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Records 1-16

Query Trace: Atrophy and GRN[orginal query]

Thalamic atrophy in frontotemporal dementia - Not just a NeuroImage. Clinical 2018 18 675-681. Bocchetta Martina, Gordon Elizabeth, Cardoso M Jorge, Modat Marc, Ourselin Sebastien, Warren Jason D, Rohrer Jonathan Similar articles in PubMed
Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study. Neurobiology of aging 2017 Nov . Galimberti Daniela, Fumagalli Giorgio G, Fenoglio Chiara, Cioffi Sara M G, Arighi Andrea, Serpente Maria, Borroni Barbara, Padovani Alessandro, Tagliavini Fabrizio, Masellis Mario, Tartaglia Maria Carmela, van Swieten John, Meeter Lieke, Graff Caroline, de Mendonça Alexandre, Bocchetta Martina, Rohrer Jonathan D, Scarpini Elio, Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
Hippocampal Sclerosis of Aging, a Common Alzheimer's Disease 'Mimic': Risk Genotypes are Associated with Brain Atrophy Outside the Temporal Lobe. Journal of Alzheimer's disease : JAD 2016 Mar . Nho Kwangsik, Saykin Andrew J, , Nelson Peter Similar articles in PubMed
Posterior cortical atrophy as a primary clinical phenotype of corticobasal syndrome with a progranulin gene rs5848 TT genotype. Orphanet journal of rare diseases 2016 11 (1): 13. Peng Guoping, Liu Ping, He Fangping, Luo Beny Similar articles in PubMed
Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort. Brain : a journal of neurology 2015 Dec . Van Mossevelde Sara, van der Zee Julie, Gijselinck Ilse, Engelborghs Sebastiaan, Sieben Anne, Van Langenhove Tim, De Bleecker Jan, Baets Jonathan, Vandenbulcke Mathieu, Van Laere Koen, Ceyssens Sarah, Van den Broeck Marleen, Peeters Karin, Mattheijssens Maria, Cras Patrick, Vandenberghe Rik, De Jonghe Peter, Martin Jean-Jacques, De Deyn Peter P, Cruts Marc, Van Broeckhoven Christine, Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
Subcortical and Deep Cortical Atrophy in Frontotemporal Dementia due to Granulin Mutations. Dementia and geriatric cognitive disorders extra 2014 Jan 4 (1): 95-102. Premi Enrico, Garibotto Valentina, Gazzina Stefano, Formenti Anna, Archetti Silvana, Gasparotti Roberto, Padovani Alessandro, Borroni Barba Similar articles in PubMed
PLD3 is accumulated on neuritic plaques in Alzheimer's disease brains. Alzheimer's research & therapy 2014 6 (9): 70. Satoh Jun-Ichi, Kino Yoshihiro, Yamamoto Yoji, Kawana Natsuki, Ishida Tsuyoshi, Saito Yuko, Arima Kunima Similar articles in PubMed
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 Similar articles in PubMed
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 Similar articles in PubMed
Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations. Journal of neuropathology and experimental neurology 2007 Feb 66 (2): 142-51. Josephs Keith A, Ahmed Zeshan, Katsuse Omi, Parisi Joseph F, Boeve Bradley F, Knopman David S, Petersen Ronald C, Davies Peter, Duara Ranjan, Graff-Radford Neill R, Uitti Ryan J, Rademakers Rosa, Adamson Jennifer, Baker Matthew, Hutton Michael L, Dickson Dennis Similar articles in PubMed

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