Zobrazeno 1 - 10
of 789
pro vyhledávání: '"A. E. Schlesinger"'
Autor:
Guilherme Rabinowits, Michael R. Migden, Todd E. Schlesinger, Robert L. Ferris, Morganna Freeman, Valerie Guild, Shlomo Koyfman, Anna C. Pavlick, Neil Swanson, Gregory T. Wolf, Scott M. Dinehart
Publikováno v:
JID Innovations, Vol 1, Iss 4, Pp 100045- (2021)
Cutaneous squamous cell carcinoma is the second most common skin cancer in the United States. Currently, there is no standardized management approach for patients with cutaneous squamous cell carcinoma who develop metastatic or locally advanced disea
Externí odkaz:
https://doaj.org/article/7bfa396119cd430f85368f3066722ea1
Autor:
Sue Peschin, Maryam M. Asgari, James E. Sligh, Sameer Malik, Lindsy Frazer-Green, David J. Leffell, Robert P. Dellavalle, Gary Goldenberg, Suzanne M. Connolly, Todd E. Schlesinger, Daniel B. Eisen, Peggy A. Wu, Daniel D. Bennett, Esther E. Freeman
Publikováno v:
Journal of the American Academy of Dermatology. 85:e209-e233
Background Actinic keratoses (AK) are rough scaly patches that arise on chronically ultraviolet-exposed skin and can progress to keratinocyte carcinoma. Objective This analysis examined the literature related to the management of AK to provide eviden
Autor:
Daniel D. Bennett, Sue Peschin, Gary Goldenberg, Todd E. Schlesinger, Daniel B. Eisen, Maryam M. Asgari, James E. Sligh, Sameer Malik, David J. Leffell, Robert P. Dellavalle, Suzanne M. Connolly, Peggy A. Wu, Esther E. Freeman, Lindsy Frazer-Green
Publikováno v:
Journal of the American Academy of Dermatology. 85:945-955
Background Actinic keratoses (AK) are rough scaly patches that arise on chronically ultraviolet-exposed skin and can progress to keratinocyte carcinoma. Treatment options for AK include topical medications, photodynamic therapy, cryosurgery, and lase
Autor:
Jennifer E. Posey, Lindsay C. Burrage, Marcus J. Miller, Pengfei Liu, Matthew T. Hardison, Sarah H. Elsea, Qin Sun, Yaping Yang, Alecia S. Willis, Alan E. Schlesinger, Carlos A. Bacino, Brendan H. Lee
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 176-183 (2014)
Lysinuric protein intolerance (LPI) is a rare autosomal recessive inborn error of metabolism caused by mutations in SLC7A7, which encodes a component of the dibasic amino acid transporter found in intestinal and renal tubular cells. Patients typicall
Externí odkaz:
https://doaj.org/article/8843537d916b4bad9f460ba4e551629d
Publikováno v:
Journal of the American Academy of Dermatology.