未登录Pathological substrate of memory impairment in multiple system atrophy多系统萎缩中记忆障碍的病理底物
Miki, Yasuo; Tanji, Kunikazu; Shinnai, Kana; Tanaka, Makoto T.; Altay, Firat; Foti, Sandrine C.; Strand, Catherine; Sasaki, Takanori; Kon, Tomoya; Shimoyama, Shuji; Furukawa, Tomonori; Nishijima, Haruo; Yamazaki, Hiromi; Asi, Yasmine T.; Bettencourt, Conceicao; Jaunmuktane, Zane; Tada, Mari; Mori, Fumiaki; Mizukami, Hiroki; Tomiyama, Masahiko; Lashuel, Hilal A.; Lashley, Tammaryn; Kakita, Akiyoshi; Ling, Helen; Lees, Andrew J.; Holton, Janice L.; Warner, Thomas T.; Wakabayashi, Koichi .png)
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收藏HnRNP K mislocalisation is a novel protein pathology of frontotemporal lobar degeneration and ageing and leads to cryptic splicingBampton, Alexander; Gatt, Ariana; Humphrey, Jack; Cappelli, Sara; Bhattacharya, Dipanjan; Foti, Sandrine; Brown, Anna-Leigh; Asi, Yasmine; Low, Yi Hua; Foiani, Marco; Raj, Towfique; Buratti, Emanuele; Fratta, Pietro; Lashley, Tammaryn 分享 收藏 Identification of multiple system atrophy mimicking Parkinson's disease or progressive supranuclear palsyMiki, Yasuo; Tsushima, Eiki; Foti, Sandrine C.; Strand, Kate M.; Asi, Yasmine T.; Yamamoto, Adam Kenji; Bettencourt, Conceicao; Oliveira, Marcos C. B.; De Pablo-Fernandez, Eduardo; Jaunmuktane, Zane; Lees, Andrew J.; Wakabayashi, Koichi; Warner, Thomas T.; Quinn, Niall; Holton, Janice L.; Ling, Helen 分享 收藏 Hippocampal α-synuclein pathology correlates with memory impairment in multiple system atrophy海马 α-突触核蛋白病理学与多系统萎缩的记忆障碍相关Miki, Yasuo; Foti, Sandrine C.; Hansen, Daniela; Strand, Kate M.; Asi, Yasmine T.; Tsushima, Eiki; Jaunmuktane, Zane; Lees, Andrew J.; Warner, Thomas T.; Quinn, Niall; Ling, Helen; Holton, Janice L. 分享 收藏 分享 收藏 Alzheimer's disease phospholipase C-gamma-2 (PLCG2) protective variant is a functional hypermorphMagno, Lorenza; Lessard, Christian B.; Martins, Marta; Lang, Verena; Cruz, Pedro; Asi, Yasmine; Katan, Matilda; Bilsland, Jamie; Lashley, Tammaryn; Chakrabarty, Paramita; Golde, Todd E.; Whiting, Paul J. 分享 收藏 Expanding the genetic heterogeneity of intellectual disability (vol 136, pg 1419, 2017)Anazi, Shams; Maddirevula, Sateesh; Salpietro, Vincenzo; Asi, Yasmine T.; Alsahli, Saud; Alhashem, Amal; Shamseldin, Hanan E.; AlZahrani, Fatema; Patel, Nisha; Ibrahim, Niema; Abdulwahab, Firdous M.; Hashem, Mais; Alhashmi, Nadia; Al Murshedi, Fathiya; Al Kindy, Adila; Alshaer, Ahmad; Rumayyan, Ahmed; Al Tala, Saeed; Kurdi, Wesam; Alsaman, Abdulaziz; Alasmari, Ali; Banu, Selina; Sultan, Tipu; Saleh, Mohammed M.; Alkuraya, Hisham; Salih, Mustafa A.; Aldhalaan, Hesham; Ben-Omran, Tawfeg; Al Musafri, Fatima; Ali, Rehab; Suleiman, Jehan; Tabarki, Brahim; El-Hattab, Ayman W.; Bupp, Caleb; Alfadhel, Majid; Al Tassan, Nada; Monies, Dorota; Arold, Stefan T.; Abouelhoda, Mohamed; Lashley, Tammaryn; Houlden, Henry; Faqeih, Eissa; Alkuraya, Fowzan S. 