FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W1977585235> ?p ?o ?g. }

• W1977585235 endingPage "494" @default.
• W1977585235 startingPage "493" @default.
• W1977585235 abstract "Journal of the European Academy of Dermatology and VenereologyVolume 30, Issue 3 p. 493-494 Letter to the Editor Unexpected manifestation of naevoid basal cell carcinoma (Gorlin) syndrome with a novel mutation in the PTCH1 gene in a female patient with long-lasting pemphigus vulgaris S. Goetze, Corresponding Author S. Goetze Department of Dermatology, Skin Cancer Center, Jena University Hospital, Jena, GermanyCorrespondence: S. Goetze. E-mail: [email protected]Search for more papers by this authorF. Raessler, F. Raessler Department of Dermatology, Skin Cancer Center, Jena University Hospital, Jena, GermanySearch for more papers by this authorU.C. Hipler, U.C. Hipler Department of Dermatology, Skin Cancer Center, Jena University Hospital, Jena, GermanySearch for more papers by this authorS. Schulz, S. Schulz Center for Human Genetics, Jena University Hospital, Jena, GermanySearch for more papers by this authorJ. Kohlhase, J. Kohlhase Center for Human Genetics, Freiburg, GermanySearch for more papers by this authorP. Elsner, P. Elsner Department of Dermatology, Skin Cancer Center, Jena University Hospital, Jena, GermanySearch for more papers by this author S. Goetze, Corresponding Author S. Goetze Department of Dermatology, Skin Cancer Center, Jena University Hospital, Jena, GermanyCorrespondence: S. Goetze. E-mail: [email protected]Search for more papers by this authorF. Raessler, F. Raessler Department of Dermatology, Skin Cancer Center, Jena University Hospital, Jena, GermanySearch for more papers by this authorU.C. Hipler, U.C. Hipler Department of Dermatology, Skin Cancer Center, Jena University Hospital, Jena, GermanySearch for more papers by this authorS. Schulz, S. Schulz Center for Human Genetics, Jena University Hospital, Jena, GermanySearch for more papers by this authorJ. Kohlhase, J. Kohlhase Center for Human Genetics, Freiburg, GermanySearch for more papers by this authorP. Elsner, P. Elsner Department of Dermatology, Skin Cancer Center, Jena University Hospital, Jena, GermanySearch for more papers by this author First published: 20 January 2015 https://doi.org/10.1111/jdv.12880Citations: 1Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL No abstract is available for this article. References 1Gorlin RJ. Nevoid basal cell carcinoma (Gorlin) syndrome. Genet Med 2004; 6: 530– 539. 2Kiwilsza M, Sporniak-Tutak K. Gorlin-Goltz syndrome – a medical condition requiring a multidisciplinary approach. Med Sci Monit 2012; 18: RA145– RA153. 3Ruocco V, Ruocco E, Schiavo AL et al. Pemphigus: Etiology, pathogenesis, and inducing or triggering factors: facts and controversies. Clin Dermatol 2013; 31: 374– 381. 4Shimada Y, Katsube K, Kabasawa Y et al. Integrated genotypic analysis of Hedgehog-related genes identifies subgroups of keratocystic odontogenic tumor with distinct clinicopathological features. PLoS ONE 2013; 8: e70995. 5Pastorino L, Pollio A, Pellacani G et al. Novel PTCH1 mutations in patients with keratocystic odontogenic tumors screened for nevoid basal cell carcinoma (NBCC) syndrome. PLoS ONE 2012; 7: e43827. Citing Literature Volume30, Issue3March 2016Pages 493-494 ReferencesRelatedInformation" @default.
• W1977585235 created "2016-06-24" @default.
• W1977585235 creator A5008658304 @default.
• W1977585235 creator A5017997630 @default.
• W1977585235 creator A5034101869 @default.
• W1977585235 creator A5052122388 @default.
• W1977585235 creator A5054870153 @default.
• W1977585235 creator A5076497043 @default.
• W1977585235 date "2015-01-20" @default.
• W1977585235 modified "2023-10-18" @default.
