Results 91 to 100 of about 1,059,853 (352)
Spine [PDF]
Operative Neurosurgery, 2019 Faiz U, Ahmad, Erica F, Bisson, Stephen Shelby, Burks, Jason J, Chang, A Jessey, Chugh, Ian, Côté, Jason M, Frerich, Zachary C, Gersey, Benjamin K, Hendricks, Michael, Karsy, Manish, Kasliwal, Katie L, Krause, Glen R, Manzano, Clinton D, Morgan, Laura A, Snyder, Christian C, Swinney, Khoi D, Than, Christian B, Theodotou, Anand, Veeravagu, Jacqueline, Ventura +19 moreopenaire +2 more sourcesSelf sliding growth guidance for early-onset scoliosis: Clinical and radiological results after a minimum of five years (5-13) of follow-up
Brain and Spine, 2021 Mustafa Eltayep, Recep Dincer, Ahmet Ates, Sina Coskun, Ugur Tasci, Ayhan Mutlu, Seray Gur, Sinan Kahraman, Tunay Sanli, Selhan Karadereler, Meric Enercan, Azmi Hamzaoglu +11 moredoaj +1 more sourceMultiple Regression Analysis of Factors Affecting the Mental Component Score Constituents of SF-36 in Adult Spinal Deformity
Global Spine Journal, 2016 Introduction As surgical decision-making and preoperative planning for adult spinal deformity (ASD) need strongly be interrelated to health related quality of life (HRQOL), there are multiple studies focusing on factors with an impact on it. Based on the Selim Ayhan, Selcem Yuksel, Asli Niyazi, Vugar Nabiyev, Ümit Özgür Güler, Tiro Mmopelwa, Montse Domingo Sabat, Ferran Pellise, Ahmet Alanay, Francisco Javier Sanchez Perez-Grueso, Frank Kleinstuck, Ibrahim Obeid, Emre Acaroglu, +13 moredoaj +1 more sourceExperimental Evaluation of Book Drawing Algorithms
, 2017 A $k$-page book drawing of a graph $G=(V,E)$ consists of a linear ordering of
its vertices along a spine and an assignment of each edge to one of the $k$
pages, which are half-planes bounded by the spine. In a book drawing, two edges
cross if and only if Klawitter, Jonathan, Mchedlidze, Tamara, Nöllenburg, Martin +2 morecore +2 more sourcesOnasemnogene Abeparvovec in Type I Spinal Muscular Atrophy: 24‐Month Follow‐Up From the Italian Registry
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective
Onasemnogene abeparvovec (OA) is an AAV9‐based gene therapy for spinal muscular atrophy type I (SMA I). Real‐world outcomes show increased response variability compared to clinical trials, and follow‐up data beyond 12–18 months are limited.Marika Pane, Giorgia Coratti, Chiara Cutrì, Antonio Varone, Riccardo Masson, Adele D'Amico, Valeria Sansone, Sonia Messina, Federica Ricci, Chiara Ticci, Claudio Bruno, Caterina Agosto, Francesca Benedetti, Antonella Pini, Sabrina Siliquini, Massimiliano Filosto, Alberto Zambon, Ilaria Bitetti, Maria Rosaria Manna, Claudia Dosi, Riccardo Zanin, Stefano Parravicini, Roberto De Sanctis, Giulia Stanca, Michela Catteruccia, Michele Tosi, Irene Mizzoni, Emilio Albamonte, Valentina Franchino, Maria Sframeli, Ilaria Cavallina, Elena Procopio, Michele Sacchini, Simone Morando, Noemi Brolatti, Federica Trucco, Gaia Scarpini, Elena Briganti, Beatrice Berti, Concetta Palermo, Daniela Leone, Stefano C. Previtali, Eugenio Mercuri, the ITASMAC working group +43 morewiley +1 more sourceExosomes from Bone Marrow Mesenchymal Stem Cells Inhibit Neuronal Apoptosis and Promote Motor Function Recovery via the Wnt/β-catenin Signaling Pathway
Cell Transplantation, 2019 Severe spinal cord injury (SCI) is caused by external mechanical injury, resulting in unrecoverable neurological injury. Recent studies have shown that exosomes derived from bone marrow mesenchymal stem cells (BMSCs-Exos) might be valuable paracrine ...Ci Li, Guangjun Jiao, Wenliang Wu, Hongliang Wang, Shanwu Ren, Lu Zhang, Hongming Zhou, Haichun Liu, Yunzhen Chen +8 moredoaj +1 more sourceClinical Validation of Plasma p‐217tau in Neurological Diseases
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective
Plasma p‐217tau is a minimally invasive but specific biomarker for diagnosing Alzheimer's disease (AD). However, its disease specificity remains to be clinically evaluated. We validated the reliability of the p‐217tau biomarker in 12 other neurological diseases.Takeshi Kawarabayashi, Takumi Nakamura, Ryoma Takahashi, Tetsuya Ueda, Seiji Kinoshita, Chikage Uchida, Takashi Sugawara, Kentaro Hashimoto, Kunihiko Ishizawa, Masakuni Amari, Hiroo Kasahara, Yoshio Ikeda, Masamitsu Takatama, Mikio Shoji +13 morewiley +1 more sourceSPG4 and Dementia: Expanding the Clinical Spectrum
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective
Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.Emanuele Panza, Arun Meyyazhagan, Eliseo Picchi, Gustavo Ribas, Ingrid Faber, Ryosuke Miyamoto, Preethi Basavaraju, Paolo Eusebi, Haripriya Kuchi Bhotla, Mario Stasi, Fabrizio Gaudiello, Francesco Patti, Filippo Maria Santorelli, Marcondes Cavalcante França Jr, José Luiz Pedroso, Orlando Graziani Povoas Barsottini, Hélio Afonso Ghizoni Teive, Peter Henry St George‐Hyslop, Toshitaka Kawarai, Antonio Orlacchio +19 morewiley +1 more source