Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Senait W. Dyson"'
Autor:
Elsa F. Velazquez, Elizabeth A. Montgomery, Hyemin Pomerantz, Jeremy C. Wallentine, Lester D.R. Thompson, Senait W. Dyson, Jerad M. Gardner, Cyril Fisher, Jessica M. Comstock, Sa A. Wang, Amitabh Srivastava, Artur Zembowicz, David Lucas, Thomas Mentzel, Susan Müller, Khin Thway, Francisco Vega, Cary Chisholm, Brenda L. Nelson
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b97d91299ee97d188414d367468b12a0
https://doi.org/10.1016/b978-0-323-44310-4.50004-x
https://doi.org/10.1016/b978-0-323-44310-4.50004-x
Autor:
Garrett A. Wirth, Senait W Dyson, Joshua Waltzman, Edward Shanbrom, Thomas Scholz, William J. Owens, Gregory R. D. Evans
Publikováno v:
Int Wound J
The authors sought to evaluate the ability of locally administered enhanced cryoprecipitate (eCryo) to improve the wound healing of split thickness skin grafts (STSG) and their donor sites. An STSG (5 × 5 cm) was harvested on the back of 30 rats and
Autor:
Zongqi Xia, Neil J. Korman, Sue Manos, Senait W Dyson, Stacey Brisman, Sareeta Parker, Robert A. Swerlick, Rizwana Khan, Michelle L. Pennie, Benjamin D. Korman
Publikováno v:
Journal of the American Academy of Dermatology. 59:582-588
Background There are large discrepancies in reported mortality for bullous pemphigoid (BP). Objective We sought to determine the mortality of a large cohort of patients with BP and compare this with age-matched control subjects. Methods Data were col
Autor:
Marc J. Glucksman, Maria Celeste M. Ramirez, Tanya Kormeili, Lisa E. Lindvall, Valerie Grum-Tokars, Senait W Dyson, Michael V. Zaragoza, John A. Martignetti, Elaine Chen
Publikováno v:
Journal of the American Academy of Dermatology. 58:303-307
Infantile systemic hyalinosis (ISH) is a rare, progressive autosomal recessive disease, which is usually fatal by the age of 2 years. Clinical onset typically occurs within the first few weeks of life. The disease is characterized by joint contractur
Autor:
Thomas Horn, Leila Ettefagh, Klilah Hershko, Cheryl Hull, Susan T. Nedorost, Anita C. Gilliam, Senait W Dyson
Publikováno v:
Journal of Cutaneous Pathology. 31:262-265
Nephrogenic fibrosing dermopathy (NFD) is a disorder characterized by dramatic thickening and hardening of skin in the extremities and trunk, which occurs in individuals on dialysis for renal disease. The pathophysiology is unknown. Increased transfo
Publikováno v:
The American Journal of Dermatopathology. 30:497-499
Langerhans cell histiocytosis (LCH), especially with an involvement limited to the skin, is a rare entity in adults. In formulating a differential diagnosis of a solitary skin lesion, LCH is rarely considered. Morphologically, cells seen in LCH can m
Publikováno v:
American Journal of Hematology. 81:703-705
Granulocyte colony stimulation factor (G-CSF) is commonly used in the treatment of chemotherapy-induced myelosuppression. We report the case of a 62-year-old man with chronic lymphocytic leukemia who presented with neutropenic fever and sepsis. After
Publikováno v:
Journal of the American Academy of Dermatology. 51:105-107
A healthy 58-year-old woman developed an asymptomatic papular eruption of the neck, cheek, abdomen, arms, and flexures. There was an 8-year history of the lesions, which had erupted when the patient started a strict vegetarian diet. Lesions lasted 3
Publikováno v:
Cutis. 88(1)
There are 5 subtypes of morphea that are based on disease distribution and presentation, including plaque, localized, generalized, linear, and deep morphea. We report a case of a young patient with morphea lesions in scattered locations confined to 1
Publikováno v:
Scopus-Elsevier
Billings, Tomomi; Wu, Jashin J; & Dyson, Senait. (2010). Erythematous plaques on the face, trunk, and upper arms. Dermatology Online Journal, 16(7). Retrieved from: http://www.escholarship.org/uc/item/00n8h38x
Billings, Tomomi; Wu, Jashin J; & Dyson, Senait. (2010). Erythematous plaques on the face, trunk, and upper arms. Dermatology Online Journal, 16(7). Retrieved from: http://www.escholarship.org/uc/item/00n8h38x
An 18-year-old woman presented with a one-year history of erythematous to slightly violaceous indurated papules and plaques on the face, earlobes, neck, upper arms, chest, and upper back.