Výsledky vyhledávání

[Mucosal manifestations of epidermolysis bullosa : Clinical presentation and management]

Autor: C, Prodinger, A, Diem, J W, Bauer, M, Laimer

Publikováno v: Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete. 67(10)

Mucosal lesions occur with different prevalence and severity in all subtypes of hereditary epidermolysis bullosa (EB), a group of rare genodermatoses. They are associated with increased morbidity and mortality, especially in severe junctional and dys

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e85379e8c6e9d5bac05035d23a4d112b
https://pubmed.ncbi.nlm.nih.gov/27515981

Zobrazit plný text záznamu

[Molecular diagnosis of methicillin-resistent Staphylococcus aureus: Methods and efficacy]

Autor: M, Hell, J W, Bauer, M, Laimer

Publikováno v: Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete. 67(1)

Methicillin-resistant Staphylococcus aureus (MRSA) isolates are a serious public health problem whose ever-increasing rate is commensurate with the pressure it is exerting on the healthcare system. At present, more than 20% of clinical S. aureus isol

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::18fd09bb84ac0bf8c1141b2adc084443
https://pubmed.ncbi.nlm.nih.gov/26016829

Zobrazit plný text záznamu

[Molecular diagnostics in melanoma]

Autor: R, Lang, J W, Bauer, M, Laimer

Publikováno v: Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete. 66(4)

The molecular landscape of melanoma is changing more rapidly than ever since new molecular technology approaches have made it possible to examine human melanoma for genetic alterations underlying the disease. In recent years, these approaches have id

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0ac6cee3f887be277c7a8d6be81dc431
https://pubmed.ncbi.nlm.nih.gov/25783213

Zobrazit plný text záznamu

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

Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorder

Autor: W. H. Muss, G. Pohla-Gubo, CM Lanschuetzer, Michael Emberger, J W Bauer, H Hintner, A. Klausegger

Publikováno v: Journal of Cutaneous Pathology. 30:553-560

Background: Kindler's syndrome is a rare genodermatosis mainly characterized by the onset of skin blistering in early childhood, web formation of fingers and toes, photosensitivity, and progressive poikiloderma. There is still debate whether this dis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::83924f9bcd0134650d2ddd09943946b6
https://doi.org/10.1034/j.1600-0560.2003.00119.x

Zobrazit plný text záznamu

Type XVII collagen gene mutations in junctional epidermolysis bullosa and prospects for gene therapy

Autor: C. Lanschuetzer, J. W. Bauer

Publikováno v: Clinical and Experimental Dermatology. 28:53-60

Non-Herlitz junctional epidermolysis bullosa (nH-JEB) is caused predominantly by mutations leading to premature stop codons on both alleles of the type XVII collagen gene (COL17A1). The analysis of mutations in this gene has provided a means of corre

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::575fd778ffe55f460db2997b46a9815a
https://doi.org/10.1046/j.1365-2230.2003.01192.x

Zobrazit plný text záznamu

[Darier disease]

Autor: A, Klausegger, M, Laimer, J W, Bauer

Publikováno v: Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete. 64(1)

Darier disease (Darier-White disease, dyskeratosis follicularis) is a rare autosomal dominant genodermatosis with regional differences in prevalence. The responsible mutations have been identified on chromosome 12q23-24.1. The gene encodes a calcium-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::14761b34326ad4efd8304c61a20cbe68
https://pubmed.ncbi.nlm.nih.gov/23337962

Zobrazit plný text záznamu

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

Autor: Reiner Fischer-Colbrie, J. W. Bauer, Sushil K. Mahata, Andrea Laslop, Manjula Mahata, K. W. Schmid

Publikováno v: Journal of neuroendocrinology. 4(1)

Chromogranin A, an acidic secretory protein, is widely distributed throughout diverse endocrine cells and the central and peripheral nervous systems. Chromogranin A is co-stored and co-secreted from secretory vesicles together with the endogenous hor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fbc817e91e7d546f13af9a7554afdce
https://pubmed.ncbi.nlm.nih.gov/21554587

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání