Zutt, Markus

[["dc.bibliographiccitation.firstpage","299"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Melanoma Research"],["dc.bibliographiccitation.lastpage","302"],["dc.bibliographiccitation.volume","13"],["dc.contributor.author","Emmert, Steffen"],["dc.contributor.author","Zutt, Markus"],["dc.contributor.author","Haenssle, Holger Andreas"],["dc.contributor.author","Neumann, C."],["dc.contributor.author","Kretschmer, Lutz"],["dc.date.accessioned","2018-11-07T10:38:43Z"],["dc.date.available","2018-11-07T10:38:43Z"],["dc.date.issued","2003"],["dc.description.abstract","The anti-melanoma activity of vindesine as a single or polychemotherapeutic agent has been reported previously in adjuvant and first-line melanoma treatment. In this study, we investigated the usefulness of vindesine monotherapy as salvage therapy in stage IV melanoma patients after failure of other chemotherapies. Thirteen patients with progressive disease were treated with 3 mg/m(2) vindesine every 2 weeks (median age, 61 years). Previous systemic treatment consisted of polychemotherapy or combined chemo-immunotherapy. All 13 patients suffered from visceral metastases (three lung, one liver, one adrenal gland and eight multiple visceral metastases). A median of three vindesine treatments was administered. Despite the various pretreatments, the toxicity of vindesine was mild. In all 13 patients, vindesine treatment was stopped due to disease progression. The median survival after primary tumour diagnosis was 42 months (8-151 months), the survival after entering stage IV was 11 months (3-35 months), and the survival after starting vindesine therapy was 4 months (1-22 months). We conclude that vindesine monotherapy is ineffective in stage IV melanoma patients previously treated with other chemotherapeutic agents."],["dc.identifier.doi","10.1097/00008390-200306000-00012"],["dc.identifier.isi","000183426800012"],["dc.identifier.pmid","12777986"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/45877"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.relation.issn","0960-8931"],["dc.title","Inefficacy of vindesine monotherapy in advanced stage IV malignant melanoma patients previously treated with other chemotherapeutic agents"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","244"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Clinical and Experimental Dermatology"],["dc.bibliographiccitation.lastpage","246"],["dc.bibliographiccitation.volume","29"],["dc.contributor.author","Haenssle, Holger Andreas"],["dc.contributor.author","Bertsch, Hans-Peter"],["dc.contributor.author","Emmert, Steffen"],["dc.contributor.author","Wolf, C."],["dc.contributor.author","Zutt, Markus"],["dc.date.accessioned","2018-11-07T10:49:10Z"],["dc.date.available","2018-11-07T10:49:10Z"],["dc.date.issued","2004"],["dc.description.abstract","Pityriasis rubra pilaris (PRP) is a rare papulosquamous skin disease of unknown aetiology that has been categorized into five clinical types based on age at onset, cutaneous features and prognosis. We present a patient with chronic exanthematic type II atypical adult PRP, whose skin status was significantly improved with monthly extracorporeal photochemotherapy (ECP). Various therapeutic regimens including narrow-band UV-B, bath PUVA therapy, systemic fumaric acid esters and systemic cyclosporin had failed. Oral retinoids could not be administered due to a type IIa hyperlipoproteinemia with profound hepatic steatosis and elevated liver transaminases. The observed clinical benefit may encourage future clinical studies analysing the effectiveness of ECP in otherwise unresponsive cases of type II PRP."],["dc.identifier.doi","10.1111/j.1365-2230.2004.01468.x"],["dc.identifier.isi","000221125900006"],["dc.identifier.pmid","15115502"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/48365"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Blackwell Publishing Ltd"],["dc.relation.issn","0307-6938"],["dc.title","Extracorporeal photochemotherapy for the treatment of exanthematic pityriasis rubra pilaris"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","342"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Der Hautarzt"],["dc.bibliographiccitation.lastpage","347"],["dc.bibliographiccitation.volume","54"],["dc.contributor.author","Zutt, Markus"],["dc.contributor.author","Emmert, Steffen"],["dc.contributor.author","Hanssle, H."],["dc.contributor.author","Grafe, A."],["dc.contributor.author","Domhof, S."],["dc.contributor.author","Neumann, C."],["dc.contributor.author","Kretschmer, Lutz"],["dc.date.accessioned","2018-11-07T10:39:45Z"],["dc.date.available","2018-11-07T10:39:45Z"],["dc.date.issued","2003"],["dc.description.abstract","Background