دسترسی یکساله به بیش از ۵۰۰ ژورنال روز جهان موجود در سامانه
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Chasing MOG antibodies down … assays and lumbar punctures
doi : 10.1093/brain/awad271
Brain, Volume 146, Issue 9, September 2023, Pages 3559–3560
Addressing the gaps between socioeconomic disparities and biological models of dementia
Agust?n Ib??ez1,2,3, Agustina Legaz3,4 and Manuel Ruiz-Adame5
doi : 10.1093/brain/awad236
Investigating cortico-striatal beta oscillations in Parkinson’s disease cognitive decline
Mansoureh Fahimi Hnazaee and Vladimir Litvak
doi : 10.1093/brain/awad273
Enhancing reward learning in the absence of an effect on reward
Michael Browning
doi : 10.1093/brain/awad248
Moving, fast and slow: behavioural insights into bradykinesia in Parkinson’s disease
Damian M. Herz1,2 and Peter Brown
doi : 10.1093/brain/awad069
Advances in understanding the function of alpha-synuclein: implications for Parkinson’s disease
Paolo Calabresi,1,2 Giulia Di Lazzaro,2 Gioia Marino,1 Federica Campanelli 1 and Veronica Ghiglieri
doi : 10.1093/brain/awad150
The functional role of the precuneus
Nicholas B. Dadario1 and Michael E. Sughrue
doi : 10.1093/brain/awad181
TGFβ4 alleviates the phenotype of Charcot–Marie–Tooth disease type 1A
Hyeonjin Jeon, 1,2,†So Young Jang,1,†Geon Kwak, 3,4,†Yong Weon Yi,5,†Mi-Hyeon You,6,†Na Young Park,1,†Ju Hee Jo, 1 Ji Won Yang, 1 Hye Ji Jang,1 Sun-Young Jeong,4 Seung Kee Moon, 4 Hyun Myung Doo, 3 Minyeop Nahm, 2 Donghoon Kim, 1,7 Jong Wook Chang,8 Byung-Ok Choi3,8,9 and Young Bin Hong
doi : 10.1093/brain/awad147
Rare variants in ANO1, encoding a calcium-activated chloride channel, predispose to moyamoya disease
Amélie Pinard,1,†Wenlei Ye,2,†Stuart M. Fraser,3 Jill A. Rosenfeld,4 Pavel Pichurin,5 Scott E. Hickey,6,7 Dongchuan Guo,1 Alana C. Cecchi,1 Maura L. Boerio,1 Stéphanie Guey,8 Chaker Aloui,8 Kwanghyuk Lee,4 Markus Kraemer,9,10 Saleh Omar Alyemni,11 University of Washington Center for Mendelian Genomics Michael J. Bamshad,12 Deborah A. Nickerson,13,‡ Elisabeth Tournier-Lasserve,8,14 Shozeb Haider,11,15 Sheng Chih Jin,16,17 Edward R. Smith,18 Kristopher T. Kahle,19,20,21,22 Lily Yeh Jan,2 Mu He2,23 and Dianna M. Milewicz
doi : 10.1093/brain/awad172
Transactive response DNA-binding protein 43 is enriched at the centrosome in human cells
Alexia Bodin,1,2,†Logan Greibill,3,†Julien Gouju,2 Franck Letournel,2 Silvia Pozzi,4,5 Jean-Pierre Julien,4,5 Laurence Renaud,6,7 Delphine Bohl,8 Stéphanie Millecamps,8 Christophe Verny,1,9 Julien Cassereau,1,9 Guy Lenaers,1,9 Arnaud Chevrollier,1 Anne-Marie Tassin3,‡ and Philippe Codron
doi : 10.1093/brain/awad228
Somatic variants of MAP3K3 are sufficient to cause cerebral and spinal cord cavernous malformations
