Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Gabrielle A. Morgan"'
Autor:
Jacob C. Spitznagle, Akadia Kacha-Ochana, Joan M. Cook-Mills, Gabrielle A. Morgan, Lauren M. Pachman
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-6 (2024)
Abstract Background Juvenile dermatomyositis (JDM) is a systemic vasculopathy associated with metabolic derangements and possible increased risk for premature atherosclerosis. Oxidation of low-density lipoprotein (LDL) in the endothelium is an early
Externí odkaz:
https://doaj.org/article/986ecb24e1a24bf6b775cd8a8f13fe5b
Autor:
Elisha D. O. Roberson, Rosana A. Mesa, Gabrielle A. Morgan, Li Cao, Wilfredo Marin, Lauren M. Pachman
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-22 (2022)
Abstract In juvenile dermatomyositis (JDM), the most common pediatric inflammatory myopathy, weakness is accompanied by a characteristic rash that often becomes chronic and is associated with vascular damage. We hoped to understand the molecular unde
Externí odkaz:
https://doaj.org/article/87f7f95adc9f4d5db7f9aaaaba33cec7
Autor:
Shefa M. Tawalbeh, Wilfredo Marin, Gabrielle A. Morgan, Utkarsh J. Dang, Yetrib Hathout, Lauren M. Pachman
Publikováno v:
BMC Rheumatology, Vol 4, Iss 1, Pp 1-15 (2020)
Abstract Background Blood accessible biomarkers to assess disease activity and their response to therapies in Juvenile Dermatomyositis (JDM) are urgently needed. This pilot study aims to identify serum protein biomarkers associated with clinical dise
Externí odkaz:
https://doaj.org/article/8adedddc628b4e898ac8d2a8cafc5b96
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 15, Iss 1, Pp 1-5 (2017)
Abstract Objective A pilot study to determine endothelial progenitor cells (EPC) number in children with Juvenile Dermatomyositis (JDM). Methods After obtaining informed consent, the EPC number from 34 fasting children with definite/probable JDM at v
Externí odkaz:
https://doaj.org/article/6c20e9d46f9c43feae4e091aea48f97d
Autor:
Gabrielle A. Morgan, Amer Khojah, Victoria Liu, Sonia I Savani, Lauren M. Pachman, Jackie Bellm, Richard M. Shore
Publikováno v:
Arthritis Care & Research. 74:1065-1069
Myositis-specific antibodies (MSAs) facilitate grouping children with juvenile dermatomyositis (DM) into distinct phenotypes. The first aim of this study was to investigate the link between anti-p155/140 and lipodystrophy as determined by dual x-ray
Autor:
Bhargavi Duvvuri, Lauren M. Pachman, Payton Hermanson, Ting Wang, Richard Moore, Dennis Ding-Hwa Wang, Aaron Long, Gabrielle A. Morgan, Stephen Doty, Rong Tian, Yasemin Sancak, Christian Lood
Publikováno v:
Journal of Autoimmunity. 138:103061
Publikováno v:
Journal of the American Academy of Dermatology. 84:1610-1618
Background Persistent skin manifestations, especially calcinoses, contribute to morbidity in children with juvenile dermatomyositis. Objective To compare the course of skin and muscle involvement and document frequency of calcinosis in juvenile derma
Autor:
Gabrielle A. Morgan, Yetrib Hathout, Shefa M. Tawalbeh, Wilfredo Marin, Utkarsh J. Dang, Lauren M. Pachman
Publikováno v:
BMC Rheumatology, Vol 4, Iss 1, Pp 1-15 (2020)
BackgroundBlood accessible biomarkers to assess disease activity and their response to therapies in Juvenile Dermatomyositis (JDM) are urgently needed. This pilot study aims to identify serum protein biomarkers associated with clinical disease activi
Autor:
Marisa Klein-Gitelman, Megan L. Curran, Gabrielle A. Morgan, Lauren M. Pachman, Amer Khojah, Christian Lood, Stephen B. Doty, Bhargavi Duvvuri
Publikováno v:
Arthritis & Rheumatology. 72:348-358
OBJECTIVE Neutrophils are key immune cells participating in host defense through several mechanisms, including the formation of neutrophil extracellular traps (NETs). This study was undertaken to investigate the role of neutrophils in juvenile dermat
Autor:
Victoria Hans, Petra C E Hissink Muller, Annet van Royen-Kerkhof, Lauren M. Pachman, Femke van Wijk, Maria C. Amoruso, Esther P A H Hoppenreijs, Thaschawee Arkachaisri, Gabrielle A. Morgan, Wineke Armbrust, Kyra A. Gelderman, J. Merlijn van den Berg, Judith Wienke, Sylvia Kamphuis, Joo Guan Yeo
Publikováno v:
Arthritis & rheumatology (Hoboken, N.J.), 72(7), 1214-1226. John Wiley and Sons Ltd
ARTHRITIS & RHEUMATOLOGY, 72(7), 1214-1226. John Wiley & Sons Ltd.
Arthritis & Rheumatology, 72, 1214-1226
Arthritis & Rheumatology, 72(7), 1214-1226. Wiley
Arthritis & Rheumatology, 72, 7, pp. 1214-1226
Arthritis and Rheumatology, 72(7), 1214-1226. WILEY
Arthritis & Rheumatology (Hoboken, N.j.)
ARTHRITIS & RHEUMATOLOGY, 72(7), 1214-1226. John Wiley & Sons Ltd.
Arthritis & Rheumatology, 72, 1214-1226
Arthritis & Rheumatology, 72(7), 1214-1226. Wiley
Arthritis & Rheumatology, 72, 7, pp. 1214-1226
Arthritis and Rheumatology, 72(7), 1214-1226. WILEY
Arthritis & Rheumatology (Hoboken, N.j.)
Contains fulltext : 220769.pdf (Publisher’s version ) (Open Access) OBJECTIVE: Juvenile dermatomyositis (DM) is a heterogeneous systemic immune-mediated vasculopathy. This study was undertaken to 1) identify inflammation/endothelial dysfunction-rel