Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Mollie Neason"'
Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes
Autor:
Martina Bocchetta, Juan Eugenio Iglesias, Viorica Chelban, Edwin Jabbari, Ruth Lamb, Lucy L. Russell, Caroline V. Greaves, Mollie Neason, David M. Cash, David L. Thomas, Jason D. Warren, John Woodside, Henry Houlden, Huw R. Morris, Jonathan D. Rohrer
Publikováno v:
Journal of Movement Disorders, Vol 13, Iss 1, Pp 39-46 (2020)
Objective Brainstem segmentation has been useful in identifying potential imaging biomarkers for diagnosis and progression in atypical parkinsonian syndromes (APS). However, the majority of work has been performed using manual segmentation, which is
Externí odkaz:
https://doaj.org/article/086030a0abc54efba8a6042898e6698e
Autor:
Sergi Borrego-Écija, Roser Sala-Llonch, John van Swieten, Barbara Borroni, Fermín Moreno, Mario Masellis, Carmela Tartaglia, Caroline Graff, Daniela Galimberti, Robert Laforce, Jr, James B Rowe, Elizabeth Finger, Rik Vandenberghe, Fabrizio Tagliavini, Alexandre de Mendonça, Isabel Santana, Matthis Synofzik, Simon Ducharme, Johannes Levin, Adrian Danek, Alex Gerhard, Markus Otto, Chris Butler, Giovanni Frisoni, Sandro Sorbi, Carolin Heller, Martina Bocchetta, David M Cash, Rhian S Convery, Katrina M Moore, Jonathan D Rohrer, Raquel Sanchez-Valle, Martin N. Rossor, Nick C. Fox, Ione O.C. Woollacott, Rachelle Shafei, Caroline Greaves, Mollie Neason, Rita Guerreiro, Jose Bras, David L. Thomas, Jennifer Nicholas, Simon Mead, Lieke Meeter, Jessica Panman, Janne Papma, Rick van Minkelen, Yolande Pijnenburg, Begoña Indakoetxea, Alazne Gabilondo, Mikel TaintaMD, Maria de Arriba, Ana Gorostidi, Miren Zulaica, Jorge Villanua, Zigor Diaz, Jaume Olives, Albert Lladó, Mircea Balasa, Anna Antonell, Nuria Bargallo, Enrico Premi, Maura Cosseddu, Stefano Gazzina, Alessandro Padovani, Roberto Gasparotti, Silvana Archetti, Sandra Black, Sara Mitchell, Ekaterina Rogaeva, Morris Freedman, Ron Keren, David Tang-Wai, Linn Öijerstedt, Christin Andersson, Vesna Jelic, Hakan Thonberg, Andrea Arighi, Chiara Fenoglio, Elio Scarpini MD, Giorgio Fumagalli, Thomas Cope, Carolyn Timberlake, Timothy Rittman, Christen Shoesmith, Robart Bartha, Rosa Rademakers, Carlo Wilke, Benjamin Bender, Rose Bruffaerts, Philip Vandamme, Mathieu Vandenbulcke, Carolina Maruta, Catarina B. Ferreira, Gabriel Miltenberger, Ana Verdelho, Sónia Afonso, Ricardo Taipa, Paola Caroppo, Giuseppe Di Fede, Giorgio Giaccone, Sara Prioni, Veronica Redaelli, Giacomina Rossi, Pietro Tiraboschi, Diana Duro, Maria Rosario Almeida, Miguel Castelo-Branco, Maria João Leitão, Miguel Tabuas-Pereira, Beatriz Santiago, Serge Gauthier, Pedro Rosa-Neto, Michele Veldsman, Toby Flanagan, Catharina Prix, Tobias Hoegen, Elisabeth Wlasich, Sandra Loosli, Sonja Schonecker, Elisa Semler, Sarah Anderl-Straub
Publikováno v:
NeuroImage: Clinical, Vol 29, Iss , Pp 102540- (2021)