and Objective. The objective of the study was to evaluate the use of a medical surgical zipper (Medizip(TM)) for wound closure under tension in comparison to conventional cutaneous sutures. The surgical zipper is supposed to reduce wound tension by approximating of the wound edges via epidermal traction. Patients/Methods. This prospective study included patients with a wound diameter of more than 1 cm. 45 patients were treated with the surgical zipper, 38 were randomized into a control group with conventional wound closure. Scars were assessed after 6-18 months focusing on aesthetic and functional aspects. Results. The average length of the scars in both groups was 9 cm, but after a observation time of at least 6 month, there were differences in the width of the scars. The group with the surgical zipper showed significantly thinner scars (2,74 mm versus 4,24 mm, p=0,0008). Only 17% of the Medizip(TM) patients developed unaesthetic rope ladder-like scars versus 65% in the control group. This observation was statistically significant (p<0,0001). Conclusions. Wound stabilization by approximation of the wound edges via surgical zipper results in improved scar formation in wounds with moderate tension. Using the Medizip(TM) in wounds under heavy tension is not recommended because of the possible development of to tension bullae under the zipper."],["dc.identifier.doi","10.1007/s00105-002-0460-7"],["dc.identifier.isi","000182445300006"],["dc.identifier.pmid","12669206"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/46127"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.relation.issn","0017-8470"],["dc.title","Improved scar formation after using a medical surgical zipper for wound closure under tension"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","137"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Annals of Oncology"],["dc.bibliographiccitation.lastpage","143"],["dc.bibliographiccitation.volume","31"],["dc.contributor.author","Haenssle, H.A."],["dc.contributor.author","Fink, C."],["dc.contributor.author","Toberer, F."],["dc.contributor.author","Winkler, J."],["dc.contributor.author","Stolz, W."],["dc.contributor.author","Deinlein, T."],["dc.contributor.author","Hofmann-Wellenhof, R."],["dc.contributor.author","Lallas, A."],["dc.contributor.author","Emmert, S."],["dc.contributor.author","Buhl, T."],["dc.contributor.author","Zutt, M."],["dc.contributor.author","Blum, A."],["dc.contributor.author","Abassi, M.S."],["dc.contributor.author","Thomas, L."],["dc.contributor.author","Tromme, I."],["dc.contributor.author","Tschandl, P."],["dc.contributor.author","Enk, A."],["dc.contributor.author","Rosenberger, A."],["dc.contributor.author","Alt, Christina"],["dc.contributor.author","Bachelerie, Marie"],["dc.contributor.author","Bajaj, Sonali"],["dc.contributor.author","Balcere, Alise"],["dc.contributor.author","Baricault, Sophie"],["dc.contributor.author","Barthaux, Clément"],["dc.contributor.author","Beckenbauer, Yvonne"],["dc.contributor.author","Bertlich, Ines"],["dc.contributor.author","Blum, Andreas"],["dc.contributor.author","Bouthenet, Marie-France"],["dc.contributor.author","Brassat, Sophie"],["dc.contributor.author","Marcel Buck, Philipp"],["dc.contributor.author","Buder-Bakhaya, Kristina"],["dc.contributor.author","Cappelletti, Maria-Letizia"],["dc.contributor.author","Chabbert, Cécile"],["dc.contributor.author","De Labarthe, Julie"],["dc.contributor.author","DeCoster, Eveline"],["dc.contributor.author","Deinlein, Teresa"],["dc.contributor.author","Dobler, Michèle"],["dc.contributor.author","Dumon, Daphnée"],["dc.contributor.author","Emmert, Steffen"],["dc.contributor.author","Gachon-Buffet, Julie"],["dc.contributor.author","Gusarov, Mikhail"],["dc.contributor.author","Hartmann, Franziska"],["dc.contributor.author","Hartmann, Julia"],["dc.contributor.author","Herrmann, Anke"],["dc.contributor.author","Hoorens, Isabelle"],["dc.contributor.author","Hulstaert, Eva"],["dc.contributor.author","Karls, Raimonds"],["dc.contributor.author","Kolonte, Andreea"],["dc.contributor.author","Kromer, Christian"],["dc.contributor.author","Lallas, Aimilios"],["dc.contributor.author","Le Blanc Vasseux, Céline"],["dc.contributor.author","Levy-Roy, Annabelle"],["dc.contributor.author","Majenka, Pawel"],["dc.contributor.author","Marc, Marine"],["dc.contributor.author","Bourret, Veronique