Seitz, Cornelia Sabine

[["dc.bibliographiccitation.firstpage","861"],["dc.bibliographiccitation.issue","09"],["dc.bibliographiccitation.journal","Zeitschrift für Gastroenterologie"],["dc.bibliographiccitation.lastpage","865"],["dc.bibliographiccitation.volume","55"],["dc.contributor.author","Gliem, Nina"],["dc.contributor.author","Broekaert, Sigrid"],["dc.contributor.author","Seitz, Cornelia"],["dc.contributor.author","Schön, Michael"],["dc.contributor.author","Ellenrieder, Volker"],["dc.date.accessioned","2020-12-10T18:12:26Z"],["dc.date.available","2020-12-10T18:12:26Z"],["dc.date.issued","2017"],["dc.identifier.doi","10.1055/s-0043-113833"],["dc.identifier.eissn","1439-7803"],["dc.identifier.issn","0044-2771"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/74371"],["dc.language.iso","de"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Esomeprazol-induzierter kutaner Lupus erythematodes"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","691"],["dc.bibliographiccitation.issue","9"],["dc.bibliographiccitation.journal","Der Hautarzt"],["dc.bibliographiccitation.lastpage","695"],["dc.bibliographiccitation.volume","62"],["dc.contributor.author","Meyersburg, Damian"],["dc.contributor.author","Schoen, Michael Peter"],["dc.contributor.author","Bertsch, Hans-Peter"],["dc.contributor.author","Seitz, Cornelia S."],["dc.date.accessioned","2018-11-07T08:52:36Z"],["dc.date.available","2018-11-07T08:52:36Z"],["dc.date.issued","2011"],["dc.description.abstract","Sarcoidosis is a granulomatous multisystemic disease of unclear etiology, which can affect any organ. The cutaneous manifestations are variable, but ulcerative cutaneous sarcoidosis is very yare. One must rule out other granulomatous skin diseases, especially necrobiosis lipoidica. There is no standarized therapy; usually an interdisciplinary acropachy over years taking multiple side effects into consideration is needed. A 58-year-old woman with a long history of cutaneous, nodal and pulmonary sarcoidosis suddenly developed ulcerations within the disseminated skin lesions on her legs. The combination of systemic hydroxychloroquine and modern wound management lead to complete healing of the ulcers and a significant improvement in the remaining skin lesions."],["dc.identifier.doi","10.1007/s00105-010-2120-7"],["dc.identifier.isi","000294498600012"],["dc.identifier.pmid","21656110"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/22208"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.relation.issn","0017-8470"],["dc.title","Uncommon cutaneous ulcerative and systemic sarcoidosis. Successful treatment with hydroxychloroquine and compression therapy"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.journal","JDDG Journal der Deutschen Dermatologischen Gesellschaft"],["dc.bibliographiccitation.volume","11"],["dc.contributor.author","Meyersburg, Damian"],["dc.contributor.author","Moessner, R."],["dc.contributor.author","Schoen, Michael Peter"],["dc.contributor.author","Seitz, Cornelia S."],["dc.date.accessioned","2018-11-07T09:19:11Z"],["dc.date.available","2018-11-07T09:19:11Z"],["dc.date.issued","2013"],["dc.format.extent","12"],["dc.identifier.isi","000324332500037"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/28579"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-blackwell"],["dc.publisher.place","Hoboken"],["dc.relation.issn","1610-0387"],["dc.relation.issn","1610-0379"],["dc.title","Palmar and plantar filiform Hyperkeratosis under immunosuppressive Therapy after Renal Transplantation in familial Renal Cysts"],["dc.type","conference_abstract"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","202"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Journal der Deutschen Dermatologischen Gesellschaft"],["dc.bibliographiccitation.lastpage","204"],["dc.bibliographiccitation.volume","16"],["dc.contributor.author","Lockmann, Anike"],["dc.contributor.author","Seitz, Cornelia S."],["dc.contributor.author","Schön, Michael P."],["dc.contributor.author","Mößner, Rotraut"],["dc.date.accessioned","2020-12-10T18:27:17Z"],["dc.date.available","2020-12-10T18:27:17Z"],["dc.date.issued","2018"],["dc.identifier.doi","10.1111/ddg.13414"],["dc.identifier.issn","1610-0379"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/76296"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Creeping eruption and eosinophilic folliculitis: Atypical cutaneous larva migrans"],["dc.title.alternative","Correspondence"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","193"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Allergologia