Zobrazeno 1 - 10
of 145
pro vyhledávání: '"John F, Bohnsack"'
Autor:
Margaret H. Chang, Fatima Barbar-Smiley, Shoghik Akoghlanian, Joanne Drew, Sheila T. Angeles-Han, Megan Quinlan-Waters, John F. Bohnsack, Ashley M. Cooper, Barbara Edelheit, Jennifer Twachtman-Bassett, Melissa A. Lerman, Kabita Nanda, C. Egla Rabinovich, Mindy S. Lo, for the CARRA Uveitis Workgroup and the CARRA Registry Investigators
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-10 (2024)
Abstract Background Chronic anterior uveitis (CAU) carries a significant risk for eye complications and vision loss. The Childhood Arthritis and Rheumatology Research Alliance (CARRA) introduced consensus treatment plans (CTPs) to standardize treatme
Externí odkaz:
https://doaj.org/article/52c07c9574c7440380bfed5cc81165ab
Autor:
Cecile N. Avery, Nicole D. Russell, Cody J. Steely, Aimee O. Hersh, John F. Bohnsack, Sampath Prahalad, Lynn B. Jorde
Publikováno v:
HGG Advances, Vol 5, Iss 2, Pp 100277- (2024)
Summary: Juvenile idiopathic arthritis (JIA) is a complex rheumatic disease encompassing several clinically defined subtypes of varying severity. The etiology of JIA remains largely unknown, but genome-wide association studies (GWASs) have identified
Externí odkaz:
https://doaj.org/article/2a0eec16dbe84a5baca47afb40757e3f
Autor:
Angela Taneja Kohli, Aimee O. Hersh, Lori Ponder, Lai Hin Kimi Chan, Kelly A. Rouster-Stevens, Anne E. Tebo, Subra Kugathasan, Stephen L. Guthery, John F. Bohnsack, Sampath Prahalad
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 21, Iss 1, Pp 1-7 (2023)
Abstract Background The prevalence of Celiac Disease (CD) in Juvenile Idiopathic Arthritis (JIA) has been reported to be 0.1–7% in various small studies. As a result of the limited number of research and their inconclusive results there are no clea
Externí odkaz:
https://doaj.org/article/1db3b91ec0ca45c7bdbce3df48e46e57
Autor:
Susan Shenoi, Kabita Nanda, Grant S. Schulert, John F. Bohnsack, Ashley M. Cooper, Bridget Edghill, Miriah C. Gillispie-Taylor, Baruch Goldberg, Olha Halyabar, Thomas G. Mason, Tova Ronis, Rayfel Schneider, Richard K. Vehe, Karen Onel, for the Childhood Arthritis and Rheumatology Research Alliance Systemic Juvenile Idiopathic Arthritis Workgroup
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 17, Iss 1, Pp 1-7 (2019)
Abstract Background We describe a Childhood Arthritis and Rheumatology Research Alliance (CARRA) survey of North American pediatric rheumatologists that assesses physician attitudes on withdrawal of medications in systemic juvenile idiopathic arthrit
Externí odkaz:
https://doaj.org/article/e2a409554cd54458a69d7fc5514747f2
Autor:
Hermine I Brunner, Carine Wouters, Alberto Martini, Daniel J Lovell, Nicolino Ruperto, Isabelle Kone-Paut, Dirk Elewaut, Ivan Lagunes, Andreas O Reiff, Lawrence Jung, Katerina Jarosova, Dana Němcová, Richard Mouy, Christy Sandborg, John F Bohnsack, Christos Gabriel, Gloria Higgins, Olcay Y Jones, Veronika Vargová, Elizabeth Chalom, Yanna Song
Publikováno v:
RMD Open, Vol 6, Iss 2 (2020)
Objectives Long-term safety and efficacy of adalimumab among patients with juvenile idiopathic arthritis (JIA) was evaluated through 6 years of treatment.Methods Children aged 4–17 years with polyarticular JIA were enrolled in a phase III, randomis
Externí odkaz:
https://doaj.org/article/68abdcafb58a4d59b2e9aac88106629b
Autor:
Jessica L. Bloom, Clara Lin, Lisa Imundo, Stephen Guthery, Shelly Stepenaskie, Csaba Galambos, Amy Lowichik, John F. Bohnsack
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 15, Iss 1, Pp 1-12 (2017)
Abstract Background H Syndrome is an autosomal recessive disorder characterized by cutaneous hyperpigmentation, hypertrichosis, and induration with numerous systemic manifestations. The syndrome is caused by mutations in SLC29A3, a gene located on ch
Externí odkaz:
https://doaj.org/article/03ecd118f0934d75a9d73088b84b55b9
Autor:
Andrew M. Simpson, MD, Karin Chen, MD, John F. Bohnsack, MD, Matthew N. Lamont, MD, Faizi A. Siddiqi, MD, Barbu Gociman, MD, PhD
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 6, Iss 8, p e1886 (2018)
Summary:. Leukocyte adhesion deficiency (LAD) is a rare primary immunodeficiency characterized by impairment of leukocyte migration during an inflammatory response. LAD patients can experience recurrent neutrophilic wounds similar to pyoderma gangren
Externí odkaz:
https://doaj.org/article/e24c4a27dd414043999e25ac2ed4a9ec
Autor:
John F. Bohnsack, Meagan D. Seay, Edward P. Quigley, Alison V. Crum, Kathleen B. Digre, Sravanthi Vegunta, Nick Mamalis, Judith E. A. Warner, Bradley J. Katz, Sean Kennedy
Publikováno v:
Journal of Neuro-Ophthalmology. 41:547-552
An 11-year-old boy presented with 2 weeks of intermittent headache, right orbital pain, and constant diplopia. Brain MRI showed dural thickening and enhancement of the right lateral cavernous sinus, right orbital apex, and tentorium. Initial cerebral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4d12c8977460c1d08f07ccd8c329c6d
https://doi.org/10.1097/wno.0000000000001342
https://doi.org/10.1097/wno.0000000000001342
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-10 (2021)
Pediatric Rheumatology Online Journal
Pediatric Rheumatology Online Journal
Background The transition of health care from Pediatric to Adult providers for adolescents and young adults with chronic disease is associated with poor outcomes. Despite the importance of this transition, over 80% of these patients do not receive th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e467370a660432d3b4ce23c046af6eac
https://doi.org/10.1186/s12969-022-00718-2
https://doi.org/10.1186/s12969-022-00718-2
Publikováno v:
Pediatric Critical Care Medicine
The COVID-19 pandemic has affected mortality and morbidity across all ages, including children. Neurologic manifestations of coronavirus disease 2019, ranging from headaches to cerebrovascular stroke, may involve the CNS or peripheral nervous system.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aa8e8079f9e7debc7d908307107e39d
https://doi.org/10.1097/pcc.0000000000002774
https://doi.org/10.1097/pcc.0000000000002774