Martin"],["dc.contributor.author","Michelet-Brunacci, Nadège"],["dc.contributor.author","Mitteldorf, Christina"],["dc.contributor.author","Paroissien, Jean"],["dc.contributor.author","Picard, Camille"],["dc.contributor.author","Plise, Diana"],["dc.contributor.author","Reymann, Valérie"],["dc.contributor.author","Ribeaudeau, Fabrice"],["dc.contributor.author","Richez, Pauline"],["dc.contributor.author","Roche Plaine, Hélène"],["dc.contributor.author","Salik, Deborah"],["dc.contributor.author","Sattler, Elke"],["dc.contributor.author","Schäfer, Sarah"],["dc.contributor.author","Schneiderbauer, Roland"],["dc.contributor.author","Secchi, Thierry"],["dc.contributor.author","Talour, Karen"],["dc.contributor.author","Trennheuser, Lukas"],["dc.contributor.author","Wald, Alexander"],["dc.contributor.author","Wölbing, Priscila"],["dc.contributor.author","Zukervar, Pascale"],["dc.date.accessioned","2020-12-10T14:22:24Z"],["dc.date.available","2020-12-10T14:22:24Z"],["dc.date.issued","2020"],["dc.identifier.doi","10.1016/j.annonc.2019.10.013"],["dc.identifier.issn","0923-7534"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/71599"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Man against machine reloaded: performance of a market-approved convolutional neural network in classifying a broad spectrum of skin lesions in comparison with 96 dermatologists working under less artificial conditions"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","22"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Clinical and Experimental Dermatology"],["dc.bibliographiccitation.lastpage","25"],["dc.bibliographiccitation.volume","33"],["dc.contributor.author","Zutt, Markus"],["dc.contributor.author","Emmert, Steffen"],["dc.contributor.author","Moussa, I."],["dc.contributor.author","Haas, E."],["dc.contributor.author","Mitteldorf, Christina"],["dc.contributor.author","Bertsch, Hans-Peter"],["dc.contributor.author","Neumann, C."],["dc.date.accessioned","2018-11-07T11:19:42Z"],["dc.date.available","2018-11-07T11:19:42Z"],["dc.date.issued","2008"],["dc.description.abstract","We describe the rare Stewart-Bluefarb syndrome in a 15-year-old boy. This syndrome presents as a congenital arteriovenous malformation of the lower leg with multiple arteriovenous shunts accompanied by the benign acroangiodermatitis of Mali (pseudo-Kaposi's sarcoma). The clinical features of this disorder and the treatment options are reviewed."],["dc.identifier.doi","10.1111/j.1365-2230.2007.02541.x"],["dc.identifier.isi","000251809700004"],["dc.identifier.pmid","17927784"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/55347"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Blackwell Publishing"],["dc.relation.issn","0307-6938"],["dc.title","Acroangiodermatitis Mali resulting from arteriovenous malformation: report of a case of Stewart-Bluefarb syndrome"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1166"],["dc.bibliographiccitation.issue","6"],["dc.bibliographiccitation.journal","Journal of the American Academy of Dermatology"],["dc.bibliographiccitation.lastpage","1169"],["dc.bibliographiccitation.volume","49"],["dc.contributor.author","Emmert, Steffen"],["dc.contributor.author","Kuster, W. K."],["dc.contributor.author","Zutt, Markus"],["dc.contributor.author","Hanssle, H."],["dc.contributor.author","Hallermann, Christian"],["dc.contributor.author","Kretschmer, Lutz"],["dc.contributor.author","Neumann, C."],["dc.date.accessioned","2018-11-07T10:34:27Z"],["dc.date.available","2018-11-07T10:34:27Z"],["dc.date.issued","2003"],["dc.description.abstract","We describe a new family with the rare genodermatosis keratosis punctata palmo-plantaris Buschke-Fischer-Brauer (keratoma disseminatum). in all, 3 family members in 3 generations were affected, a pattern consistent with autosomal dominant inheritance. Clinical symptoms started in the third decade with disseminated, small, round, hyperkeratotic papules on the palms and soles. Punctate keratoses coalesced into hyperkeratotic plaques on pressure points. Identification of additional families is necessary to permit definitive genetic classification of this genodermatosis."],["dc.identifier.doi","10.1016/S0190-9622(03)00472-9"],["dc.identifier.isi","000186784800035"],["dc.identifier.pmid","14639410"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/44878"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Mosby, Inc"],["dc.relation.issn","0190-9622"],["dc.title","A new family with the rare genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","72"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Dermatology"],["dc.bibliographiccitation.lastpage","76"],["dc.bibliographiccitation.volume","207"],["dc.contributor.author","Zutt, Markus"],["dc.contributor.author","Strutz, Frank