HuGE Literature Finder
Records 1-20
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Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study.
The Lancet. Neurology 2019 Dec 18 (12): 1103-1111. van der Ende Emma L, Meeter Lieke H, Poos Jackie M, Panman Jessica L, Jiskoot Lize C, Dopper Elise G P, Papma Janne M, de Jong Frank Jan, Verberk Inge M W, Teunissen Charlotte, Rizopoulos Dimitris, Heller Carolin, Convery Rhian S, Moore Katrina M, Bocchetta Martina, Neason Mollie, Cash David M, Borroni Barbara, Galimberti Daniela, Sanchez-Valle Raquel, Laforce Robert, Moreno Fermin, Synofzik Matthis, Graff Caroline, Masellis Mario, Carmela Tartaglia Maria, Rowe James B, Vandenberghe Rik, Finger Elizabeth, Tagliavini Fabrizio, de Mendonça Alexandre, Santana Isabel, Butler Chris, Ducharme Simon, Gerhard Alex, Danek Adrian, Levin Johannes, Otto Markus, Frisoni Giovanni B, Cappa Stefano, Pijnenburg Yolande A L, Rohrer Jonathan D, van Swieten John C, |
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Analysis of GWAS-linked variants in multiple system atrophy.
Neurobiology of aging 2018 Mar . Gu XiaoJing, Chen YongPing, Zhou QingQing, Lu Ying-Che, Cao Bei, Zhang LingYu, Kuo Ming-Che, Wu Yih-Ru, Wu Ruey-Meei, Tan Eng-King, Shang Hui-Fang, |
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Thalamic atrophy in frontotemporal dementia - Not just a C9orf72 problem.
NeuroImage. Clinical 2018 18 675-681. Bocchetta Martina, Gordon Elizabeth, Cardoso M Jorge, Modat Marc, Ourselin Sebastien, Warren Jason D, Rohrer Jonathan |
A genome-wide association study in multiple system atrophy.
Neurology 2016 Sep . Sailer Anna, Scholz Sonja W, Nalls Michael A, Schulte Claudia, Federoff Monica, Price T Ryan, Lees Andrew, Ross Owen A, Dickson Dennis W, Mok Kin, Mencacci Niccolo E, Schottlaender Lucia, Chelban Viorica, Ling Helen, O'Sullivan Sean S, Wood Nicholas W, Traynor Bryan J, Ferrucci Luigi, Federoff Howard J, Mhyre Timothy R, Morris Huw R, Deuschl Günther, Quinn Niall, Widner Hakan, Albanese Alberto, Infante Jon, Bhatia Kailash P, Poewe Werner, Oertel Wolfgang, Höglinger Günter U, Wüllner Ullrich, Goldwurm Stefano, Pellecchia Maria Teresa, Ferreira Joaquim, Tolosa Eduardo, Bloem Bastiaan R, Rascol Olivier, Meissner Wassilios G, Hardy John A, Revesz Tamas, Holton Janice L, Gasser Thomas, Wenning Gregor K, Singleton Andrew B, Houlden Henry, |
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Neurofilament light chain: a biomarker for genetic frontotemporal dementia.
Annals of clinical and translational neurology 2016 Aug 3 (8): 623-36. Meeter Lieke H, Dopper Elise G, Jiskoot Lize C, Sanchez-Valle Raquel, Graff Caroline, Benussi Luisa, Ghidoni Roberta, Pijnenburg Yolande A, Borroni Barbara, Galimberti Daniela, Laforce Robert Jr, Masellis Mario, Vandenberghe Rik, Ber Isabelle Le, Otto Markus, van Minkelen Rick, Papma Janne M, Rombouts Serge A, Balasa Mircea, Öijerstedt Linn, Jelic Vesna, Dick Katrina M, Cash David M, Harding Sophie R, Jorge Cardoso M, Ourselin Sebastien, Rossor Martin N, Padovani Alessandro, Scarpini Elio, Fenoglio Chiara, Tartaglia Maria C, Lamari Foudil, Barro Christian, Kuhle Jens, Rohrer Jonathan D, Teunissen Charlotte E, van Swieten John |
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Serum neurofilament light chain protein is a measure of disease intensity in frontotemporal dementia.
Neurology 2016 Aug . Rohrer Jonathan D, Woollacott Ione O C, Dick Katrina M, Brotherhood Emilie, Gordon Elizabeth, Fellows Alexander, Toombs Jamie, Druyeh Ronald, Cardoso M Jorge, Ourselin Sebastien, Nicholas Jennifer M, Norgren Niklas, Mead Simon, Andreasson Ulf, Blennow Kaj, Schott Jonathan M, Fox Nick C, Warren Jason D, Zetterberg Henr |
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MAPT haplotype diversity in multiple system atrophy.
Parkinsonism & related disorders 2016 09 30 40-5. Labbé Catherine, Heckman Michael G, Lorenzo-Betancor Oswaldo, Murray Melissa E, Ogaki Kotaro, Soto-Ortolaza Alexandra I, Walton Ronald L, Fujioka Shinsuke, Koga Shunsuke, Uitti Ryan J, van Gerpen Jay A, Petersen Ronald C, Graff-Radford Neill R, Younkin Steven G, Boeve Bradley F, Cheshire William P, Low Phillip A, Sandroni Paola, Coon Elizabeth A, Singer Wolfgang, Wszolek Zbigniew K, Dickson Dennis W, Ross Owen |
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Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutations.
