Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Charles K. Li"'
Autor:
Sonia Shah, Paul Knopp, Bhanu P. Singh, Halima Moncrieffe, Charles K. Li, Bin Gao, Lucy R. Wedderburn, Kanneboyina Nagaraju, Hemlata Varsani
Publikováno v:
The American Journal of Pathology. 175:1030-1040
Folding and transport of proteins, such as major histocompatibility complex (MHC) class I, through the endoplasmic reticulum (ER) is tightly regulated in all cells, including muscle tissue, where the specialized ER sarcoplasmic reticulum is also crit
Autor:
Charles K. Li, David A. Isenberg
Publikováno v:
Medicine. 34:445-452
Systemic lupus erythematosus (SLE) is a diverse autoimmune rheumatic disease principally affecting women during childbearing years. The female-to-male ratio is around 9:1. Although virtually all patients have skin and joint disease between 30 and 50%
Autor:
Charles K. Li, Lucy R. Wedderburn
Publikováno v:
Best Practice & Research Clinical Rheumatology. 18:345-358
The paediatric idiopathic inflammatory myopathies (IIMs) are a group of rare but serious systemic autoimmune conditions of childhood. The most common of the paediatric IIMs is juvenile dermatomyositis (JDM), while polymyositis and inclusion body myos
Autor:
Charles K. Li, Lucy R. Wedderburn, Janice L. Holton, Hemlata Varsani, Katy Newton, Brian Harding
Publikováno v:
Muscle & Nerve. 37:259-261
The aim of this study was to define normal ranges of histological features in pediatric muscle in comparison with muscle demonstrating inflammatory changes. Sixteen pediatric muscle biopsy samples, considered normal by standard histology, were analyz
Autor:
Hemlata, Varsani, Susan C, Charman, Charles K, Li, Suely K N, Marie, Anthony A, Amato, Brenda, Banwell, Kevin E, Bove, Andrea M, Corse, Alison M, Emslie-Smith, Thomas S, Jacques, Ingrid E, Lundberg, Carlo, Minetti, Inger, Nennesmo, Elisabeth J, Rushing, Adriana M E, Sallum, Caroline, Sewry, Clarissa A, Pilkington, Janice L, Holton, Lucy R, Wedderburn, Linda, Suffiel
Publikováno v:
Annals of the Rheumatic Diseases
ObjectivesTo study muscle biopsy tissue from patients with juvenile dermatomyositis (JDM) in order to test the reliability of a score tool designed to quantify the severity of histological abnormalities when applied to biceps humeri in addition to qu
Juvenile dermatomyositis (JDM) is a rare but complex and potentially life-threatening autoimmune disease of childhood, primarily affecting proximal muscles and skin. Although the cause of JDM remains unknown it is clear that genetic and environmental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f68f8f80d23a9e004e9eed717d47a3d6
https://europepmc.org/articles/PMC3383527/
https://europepmc.org/articles/PMC3383527/
Autor:
Kanneboyina Nagaraju, Shi-Jin Zhang, Håkan Westerblad, Cecilia Grundtman, Charles K. Li, Abram Katz, Lucy R. Wedderburn, Johanna T. Lanner, S Salomonsson, Ingrid E. Lundberg
Publikováno v:
Musclenerve. 39(5)
Expression of major histocompatibility complex (MHC) class I in skeletal muscle fibers is an early and consistent finding in inflammatory myopathies. To test if MHC class I has a primary role in muscle impairment, we used transgenic mice with inducib
Autor:
Hemlata, Varsani, Katy R, Newton, Charles K, Li, Brian, Harding, Janice L, Holton, Lucy R, Wedderburn
Publikováno v:
Musclenerve. 37(2)
The aim of this study was to define normal ranges of histological features in pediatric muscle in comparison with muscle demonstrating inflammatory changes. Sixteen pediatric muscle biopsy samples, considered normal by standard histology, were analyz
Autor:
Suely Kazue Nagahashi Marie, Carlo Minetti, Elisabeth J. Rushing, Susan C. Charman, Andrea M. Corse, Lucy R. Wedderburn, Katy Newton, Clarissa Pilkington, Ingrid E. Lundberg, Anthony A. Amato, Janice L. Holton, Charles K. Li, Brian Harding, Jessica E. Hoogendijk, Alison M. Emslie-Smith, Brenda Banwell, Inger Nennesmo, Hemlata Varsani, Kevin E. Bove, Caroline Sewry
Objective To devise and test a system with which to evaluate abnormalities on muscle biopsy samples obtained from children diagnosed with juvenile dermatomyositis (DM). Methods We established an International Consensus Group on Juvenile DM Biopsy and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f3ad717ef020fd08a0e99d8e62834e5
http://hdl.handle.net/11567/222532
http://hdl.handle.net/11567/222532
Autor:
Jill Moss, Russell J.M. Lane, Poonam Singh, Chiara Marini-Bettolo, Federico Roncaroli, Peter Charles, Charles K. Li
Publikováno v:
Annals of the Rheumatic Diseases. 71:A47.2-A48
Immune mediated inflammatory myopathies are a heterogeneous group of acquired diseases characterised by inflammation of skeletal muscle. In recent years, this group of conditions has become better characterised by the detection of autoantibodies to a