Mutations in the granulin gene (GRN) cause familial frontotemporal dementia. Understanding the structural brain changes in presymptomatic GRN carriers would enforce the use of neuroimaging biomarkers for early diagnosis and monitoring. We studied 100
Externí odkaz:
https://doaj.org/article/72b369b73dcc4f09a097d911ba639780
Autor:
Carole H. Sudre, Martina Bocchetta, Carolin Heller, Rhian Convery, Mollie Neason, Katrina M. Moore, David M. Cash, David L. Thomas, Ione O.C. Woollacott, Martha Foiani, Amanda Heslegrave, Rachelle Shafei, Caroline Greaves, John van Swieten, Fermin Moreno, Raquel Sanchez-Valle, Barbara Borroni, Robert Laforce, Jr, Mario Masellis, Maria Carmela Tartaglia, Caroline Graff, Daniela Galimberti, James B. Rowe, Elizabeth Finger, Matthis Synofzik, Rik Vandenberghe, Alexandre de Mendonça, Fabrizio Tagliavini, Isabel Santana, Simon Ducharme, Chris Butler, Alex Gerhard, Johannes Levin, Adrian Danek, Giovanni B. Frisoni, Sandro Sorbi, Markus Otto, Henrik Zetterberg, Sebastien Ourselin, M. Jorge Cardoso, Jonathan D. Rohrer
Publikováno v:
NeuroImage: Clinical, Vol 24, Iss , Pp - (2019)
Frontotemporal dementia (FTD) is a heterogeneous group of neurodegenerative disorders with both sporadic and genetic forms. Mutations in the progranulin gene (GRN) are a common cause of genetic FTD, causing either a behavioural presentation or, less
Externí odkaz:
https://doaj.org/article/b08168152a4e4c0a9f0049681ce3c06c
Autor:
Jonathan D. Rohrer, Mollie Neason, Martina Bocchetta, Juan Eugenio Iglesias, Jason D. Warren, David M. Cash
Publikováno v:
Human Brain Mapping
Thalamic atrophy is a common feature across all forms of FTD but little is known about specific nuclei involvement. We aimed to investigate in vivo atrophy of the thalamic nuclei across the FTD spectrum. A cohort of 402 FTD patients (age: mean(SD) 64
Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes
Autor:
David L. Thomas, Jonathan D. Rohrer, Viorica Chelban, John Woodside, Juan Eugenio Iglesias, Edwin Jabbari, Caroline V. Greaves, Martina Bocchetta, Henry Houlden, Ruth Lamb, Mollie Neason, Lucy L. Russell, David M. Cash, Huw R. Morris, Jason D. Warren
Publikováno v:
Journal of Movement Disorders
Journal of Movement Disorders, Vol 13, Iss 1, Pp 39-46 (2020)
Journal of Movement Disorders, Vol 13, Iss 1, Pp 39-46 (2020)
OBJECTIVE: Brainstem segmentation has been useful in identifying potential imaging biomarkers for diagnosis and progression in atypical parkinsonian syndromes (APS). However, the majority of work has been performed using manual segmentation, which is
Autor:
