Zobrazeno 1 - 10
of 80
pro vyhledávání: '"D. Martin Carter"'
Autor:
Andrew N. Lin, D. Martin Carter
Because skin blisters are the initial manifestation of epidermolysis bullosa (EB), patients invariably present to the dermatologist for diagnosis and treatment. However, EB is a systemic disease whose management requires input from clinicians in virt
Publikováno v:
American Journal of Ophthalmology. 118:384-390
Surgical excision of subfoveal neovascular membranes may result in recovery of excellent visual acuity in patients with presumed ocular histoplasmosis but not in patients with age-related macular degeneration. To provide an explanation for this discr
Publikováno v:
New England Journal of Medicine. 327:163-167
Background. Recessive dystrophic epidermolysis bullosa is an uncommon, severely disabling, heritable disorder characterized by abnormal fragility of the skin. Open trials have suggested th...
Publikováno v:
Medicine. 71:121-127
One hundred one patients with EB were evaluated by a combination of prospective and retrospective review, and analyzed regarding the nature, incidence, and prevalence of their gastrointestinal (GI) manifestations. Involvement of the GI tract is a wel
Publikováno v:
Journal of Investigative Dermatology. 97(5):849-861
An unusual, elongated, refractile cell morphology was observed in keratinocytes cultured from three patients with non-lethalis forms of junctional epidermolysis bullosa (JEB). To determine whether these changes might be related to altered cell adhesi
Autor:
Karen A. Holbrook, Eugene A. Bauer, Robert A. Briggaman, Sidney Hurwitz, Nancy B. Esterly, Andrew N. Lin, Robin A.J. Eady, D. Martin Carter, Jo-David Fine, Roger W. Pearson, Lorraine Johnson, Virginia P. Sybert
Publikováno v:
Journal of the American Academy of Dermatology. 24:119-135
Inherited epidermolysis bullosa encompasses a number of diseases, with the common finding of blister formation, after minor mechanical trauma to the skin. In some forms significant, if not eventually fatal, extracutaneous disease activity may occur.
Publikováno v:
Journal of Investigative Dermatology. 94(6):s135-s140
Psoriasis is characterized by epidermal hyperplasia, altered epidermal maturation, and local accumulation of acute and chronic inflammatory cells. Keratinocyte hyperplasia in psoriasis may be explained in part by overproduction of growth factors or c
Publikováno v:
Journal of the American Academy of Dermatology. 30(3)
Background: Anesthestic and monitoring instrumentations such as endotracheal intubation may cause skin and mucosal damage with potentially serious consequences in patients with epidermolysis bullosa (EB). Objective: This study defines the risks of sk
Autor:
Pravinkumar B. Sehgal, Shu Man Fu, Angela Granelli-Piperno, Rachel Grossman, James G. Krueger, Alice B. Gottlieb, D. Martin Carter, Lakshmi Khandke, Lance Barazani, Miriam V. Rivas
Publikováno v:
The Journal of investigative dermatology. 98(3)
Cyclosporine (CSA) decreases lymphokine synthesis and keratinocyte proliferation in vitro, but its in vivo mechanism of action in treating recalcitrant psoriasis is incompletely understood. Ten psoriasis patients were treated with CSA (27.5 mg/kg/d)
Autor:
D. Martin Carter, Andrew N. Lin
Publikováno v:
Epidermolysis Bullosa ISBN: 9781461277170
Junctional epidermolysis bullosa is an autosomal recessive disorder characterized by the formation of blisters at the lamina lucida, an electron-lucent zone located between the basal cell plasma membrane and the lamina densa (Fig. 8.1). Like other fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd2b58d327488c8018b1a595545ef3a2
https://doi.org/10.1007/978-1-4612-2914-8_8
https://doi.org/10.1007/978-1-4612-2914-8_8