et Immunopathologia"],["dc.bibliographiccitation.lastpage","199"],["dc.bibliographiccitation.volume","39"],["dc.contributor.author","Seitz, Cornelia S."],["dc.contributor.author","Broecker, Eva-B."],["dc.contributor.author","Trautmann, Axel"],["dc.date.accessioned","2018-11-07T08:54:31Z"],["dc.date.available","2018-11-07T08:54:31Z"],["dc.date.issued","2011"],["dc.description.abstract","Background: Macrolides are useful in a wide range of bacterial infections including upper and lower respiratory tract, skin, and sexually transmitted diseases and are used in Helicobacter pylori eradication regimen. Skin symptoms occurring during drug therapy are mostly attributed to the antibiotic, causing considerable limitations of future therapeutic options. The aim of this retrospective analysis was to demonstrate results of diagnostic testing in cases of clinically suspected immediate and delayed macrolide hypersensitivity. Methods: A total of 125 patients with a history of immediate or delayed hypersensitivity symptoms in temporal relation to treatment with a macrolide antibiotic were studied using standardised skin tests followed by oral challenges. Selected patients with severe symptoms were further evaluated with in vitro tests. Results:. Macrolide hypersensitivity was excluded in 109 patients (87.2%) by tolerated oral challenge tests. During 113 challenges in four patients an exanthema was provoked by the suspected macrolide. Only one patient developed a positive late skin test reaction. Out of the 28 Helicobacter pylori-treated patients, one patient with clarithromycin allergy was identified, whereas in eight cases amoxicillin allergy caused the exanthema. Laboratory tests using the suspected macrolides were constantly negative. Conclusions: History alone leads to an over-estimation of macrolide hypersensitivity. Moreover, skin and in vitro tests seem to be not very useful in identifying hypersensitive patients. Challenge tests appear to be necessary for definitely confirming or ruling out macrolide allergy. (C) 2010 SEICAP. Published by Elsevier Espana, S.L. All rights reserved."],["dc.identifier.doi","10.1016/j.aller.2010.06.008"],["dc.identifier.isi","000293608200002"],["dc.identifier.pmid","21269750"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/22689"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Elsevier Doyma Sl"],["dc.relation.issn","1578-1267"],["dc.relation.issn","0301-0546"],["dc.title","Suspicion of macrolide allergy after treatment of infectious diseases including Helicobacter pylori: Results of allergological testing"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1201"],["dc.bibliographiccitation.issue","12"],["dc.bibliographiccitation.journal","Journal der Deutschen Dermatologischen Gesellschaft"],["dc.bibliographiccitation.lastpage","1202"],["dc.bibliographiccitation.volume","14"],["dc.contributor.author","Patschan, Susann"],["dc.contributor.author","Seitz, Cornelia S."],["dc.date.accessioned","2020-12-10T18:27:15Z"],["dc.date.available","2020-12-10T18:27:15Z"],["dc.date.issued","2016"],["dc.identifier.doi","10.1111/ddg.13162"],["dc.identifier.issn","1610-0379"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/76287"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Haut und Rheuma"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","121"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Experimental Dermatology"],["dc.bibliographiccitation.lastpage","128"],["dc.bibliographiccitation.volume","28"],["dc.contributor.author","Priebe, Marie K."],["dc.contributor.author","Dewert, Nadin"],["dc.contributor.author","Amschler, Katharina"],["dc.contributor.author","Erpenbeck, Luise"],["dc.contributor.author","Heinzerling, Lucie"],["dc.contributor.author","Schön, Michael P."],["dc.contributor.author","Seitz, Cornelia S."],["dc.contributor.author","Lorenz, Verena N."],["dc.date.accessioned","2020-12-10T18:28:40Z"],["dc.date.available","2020-12-10T18:28:40Z"],["dc.date.issued","2018"],["dc.identifier.doi","10.1111/exd.13848"],["dc.identifier.issn","0906-6705"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/76375"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","c-Rel is a cell cycle modulator in human melanoma cells"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2055"],["dc.bibliographiccitation.issue","8"],["dc.bibliographiccitation.journal","Journal of Investigative Dermatology"],["dc.bibliographiccitation.lastpage","2068"],["dc.bibliographiccitation.volume","128"],["dc.contributor.author","Inui, Hiroki"],["dc.contributor.author","Oh, Kyu-Seon"],["dc.contributor.author","Nadem, Carine"],["dc.contributor.author","Ueda, Takahiro"],["dc.contributor.author","Khan, Sikandar C."],["dc.contributor.author","Metin, Ahmet"],["dc.contributor.author","Gozukara, Engm"],["dc.contributor.author","Emmert, Steffen"],["dc.contributor.author","Slor, Hanoch"],["dc.contributor.author","Busch, David B."],["dc.contributor.author","Baker, Carl C."],["dc.contributor.author","DiGiovanna, John J."],["dc.contributor.author","Tamura, Deborah"],["dc.contributor.author","Seitz, Cornelia S."],["dc.contributor.author","Gratchev, Alexei"],["dc.contributor.author","Wu, W."],["dc.contributor.author","Chung, Kee Yang"],["dc.contributor.author","Chung, Hye Jin"],["dc.contributor.author","Azizi, Esther"],["dc.contributor.author","Woodgate, Roger"],["dc.contributor.author","Schneider, Thomas D."],["dc.contributor.author","Kraemer, Kenneth H."],["dc.date.accessioned","2018-11-07T11:12:33Z"],["dc.date.available","2018-11-07T11:12:33Z"],["dc.date.issued","2008"],["dc.description.abstract","Xeroderma pigmentosum-variant (XP-V) patients have sun sensitivity and increased skin cancer risk. Their cells have normal nucleotide excision repair, but have defects in the POLH gene encoding an error-prone polymerase, DNA polymerase eta (pol eta). To survey the molecular basis of XP-V worldwide, we measured pol eta protein in skin fibroblasts from putative XP-V patients (aged 8-66 years) from 10 families in North America, Turkey, Israel, Germany, and Korea. Pol eta was undetectable in cells from patients in eight families, whereas two showed faint bands. DNA sequencing identified 10 different POLH mutations. There were two splicing, one nonsense, five frameshift (3 deletion and 2 insertion), and two missense mutations. Nine of these mutations involved the catalytic domain. Although affected siblings had similar clinical features, the relation between the clinical features and the mutations was not clear. POLH mRNA levels were normal or reduced by 50% in three cell strains with undetectable levels of pol eta protein, indicating that nonsense-mediated message decay was limited. We found a wide spectrum of mutations in the POLH gene among XP-V patients in different countries, suggesting that many of these mutations arose independently."],["dc.description.sponsorship","Intramural NIH HHS [Z01 BC008396-18, Z01 HD001500-25]"],["dc.identifier.doi","10.1038/jid.2008.48"],["dc.identifier.isi","258031700027"],["dc.identifier.pmid","18368133"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/53695"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Nature Publishing Group"],["dc.relation.issn","0022-202X"],["dc.title","Xeroderma pigmentosum-variant patients from America, Europe, and Asia"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2071"],["dc.bibliographiccitation.issue","11"],["dc.bibliographiccitation.journal","Rheumatology"],["dc.bibliographiccitation.lastpage","2073"],["dc.bibliographiccitation.volume","58"],["dc.contributor.author","Korsten, Peter"],["dc.contributor.author","Seitz, Cornelia S"],["dc.contributor.author","Sahlmann, Carsten O"],["dc.contributor.author","Schmidt, Jens"],["dc.date.accessioned","2020-12-10T18:19:41Z"],["dc.date.available","2020-12-10T18:19:41Z"],["dc.date.issued","2019"],["dc.identifier.doi","10.1093/rheumatology/kez313"],["dc.identifier.eissn","1462-0332"],["dc.identifier.issn","1462-0324"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/75335"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Comment on: The temporal relationship between cancer and adult onset anti-transcriptional intermediary factor 1 antibody–positive dermatomyositis"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.journal","JDDG Journal der Deutschen Dermatologischen Gesellschaft"],["dc.bibliographiccitation.volume","11"],["dc.contributor.author","Seitz, Cornelia S."],["dc.date.accessioned","2018-11-07T09:25:22Z"],["dc.date.available","2018-11-07T09:25:22Z"],["dc.date.issued","2013"],["dc.format.extent","32"],["dc.identifier.isi","000318116100096"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/30049"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-blackwell"],["dc.publisher.place","Hoboken"],["dc.relation.issn","1610-0379"],["dc.title","Vasculitis in dermatological Practice - what is important for my Patients?"],["dc.type","conference_abstract"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]