Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Mona Z. Mofid"'
Autor:
Foad Nahai
Publikováno v:
Plastic and Reconstructive Surgery. 111:2443-2444
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
Autor:
Nahai, Foad
Publikováno v:
Plastic and Reconstructive Surgery; June 2003, Vol. 111 Issue: 7 p2443-2444, 2p
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