Genetics of dementia von Loy, Clement T, FRACP, Schofield, Peter R, Prof, Turner, Anne M, FRACP, Kwok, John BJ, Dr

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Role of the Long Non-Coding RNA MAPT-AS1 in Regulation of Microtubule Associated Protein Tau (MAPT) Expression in Parkinson's Disease von Coupland, Kirsten G, Kim, Woojin S, Halliday, Glenda M, Hallupp, Marianne, Dobson-Stone, Carol, Kwok, John B J

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Stepping into the Role of Editor-In-Chief von Kwok, John B.

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Cerebellar integrity in the amyotrophic lateral sclerosis-frontotemporal dementia continuum von Tan, Rachel H, Devenney, Emma, Dobson-Stone, Carol, Kwok, John B, Hodges, John R, Kiernan, Matthew C, Halliday, Glenda M, Hornberger, Michael

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DNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E In Vitro von Coupland, Kirsten G., Mellick, George D., Silburn, Peter A., Mather, Karen, Armstrong, Nicola J., Sachdev, Perminder S., Brodaty, Henry, Huang, Yue, Halliday, Glenda M., Hallupp, Marianne, Kim, Woojin S., Dobson-Stone, Carol, Kwok, John B.J.

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The underacknowledged PPA-ALS: A unique clinicopathologic subtype with strong heritability von Tan, Rachel H, Guennewig, Boris, Dobson-Stone, Carol, Kwok, John B.J, Kril, Jillian J, Kiernan, Matthew C, Hodges, John R, Piguet, Olivier, Halliday, Glenda M

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C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts von DOBSON-STONE, Carol, HALLUPP, Marianne, BARTLEY, Lauren, SHEPHERD, Claire E, HALLIDAY, Glenda M, SCHOFIELD, Peter R, HODGES, John R, KWOK, John B. J

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The Role of White Matter Dysfunction and Leukoencephalopathy/Leukodystrophy Genes in the Aetiology of Frontotemporal Dementias: Implications for Novel Approaches to Therapeutics von Lok, Hiu Chuen, Kwok, John B

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C9ORF72 repeat expansion in Australian and Spanish frontotemporal dementia patients von Dobson-Stone, Carol, Hallupp, Marianne, Loy, Clement T, Thompson, Elizabeth M, Haan, Eric, Sue, Carolyn M, Panegyres, Peter K, Razquin, Cristina, Seijo-Martínez, Manuel, Rene, Ramon, Gascon, Jordi, Campdelacreu, Jaume, Schmoll, Birgit, Volk, Alexander E, Brooks, William S, Schofield, Peter R, Pastor, Pau, Kwok, John B J

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Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies von Forrest, Shelley L, Kril, Jillian J, Stevens, Claire H, Kwok, John B, Hallupp, Marianne, Kim, Woojin S, Huang, Yue, McGinley, Ciara V, Werka, Hellen, Kiernan, Matthew C, Götz, Jürgen, Spillantini, Maria Grazia, Hodges, John R, Ittner, Lars M, Halliday, Glenda M

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TDP-43 proteinopathies: pathological identification of brain regions differentiating clinical phenotypes von Tan, Rachel H, Kril, Jillian J, Fatima, Manaal, McGeachie, Andrew, McCann, Heather, Shepherd, Claire, Forrest, Shelley L, Affleck, Andrew, Kwok, John B J, Hodges, John R, Kiernan, Matthew C, Halliday, Glenda M

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Detecting and Validating MAPT Mutations in Neurodegeneration Patients and Analysis of Exon Splicing Consequences von Dobson-Stone, Carol, Guennewig, Boris, Mundell, Hamish, Kwok, John B.

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A role for transcription factor GTF2IRD2 in executive function in Williams-Beuren syndrome von Porter, Melanie A, Dobson-Stone, Carol, Kwok, John B J, Schofield, Peter R, Beckett, William, Tassabehji, May

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GSK3B polymorphisms alter transcription and splicing in Parkinson's disease von Kwok, John B. J., Hallupp, Marianne, Loy, Clement T., Chan, Daniel K. Y., Woo, Jean, Mellick, George D., Buchanan, Daniel D., Silburn, Peter A., Halliday, Glenda M., Schofield, Peter R.

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Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration-motor neuron disease von Luty, Agnes A., Kwok, John B.J., Dobson-Stone, Carol, Loy, Clement T., Coupland, Kirsten G., Karlström, Helena, Sobow, Tomasz, Tchorzewska, Joanna, Maruszak, Aleksandra, Barcikowska, Maria, Panegyres, Peter K., Zekanowski, Cezary, Brooks, William S., Williams, Kelly L., Blair, Ian P., Mather, Karen A., Sachdev, Perminder S., Halliday, Glenda M., Schofield, Peter R.

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Srp20 regulates TrkB pre-mRNA splicing to generate TrkB-Shc transcripts with implications for Alzheimer's disease von Wong, Jenny, Garner, Brett, Halliday, Glenda M., Kwok, John B. J.

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Reduced glucocerebrosidase activity in monocytes from patients with Parkinson’s disease von Atashrazm, Farzaneh, Hammond, Deborah, Perera, Gayathri, Dobson-Stone, Carol, Mueller, Nicole, Pickford, Russell, Kim, Woojin Scott, Kwok, John B., Lewis, Simon J. G., Halliday, Glenda M., Dzamko, Nicolas

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Finding MAPT Mutations in Frontotemporal Dementia and Other Tauopathies von Dobson-Stone, Carol, Kwok, John B. J.

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Heritability in frontotemporal dementia: more missing pieces? von Po, Kieren, Leslie, Felicity V. C., Gracia, Natalie, Bartley, Lauren, Kwok, John B. J., Halliday, Glenda M., Hodges, John R., Burrell, James R.

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The complex relationship between genotype, pathology and phenotype in familial dementia von Kwok, John B., Loy, Clement T., Dobson-Stone, Carol, Halliday, Glenda M.

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