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Publikováno v:
Connective Tissue Research. 34:271-279
Epidermolysis bullosa (EB) is a group of conditions characterized by basement membrane and cellular defects that result in skin fragility and variable extra-cutaneous involvement. The teeth can be severely affected with marked enamel malformations. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0d71351e97f645eb739305b4ff0dea9
https://doi.org/10.3109/03008209609005271
https://doi.org/10.3109/03008209609005271
Autor:
Y. Horiguchi, T. Maruguchi, Y. Maruguchi, S. Suzuki, J. -D. Fine, I. M. Leigh, T. Yoshiki, M. Ueda, K. -I. Toda, N. Isshiki, S. Imamura
Publikováno v:
Archives of Dermatological Research. 286:53-61
Keratinocytes were cultured on fibroblast-free dermal substitutes made of type I collagen film (collagen dermal substitute) and an extracellular matrix gel film (matrix dermal substitute), each of which was laid on a lyophilized type I collagen spong
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7f67d8358471a6827d133182d3946d5
https://doi.org/10.1007/bf00375844
https://doi.org/10.1007/bf00375844
Publikováno v:
Rook's Textbook of Dermatology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6faabf894c9b43bd8fbdc1de04ad7986
https://doi.org/10.1002/9780470750520.ch40
https://doi.org/10.1002/9780470750520.ch40
Publikováno v:
Archives of Dermatology. 126:1587-1593
The expression of type VII collagen and 19-DEJ-1 antigen was examined in 73 and 71 patients, respectively, with recessive dystrophic epidermolysis bullosa (RDEB), comprising gravis, mitis, inversa, and indeterminant subsets, to better determine the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a5b065e0f042280a7f870604ed74c0c
https://doi.org/10.1001/archderm.126.12.1587
https://doi.org/10.1001/archderm.126.12.1587
Autor:
J. D. Fine
Publikováno v:
Archives of Dermatology. 126:1187-1190
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13680517f43249bb4e01bc134f7ea05e
https://doi.org/10.1001/archderm.126.9.1187
https://doi.org/10.1001/archderm.126.9.1187
Autor:
J D, Fine, R A, Eady, E A, Bauer, R A, Briggaman, L, Bruckner-Tuderman, A, Christiano, A, Heagerty, H, Hintner, M F, Jonkman, J, McGrath, J, McGuire, A, Moshell, H, Shimizu, G, Tadini, J, Uitto
Publikováno v:
Journal of the American Academy of Dermatology. 42(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8f8bf11c0c18b6e137a6735273cdc41c
https://pubmed.ncbi.nlm.nih.gov/10827412
https://pubmed.ncbi.nlm.nih.gov/10827412
Publikováno v:
British Journal of Dermatology. 150:613-614
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29e7cd1fa96cb82464ed7a54eae6593d
https://doi.org/10.1046/j.1365-2133.2004.05816.x
https://doi.org/10.1046/j.1365-2133.2004.05816.x
Autor:
J D, Fine
Publikováno v:
Dermatologic clinics. 13(3)
The study of rare diseases may provide unique insights into new mechanisms of disease. Such research is difficult to perform, however, owing to a variety of problems associated with patient recruitment and classification, and the biases that are freq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::54e06186a67bad2a1324729033c68d85
https://pubmed.ncbi.nlm.nih.gov/7554513
https://pubmed.ncbi.nlm.nih.gov/7554513