Jian Ren,1,†Yazi Huang, 2,†Yeqing Ren, 1,†Tianqi Tu,1 Baoshan Qiu,2,3 Daosheng Ai, 2,4 Zhanying Bi,2,5 Xue Bai,2 Fengzhi Li, 2 Jun-Liszt Li, 2,4 Xing-jun Chen,2,4 Ziyan Feng, 2 Zongpei Guo,2 Jianfeng Lei,6 An Tian,1 Ziwei Cui,1 Volkhard Lindner,7 Ralf H. Adams, 8 Yibo Wang, 9 Fei Zhao,2 Jakob K?rbelin, 10 Wenzhi Sun,2,11 Yilong Wang,3 Hongqi Zhang,1 Tao Hong 1 and Woo-ping Ge
doi : 10.1093/brain/awad104
Thalamocortical disconnection involved in pusher syndrome
Hannah Rosenzopf,1,†Julian Klingbeil,2,†Max Wawrzyniak, 2 Lisa R?hrig, 1 Christoph Sperber,1,‡ Dorothee Saur2 and Hans-Otto Karnath
doi : 10.1093/brain/awad096
Corticostriatal beta oscillation changes associated with cognitive function in Parkinson’s disease
Danika L. Paulo,1,†Helen Qian,1,2,†Deeptha Subramanian,1 Graham W. Johnson,1,3 Zixiang Zhao,1 Kilian Hett,4 Hakmook Kang,5 C. Chris Kao,1 Noah Roy,1 Jessica E. Summers,4 Daniel O. Claassen,4 Kaltra Dhima4 and Sarah K. Bick
doi : 10.1093/brain/awad206
Impulse control disorder in Parkinson’s disease is associated with abnormal frontal value signalling
Jorryt G. Tichelaar,1,2 Ceyda Sayal?, 3 Rick C. Helmich 1,2 and Roshan Cools
doi : 10.1093/brain/awad162
Severe cholinergic terminal loss in newly diagnosed dementia with Lewy bodies
Niels Okkels,1,2,3,†Jacob Horsager,1,2,†Miguel Labrador-Espinosa,4,5 Pernille L. Kjeldsen,1,2,6 Malene F. Damholdt,2 Janne Mortensen,3 Karsten Vesterg?rd,6 Karoline Knudsen,1,2 Katrine B. Andersen,1,2 Tatyana D. Fedorova,1,2 Casper Skj?rb?k,1,2 Hanne Gottrup,3 Allan K. Hansen,1,7 Michel J. Grothe4,5 and Per Borghammer
doi : 10.1093/brain/awad192
Rigidity in Parkinson’s disease: evidence from biomechanical and neurophysiological measures
Francesco Asci,1,2,†Marco Falletti, 1,†Alessandro Zampogna,1 Martina Patera,1 Mark Hallett, 3 John Rothwell 4 and Antonio Suppa
doi : 10.1093/brain/awad114
Determinants of cognitive and brain resilience to tau pathology: a longitudinal analysis
Diana I. Bocancea,1,2 Anna L. Svenningsson,3 Anna C. van Loenhoud, 1,2 Colin Groot, 1,2,3 Frederik Barkhof,4,5 Olof Strandberg, 3 Ruben Smith,3,6 for the Alzheimer’s Disease Neuroimaging Initiative Renaud La Joie,7 Howard J. Rosen,7 Michael J. Pontecorvo,8 Gil D. Rabinovici,7,9,10 Wiesje M. van der Flier,1,2,11 Oskar Hansson 3,12 and Rik Ossenkoppele
doi : 10.1093/brain/awad100
Genetically identical twin-pair difference models support the amyloid cascade hypothesis
Emma M. Coomans,1,2,†Jori Tomassen, 3,4,†Rik Ossenkoppele,3,4,5 Betty M. Tijms, 3,4 Luigi Lorenzini, 1,2 Mara ten Kate,1,2 Lyduine E. Collij, 1,2 Fiona Heeman,1,2,6,7 Roos M. Rikken, 1,2 Sophie M. van der Landen,3,4 Marijke E. den Hollander,1,2 Sandeep S. V. Golla,1,2 Maqsood Yaqub,1,2 Albert D. Windhorst,1,2 Frederik Barkhof, 1,2,8 Philip Scheltens,3,4 Eco J. C. de Geus,9 Pieter Jelle Visser, 3,4,10,11 Bart N. M. van Berckel 1,2 and Anouk den Braber3,4,7
