日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Inhaled Corticosteroids Alone and in Combination With Long-Acting β2 Receptor Agonists to Treat Reduced Lung Function in Preterm-Born Children: A Randomized Clinical Trial

单独使用吸入性皮质类固醇和联合长效β2受体激动剂治疗早产儿肺功能减退:一项随机临床试验

Goulden, Nia; Cousins, Michael; Hart, Kylie; Jenkins, Alison; Willetts, Gill; Yendle, Louise; Doull, Iolo; Williams, E Mark; Hoare, Zoe; Kotecha, Sailesh

Temporary reduction in fine particulate matter due to 'anthropogenic emissions switch-off' during COVID-19 lockdown in Indian cities

印度城市在新冠疫情封锁期间,由于“人为排放停止”,细颗粒物浓度暂时下降

Kumar, Prashant; Hama, Sarkawt; Omidvarborna, Hamid; Sharma, Ashish; Sahani, Jeetendra; Abhijith, K V; Debele, Sisay E; Zavala-Reyes, Juan C; Barwise, Yendle; Tiwari, Arvind

Mutations in KCNT1 cause a spectrum of focal epilepsies

KCNT1基因突变会导致一系列局灶性癫痫。

Møller, Rikke S; Heron, Sarah E; Larsen, Line H G; Lim, Chiao Xin; Ricos, Michael G; Bayly, Marta A; van Kempen, Marjan J A; Klinkenberg, Sylvia; Andrews, Ian; Kelley, Kent; Ronen, Gabriel M; Callen, David; McMahon, Jacinta M; Yendle, Simone C; Carvill, Gemma L; Mefford, Heather C; Nabbout, Rima; Poduri, Annapurna; Striano, Pasquale; Baglietto, Maria G; Zara, Federico; Smith, Nicholas J; Pridmore, Clair; Gardella, Elena; Nikanorova, Marina; Dahl, Hans Atli; Gellert, Pia; Scheffer, Ingrid E; Gunning, Boudewijn; Kragh-Olsen, Bente; Dibbens, Leanne M

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology

Dravet综合征作为癫痫性脑病:来自长期病程和神经病理学的证据

Catarino, Claudia B; Liu, Joan Y W; Liagkouras, Ioannis; Gibbons, Vaneesha S; Labrum, Robyn W; Ellis, Rachael; Woodward, Cathy; Davis, Mary B; Smith, Shelagh J; Cross, J Helen; Appleton, Richard E; Yendle, Simone C; McMahon, Jacinta M; Bellows, Susannah T; Jacques, Thomas S; Zuberi, Sameer M; Koepp, Matthias J; Martinian, Lillian; Scheffer, Ingrid E; Thom, Maria; Sisodiya, Sanjay M

De novo SCN1A mutations in migrating partial seizures of infancy

婴儿游走性部分性癫痫中的新生SCN1A突变

Carranza Rojo, D; Hamiwka, L; McMahon, J M; Dibbens, L M; Arsov, T; Suls, A; Stödberg, T; Kelley, K; Wirrell, E; Appleton, B; Mackay, M; Freeman, J L; Yendle, S C; Berkovic, S F; Bienvenu, T; De Jonghe, P; Thorburn, D R; Mulley, J C; Mefford, H C; Scheffer, I E

Rare copy number variants are an important cause of epileptic encephalopathies

罕见拷贝数变异是癫痫性脑病的重要病因。

Mefford, Heather C; Yendle, Simone C; Hsu, Cynthia; Cook, Joseph; Geraghty, Eileen; McMahon, Jacinta M; Eeg-Olofsson, Orvar; Sadleir, Lynette G; Gill, Deepak; Ben-Zeev, Bruria; Lerman-Sagie, Tally; Mackay, Mark; Freeman, Jeremy L; Andermann, Eva; Pelakanos, James T; Andrews, Ian; Wallace, Geoffrey; Eichler, Evan E; Berkovic, Samuel F; Scheffer, Ingrid E

Monoclonal antibodies to the membrane domain of the human erythrocyte anion transport protein. Localization of the C-terminus of the protein to the cytoplasmic side of the red cell membrane and distribution of the protein in some human tissues

针对人红细胞阴离子转运蛋白膜结构域的单克隆抗体。该蛋白C端定位于红细胞膜胞质侧,并分布于某些人体组织中。

Wainwright, S D; Tanner, M J; Martin, G E; Yendle, J E; Holmes, C