• W1977585235 title "Unexpected manifestation of naevoid basal cell carcinoma (Gorlin) syndrome with a novel mutation in the <i>PTCH1</i> gene in a female patient with long-lasting pemphigus vulgaris" @default.
• W1977585235 cites W1998240959 @default.
• W1977585235 cites W1998996879 @default.
• W1977585235 cites W2010462296 @default.
• W1977585235 cites W2061504587 @default.
• W1977585235 cites W2097695197 @default.
• W1977585235 doi "https://doi.org/10.1111/jdv.12880" @default.
• W1977585235 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25600101" @default.
• W1977585235 hasPublicationYear "2015" @default.
• W1977585235 type Work @default.
• W1977585235 sameAs 1977585235 @default.
• W1977585235 citedByCount "2" @default.
• W1977585235 countsByYear W19775852352018 @default.
• W1977585235 countsByYear W19775852352022 @default.
• W1977585235 crossrefType "journal-article" @default.
• W1977585235 hasAuthorship W1977585235A5008658304 @default.
• W1977585235 hasAuthorship W1977585235A5017997630 @default.
• W1977585235 hasAuthorship W1977585235A5034101869 @default.
• W1977585235 hasAuthorship W1977585235A5052122388 @default.
• W1977585235 hasAuthorship W1977585235A5054870153 @default.
• W1977585235 hasAuthorship W1977585235A5076497043 @default.
• W1977585235 hasConcept C104317684 @default.
• W1977585235 hasConcept C121608353 @default.
• W1977585235 hasConcept C126322002 @default.
• W1977585235 hasConcept C16005928 @default.
• W1977585235 hasConcept C2777789703 @default.
• W1977585235 hasConcept C2778539099 @default.
• W1977585235 hasConcept C2778804307 @default.
• W1977585235 hasConcept C2779477247 @default.
• W1977585235 hasConcept C3019992690 @default.
• W1977585235 hasConcept C54355233 @default.
• W1977585235 hasConcept C71924100 @default.
• W1977585235 hasConcept C86803240 @default.
• W1977585235 hasConceptScore W1977585235C104317684 @default.
• W1977585235 hasConceptScore W1977585235C121608353 @default.
• W1977585235 hasConceptScore W1977585235C126322002 @default.
• W1977585235 hasConceptScore W1977585235C16005928 @default.
• W1977585235 hasConceptScore W1977585235C2777789703 @default.
• W1977585235 hasConceptScore W1977585235C2778539099 @default.
• W1977585235 hasConceptScore W1977585235C2778804307 @default.
• W1977585235 hasConceptScore W1977585235C2779477247 @default.
• W1977585235 hasConceptScore W1977585235C3019992690 @default.
• W1977585235 hasConceptScore W1977585235C54355233 @default.
• W1977585235 hasConceptScore W1977585235C71924100 @default.
• W1977585235 hasConceptScore W1977585235C86803240 @default.
• W1977585235 hasIssue "3" @default.
• W1977585235 hasLocation W19775852351 @default.
• W1977585235 hasLocation W19775852352 @default.
• W1977585235 hasOpenAccess W1977585235 @default.
• W1977585235 hasPrimaryLocation W19775852351 @default.
• W1977585235 hasRelatedWork W10191283 @default.
• W1977585235 hasRelatedWork W2029706239 @default.
• W1977585235 hasRelatedWork W2051704735 @default.
• W1977585235 hasRelatedWork W2116661571 @default.
• W1977585235 hasRelatedWork W2140085404 @default.
• W1977585235 hasRelatedWork W3092255352 @default.
• W1977585235 hasRelatedWork W3093398530 @default.
• W1977585235 hasRelatedWork W3153553021 @default.
• W1977585235 hasRelatedWork W4361252764 @default.
• W1977585235 hasRelatedWork W4384787935 @default.
• W1977585235 hasVolume "30" @default.
• W1977585235 isParatext "false" @default.
• W1977585235 isRetracted "false" @default.
• W1977585235 magId "1977585235" @default.
• W1977585235 workType "article" @default.