Pietro Tiraboschi, Katrina M. Moore, Nick C. Fox, David L. Thomas, Jonathan D. Rohrer, Begoña Indakoetxea, Serge Gauthier, Thomas E. Cope, Mikel TaintaMD, Enrico Premi, Philip Vandamme, Giorgio Giaccone, Mircea Balasa, Sandra E. Black, John C. van Swieten, Catharina Prix, Sergi Borrego-Écija, Sandro Sorbi, Håkan Thonberg, Roser Sala-Llonch, Rick van Minkelen, Maria de Arriba, Elizabeth Finger, Michele Veldsman, Raquel Sánchez-Valle, Vesna Jelic, Veronica Redaelli, Zigor Diaz, James B. Rowe, Daniela Galimberti, Rhian S Convery, Anna Antonell, Miren Zulaica, Jennifer M. Nicholas, Alessandro Padovani, Diana Duro, Giuseppe Di Fede, Albert Lladó, Núria Bargalló, Pedro Rosa-Neto, Sara Prioni, Alazne Gabilondo, C. Ferreira, Andrea Arighi, Sara Mitchell, Mario Masellis, Chiara Fenoglio, Rachelle Shafei, Benjamin Bender, Rik Vandenberghe, Isabel Santana, Carlo Wilke, Christen Shoesmith, Janne M. Papma, Mathieu Vandenbulcke, Robart Bartha, Sandra V. Loosli, Giorgio Fumagalli, Ana Verdelho, Robert Laforce, Paola Caroppo, Adrian Danek, Jessica L. Panman, Maria Rosário Almeida, Carolin Heller, Jorge Villanua, Johannes Levin, Rita Guerreiro, Stefano Gazzina, Jose Bras, Miguel Castelo-Branco, Ekaterina Rogaeva, Fabrizio Tagliavini, Giacomina Rossi, Markus Otto, Timothy Rittman, Beatriz Santiago, Simon Mead, Rosa Rademakers, Maria João Leitão, Simon Ducharme, Sarah Anderl-Straub, Ron Keren, Ione O.C. Woollacott, Morris Freedman, Gabriel Miltenberger, Fermin Moreno, Martin N. Rossor, Tobias Hoegen, Jaume Olives, Carolyn Timberlake, Barbara Borroni, Ricardo Taipa, Elio Scarpini, David M. Cash, Miguel Tábuas-Pereira, Roberto Gasparotti, Sonja Schönecker, Martina Bocchetta, Lieke H.H. Meeter, Alexander Gerhard, Rose Bruffaerts, Carmela Tartaglia, Caroline V. Greaves, Christopher C Butler, Toby Flanagan, Sónia Afonso, Matthis Synofzik, Linn Öijerstedt, David F. Tang-Wai, Yolande A.L. Pijnenburg, Maura Cosseddu, Carolina Maruta, Alexandre de Mendonça, Christin Andersson, Caroline Graff, Ana Gorostidi, Silvana Archetti, Giovanni B. Frisoni, Elisabeth Wlasich, Mollie Neason, Elisa Semler
Publikováno v:
NeuroImage: Clinical, 29:102540. Elsevier BV
NeuroImage: Clinical, 29:102540. Elsevier
NeuroImage: Clinical 29, 102540-(2021). doi:10.1016/j.nicl.2020.102540
Medical Biophysics Publications
NeuroImage : Clinical
Borrego-Écija, S, Sala-Llonch, R, van Swieten, J, Borroni, B, Moreno, F, Masellis, M, Tartaglia, C, Graff, C, Galimberti, D, Laforce, R, Rowe, J B, Finger, E, Vandenberghe, R, Tagliavini, F, de Mendonça, A, Santana, I, Synofzik, M, Ducharme, S, Levin, J, Danek, A, Gerhard, A, Otto, M, Butler, C, Frisoni, G, Sorbi, S, Heller, C, Bocchetta, M, Cash, D M, Convery, R S, Moore, K M, Rohrer, J D, Sanchez-Valle, R, Rossor, M N, Fox, N C, Woollacott, I O C, Shafei, R, Greaves, C, Neason, M, Guerreiro, R, Bras, J, Thomas, D L, Nicholas, J, Mead, S, Meeter, L, Panman, J, Papma, J, van Minkelen, R, Pijnenburg, Y, Indakoetxea, B, Gabilondo, A, TaintaMD, M, de Arriba, M, Gorostidi, A, Zulaica, M, Villanua, J, Diaz, Z, Olives, J, Lladó, A, Balasa, M, Antonell, A, Bargallo, N, Premi, E, Cosseddu, M, Gazzina, S, Padovani, A, Gasparotti, R, Archetti, S, Black, S, Mitchell, S, Rogaeva, E, Freedman, M, Keren, R, Tang-Wai, D, Öijerstedt, L, Andersson, C, Jelic, V, Thonberg, H, Arighi, A, Fenoglio, C, Scarpini