Amyotrophic lateral sclerosis & frontotemporal degeneration 2015 Oct 1-9. Snowden Julie S, Adams Jennifer, Harris Jennifer, Thompson Jennifer C, Rollinson Sara, Richardson Anna, Jones Matthew, Neary David, Mann David M, Pickering-Brown Stua |
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Evaluating pathogenic dementia variants in posterior cortical atrophy.
Neurobiology of aging 2015 Oct . Carrasquillo Minerva M, Barber Imelda, Lincoln Sarah J, Murray Melissa E, Camsari Gamze Balci, Khan Qurat Ul Ain, Nguyen Thuy, Ma Li, Bisceglio Gina D, Crook Julia E, Younkin Steven G, Dickson Dennis W, Boeve Bradley F, Graff-Radford Neill R, Morgan Kevin, Ertekin-Taner Nilüf |
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Pain and temperature processing in dementia: a clinical and neuroanatomical analysis.
Brain : a journal of neurology 2015 Oct . Fletcher Phillip D, Downey Laura E, Golden Hannah L, Clark Camilla N, Slattery Catherine F, Paterson Ross W, Rohrer Jonathan D, Schott Jonathan M, Rossor Martin N, Warren Jason |
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Association analysis of the GRN ?rs5848 and MAPT rs242557 polymorphisms in Parkinson's disease and multiple system atrophy: a large-scale population-based study and meta-analysis.
The International journal of neuroscience 2015 Sep 1-8. Chen YongPing, Cao Bei, Ou RuWei, Chen XuePing, Zhao Bi, Wei QianQian, Wu Ying, Shang Hui-Fa |
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Temporal Variant Frontotemporal Dementia is Associated with Globular Glial Tauopathy.
Cognitive and behavioral neurology : official journal of the Society for Behavioral and Cognitive Neurology 2015 Jun 28 (2): 92-7. Clark Camilla N, Lashley Tammaryn, Mahoney Colin J, Warren Jason D, Revesz Tamas, Rohrer Jonathan |
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Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance images.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2015 May 22 (5): 745-52. Whitwell J L, Boeve B F, Weigand S D, Senjem M L, Gunter J L, Baker M C, DeJesus-Hernandez M, Knopman D S, Wszolek Z K, Petersen R C, Rademakers R, Jack C R, Josephs K |
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Profiles of white matter tract pathology in frontotemporal dementia.
Human brain mapping 2014 Aug 35 (8): 4163-79. Mahoney Colin J, Ridgway Gerard R, Malone Ian B, Downey Laura E, Beck Jonathan, Kinnunen Kirsi M, Schmitz Nicole, Golden Hannah L, Rohrer Jonathan D, Schott Jonathan M, Rossor Martin N, Ourselin Sebastien, Mead Simon, Fox Nick C, Warren Jason |
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MAPT1 gene rs1052553 variant is unrelated with the risk for restless legs syndrome.
Journal of neural transmission (Vienna, Austria : 1996) 2013 Mar 120 (3): 463-7. Roco Angela, Jiménez-Jiménez Félix Javier, Alonso-Navarro Hortensia, Martínez Carmen, Zurdo Martín, Turpín-Fenoll Laura, Millán Jorge, Adeva-Bartolomé Teresa, Cubo Esther, Navacerrada Francisco, Rojo-Sebastián Ana, Rubio Lluisa, Calleja Marisol, Plaza-Nieto José Francisco, Pilo-de-la-Fuente Belén, Arroyo-Solera Margarita, García-Martín Elena, Agúndez José A |
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Selective brain gray matter atrophy associated with APOE e4 and MAPT H1 in subjects with mild cognitive impairment.
Journal of Alzheimer's disease : JAD 2012 Oct . Goñi J, Cervantes S, Arrondo G, Lamet I, Pastor P, Pastor MA |
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Trajectories of brain and hippocampal atrophy in FTD with mutations in MAPT or GRN.
Neurology 2011 Jul 77 (4): 393-8. Whitwell J L, Weigand S D, Gunter J L, Boeve B F, Rademakers R, Baker M, Knopman D S, Wszolek Z K, Petersen R C, Jack C R, Josephs K |
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Synaptic changes in frontotemporal lobar degeneration: correlation with MAPT haplotype and APOE genotype.
Neuropathology and applied neurobiology 2011 Jun 37 (4): 366-80. Connelly S J, Mukaetova-Ladinska E B, Abdul-All Z, Alves da Silva J, Brayne C, Honer W G, Mann D M |
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Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide.
Neurobiology of disease 2009 Mar 33 (3): 379-85. Benussi Luisa, Ghidoni Roberta, Pegoiani Eleonora, Moretti Davide V, Zanetti Orazio, Binetti Giulia |
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A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series.
Brain : a journal of neurology 2008 Mar 131 (Pt 3): 706-20. Beck Jonathan, Rohrer Jonathan D, Campbell Tracy, Isaacs Adrian, Morrison Karen E, Goodall Emily F, Warrington Elizabeth K, Stevens John, Revesz Tamas, Holton Janice, Al-Sarraj Safa, King Andrew, Scahill Rachael, Warren Jason D, Fox Nick C, Rossor Martin N, Collinge John, Mead Sim |
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- Page last updated:Sep 23, 2021
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