Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Mona Z. Mofid"'
Autor:
David James Savage, Lisa A. Tushla, Katie Guenin, Isabel Gross, Nina Kanakarajavelu, Rebecca Young, Deysi Merino-Gonzalez, Nannette Stamm, Susan M. Swetter, Susan Boiko, Mona Z Mofid, Samantha Guild, Sara A Quandt, Thomas Arcury
Publikováno v:
Journal of Clinical Oncology. 40:113-113
113 Background: Farmworkers are at increased risk for skin cancer because of occupational exposure to sun and pesticides. In 2017/2018, Farmworker Justice conducted the Unidos community mobilization project to raise skin-cancer awareness and promote
Publikováno v:
Plastic and Reconstructive Surgery. 111:2434-2442
Publikováno v:
Journal of the American Academy of Dermatology. 38:825-830
We describe a kindred in whom epidermolytic palmoplantar keratoderma occurred in association with Ehlers-Danlos syndrome type III (benign hypermobility syndrome). This kindred consisted of 27 members of four generations, 14 of whom had palmoplantar k
Publikováno v:
Journal of the American Academy of Dermatology. 46:S16-S18
Primary hyperoxaluria encompasses 3 rare genetic disorders of glyoxylate metabolism characterized by excessive urinary excretion of oxalic acid, resulting in oxalosis. Patients typically have recurrent calcium oxalate nephrolithiasis and nephrocalcin
Autor:
Mona Z. Mofid, Daniel N. Sauder
Publikováno v:
Dermatologic clinics. 23(2)
Further understanding of the pathogenesis of dermatologic conditions at a molecular level has led to targeted therapies. The topical immune response modifiers have contributed significantly to the treatment of cutaneous diseases. New topical remedies
Publikováno v:
Journal of the American Academy of Dermatology. 47
Urticarial vasculitis, a form of leukocytoclastic vasculitis involving the postcapillary venules, is classified as a type III hypersensitivity reaction and has been associated with connective tissue disease. The lesions resemble urticaria and typical
Publikováno v:
International journal of dermatology. 41(6)
Background The occurrence of bullous lesions in localized or systemic scleroderma is rare. Three histologic patterns have been reported: lichen sclerosus et atrophicus-like, lymphangiectatic blisters and autoimmune blistering diseases. Objective To i
Autor:
Mona Z. Mofid, Andrew M. Munster, Hossein C. Nousari, Constantino Costarangos, Benjamin Bernstein, Lesley Wong
Publikováno v:
Journal of Burn Care & Rehabilitation. 21:246-247
Drug-induced linear immunoglobulin A bullous disease is a subepidermal blistering disorder that most commonly occurs after exposure to vancomycin. It can clinically mimic toxic epidermolytic necrolysis. We describe an 87-year-old white woman in whom
Publikováno v:
JAMA. 281:640
ContextIn cutaneous melanoma, tumor depth remains the best biologic predictor of patient survival. Detection of prognostically favorable lesions may be associated with improved survival in patients with melanoma.ObjectiveTo determine melanoma detecti
Publikováno v:
Plastic & Reconstructive Surgery; Jun2003, Vol. 111 Issue 7, p2434, 9p