MD, E, Fumagalli, G, Cope, T, Timberlake, C, Rittman, T, Shoesmith, C, Bartha, R, Rademakers, R, Wilke, C, Bender, B, Bruffaerts, R, Vandamme, P, Vandenbulcke, M, Maruta, C, Ferreira, C B, Miltenberger, G, Verdelho, A, Afonso, S N, Taipa, R, Caroppo, P, di Fede, G, Giaccone, G, Prioni, S, Redaelli, V, Rossi, G, Tiraboschi, P, Duro, D, Rosario Almeida, M, Castelo-Branco, M, João Leitão, M, Tabuas-Pereira, M, Santiago, B, Gauthier, S, Rosa-Neto, P, Veldsman, M, Flanagan, T, Prix, C, Hoegen, T, Wlasich, E, Loosli, S, Schonecker, S, Semler, E & Anderl-Straub, S 2021, ' Disease-related cortical thinning in presymptomatic granulin mutation carriers ', NeuroImage: Clinical, vol. 29, 102540 . https://doi.org/10.1016/j.nicl.2020.102540
NeuroImage: Clinical, Vol 29, Iss, Pp 102540-(2021)
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
NeuroImage: Clinical, 29:102540. Elsevier
NeuroImage: Clinical 29, 102540-(2021). doi:10.1016/j.nicl.2020.102540
Medical Biophysics Publications
NeuroImage : Clinical
Borrego-Écija, S, Sala-Llonch, R, van Swieten, J, Borroni, B, Moreno, F, Masellis, M, Tartaglia, C, Graff, C, Galimberti, D, Laforce, R, Rowe, J B, Finger, E, Vandenberghe, R, Tagliavini, F, de Mendonça, A, Santana, I, Synofzik, M, Ducharme, S, Levin, J, Danek, A, Gerhard, A, Otto, M, Butler, C, Frisoni, G, Sorbi, S, Heller, C, Bocchetta, M, Cash, D M, Convery, R S, Moore, K M, Rohrer, J D, Sanchez-Valle, R, Rossor, M N, Fox, N C, Woollacott, I O C, Shafei, R, Greaves, C, Neason, M, Guerreiro, R, Bras, J, Thomas, D L, Nicholas, J, Mead, S, Meeter, L, Panman, J, Papma, J, van Minkelen, R, Pijnenburg, Y, Indakoetxea, B, Gabilondo, A, TaintaMD, M, de Arriba, M, Gorostidi, A, Zulaica, M, Villanua, J, Diaz, Z, Olives, J, Lladó, A, Balasa, M, Antonell, A, Bargallo, N, Premi, E, Cosseddu, M, Gazzina, S, Padovani, A, Gasparotti, R, Archetti, S, Black, S, Mitchell, S, Rogaeva, E, Freedman, M, Keren, R, Tang-Wai, D, Öijerstedt, L, Andersson, C, Jelic, V, Thonberg, H, Arighi, A, Fenoglio, C, Scarpini MD, E, Fumagalli, G, Cope, T, Timberlake, C, Rittman, T, Shoesmith, C, Bartha, R, Rademakers, R, Wilke, C, Bender, B, Bruffaerts, R, Vandamme, P, Vandenbulcke, M, Maruta, C, Ferreira, C B, Miltenberger, G, Verdelho, A, Afonso, S N, Taipa, R, Caroppo, P, di Fede, G, Giaccone, G, Prioni, S, Redaelli, V, Rossi, G, Tiraboschi, P, Duro, D, Rosario Almeida, M, Castelo-Branco, M, João Leitão, M, Tabuas-Pereira, M, Santiago, B, Gauthier, S, Rosa-Neto, P, Veldsman, M, Flanagan, T, Prix, C, Hoegen, T, Wlasich, E, Loosli, S, Schonecker, S, Semler, E & Anderl-Straub, S 2021, ' Disease-related cortical thinning in presymptomatic granulin mutation carriers ', NeuroImage: Clinical, vol. 29, 102540 . https://doi.org/10.1016/j.nicl.2020.102540
NeuroImage: Clinical, Vol 29, Iss, Pp 102540-(2021)
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
© 2020 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license.