doi : 10.1093/brain/awad077
Cerebrospinal fluid transcripts may predict shunt surgery responses in normal pressure hydrocephalus
Zachary Levin,1,2 Owen P. Leary,3 Victor Mora, 1,2 Shawn Kant, 3 Sarah Brown,3 Konstantina Svokos,3 Umer Akbar, 4 Thomas Serre,2,5 Petra Klinge,3 Alexander Fleischmann1,2 and Maria Grazia Ruocco
doi : 10.1093/brain/awad109
Genetic variability in sporadic amyotrophic lateral sclerosis
Sien Hilde Van Daele,1,2,3,4 Matthieu Moisse,1,2 Joke J. F. A. van Vugt, 5 Ramona A. J. Zwamborn, 5 Rick van der Spek,5 Wouter van Rheenen, 5 Kristel Van Eijk, 5 Kevin Kenna,5 Philippe Corcia,6,7 Patrick Vourc’h,7 Philippe Couratier, 8 Orla Hardiman,9 Russell McLaughin,10 Marc Gotkine,11 Vivian Drory,12 Nicola Ticozzi,13,14 Vincenzo Silani, 13,14 Antonia Ratti,13,15 Mamede de Carvalho,16 Jes?s S. Mora Pardina,17 Monica Povedano, 18 Peter M. Andersen, 19 Markus Weber, 20 Nazli A. Bas? ak,21 Chris Shaw,22 Pamela J. Shaw, 23 Karen E. Morrison, 24 John E. Landers, 25 Jonathan D. Glass, 26 Michael A. van Es,5 Leonard H. van den Berg, 5 Ammar Al-Chalabi,22 Jan Veldink 5 and Philip Van Damme1,2,3 , on behalf of Project MinE ALS Sequencing Consortium
doi : 10.1093/brain/awad120
Multiomics and machine-learning identify novel transcriptional and mutational signatures in amyotrophic lateral sclerosis
Alberto Catanese,1,2,†Sandeep Rajkumar, 1 Daniel Sommer,1 Pegah Masrori, 3,4,5 Nicole Hersmus,3,4,5 Philip Van Damme, 3,4,5 Simon Witzel, 6 Albert Ludolph,2,6 Ritchie Ho, 7,8,9,10 Tobias M. Boeckers 1,2 and Medhanie Mulaw
doi : 10.1093/brain/awad075
CDNF rescues motor neurons in models of amyotrophic lateral sclerosis by targeting endoplasmic reticulum stress
Francesca De Lorenzo, 1,2 Patrick Lüningschr?r,3 Jinhan Nam,1,2 Liam Beckett,1,2 Federica Pilotto,4 Emilia Galli,1 P?ivi Lindholm, 1 Cora Rüdt von Collenberg,3 Simon Tii Mungwa, 3 Sibylle Jablonka,3 Julia Kauder,5 Nadine Thau-Habermann,5 Susanne Petri,5 Dan Lindholm,6,7 Smita Saxena, 4 Michael Sendtner,3 Mart Saarma 1,†and Merja H. Voutilainen
doi : 10.1093/brain/awad087
Anoctamin-5 related muscle disease: clinical and genetic findings in a large European cohort
Alexander de Bruyn,1 Federica Montagnese, 2 Sonja Holm-Yildiz,3 Nanna Scharff Poulsen,3 Tanya Stojkovic, 4 Anthony Behin,4 Johanna Palmio, 5 Manu Jokela, 5,6 Jan L. De Bleecker,7 Marianne de Visser,8 Anneke J. van der Kooi,8 Leroy ten Dam,8 Cristina Dom?nguez Gonz?lez,9 Lorenzo Maggi, 10 Annamaria Gallone, 10 Anna Kostera-Pruszczyk, 11 Anna Macias, 11 Anna ?usakowska,11 Velina Nedkova,12 Montse Olive, 13,14 Rodrigo ?lvarez-Velasco, 13,14 Julia Wanschitz,15 Carmen Paradas,16,17 Fabiola Mavillard,16,17 Giorgia Querin,18 Gorka Fern?ndez-Eulate,4 Ros Quinlivan,19 Maggie C. Walter,2 Christophe E. Depuydt,20 Bjarne Udd,5 John Vissing,3 Benedikt Schoser2 and Kristl G. Claeys
