Results 121 to 130 of about 698,332 (299)
dataset related to article "Dysregulation of Muscle-Specific MicroRNAs as Common Pathogenic Feature Associated with Muscle Atrophy in ALS, SMA and SBMA: Evidence from Animal Models and Human Patients"
, 2021 Claudia Malacarne, M. Galbiati, Eleonora Giagnorio, Paola Cavalcante, Franco Salerno, Francesca Andreetta, Cinzia Cagnoli, Michela Taiana, Monica Nizzardo, Stefania Corti, Viviana Pensato, Anna Venerando, Cinzia Gellera, Silvia Fenu, Davide Pareyson, Riccardo Masson, Lorenzo Maggi, Eleonora Dalla Bella, Giuseppe Lauria, Renato Mantegazza, Pia Bernasconi, Angelo Poletti, Silvia Bonanno, Stefania Marcuzzo +23 moreopenalex +1 more sourceLongitudinal Brain Atrophy Rates in Presymptomatic Carriers of Genetic Frontotemporal Dementia [PDF]
, 2022 Jackie M. Poos, Leonie D. M. Grandpierre, Emma L. van der Ende, Jessica Panman, Janne M. Papma, Harro Seelaar, Esther van den Berg, Ronald van ’t Klooster, Esther E. Bron, Rebecca M. E. Steketee, Meike W. Vernooij, Yolande A.L. Pijnenburg, Serge A.R.B. Rombouts, John C. van Swieten, Lize C. Jiskoot +14 moreopenalex +1 more sourcePortable Low‐Field Magnetic Resonance Imaging in People With Human Immunodeficiency Virus
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective
The aging population of people with HIV (PWH) raises heightened concerns regarding accelerated aging and dementia. Portable, low‐field MRI (LF‐MRI) is an innovative technology that could enhance access and facilitate routine monitoring of PWH.Annabel Sorby‐Adams, Malachi Keo, Jennifer Guo, Daire Daly, Richard Ahern, Kimon Zachary, Gregory Robbins, Rajesh T. Gandhi, Bragi Sveinsson, Adam de Havenon, Kevin N. Sheth, Otto Rapalino, Juan Eugenio Iglesias Gonzales, W. Taylor Kimberly, Shibani S. Mukerji +14 morewiley +1 more sourceSecond consensus statement on the diagnosis of multiple system atrophy
Neurology, 2008 S. Gilman, G. Wenning, Phillip A. Low, D. Brooks, C. Mathias, J. Trojanowski, N. Wood, C. Colosimo, A. Durr, C. Fowler, H. Kaufmann, T. Klockgether, A. Lees, W. Poewe, N. Quinn, T. Révész, D. Robertson, P. Sandroni, K. Seppi, M. Vidailhet +19 moresemanticscholar +1 more sourceDiscriminating α-synuclein strains in Parkinson’s disease and multiple system atrophy
Nature, 2020 M. Shahnawaz, Abhisek Mukherjee, S. Pritzkow, Nicolas Mendez, Prakruti Rabadia, Xiangan Liu, Bo Hu, A. Schmeichel, W. Singer, Gang Wu, A. Tsai, Hamid Shirani, K. Nilsson, Phillip A. Low, C. Soto +14 moresemanticscholar +1 more sourceInsights Into the Antigenic Repertoire of Unclassified Synaptic Antibodies
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective
We sought to characterize the sixth most common finding in our neuroimmunological laboratory practice (tissue assay‐observed unclassified neural antibodies [UNAs]), combining protein microarray and phage immunoprecipitation sequencing (PhIP‐Seq). Methods
Patient specimens (258; 133 serums; 125 CSF) meeting UNA criteria were profiled; Michael Gilligan, John R. Mills, Paulina Vargas, Naveen K. Paramasivan, Connie E. Lesnick, Eati Basal, Surendra Dasari, James P. Fryer, Shannon R. Hinson, Joseph Laporta, Amy Espinal, Dennis Fitzgerald, Carolina Garcia, Anna E. Morenkova, Paola Pergami, Anna Shah, Andrew Knight, Reghann LaFrance Corey, Vanda A. Lennon, Anastasia Zekeridou, Sean J. Pittock, Divyanshu Dubey, Andrew McKeon +22 morewiley +1 more sourceFrailty Exacerbates Disability in Progressive Multiple Sclerosis
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background
To evaluate frailty in severe progressive multiple sclerosis (PMS) and to investigate the underlying mechanisms. Methods
This prospective, cross‐sectional, multicenter study enrolled a late severe PMS group requiring skilled nursing (n = 53) and an age, sex, and disease duration‐matched control PMS group (n = 53).Taylor R. Wicks, Anna Wolska, Diala Ghazal, Dejan Jakimovski, Bianca Weinstock‐Guttman, Alexander Burnham, Niels Bergsland, Michael G. Dwyer, Alan T. Remaley, Robert Zivadinov, Murali Ramanathan +10 morewiley +1 more sourceSingle‐Dose Gene‐Replacement Therapy for Spinal Muscular Atrophy
New England Journal of Medicine, 2017 J. Mendell, S. Al-Zaidy, R. Shell, W. Arnold, L. Rodino-Klapac, T. Prior, L. Lowes, L. Alfano, K. Berry, K. Church, J. Kissel, S. Nagendran, J. L'italien, D. Sproule, C. Wells, J. Cardenas, M. Heitzer, A. Kaspar, Sarah E. Corcoran, L. Braun, S. Likhite, Carlos J. Miranda, K. Meyer, K. Foust, A. Burghes, B. Kaspar +25 moresemanticscholar +1 more sourceHealth‐Related Quality of Life in Rare Forms of Childhood‐Onset Hereditary Spastic Paraplegia
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT
We assessed health‐related quality of life (HRQoL) in 80 children with rare hereditary spastic paraplegias using the Caregiver Priorities and Child Health Index of Life with Disabilities and clinician‐reported outcomes. HRQoL was consistently reduced, particularly in relation to motor, autonomic, and bulbar symptoms.Henri J. D. Schmidt, Nicole Battaglia, Joshua Rong, Amy Tam, Siofra Carty, Vicente Quiroz, Kathryn Yang, Zainab Zaman, Luca Schierbaum, Katerina Bernardi, Julian E. Alecu, Darius Ebrahimi‐Fakhari +11 morewiley +1 more source