwoodie, Sally L, Cheung, Sau Wai, Zhang, Xue, Jin, Li, Lupski, James R, Qiu, Guixing, Zhang, Feng

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