doi : 10.1093/brain/awad088
Clinical features and prognostic factors in adults with viral meningitis
Pelle Trier Petersen,1,2 Jacob Bodilsen, 3,4 Micha Phill Gr?nholm Jepsen, 1 Lykke Larsen, 5 Merete Storgaard,6 Birgitte R?nde Hansen, 7 Jannik Helweg-Larsen,8 Lothar Wiese, 9 Hans Rudolf Lüttichau,10 Christian ?stergaard Andersen, 11 Henrik Nielsen, 3,4 Christian Thomas Brandtand 9 for the Danish Study Group of Infections of the Brain (DASGIB)
doi : 10.1093/brain/awad089
Neuropathy due to bi-allelic SH3TC2 variants: genotype-phenotype correlation and natural history
Tyler Rehbein,1 Tong Tong Wu, 2 Simona Treidler, 3 Davide Pareyson, 4 Richard Lewis, 5 Sabrina W. Yum, 6,7 Brett A. McCray, 8 Sindhu Ramchandren, 9 Joshua Burns, 10 Jun Li, 11 Richard S. Finkel, 12 Steven S. Scherer, 6 Stephan Zuchner, 13 Michael E. Shy, 14 Mary M. Reilly 15 and David N. Herrmann 1 on behalf of the Inherited Neuropathy Consortium-Rare Diseases Clinical Research Network (INC-RDCRN)
doi : 10.1093/brain/awad095
Mitochondrial dysfunction and calcium dysregulation in COQ8A-ataxia Purkinje neurons are rescued by CoQ10 treatment
Ioannis Manolaras, 1,2,3,4 Andrea Del Bondio,5,6 Olivier Griso,1,2,3,4 Laurence Reutenauer,1,2,3,4,5,6 Aurélie Eisenmann,1,2,3,4 Bianca H. Habermann 7 and Hélène Puccio
doi : 10.1093/brain/awad099
Molecular basis of FAAH-OUT-associated human pain insensitivity
Hajar Mikaeili,1 Abdella M. Habib, 2 Charlix Wai-Lok Yeung,1 Sonia Santana-Varela,1 Ana P. Luiz, 1 Kseniia Panteleeva, 1 Sana Zuberi, 1 Alkyoni Athanasiou-Fragkouli,3 Henry Houlden, 3 John N. Wood,1 Andrei L. Okorokov1 and James J. Cox 1
doi : 10.1093/brain/awad098
A sensory neuron-specific long non-coding RNA reduces neuropathic pain by rescuing KCNN1 expression
Bing Wang,1,†Longfei Ma,1,†Xinying Guo,1,†Shibin Du,1,†Xiaozhou Feng,1,†Yingping Liang,1,†Gokulapriya Govindarajalu, 1 Shaogen Wu,1 Tong Liu,2 Hong Li,2 Shivam Patel,1 Alex Bekker,1 Huijuan Hu 1,3 and Yuan-Xiang Tao
doi : 10.1093/brain/awad110
Widespread genomic influences on phenotype in Dravet syndrome, a ‘monogenic’ condition
Helena Martins Custodio, 1,2,†Lisa M. Clayton, 1,2,†Ravishankara Bellampalli,1,2 Susanna Pagni,1,2 Katri Silvennoinen,1,2,3 Richard Caswell,4 Genomics England Research Consortium Andreas Brunklaus,5,6 Renzo Guerrini,7 Bobby P. C. Koeleman, 8 Johannes R. Lemke,9,10 Rikke S. M?ller, 11,12 Ingrid E. Scheffer,13,14 Sarah Weckhuysen,15,16,17,18 Federico Zara,19,20 Sameer Zuberi, 5,6 Karoline Kuchenbaecker,21 Simona Balestrini, 1,2,7 James D. Mills 1,2,22,‡ and Sanjay M. Sisodiya1,
