Zobrazeno 1 - 10
of 540
pro vyhledávání: '"R Hametner"'
Autor:
Scorziello, Antonella1 (AUTHOR) rossana.sirabella@unina.it, Sirabella, Rossana1 (AUTHOR) michele.tufano@unina.it, Sisalli, Maria Josè2 (AUTHOR) mariajose.sisalli@unina.it, Tufano, Michele1 (AUTHOR) lgiacciol@gmail.com, Giaccio, Lucia1 (AUTHOR) elena.dapolito@unina.it, D'Apolito, Elena1 (AUTHOR) lorenzo.castellano@unina.it, Castellano, Lorenzo1 (AUTHOR), Annunziato, Lucio3 (AUTHOR) scorziel@unina.it
Publikováno v:
International Journal of Molecular Sciences. Nov2024, Vol. 25 Issue 21, p11490. 21p.
Autor:
G Pohla-Gubo, Takashi Hashimoto, B. Schafleitner, J W Bauer, CM Lanschuetzer, H Hintner, R Hametner, Wolfgang Salmhofer
Publikováno v:
Journal of Telemedicine and Telecare. 10:39-43
We evaluated low-cost, store-and-forward telepathology interpretation of digital images of skin sections stained immunohistochemically, using immunofluorescence (IF) and immunoperoxidase (IP). The sample comprised 17 patients with skin diseases chara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bd3af1cab106e743ccda9016ac606cf
https://doi.org/10.1258/135763304322764185
https://doi.org/10.1258/135763304322764185
Autor:
H Hintner, Klemens Rappersberger, Johann W. Bauer, R. Hametner, Wolfgang Salmhofer, Dieter Metze, H. Schaeppi, Susana Ortiz-Urda
Publikováno v:
British Journal of Dermatology. 144:1249-1254
We report a 72-year-old male patient with a nodular malignant melanoma that was associated with focal suprabasal acantholysis (FSA). This phenomenon, which is regarded as an incidental finding by dermatopathologists, may be associated with inflammato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a07ed6a6bcbe325ac9b5f2c62aa2ffb6
https://doi.org/10.1046/j.1365-2133.2001.04243.x
https://doi.org/10.1046/j.1365-2133.2001.04243.x
Autor:
Günther Grabner, H Hintner, Wolfgang Muss, Johann W. Bauer, R. Hametner, H. Schaeppi, G. Pohla-Gubo, Dieter Metze, J. Ruckhofer
Publikováno v:
British Journal of Dermatology. 141:887-892
Summary Epidermolysis bullosa acquisita (EBA) is an autoimmune bullous disease with frequent ocular involvement, but visual loss is rare. In contrast, EBA patients with predominant IgA autoantibodies more frequently develop severe ocular involvement,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cdec308f2493ee5c99a4782c1626904
https://doi.org/10.1046/j.1365-2133.1999.03163.x
https://doi.org/10.1046/j.1365-2133.1999.03163.x
Autor:
B. Schafleitner, R. Hametner, Helmut Hintner, Martin Laimer, G. Pohla-Gubo, Elke Sadler, Johann W. Bauer, CM Lanschuetzer
Publikováno v:
British Journal of Dermatology. 157:417-419
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6d549f6ae0e676668ced9beef266025
https://doi.org/10.1111/j.1365-2133.2007.08048.x
https://doi.org/10.1111/j.1365-2133.2007.08048.x
Autor:
R. Jones, Barbara Kofler, R. Hametner, Tiina P. Iismaa, C. Tuechler, Wolfgang Sperl, N. R. Jones
Publikováno v:
Annals of the New York Academy of Sciences. 863:438-441
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a239621edc6868bd02d8948215705dd8
https://doi.org/10.1111/j.1749-6632.1998.tb10718.x
https://doi.org/10.1111/j.1749-6632.1998.tb10718.x
Autor:
E. Sadler, Michael Emberger, V. Wally, A. Klausegger, CM Lanschuetzer, H Hintner, G. Pohla-Gubo, Wolfgang Muss, Martin Laimer, Johann W. Bauer, R. Hametner, K. Oender, J. Koller
Publikováno v:
British Journal of Dermatology. 154:185-187
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1273e70f77be8933e29de950089a67b
https://doi.org/10.1111/j.1365-2133.2005.06988.x
https://doi.org/10.1111/j.1365-2133.2005.06988.x
Autor:
R Hametner, Jouni Uitto, J W Bauer, H Hintner, CM Lanschuetzer, G Pohla-Gubo, G. Richard, A Klausegger
Publikováno v:
Clinical and Experimental Dermatology. 28:77-79
We report the sixth case of a human keratin 14 'knockout' mutation resulting in recessive epidermolysis bullosa simplex (EBS). A novel, homozygous nonsense mutation resulting from a deletion/insertion mutation (744delC/insAG) leads to a premature ter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8525ad522e66197d919200dd23a1113
https://doi.org/10.1046/j.1365-2230.2003.01218.x
https://doi.org/10.1046/j.1365-2230.2003.01218.x
Autor:
Culicetto, Laura1 (AUTHOR), Formica, Caterina1 (AUTHOR) katia.formica@irccsme.it, Lo Buono, Viviana1 (AUTHOR), Latella, Desirèe1 (AUTHOR), Maresca, Giuseppa1 (AUTHOR), Brigandì, Amelia1 (AUTHOR), Sorbera, Chiara1 (AUTHOR), Di Lorenzo, Giuseppe1 (AUTHOR), Quartarone, Angelo1 (AUTHOR), Marino, Silvia1 (AUTHOR), Witt, Karsten1 (AUTHOR)
Publikováno v:
Parkinson's Disease (20420080). 8/27/2024, Vol. 2024, p1-10. 10p.
Autor:
Turcu-Stiolica, Adina1 (AUTHOR) adina.turcu@umfcv.ro, Naidin, Mihaela-Simona1 (AUTHOR) mihaela.subtirelu@umfcv.ro, Halmagean, Steliana2 (AUTHOR) steliana.halmagean@neurotherapy.ro, Ionescu, Ana Maria3 (AUTHOR) ana.maria.ionescu@univ-ovidius.ro, Pirici, Ionica4 (AUTHOR) ionica.pirici@umfcv.ro
Publikováno v:
Diagnostics (2075-4418). Aug2024, Vol. 14 Issue 15, p1609. 12p.