Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sharifeh Farasat"'
Autor:
Arthur J. Sober, Timothy M. Johnson, Anthony P. Tufaro, Victor A. Neel, William H. Sharfman, Sharifeh Farasat, Nanette J. Liégeois, Martin C. Mihm, Paul Nghiem, Jatin P. Shah, Kishwer S. Nehal, Siegrid S. Yu, Clark C. Otley, Joseph A. Califano, Charles M. Balch, David R. Byrd, Thomas Lardaro, Alice Y. Chuang
Publikováno v:
Journal of the American Academy of Dermatology. 64:1051-1059
Background The incidence of cutaneous squamous cell carcinoma (cSCC) is increasing. Although most patients achieve complete remission with surgical treatment, those with advanced disease have a poor prognosis. The American Joint Committee on Cancer (
Autor:
Sharifeh Farasat, Patrick W. Blake, Matthew L. Herman, Peter J. Steinbach, Ming Hui Wei, Sherri J. Bale, Philip Fleckman, Ousmane Toure, Jorge R. Toro
Publikováno v:
Human Mutation. 30:537-547
Autosomal recessive congenital ichthyosis (ARCI) is a heterogeneous group of rare cornification diseases. Germline mutations in TGM1 are the most common cause of ARCI in the United States. TGM1 encodes for the TGase-1 enzyme that functions in the for
Publikováno v:
Archives of dermatology. 144(3)
We conducted a literature review to investigate the recent advances in genetics, molecular biology, clinical manifestations, and therapy of 7 inherited diseases that are characterized by seemingly unprovoked inflammation. These autoinflammatory disea
Autor:
Diana J. Pillas, Sharifeh Farasat, James E. Rubenstein, John M. Freeman, Eileen P.G. Vining, Eric H. Kossoff
Publikováno v:
Epilepsybehavior : EB. 8(2)
Although the success rates and complications of various treatment options for children with intractable epilepsy have been described, the actual expectations of parents for these treatments are less clear. Since 1998, parents at our institution have