Mutations in the granulin gene (GRN) cause familial frontotemporal dementia. Understanding the structural brain changes in presymptomat
Mutations in the granulin gene (GRN) cause familial frontotemporal dementia. Understanding the structural brain changes in presymptomat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::206c236cf6771818dba529a883b4673f
https://research.vumc.nl/en/publications/f32bfcad-31e0-49f2-b957-578f21195ea2
https://research.vumc.nl/en/publications/f32bfcad-31e0-49f2-b957-578f21195ea2
Autor:
Sandro Sorbi, James B. Rowe, Matthis Synofzik, A. Danek, Martina Bocchetta, Johannes Levin, Markus Otto, Rhian S Convery, Fabrizio Tagliavini, Steven Williams, Daniel C. Alexander, Barbara Borroni, Mollie Neason, David L. Thomas, Jonathan D. Rohrer, Carmela Tartaglia, Alexandre de Mendonça, Giovanni B. Frisoni, David M. Cash, Katrina M. Moore, Roberta Ghidoni, Alexander Gerhard, Elizabeth Finger, Alexandra L. Young, Isabel Santana, Christopher C Butler, Fermin Moreno, Caroline Graff, John C. van Swieten, Mario Masellis, Raquel Sánchez-Valle, Robert Laforce, Simon Ducharme, Daniela Galimberti, Rik Vandenberghe
Publikováno v:
Alzheimer's & Dementia. 16
Autor:
Anthony G Marson, Kumar Das, Mollie Neason, Barbara A. K. Kreilkamp, Besa Ziso, Samia Elkommos, C. de Bezenac, Nicola J. Leek, Simon S. Keller
Publikováno v:
European journal of neurology
BackgroundPatients with chronic focal epilepsy may have atrophy of brain structures important for the generation and maintenance of seizures. However, little research has been conducted in patients with newly diagnosed focal epilepsy (NDfE), despite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48687de4aadfd23418ea9cd2555682ca
https://doi.org/10.1101/2020.07.24.20159368
https://doi.org/10.1101/2020.07.24.20159368
Autor:
Elise G.P. Dopper, Desheng Xu, Christopher C Butler, Alexandre de Mendonça, James B. Rowe, Isabel Santana, Fabrizio Tagliavini, Barbara Borroni, Lize C. Jiskoot, Robert Laforce, Jessica L. Panman, Jackie M. Poos, Yolande A.L. Pijnenburg, Lieke H.H. Meeter, Emma L. van der Ende, Harro Seelaar, Georgia Peakman, Alexander Gerhard, Daniela Galimberti, Jonathan D. Rohrer, Simon Ducharme, Janne M. Papma, Mollie Neason, Charlotte E. Teunissen, Rik Vandenberghe, Meifang Xiao, Elizabeth Finger, Maria Carmela Tartaglia, Adrian Danek, Raquel Sánchez-Valle, Johannes Levin, Markus Otto, Paul F. Worley, Fermin Moreno, Carolin Heller, David M. Cash, Katrina M. Moore, Martina Bocchetta, Rhian S Convery, Caroline Graff, Matthis Synofzik, John C. van Swieten, Mario Masellis
Publikováno v:
Journal of Neurology Neurosurgery and Psychiatry, 91(6), 612-621. BMJ Publishing Group