M."],["dc.contributor.author","Happle, R."],["dc.contributor.author","Habenicht, E. M."],["dc.contributor.author","Emmert, Steffen"],["dc.contributor.author","Haenssle, Holger Andreas"],["dc.contributor.author","Kretschmer, Lutz"],["dc.contributor.author","Neumann, C."],["dc.date.accessioned","2018-11-07T10:42:19Z"],["dc.date.available","2018-11-07T10:42:19Z"],["dc.date.issued","2003"],["dc.description.abstract","The Schimmelpenning-Feuerstein-Mims syndrome (SFM syndrome) is a rare and variable multisystem defect consisting of congenital, extensive linear nevus sebaceus and associated abnormalities in different neuroectodermal organ systems. We present the history of a 52-year-old female patient with disproportionate hyposomia and asymmetric constitution. From birth she suffered from a right-sided, extensive nevus sebaceus following Blaschko's lines extending on the scalp, neck, right arm and trunk. At the age of 5 years, she developed a generalized growth retardation, along with deformations of bones. At the age of 11, hypophosphatemic rickets was diagnosed causing this growth retardation. Moreover, the patient developed a precocious puberty at the age of 9 years. When we saw the patient 40 years after the diagnosis had been made, phosphaturia had returned to normal. Specific therapy of hypophosphatemic rickets is straightforward and efficient in preventing late complications like growth retardation. We suggest to conduct appropriate laboratory tests in early childhood in patients with an extensive systematized sebaceous nevus or with additional signs of growth retardation or skeletal involvement, in order to exclude hypophosphatemic rickets associated with SFM syndrome. Copyright (C) 2003 S. Karger AG, Basel."],["dc.identifier.doi","10.1159/000070948"],["dc.identifier.isi","000183981800018"],["dc.identifier.pmid","12835555"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/46766"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Karger"],["dc.relation.issn","1018-8665"],["dc.title","Schimmelpenning-Feuerstein-Mims syndrome with hypophosphatemic rickets"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","222"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Contact Dermatitis"],["dc.bibliographiccitation.lastpage","227"],["dc.bibliographiccitation.volume","80"],["dc.contributor.author","Bauer, Andrea"],["dc.contributor.author","Geier, Johannes"],["dc.contributor.author","Schreiber, Sophie"],["dc.contributor.author","Schubert, Steffen"],["dc.contributor.author","Beiteke, Ulrike"],["dc.contributor.author","Dissemond, Joachim"],["dc.contributor.author","Buhl, Timo"],["dc.contributor.author","Schäkel, Knut"],["dc.contributor.author","Pföhler, Claudia"],["dc.contributor.author","Brasch, Jochen"],["dc.contributor.author","Worm, Margitta"],["dc.contributor.author","Kreft, Burkhard"],["dc.contributor.author","Schliemann, Sibylle"],["dc.contributor.author","Darsow, Ulf"],["dc.contributor.author","Becker, Detlef"],["dc.contributor.author","Forchhammer, Stephan"],["dc.contributor.author","Hartmann, Karin"],["dc.contributor.author","Witte, Jana"],["dc.contributor.author","Pfützner, Wolfgang"],["dc.contributor.author","Coras‐Stepanek, Brigitte"],["dc.contributor.author","Skudlik, Christoph"],["dc.contributor.author","Wagner, Nicola"],["dc.contributor.author","Aberer, Werner"],["dc.contributor.author","Emmert, Steffen"],["dc.contributor.author","Baron, Jens Malte"],["dc.contributor.author","Siedlecki, Katharina"],["dc.contributor.author","Baur, Vera"],["dc.contributor.author","Schmieder, Astrid"],["dc.contributor.author","Weisshaar, Elke"],["dc.contributor.author","Grunwald‐Delitz, Heidrun"],["dc.contributor.author","Trautmann, Axel"],["dc.contributor.author","Bircher, Andreas"],["dc.contributor.author","Szliska, Christiane"],["dc.contributor.author","Weiß, Johannes"],["dc.contributor.author","Effendy, Isaak"],["dc.contributor.author","Jünger, Michael"],["dc.contributor.author","Brehler, Randolf"],["dc.contributor.author","Molin, Sonja"],["dc.contributor.author","Werfel, Thomas"],["dc.contributor.author","Dickel, Heinrich"],["dc.contributor.author","Rieker‐Schwienbacher, Juliane"],["dc.contributor.author","Vieluf, Dieter"],["dc.contributor.author","Stadler, Rudolf"],["dc.contributor.author","Simon, Dagmar"],["dc.contributor.author","Fartasch, Manigé"],["dc.contributor.author","Navarini, Alexander"],["dc.contributor.author","Treudler, Regina"],["dc.contributor.author","Nestoris, Stefan"],["dc.contributor.author","Mechtel, Dirk"],["dc.contributor.author","Schröder‐Kraft, Claudia"],["dc.contributor.author","Löffler, Harald"],["dc.contributor.author","Fischer, Matthias"],["dc.contributor.author","Koch, André"],["dc.contributor.author","Raap, Ulrike"],["dc.contributor.author","Grabbe, Jürgen"],["dc.contributor.author","Lucca, Julie"],["dc.contributor.author","Zutt, Markus"],["dc.contributor.author","Spring, Philipp"],["dc.contributor.author","Prager, Welf"],["dc.date.accessioned","2020-12-10T18:27:12Z"],["dc.date.available","2020-12-10T18:27:12Z"],["dc.date.issued","2019"],["dc.identifier.doi","10.1111/cod.13169"],["dc.identifier.eissn","1600-0536"],["dc.identifier.issn","0105-1873"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/76272"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Contact