doi : 10.1093/brain/awad111
Spike propagation mapping reveals effective connectivity and predicts surgical outcome in epilepsy
Margherita A. G. Matarrese,1,2,3 Alessandro Loppini, 2 Lorenzo Fabbri,1,3 Eleonora Tamilia,4 M. Scott Perry, 1 Joseph R. Madsen,5 Jeffrey Bolton,6 Scellig S. D. Stone, 5 Phillip L. Pearl, 6 Simonetta Filippi 2 and Christos Papadelis
doi : 10.1093/brain/awad118
Structural disconnection relates to functional changes after temporal lobe epilepsy surgery
Lucas E. Sainburg,1,2 Andrew P. Janson, 2 Graham W. Johnson, 1,2 Jasmine W. Jiang, 2,3 Baxter P. Rogers,1,2 Catie Chang,1,2,4 Dario J. Englot 1,2,3,4 and Victoria L. Morgan
doi : 10.1093/brain/awad117
Cortical microstructural gradients capture memory network reorganization in temporal lobe epilepsy
Jessica Royer,1,2 Sara Larivière,1 Raul Rodriguez-Cruces, 1 Donna Gift Cabalo,1 Shahin Tavakol, 1 Hans Auer,1 Alexander Ngo,1 Bo-yong Park,1,3,4 Casey Paquola, 5 Jonathan Smallwood,6 Elizabeth Jefferies, 7 Lorenzo Caciagli,8 Andrea Bernasconi, 9 Neda Bernasconi, 9 Birgit Frauscher2 and Boris C. Bernhardt
doi : 10.1093/brain/awad125
Diagnostic implications of MOG-IgG detection in sera and cerebrospinal fluids
Yuki Matsumoto,1,†Kimihiko Kaneko, 1,2,†Toshiyuki Takahashi,3 Yoshiki Takai, 1,2 Chihiro Namatame,1 Hiroshi Kuroda, 1 Tatsuro Misu,1,2 Kazuo Fujihara 4 and Masashi Aoki 1
doi : 10.1093/brain/awad122
Disease, disorder, condition or enigma? Epilepsy and its modern history re-examined
Walter van Emde Boas
doi : 10.1093/brain/awad168
Presymptomatic spinal muscular atrophy: a cautionary approach to the proposed new terminology
Michelle A. Farrar, 1,2 Matthew C. Kiernan3,4 and Didu S. Kariyawasam
doi : 10.1093/brain/awad061
The Italian reappraisal of the most frequent genetic defects in hereditary optic neuropathies and the global top 10
Claudio Fiorini, 1,†Danara Ormanbekova,1,†Flavia Palombo, 1,†Michele Carbonelli, 2 Giulia Amore, 2 Martina Romagnoli,1 Pietro d’Agati, 1 Maria Lucia Valentino,1,2 Piero Barboni,3 Maria Lucia Cascavilla, 3 Annamaria De Negri, 4 Federico Sadun,5 Arturo Carta, 6 Francesco Testa,7 Vittoria Petruzzella, 8 Silvana Guerriero, 8 Stefania Bianchi Marzoli, 9 Valerio Carelli,1,2,†Chiara La Morgia 1,2,†and Leonardo Caporali
doi : 10.1093/brain/awad080
Lecanemab: turning point, or status quo? An ethics perspective
Timothy Daly
doi : 10.1093/brain/awad094
Reply: Lecanemab: turning point, or status quo? An ethics perspective
John Hardy 1,2,3 and Catherine Mummery
doi : 10.1093/brain/awad102
Correction to: Rare variants in ANO1, encoding a calcium-activated chloride channel, predispose to moyamoya disease
doi : 10.1093/brain/awad270
