Zobrazeno 1 - 8
of 8
pro vyhledávání: '"J E, Muhlbauer"'
Autor:
D. M. Elston, W. F. Bergfeld, D. A. Whiting, J. T. McMahon, D. M. Dawson, K. L. Quint, J. E. Muhlbauer
Publikováno v:
Journal of cutaneous pathology. 19(5)
An unusual hair dystrophy was studied by means of light and electron microscopy. Hair fibers demonstrated a boomerang deformity containing small and large "bubbles". Electron microscopy revealed a loss of cortical cells and medulla at these sites. Cr
Autor:
J E, Muhlbauer
Publikováno v:
Journal of the American Academy of Dermatology. 3:217-230
Granuloma annular (GA) is a benign inflammatory skin disease usually localized to the distal extremities, although generalized, perforating, and subcutaneous variants have also been identified. A regular histopathologic feature is the presence of mon
Autor:
J. E. Muhlbauer
Publikováno v:
JAMA: The Journal of the American Medical Association. 247:3095-3102
Publikováno v:
Archives of Dermatological Research. 277:499-501
Basement-membrane-zone (BMZ) components are altered in basal-cell carcinoma (BCC). Electron microscopy has identified areas of normal, discontinuous, or absent BMZ components in human BCC [13, 15, 26]. In the present study, we used new monoclonal ant
Autor:
J. E. Muhlbauer
Publikováno v:
Archives of Dermatology. 120:866-868
Publikováno v:
JAMA. 252(7)
Cat-scratch disease is a zoonotic infection characterized by a skin papule at the site of the scratch followed by regional lymphadenitis. Recently, small gram-negative pleomorphic bacilli were demonstrated in sections of lymph node from patients with
Publikováno v:
Archives of dermatology. 120(7)
Biopsy specimens of papules taken from eight patients with polymorphous light eruption ( PMLE ) were examined by a direct immunofluorescence technique. Extensive intervascular and focal perivascular deposits of fibrin were detected in each case. Slig
Publikováno v:
JAMA. 247(22)
Variegate porphyria (VP) is an autosomal dominant disease characterized in adults by mechanical fragility and blistering of sun-exposed skin or acute visceral and neurological manifestations. The laboratory diagnosis of VP depends on a search for hig