Zobrazeno 1 - 10
of 676
pro vyhledávání: '"G, Micheletti"'
Autor:
S. Ingen-Housz-Oro, V. Schmidt, M. M. Ameri, R. Abe, A. Brassard, A. Mostaghimi, A. S. Paller, A. Romano, B. Didona, B. H. Kaffenberger, B. Ben Said, B. Y. H. Thong, B. Ramsay, E. Brezinova, B. Milpied, C. G. Mortz, C. Y. Chu, C. Sotozono, J. Gueudry, D. G. Fortune, S. M. Dridi, D. Tartar, G. Do-Pham, E. Gabison, E. J. Phillips, F. Lewis, C. Salavastru, B. Horvath, J. Dart, J. Setterfield, J. Newman, J. T. Schulz, A. Delcampe, K. Brockow, L. Seminario-Vidal, L. Jörg, M. P. Watson, M. Gonçalo, M. Lucas, M. Torres, M. H. Noe, N. Hama, N. H. Shear, P. O’Reilly, P. Wolkenstein, P. Romanelli, R. P. Dodiuk-Gad, R. G. Micheletti, G. S. Tiplica, R. Sheridan, S. Rauz, S. Ahmad, S. L. Chua, T. H. Flynn, W. Pichler, S. T. Le, E. Maverakis, S. Walsh, L. E. French, M. C. Brüggen
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Background Long-term sequelae are frequent and often disabling after epidermal necrolysis (Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN)). However, consensus on the modalities of management of these sequelae is lacking.
Externí odkaz:
https://doaj.org/article/03fab2d6e5c44c33a299e7696bc863e7
Autor:
Jay R. Patel, MD, Daniel J. Lewis, MD, Jenny Wei, MD, Alexandra Coromilas, MD, Robert G. Micheletti, MD
Publikováno v:
JAAD Case Reports, Vol 35, Iss , Pp 46-48 (2023)
Externí odkaz:
https://doaj.org/article/8429d5d9ae5448a3bf7c82e5e46627df
Autor:
Madeline E. Marks, Ramya Krishna Botta, Riichiro Abe, Thomas M. Beachkofsky, Isabelle Boothman, Bruce C. Carleton, Wen-Hung Chung, Ricardo R. Cibotti, Roni P. Dodiuk-Gad, Christian Grimstein, Akito Hasegawa, Jay H. Hoofnagle, Shuen-Iu Hung, Benjamin Kaffenberger, Daniela Kroshinsky, Rannakoe J. Lehloenya, Michelle Martin-Pozo, Robert G. Micheletti, Maja Mockenhaupt, Keisuke Nagao, Suman Pakala, Amy Palubinsky, Helena B. Pasieka, Jonathan Peter, Munir Pirmohamed, Melissa Reyes, Hajirah N. Saeed, Jeffery Shupp, Chonlaphat Sukasem, Jhih Yu Syu, Mayumi Ueta, Li Zhou, Wan-Chun Chang, Patrice Becker, Teresa Bellon, Kemberlee Bonnet, Gianpiero Cavalleri, James Chodosh, Anna K. Dewan, Arturo Dominguez, Xinzhong Dong, Elena Ezhkova, Esther Fuchs, Jennifer Goldman, Sonia Himed, Simon Mallal, Alina Markova, Kerry McCawley, Allison E. Norton, David Ostrov, Michael Phan, Arthur Sanford, David Schlundt, Daniel Schneider, Neil Shear, Kanade Shinkai, Eric Tkaczyk, Jason A. Trubiano, Simona Volpi, Charles S. Bouchard, Sherrie J. Divito, Elizabeth J. Phillips
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis (SJS/TEN) is a predominantly drug-induced disease, with a mortality rate of 15–20%, that engages the expertise of multiple disciplines: dermatology, allergy, immunology, clinical pharmacology, bur
Externí odkaz:
https://doaj.org/article/83a942713faf4a3ab1f40a9ad2a0e4a0
Autor:
Alexandra J. Coromilas, MD, Sherrie J. Divito, MD, PhD, Elizabeth J. Phillips, MD, Robert G. Micheletti, MD
Publikováno v:
JAAD International, Vol 11, Iss , Pp 88-89 (2023)
Externí odkaz:
https://doaj.org/article/435590c8a76f4a5fbd0ecdb4ce8efe32
Publikováno v:
International Journal of Women's Dermatology, Vol 7, Iss 5, Pp 545-551 (2021)
Glucocorticoid-induced osteoporosis (GIOP) is a frequently encountered and serious side effect of glucocorticoid use. Bone loss leading to an increased risk for fracture occurs early in the use of glucocorticoids, yet patients at risk for this compli
Externí odkaz:
https://doaj.org/article/c56d1f67b63049baa7c4e87e799843cf
Autor:
Shreya Bhattacharya, Sayon Basu, Emily Sheng, Christina Murphy, Jenny Wei, Anna E. Kersh, Caroline A. Nelson, Joshua S. Bryer, Hovik A. Ashchyan, Katherine Steele, Amy Forrestel, John T. Seykora, Robert G. Micheletti, William D. James, Misha Rosenbach, Thomas H. Leung
Publikováno v:
The Journal of Clinical Investigation, Vol 133, Iss 1 (2023)
Background Acute febrile neutrophilic dermatosis (Sweet syndrome) is a potentially fatal multiorgan inflammatory disease characterized by fever, leukocytosis, and a rash with a neutrophilic infiltrate. The disease pathophysiology remains elusive, and
Externí odkaz:
https://doaj.org/article/a0c5dcf981104343b387ffb3f44bf29b
Autor:
Vima M. Patel, Brian Chu, Keith W. Hamilton, Cassandra Bellamy, Christina Harker, Joshua S. Bryer, Bridget Shields, Rebecca L. Hirsh, Olajumoke O. Fadugba, Robert G. Micheletti
Publikováno v:
Antimicrobial Stewardship & Healthcare Epidemiology, Vol 3 (2023)
A penicillin allergy testing service (PATS) assessed penicillin allergy in patients with hematologic malignancies; 17 patients who met criteria had negative skin testing. Patients who underwent penicillin challenge passed and were delabeled. Of delab
Externí odkaz:
https://doaj.org/article/6b9cd0dc419a4711a4f9d035f0df4c50
Autor:
Robert G. Micheletti
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Cutaneous vasculitis encompasses a spectrum of disease states, with varied morphology, severity, and potential for systemic involvement. Even vasculitis which is skin-limited can have a significant quality-of-life impact, necessitating treatment. Thi
Externí odkaz:
https://doaj.org/article/6c65e846fc0f40979af9a6d3ceb34de6
Autor:
Robert G. Micheletti, Christian Pagnoux, Roy N. Tamura, Peter C. Grayson, Carol A. McAlear, Renee Borchin, Jeffrey P. Krischer, Peter A. Merkel, for the Vasculitis Clinical Research Consortium
Publikováno v:
Trials, Vol 21, Iss 1, Pp 1-9 (2020)
Abstract Background Skin-limited forms of vasculitis, while lacking systemic manifestations, can persist or recur indefinitely, cause pain, itch, or ulceration, and be complicated by infection or scarring. High-quality evidence on how to treat these
Externí odkaz:
https://doaj.org/article/9c5aba9c9d7540e494956781ad6f8690
Autor:
Amit Garg, Sahil Rawal, Oleg Akilov, Afsaneh Alavi, Christine Ardon, Falk G Bechara, Arnon D Cohen, Steven R Cohen, Steven Daveluy, Véronique del Marmol, Maïa Delage, Solveig Esmann, Shani Fisher, Evangelos J Giamarellos-Bourboulis, Amelia Glowaczewska, Noah Goldfarb, Elena Gonzalez Brant, Øystein Grimstad, Sandra Guilbault, Iltefat Hamzavi, Rosalind Hughes, John R Ingram, Gregor B E Jemec, Qiang Ju, Naomi Kappe, Brian Kirby, Joslyn S Kirby, Michelle A Lowes, Lukasz Matusiak, Stella Micha, Robert G Micheletti, Angela P Miller, Dagfinn Moseng, Haley B Naik, Aude Nassif, Georgios Nikolakis, So Yeon Paek, Jose Carlos Pascual, Errol Prens, Barry Resnik, Hassan Riad, Christopher Sayed, Saxon D Smith, Yssra Soliman, Jacek C Szepietowski, Jerry Tan, Linnea Thorlacius, Thrasyvoulos Tzellos, Hessel H van der Zee, Bente Villumsen, Lanqi Wang, Christos C Zouboulis, Andrew Strunk
Publikováno v:
British Journal of Dermatology. 188:808-810
Patients with hidradenitis suppurativa experience significant life impact related to their disease. Younger age, Black race, high BMI, active smoking, flares, depression, anxiety, high comorbidity burden, disability, and difficult access to a dermato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::460a9d966897825035aeb1015abebdbc
https://doi.org/10.1093/bjd/ljad069
https://doi.org/10.1093/bjd/ljad069