分享 收藏 Expanding the genetic heterogeneity of intellectual disabilityAnazi, Shams; Maddirevula, Sateesh; Salpietro, Vincenzo; Asi, Yasmine T.; Alsahli, Saud; Alhashem, Amal; Shamseldin, Hanan E.; AlZahrani, Fatema; Patel, Nisha; Ibrahim, Niema; Abdulwahab, Firdous M.; Hashem, Mais; Alhashmi, Nadia; Al Murshedi, Fathiya; Al Kindy, Adila; Alshaer, Ahmad; Rumayyan, Ahmed; Al Tala, Saeed; Kurdi, Wesam; Alsaman, Abdulaziz; Alasmari, Ali; Banu, Selina; Sultan, Tipu; Saleh, Mohammed M.; Alkuraya, Hisham; Salih, Mustafa A.; Aldhalaan, Hesham; Ben-Omran, Tawfeg; Al Musafri, Fatima; Ali, Rehab; Suleiman, Jehan; Tabarki, Brahim; El-Hattab, Ayman W.; Bupp, Caleb; Alfadhel, Majid; Al Tassan, Nada; Monies, Dorota; Arold, Stefan T.; Abouelhoda, Mohamed; Lashley, Tammaryn; Houlden, Henry; Faqeih, Eissa; Alkuraya, Fowzan S. 分享 收藏 Heterogeneous ribonuclear protein E2 (hnRNP E2) is associated with TDP-43-immunoreactive neurites in Semantic Dementia but not with other TDP-43 pathological subtypes of Frontotemporal Lobar DegenerationDavidson, Yvonne S.; Robinson, Andrew C.; Flood, Louis; Rollinson, Sara; Benson, Bridget C.; Asi, Yasmine T.; Richardson, Anna; Jones, Matthew; Snowden, Julie S.; Pickering-Brown, Stuart; Lashley, Tammaryn; Mann, David M. A. 分享 收藏 Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutationKiely, Aoife P.; Ling, Helen; Asi, Yasmine T.; Kara, Eleanna; Proukakis, Christos; Schapira, Anthony H.; Morris, Huw R.; Roberts, Helen C.; Lubbe, Steven; Limousin, Patricia; Lewis, Patrick A.; Lees, Andrew J.; Quinn, Niall; Hardy, John; Love, Seth; Revesz, Tamas; Houlden, Henry; Holton, Janice L. 分享 收藏 Minimal change multiple system atrophy: An aggressive variant?Ling, Helen; Asi, Yasmine T.; Petrovic, Igor N.; Ahmed, Zeshan; Prashanth, L. K.; Hazrati, Lili-Naz; Nishizawa, Masatoyo; Ozawa, Tetsutaro; Lang, Anthony; Lees, Andrew J.; Revesz, Tamas; Holton, Janice L. 分享 收藏 分享 收藏 分享 收藏 α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?与G51D SNCA突变相关的 α-突触核蛋白病: 帕金森病与多系统萎缩之间的联系？Kiely, Aoife P.; Asi, Yasmine T.; Kara, Eleanna; Limousin, Patricia; Ling, Helen; Lewis, Patrick; Proukakis, Christos; Quinn, Niall; Lees, Andrew J.; Hardy, John; Revesz, Tamas; Houlden, Henry; Holton, Janice L. 分享 收藏 分享 收藏 Multiple system atrophy-parkinsonism with slow progression and prolonged survival: A diagnostic catchPetrovic, Igor N.; Ling, Helen; Asi, Yasmine; Ahmed, Zeshan; Kukkle, Prashanth L.; Hazrati, Lili-Naz; Lang, Anthony E.; Revesz, Tamas; Holton, Janice L.; Lees, Andrew J. 分享 收藏 分享 收藏 
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