Van Der Ende, E L, Xiao, M, Xu, D, Poos, J M, Panman, J L, Jiskoot, L C, Meeter, L H, Dopper, E G P, Papma, J M, Heller, C, Convery, R, Moore, K, Bocchetta, M, Neason, M, Peakman, G, Cash, D M, Teunissen, C E, Graff, C, Synofzik, M, Moreno, F, Finger, E, Sánchez-Valle, R, Vandenberghe, R, Laforce, R, Masellis, M, Tartaglia, M C, Rowe, J B, Butler, C R, Ducharme, S, Gerhard, A, Danek, A, Levin, J, Pijnenburg, Y A L, Otto, M, Borroni, B, Tagliavini, F, De Mendonca, A, Santana, I, Galimberti, D, Seelaar, H, Rohrer, J D, Worley, P F & Van Swieten, J C 2020, ' Neuronal pentraxin 2 : A synapse-derived CSF biomarker in genetic frontotemporal dementia ', Journal of Neurology, Neurosurgery and Psychiatry, vol. 91, no. 6, pp. 612-621 . https://doi.org/10.1136/jnnp-2019-322493
Journal of neurology, neurosurgery, and psychiatry 91(6), 612-621 (2020). doi:10.1136/jnnp-2019-322493
Journal of Neurology, Neurosurgery, and Psychiatry
Journal of Neurology, Neurosurgery and Psychiatry, 91(6), 612-621. BMJ PUBLISHING GROUP
Journal of Neurology, Neurosurgery and Psychiatry, 91(6), 612-621. BMJ Publishing Group
Van Der Ende, E L, Xiao, M, Xu, D, Poos, J M, Panman, J L, Jiskoot, L C, Meeter, L H, Dopper, E G P, Papma, J M, Heller, C, Convery, R, Moore, K, Bocchetta, M, Neason, M, Peakman, G, Cash, D M, Teunissen, C E, Graff, C, Synofzik, M, Moreno, F, Finger, E, Sánchez-Valle, R, Vandenberghe, R, Laforce, R, Masellis, M, Tartaglia, M C, Rowe, J B, Butler, C R, Ducharme, S, Gerhard, A, Danek, A, Levin, J, Pijnenburg, Y A L, Otto, M, Borroni, B, Tagliavini, F, De Mendonca, A, Santana, I, Galimberti, D, Seelaar, H, Rohrer, J D, Worley, P F & Van Swieten, J C 2020, ' Neuronal pentraxin 2 : A synapse-derived CSF biomarker in genetic frontotemporal dementia ', Journal of Neurology, Neurosurgery and Psychiatry, vol. 91, no. 6, pp. 612-621 . https://doi.org/10.1136/jnnp-2019-322493
Journal of neurology, neurosurgery, and psychiatry 91(6), 612-621 (2020). doi:10.1136/jnnp-2019-322493
Journal of Neurology, Neurosurgery, and Psychiatry
Journal of Neurology, Neurosurgery and Psychiatry, 91(6), 612-621. BMJ PUBLISHING GROUP
Journal of Neurology, Neurosurgery and Psychiatry, 91(6), 612-621. BMJ Publishing Group
IntroductionSynapse dysfunction is emerging as an early pathological event in frontotemporal dementia (FTD), however biomarkers are lacking. We aimed to investigate the value of cerebrospinal fluid (CSF) neuronal pentraxins (NPTXs), a family of prote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bd6338ac207f600d9f1f0a1164c22d7
https://pure.eur.nl/en/publications/189c930b-79f4-475b-98ab-b63379aa9ab3
https://pure.eur.nl/en/publications/189c930b-79f4-475b-98ab-b63379aa9ab3
Autor:
David M. Cash, Mollie Neason, Martina Bocchetta, Rhian S Convery, Sebastien Ourselin, Jason D. Warren, M. Jorge Cardoso, Marc Modat, Jonathan D. Rohrer
Publikováno v:
NeuroImage : Clinical
NeuroImage: Clinical, Vol 26, Iss, Pp-(2020)
NeuroImage: Clinical, Vol 26, Iss, Pp-(2020)
Background: The basal forebrain is a subcortical structure that plays an important role in learning, attention, and memory. Despite the known subcortical involvement in frontotemporal dementia (FTD), there is little research into the role of the basa