sensitization to plants of the Compositae family: Data of the Information Network of Departments of Dermatology (IVDK) from 2007 to 2016"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","980"],["dc.bibliographiccitation.issue","5"],["dc.bibliographiccitation.journal","Journal of Investigative Dermatology"],["dc.bibliographiccitation.lastpage","985"],["dc.bibliographiccitation.volume","126"],["dc.contributor.author","Haenssle, Holger Andreas"],["dc.contributor.author","Krueger, Ullrich"],["dc.contributor.author","Vente, Claudia"],["dc.contributor.author","Thoms, Kai-Martin"],["dc.contributor.author","Bertsch, Hans-Peter"],["dc.contributor.author","Zutt, Markus"],["dc.contributor.author","Rosenberger, Albert"],["dc.contributor.author","Neumann, Christine"],["dc.contributor.author","Emmert, Steffen"],["dc.date.accessioned","2018-11-07T09:53:11Z"],["dc.date.available","2018-11-07T09:53:11Z"],["dc.date.issued","2006"],["dc.description.abstract","We analyzed the value of digital epiluminescence microscopy (DELM) for the long-term follow-up of atypical nevi. Patients (n = 530) were prospectively categorized into defined melanoma risk groups and followed by clinical and epiluminescence microscopy (ELM) examinations. Atypical nevi (n = 7001) were additionally followed by DELM. During follow-up (median 32.2 months), we detected 53 melanomas among 637 excised lesions (8.3% overall chance of success). The chance of success for melanoma detection among lesions suspicious by ELM criteria was increased to 17% when additional DELM-documented changes were present. Moreover, 18 of the 53 melanomas were exclusively identified by DELM-documented changes, indicating that DELM increased the sensitivity of the ELM analysis by identifying additional melanomas. However, for lesions exclusively excised due to DELM changes, the chance of success was lower than for ELM (5.2 vs 11.8%). Excisions due to mere DELM changes detected 66.7% of melanomas in familial atypical mole and multiple melanoma (FAMMM) and 32.5% of melanomas in atypical mole syndrome (AMS) patients. We conclude that DELM is a valuable tool for the long- term follow- up of atypical nevi, especially in the high- risk groups of FAMMM and AMS patients. Randomized controlled trials are needed to validate the data from this clinical trial."],["dc.identifier.doi","10.1038/sj.jid.5700119"],["dc.identifier.isi","000238968700010"],["dc.identifier.pmid","16514414"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/36280"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Nature Publishing Group"],["dc.relation.issn","0022-202X"],["dc.title","Results from an observational trial: Digital epiluminescence Microscopy follow-up of atypical nevi increases the sensitivity and the chance of success of conventional dermoscopy in detecting melanoma"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1592"],["dc.bibliographiccitation.issue","10"],["dc.bibliographiccitation.journal","Dermatologic Surgery"],["dc.bibliographiccitation.lastpage","1595"],["dc.bibliographiccitation.volume","35"],["dc.contributor.author","Kaune, Kjell Matthias"],["dc.contributor.author","Haas, Ellen"],["dc.contributor.author","Emmert, Steffen"],["dc.contributor.author","Schoen, Michael Peter"],["dc.contributor.author","Zutt, Markus"],["dc.date.accessioned","2018-11-07T11:23:28Z"],["dc.date.available","2018-11-07T11:23:28Z"],["dc.date.issued","2009"],["dc.description.abstract","The authors have indicated no significant interest with commercial supporters."],["dc.identifier.doi","10.1111/j.1524-4725.2009.01282.x"],["dc.identifier.isi","000270397300024"],["dc.identifier.pmid","19681988"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/56202"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-blackwell Publishing, Inc"],["dc.relation.issn","1076-0512"],["dc.title","Successful Treatment of Severe Keratosis Pilaris Rubra with a 595-nm Pulsed Dye Laser"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]