Results 71 to 80 of about 982,800 (303)

What Works? How Federal Contractors are Implementing Section 503: Executive Summary [PDF]

, 2018
This survey is part of a larger project entitled “Initial Impact of Section 503 Rules: Identifying Effective Employer Practices and Trends in Disability Violations among Federal Contractors” funded by the US Department of Labor, Chief Evaluation Office ...
Bruyere, Susanne M, Dr., von Schrader, Sarah   +1 more
core   +1 more source

Predicting Loss of Ambulation in Limb Girdle Muscular Dystrophy R9

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Limb girdle muscular dystrophy type R9 (LGMDR9) results from biallelic variants in FKRP. There is limited data to predict loss of ambulation (LOA) among those with LGMDR9. Methods Participants in an ongoing dystroglycanopathy natural history study (NCT00313677) with FKRP variants who had achieved ambulation and were more than 3 ...
Chandra L. Miller, Lauren N. Coffey, Shelley R. H. Mockler, Katie M. Laubscher, Carrie M. Stephan, M. Bridget Zimmerman, Katherine D. Mathews   +6 more
wiley   +1 more source

An interdisciplinary clinical practice model for the management of low-back pain in primary care: the CLIP project [PDF]

, 2008
Background Low-back pain is responsible for significant disability and costs in industrialized countries. Only a minority of subjects suffering from low-back pain will develop persistent disability.
Stéphane Poitras, Michel Rossignol, Clermont Dionne, Michel Tousignant, Manon Truchon, Bertrand Arsenault, Pierre Allard, Manon Coté, Alain Neveu, LH Pengel, G Waddell, J Borkan, K Karjalainen, MW van Tulder, AC Breen, Royal College of General Practitioners (RCGP), AD Oxman, BW Koes, S Weiser, P Loisel, WE van der Weide, MW van Tulder, JG Jarvik, J Breslau, JW Frank, WS Shaw, CE Dionne, CE Dionne, JA Kopec, M Roland, JC Fairbank, JB Staal, MJL Sullivan, SH Kori, G Waddell, MJL Sullivan, M Davidson, AK Burton, P Little, L Abenhaim, L Butler, L Li, AK Burton, KB Hagen, G Hilde, S Stock, G Pransky, K Karjalainen, MJ Durand, RW Ostelo, JA Hayden, MJL Sullivan, GE Bekkering, V Gonzalez-Urzelai, PB Bishop, A Espeland, T Overmeer, H Schers, ID Graham, MW van Tulder, N Bogduk, MW van Tulder, KC Jackson, G Bronfort, WJ Assendelft, DC Cherkin, SF Nadler, M van Tulder, MW van Tulder, TJ Schnitzer, AD Furlan, E Manheimer, MW Heymans, HA Clare, AD Furlan, KB Hagen, P Philadelphia, AA Harte, P Jellema, L Niemisto, PJ Nelemans, J Guzman, M van Tulder, CG Maher, MJ Yelland, G Urrutia, CW Slipman, A Khadilkar   +87 more
core   +1 more source

Immune‐Driven Expression in Inclusion Body Myositis With T‐Cell Large Granular Lymphocytic Leukemia

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives T‐cell large granular lymphocytic leukemia (T‐LGLL), reported in up to 58% of inclusion body myositis (IBM) patients, is a rare leukemia of cytotoxic or less commonly helper T cells. The range of myopathies in T‐LGLL and the impact of coexisting T‐LGLL in IBM are not well understood. Our objectives are to investigate the spectrum of
Pannathat Soontrapa, Iago Pinal‐Fernandez, Pritikanta Paul, Michael P. Skolka, Margherita Milone, Min Shi, Mithun V. Shah, Maria Casal‐Dominguez, Katherine Pak, Andrew L. Mammen, Teerin Liewluck   +10 more
wiley   +1 more source

