Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Alice Frigerio"'
Publikováno v:
Journal of Diabetes Research, Vol 2018 (2018)
Background. Metabolic alterations as hyperglycemia and inflammation induce myocardial molecular events enhancing oxidative stress and mitochondrial dysfunction. Those alterations are responsible for a progressive loss of cardiomyocytes, cardiac stem
Externí odkaz:
https://doaj.org/article/00ae70cc90904d98be05f1e9c38a7161
Autor:
Alice Frigerio, Karol Wright, Whitney Wooderchak-Donahue, Oon T Tan, Rebecca Margraf, David A Stevenson, J Fredrik Grimmer, Pinar Bayrak-Toydemir
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0133158 (2015)
Port-wine stains (PWS) are capillary malformations, typically located in the dermis of the head and neck, affecting 0.3% of the population. Current theories suggest that port-wine stains are caused by somatic mutations that disrupt vascular developme
Externí odkaz:
https://doaj.org/article/9d44737acfd34b0d9148837db4481c6c
Publikováno v:
Journal of drugs in dermatology : JDD. 21(5)
The intent of this brief communication is to describe a unique incomplete staining frozen section pathology artifact encountered during Mohs Micrographic Surgery. At the authorsrsquo; institution, an amorphous, eosinophilic artifact that obscured cel
Autor:
Allison T. Vidimos, Shlomo A. Koyfman, Giovanni Damiani, Brian R. Gastman, Thomas Chu, Sheena Tsai, G. Thomas Budd, Alice Frigerio, Rosalynn R.Z. Conic, Nikhil P. Joshi, Natasha Atanaskova Mesinkovska, Nicola Luigi Bragazzi
Publikováno v:
Journal of the American Academy of Dermatology. 83:809-816
Background Cutaneous angiosarcoma (CAS) is a rare, malignant tumor of vascular mesenchymal origin accounting for less than 1% of all sarcomas. Objective To examine epidemiologic trends and outcomes in CAS. Methods In this retrospective, population-ba
Autor:
Josue A, Flores Daboub, Johanes Fred, Grimmer, Alice, Frigerio, Whitney, Wooderchak-Donahue, Ryan, Arnold, Jeff, Szymanski, Nicola, Longo, Pinar, Bayrak-Toydemir
Publikováno v:
Cold Spring Harbor Molecular Case Studies
Parkes Weber syndrome is associated with autosomal dominant inheritance, caused by germline heterozygous inactivating changes in the RASA1 gene, characterized by multiple micro arteriovenous fistulas and segmental overgrowth of soft tissue and skelet
Autor:
Josh Bleicher, Alice Frigerio, Sheryll L. Vanderhooft, Jo Anna Reems, Giavonni M. Lewis, Jan Pierce
Publikováno v:
JAAD Case Reports
Publikováno v:
JAAD Case Reports
Publikováno v:
JAAD Case Reports
A case of facial acute localized exanthematous pustulosis (ALEP) secondary to lamotrigine is presented. Upon rechallenge with the culprit medication, the patient had acute generalized exanthematous pustulosis (AGEP). This case highlights lamotrigine
Publikováno v:
Pediatric Dermatology.
A case of a 15-year-old male patient with a 3-year history of linear, segmental amyopathic dermatomyositis with calcinosis cutis is presented. The calcinosis was recalcitrant to treatment with topical steroids and hydroxychloroquine. Topical 10% sodi
Publikováno v:
Varedi, Danny; Frigerio, Alice; Scaife, Courtney; & Hull, Christopher. (2019). A novel case of TIF1 gamma autoantibody positive dermatomyositis associated with a non-functional pancreatic neuroendocrine tumor. Dermatology Online Journal, 25(3). Retrieved from: http://www.escholarship.org/uc/item/4fc9p1bd
Dermatomyositis (DM) is an idiopathic inflammatory myopathy characterized by proximal muscle weakness associated with a distinct cutaneous eruption. The association of DM with malignancy has been extensively described in the literature. Patients with