Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Sonal D, Shah"'
Publikováno v:
JAAD Case Reports, Vol 26, Iss , Pp 9-12 (2022)
Externí odkaz:
https://doaj.org/article/51346c2147e043d8a932c82def9c0900
Autor:
Esteban, Fernández Faith, Sonal D, Shah, Mitchell, Braun, Elena, Pope, Irene, Lara-Corrales, Patricia M, Witman, Katya, Harfmann, Flora, Bradley, Rohali, Keesari, Kenneth, Jackson, Alexandra, Hallagan, Ilona J, Frieden
Publikováno v:
Journal of the American Academy of Dermatology. 88:414-420
Ulceration is an important complication in infantile hemangiomas (IHs). Prior to the use of β-blockers, the estimated incidence of this complication in a referral population was between 15% and 30%. The incidence and factors associated with ulcerati
Publikováno v:
Pediatric Dermatology. 40:507-510
Autor:
David X, Zheng, Thomas B, Cwalina, Tarun K, Jella, Christopher R, Cullison, Sonal D, Shah, Jeffrey F, Scott, Carlos A, Camargo
Publikováno v:
Journal of the American Academy of Dermatology. 87:1169-1172
Autor:
David X. Zheng, Thomas B. Cwalina, Kathleen M. Mulligan, Benjamin Gallo Marin, Katie A. O'Connell, Sonal D. Shah, Shawn G. Kwatra, Arash Mostaghimi
Publikováno v:
Pediatric Dermatology. 39:927-930
Our objective was to examine the prevalence and predictors of delayed medical care due to transportation barriers among children with atopic dermatitis (AD) living in the United States (US). We analyzed data from the 1998-2018 National Health Intervi
Autor:
Johanna Sheu Song, Jennifer T. Huang, Maria del Carmen Fraile Alonso, Richard J. Antaya, Harper N. Price, Tracy Funk, Rony A. Francois, Sonal D. Shah
Publikováno v:
Pediatric Dermatology. 39:889-895
Complications of hematopoietic stem cell transplant (HSCT) include acute graft-versus-host disease (aGVHD). Severe cutaneous aGVHD can present with generalized erythroderma, desquamation, and bullae which can mimic toxic epidermal necrolysis (TEN). T
Autor:
Mitchell Braun, Micah Pascual, Thaddeus Mully, Andrew Phelps, Lori Prok, Sonal D. Shah, Lucinda L. Kohn
Publikováno v:
Pediatric Dermatology. 39:438-442
Autor:
Lucinda L. Kohn, Mitchell Braun, Kelly M. Cordoro, Timothy H. McCalmont, Sonal D. Shah, Ilona J. Frieden, Anubhav N. Mathur
Publikováno v:
Pediatric Dermatology. 39:84-90
To characterize the skin and mucosal findings of NEMO syndrome.Retrospective review of clinical characteristics from a cohort of two families with mutations in IKBKG (the NEMO-encoding gene). A literature review identified 86 studies describing 192 p
KAT6A, a histone/lysine acetyltransferase is located on 8p11 and has been reported in association with a variety of partner genes like CREBBP (16p13), EP300 (22q13), LEUTX (9q13), NCOA2, NCOA3, and ASXL2. Favorable prognosis and spontaneous remission
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b63f661448f7abc695dfc339ba595dd0
https://doi.org/10.22541/au.167271430.01219149/v1
https://doi.org/10.22541/au.167271430.01219149/v1
Publikováno v:
Pediatric Dermatology. 38:1272-1275
BACKGROUND Onychoheterotopia, or ectopic nail, is a rare nail condition in which nail growth occurs in areas other than the distal phalanges. The majority of cases in the literature are noted to be congenital; however, acquired cases have less common