Characterization of Clinical Phenotype to Glial Fibrillary Acidic Protein Concentrations in Alexander Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To determine the concentration of glial fibrillary acidic protein (GFAP) in cerebrospinal fluid (CSF) and plasma in Alexander disease (AxD) and whether GFAP levels are predictive of disease phenotypes. Methods CSF and plasma were collected (longitudinally when available) from AxD participants and non‐AxD controls.
Amy T. Waldman, Asako Takanohashi, Joshua Y. Joung, Geraldine W. Liu, Kaley Arnold, Amy Pizzino, Walter Faig, Sarah Woidill, Sona Narula, Adeline L. Vanderver   +9 more
wiley   +1 more source

Protocolo de avaliação da amusia: exemplo português Evaluation protocol for amusia: portuguese sample

Brazilian Journal of Otorhinolaryngology, 2012
A amusia é uma disfunção que compromete o processamento musical. Parte desse processamento é feito a nível do cortéx auditivo primário. O estudo dessa afecção permite-nos avaliar também as vias auditivas centrais.
Maria Conceição Peixoto, Jorge Martins, Pedro Teixeira, Marisa Alves, José Bastos, Carlos Ribeiro   +5 more
doaj   +1 more source

Battling Red Tape: Veterans Struggle for Care and Benefits [PDF]

, 2008
More than 1.5 million troops have served in Iraq and Afghanistan. 30,000 troops are counted among those wounded in action. But hundreds of thousands of others have suffered injuries not recorded in the official tally, including the many veterans with ...
Vanessa Williamson
core  

Spinal Cord Infarction Versus Idiopathic Transverse Myelitis: Clinical, Radiological, and Functional Insights From a Retrospective Cohort Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Introduction Spinal cord infarction (SCI) is a rare but devastating myelopathy, characterized by a high disability rate and an unfavorable prognosis. It has often been underdiagnosed and misdiagnosed as idiopathic transverse myelitis (ITM). This study aimed to describe the clinical features, radiological biomarkers, treatments, and functional ...
Zeqiang Ji, Jianlong Zhang, Yiming Shi, Shiyu Shan, Yang Du, Guangshuo Li, Ying Jin, Yani Zhang, Chuanying Wang, Yijun Lin, Yuhao Guo, Decai Tian, Xingquan Zhao, Tian Song   +13 more
wiley   +1 more source

Coordinated and tailored work rehabilitation: a randomized controlled trial with economic evaluation undertaken with workers on sick leave due to musculoskeletal disorders [PDF]

, 2009
Introduction In Denmark, the magnitude and impact of work disability on the individual worker and society has prompted the development of a new "coordinated and tailored work rehabilitation" (CTWR) approach.
A Bandura, C Briand, Carl Lysbeck Hansen, David Sherson, EL Hultberg, G Waddell, G Waddell, HH Lauridsen, HH Lauridsen, IA Steenstra, IA Steenstra, J Frank, J Hogelund, J Karrholm, JAL Gorringe, Jens Olsen, JR Anema, Jørgen Kilsgaard, M Kivimaki, M Labriola, M Sculpher, MJ Durand, MJ Durand, N Krause, N Krause, N Krause, P Loisel, P Loisel, P Loisel, RL Franche, RL Franche, S Gjesdal, S Gjesdal, SJ Linton, T Lund, TH Hansson, Thomas Lund, Ute Bültmann   +37 more
core   +4 more sources

Remote Assessment of Ataxia Severity in SCA3 Across Multiple Centers and Time Points

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Spinocerebellar ataxia type 3 (SCA3) is a genetically defined ataxia. The Scale for Assessment and Rating of Ataxia (SARA) is a clinician‐reported outcome that measures ataxia severity at a single time point. In its standard application, SARA fails to capture short‐term fluctuations, limiting its sensitivity in trials.
Marcus Grobe‐Einsler, Vivian Maas, Arian Taheri Amin, Jennifer Faber, Tamara Schaprian, Katharina Hill, Matthis Synofzik, Lisa H. Graf, Heike Jacobi, Manuela Lima, Ana F. Ferreira, Bart P. van de Warrenburg, Ilse H. J. Willemse, Dagmar Timmann, Andreas Thieme, Paola Giunti, Hector Garcia‐Moreno, Magda M. Santana, Jeannette Hübener‐Schmid, Elin H. Davies, Thomas Klockgether   +20 more
wiley   +1 more source