Zobrazeno 1 - 10 of 56 pro vyhledávání: '"R. Hametner"'
1
Telepathology using immunofluorescence/immunoperoxidase microscopy
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
Zobrazit plný text záznamu
2
A localized variant of paraneoplastic pemphigus: acantholysis associated with malignant melanoma
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
Zobrazit plný text záznamu
3
Ocular involvement in IgA-epidermolysis bullosa acquisita
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
Zobrazit plný text záznamu
7
A novel homozygous nonsense deletion/insertion mutation in the keratin 14 gene (Y248X; 744delC/insAG) causes recessive epidermolysis bullosa simplex type Köbner
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
Zobrazit plný text záznamu
9
A novel homozygous nonsense deletion/insertion mutation in the keratin 14 gene (Y248X; 744delC/insAG) causes recessive epidermolysis bullosa simplex type Köbner
Autor: C M, Lanschuetzer, A, Klausegger, G, Pohla-Gubo, R, Hametner, G, Richard, J, Uitto, H, Hintner, J W, Bauer
Publikováno v: Clinical and experimental dermatology. 28(1)
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=pmid________::4bd1c5fa195e1f19f6e56ab30fc44f92
https://pubmed.ncbi.nlm.nih.gov/12558637
Zobrazit plný text záznamu
10
Kniha
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje