TDP-43 extracted from frontotemporal lobar degeneration subject brains displays distinct aggregate assemblies and neurotoxic effects reflecting disease progression rates von Laferrière, Florent, Maniecka, Zuzanna, Pérez-Berlanga, Manuela, Hruska-Plochan, Marian, Gilhespy, Larissa, Hock, Eva-Maria, Wagner, Ulrich, Afroz, Tariq, Boersema, Paul J., Barmettler, Gery, Foti, Sandrine C., Asi, Yasmine T., Isaacs, Adrian M., Al-Amoudi, Ashraf, Lewis, Amanda, Stahlberg, Henning, Ravits, John, De Giorgi, Francesca, Ichas, François, Bezard, Erwan, Picotti, Paola, Lashley, Tammaryn, Polymenidou, Magdalini

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Improving diagnostic accuracy of multiple system atrophy: a clinicopathological study von Miki, Yasuo, Foti, Sandrine C, Asi, Yasmine T, Tsushima, Eiki, Quinn, Niall, Ling, Helen, Holton, Janice L

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Heterogeneous Nuclear Ribonucleoproteins: Implications in Neurological Diseases von Low, Yi-Hua, Asi, Yasmine, Foti, Sandrine C., Lashley, Tammaryn

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Alpha-synuclein mRNA expression in oligodendrocytes in MSA von Asi, Yasmine T., Simpson, Julie E., Heath, Paul R., Wharton, Stephen B., Lees, Andrew J., Revesz, Tamas, Houlden, Henry, Holton, Janice L.

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Expanding the genetic heterogeneity of intellectual disability von 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.

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[alpha]-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy? von 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

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α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson’s disease and multiple system atrophy? von 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.

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Identification of multiple system atrophy mimicking Parkinson's disease or progressive supranuclear palsy von Miki, 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

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Identification and Quantification of Oligodendrocyte Precursor Cells in Multiple System Atrophy, Progressive Supranuclear Palsy and Parkinson's Disease von Ahmed, Zeshan, Asi, Yasmine T., Lees, Andrew J., Revesz, Tamas, Holton, Janice L.

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Hippocampal alpha-synuclein pathology correlates with memory impairment in multiple system atrophy von 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.

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HnRNP K mislocalisation is a novel protein pathology of frontotemporal lobar degeneration and ageing and leads to cryptic splicing von Bampton, 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

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Alzheimer’s disease phospholipase C-gamma-2 (PLCG2) protective variant is a functional hypermorph von Magno, 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.

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Pathological substrate of memory impairment in multiple system atrophy von 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, Conceição, 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

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Minimal change multiple system atrophy: An aggressive variant? von 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.

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Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation von Kiely, 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

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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 Frontotemp... von Davidson, 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

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Correction to: Expanding the genetic heterogeneity of intellectual disability von 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.

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Multiple system atrophy-parkinsonism with slow progression and prolonged survival: A diagnostic catch von Petrovic, 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.

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Identification of multiple system atrophy mimicking Parkinson's disease or progressive supranuclear palsy von Miki, 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

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TDP-43 extracted from frontotemporal lobar degeneration subject brains displays distinct aggregate assemblies and neurotoxic effects reflecting disease progression rates von Laferrière, Florent, Maniecka, Zuzanna, Pérez-Berlanga, Manuela, Hruska-Plochan, Marian, Gilhespy, Larissa, Hock, Eva-Maria, Wagner, Ulrich, Afroz, Tariq, Boersema, Paul J, Barmettler, Gery, Foti, Sandrine C, Asi, Yasmine T, Isaacs, Adrian M, Al-Amoudi, Ashraf, Lewis, Amanda, Stahlberg, Henning, Ravits, John, De Giorgi, Francesca, Ichas, François, Bezard, Erwan, Picotti, Paola, Lashley, Tammaryn, Polymenidou, Magdalini

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