Search

Your search keyword '"Gudat, F."' showing total 423 results
Start Over Author "Gudat, F."
423 results on '"Gudat, F."'

2. Immunocytochemistry in Diagnostic Cytology

Author

Dalquen, P., Sauter, G., Epper, R., Kleiber, B., Feichter, G., Gudat, F., Herfarth, Ch., editor, Senn, H.-J., editor, Baum, M., editor, Diehl, V., editor, Gutzwiller, F., editor, Rajewsky, M. F., editor, Wannenmacher, M., editor, Pfitzer, Peter, editor, and Grundmann, E., editor

Published
1993
Full Text
View/download PDF

26. Histochemical and Electron-Microscopic Aspects of Bone Tumor Diagnosis

Author

Remagen, W., Gudat, F., Heitz, P., Allfrey, V. G., editor, Allgöwer, M., editor, Bauer, K. H., editor, Berenblum, I., editor, Bergel, F., editor, Bernard, J., editor, Bernhard, W., editor, Blokhin, N. N., editor, Bock, H. E., editor, Braun, W., editor, Bucalossi, P., editor, Chaklin, A. V., editor, Chorazy, M., editor, Cunningham, G. J., editor, Della Porta, G., editor, Denoix, P., editor, Dulbecco, R., editor, Eagle, H., editor, Eker, R., editor, Good, R. A., editor, Grabar, P., editor, Hamperl, H., editor, Harris, R. J. C., editor, Hecker, E., editor, Herbeuval, R., editor, Higginson, J., editor, Hueper, W. C., editor, Isliker, H., editor, Kieler, J., editor, Klein, G., editor, Koprowski, H., editor, Koss, L. G., editor, Martz, G., editor, Mathé, G., editor, Mühlbock, O., editor, Nakahara, W., editor, Old, L. J., editor, Potter, V. R., editor, Sabin, A. B., editor, Sachs, L., editor, Saxén, E. A., editor, Schmidt, C. G., editor, Spiegelman, S., editor, Szybalski, W., editor, Tagnon, H., editor, Taylor, R. M., editor, Tissières, A., editor, Uehlinger, E., editor, Wissler, R. W., editor, Rentchnick, P., editor, and Grundmann, Ekkehard, editor

Published
1976
Full Text
View/download PDF

47. Primary Gelatinous Drop-Like Corneal Dystrophy in a White Woman

Author

Gudat F, Büchi Er, Uffer S, and Daicker B

Subjects
Adult, Reoperation, Pathology, medicine.medical_specialty, Corneal dystrophy, Corneal Diseases, law.invention, law, mental disorders, Keratin, medicine, Humans, Longitudinal Studies, Corneal Dystrophies, Hereditary, chemistry.chemical_classification, Histology, Amyloidosis, medicine.disease, Ophthalmology, chemistry, Ultrastructure, Immunohistochemistry, Female, Gelatinous drop-like corneal dystrophy, Electron microscope, Amyloid (mycology), Keratoplasty, Penetrating, Follow-Up Studies
Abstract

A white female with primary gelatinous drop-like corneal dystrophy (PGDD) was followed from the ages of 8 to 37 years. During this time, she underwent repeated lamellar and penetrating keratoplasties on both sides due to relapsing bilateral corneal opacifications. The diagnosis of PGDD was based on the histology of the corneal specimens obtained at 10 and 36 years of age, as well as on the characteristic clinical appearance and course. Electron microscopy showed typical amyloid fibrils. Immunohistochemical staining was mildly positive for amyloid AL (light chain), but negative for amyloid AA, AF, AB, and keratin. Thus, the precursor protein of the amyloid deposits in PGDD might derive from immunoglobulins, e.g., from the tear film. However, the precursor protein might derive from a different origin altogether. In that case, the positive staining for amyloid AL would translate nonspecific absorption of fragments of light chains.

Published
1994
Full Text
View/download PDF

Catalog

Books, media, physical & digital resources
See catalog results