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1986 1
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29 results

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European consensus-based interdisciplinary guideline for diagnosis and treatment of basal cell carcinoma-update 2023.
Peris K, Fargnoli MC, Kaufmann R, Arenberger P, Bastholt L, Seguin NB, Bataille V, Brochez L, Del Marmol V, Dummer R, Forsea AM, Gaudy-Marqueste C, Harwood CA, Hauschild A, Höller C, Kandolf L, Kellerners-Smeets NWJ, Lallas A, Leiter U, Malvehy J, Marinović B, Mijuskovic Z, Moreno-Ramirez D, Nagore E, Nathan P, Stratigos AJ, Stockfleth E, Tagliaferri L, Trakatelli M, Vieira R, Zalaudek I, Garbe C; EADO”A, EDF”B, ESTRO”C, UEMS”D and EADV”E. Peris K, et al. Eur J Cancer. 2023 Oct;192:113254. doi: 10.1016/j.ejca.2023.113254. Epub 2023 Jul 28. Eur J Cancer. 2023. PMID: 37604067 Free article. Review.
Photodynamic therapy is an effective treatment for superficial and low-risk nodular BCCs. ...Long-term follow-up is recommended in patients with high-risk BCC, multiple BCCs, and Gorlin syndrome....
Photodynamic therapy is an effective treatment for superficial and low-risk nodular BCCs. ...Long-term follow-up is recommended in pa …
Gorlin Syndrome: Recent Advances in Genetic Testing and Molecular and Cellular Biological Research.
Onodera S, Nakamura Y, Azuma T. Onodera S, et al. Int J Mol Sci. 2020 Oct 13;21(20):7559. doi: 10.3390/ijms21207559. Int J Mol Sci. 2020. PMID: 33066274 Free PMC article. Review.
Gorlin syndrome is a skeletal disorder caused by a gain of function mutation in Hedgehog (Hh) signaling. ...It is also the major driver gene in the development of basal cell carcinoma and medulloblastoma. In this review, we first present the recent advances in Go …
Gorlin syndrome is a skeletal disorder caused by a gain of function mutation in Hedgehog (Hh) signaling. ...It is also the maj …
SHH inhibitors for the treatment of medulloblastoma.
Samkari A, White J, Packer R. Samkari A, et al. Expert Rev Neurother. 2015;15(7):763-70. doi: 10.1586/14737175.2015.1052796. Epub 2015 May 31. Expert Rev Neurother. 2015. PMID: 26027634 Review.
Hereditary gynaecological malignancies: advances in screening and treatment.
Folkins AK, Longacre TA. Folkins AK, et al. Histopathology. 2013 Jan;62(1):2-30. doi: 10.1111/his.12028. Histopathology. 2013. PMID: 23240667 Review.
Other, less common hereditary conditions associated with gynaecological tract manifestations, such as Cowden syndrome, Peutz-Jeghers syndrome, Gorlin syndrome and hereditary leiomyomatosis and renal cell carcinoma, are also summarized briefly....
Other, less common hereditary conditions associated with gynaecological tract manifestations, such as Cowden syndrome, Peutz-Jeghers …
First evidence of genotype-phenotype correlations in Gorlin syndrome.
Evans DG, Oudit D, Smith MJ, Rutkowski D, Allan E, Newman WG, Lear JT. Evans DG, et al. J Med Genet. 2017 Aug;54(8):530-536. doi: 10.1136/jmedgenet-2017-104669. Epub 2017 Jun 8. J Med Genet. 2017. PMID: 28596197
BACKGROUND: Gorlin syndrome (GS) is an autosomal dominant syndrome characterised by multiple basal cell carcinomas (BCCs) and an increased risk of jaw cysts and early childhood medulloblastoma. ...
BACKGROUND: Gorlin syndrome (GS) is an autosomal dominant syndrome characterised by multiple basal cell carcinomas (BCC …
Digital pathology-based artificial intelligence models for differential diagnosis and prognosis of sporadic odontogenic keratocysts.
Cai X, Zhang H, Wang Y, Zhang J, Li T. Cai X, et al. Int J Oral Sci. 2024 Feb 26;16(1):16. doi: 10.1038/s41368-024-00287-y. Int J Oral Sci. 2024. PMID: 38403665 Free PMC article.
OKC combined with basal cell carcinoma as well as skeletal and other developmental abnormalities is thought to be associated with Gorlin syndrome. Moreover, OKC needs to be differentiated from orthokeratinized odontogenic cyst and other jaw cysts. ...
OKC combined with basal cell carcinoma as well as skeletal and other developmental abnormalities is thought to be associated with Gorlin …
A contemporary review of molecular candidates for the development and treatment of childhood medulloblastoma.
Sümer-Turanlıgil NC, Cetin EÖ, Uyanıkgil Y. Sümer-Turanlıgil NC, et al. Childs Nerv Syst. 2013 Mar;29(3):381-8. doi: 10.1007/s00381-012-2014-3. Epub 2013 Jan 6. Childs Nerv Syst. 2013. PMID: 23292496 Review.
Occurrence of pediatric brain tumors including medulloblastoma are mostly sporadic, but some hereditary diseases like Li-Fraumeni syndrome, Gorlin's syndrome, Turcot's syndrome, and Rubenstein-Tarbi syndrome are known to contribute their develop …
Occurrence of pediatric brain tumors including medulloblastoma are mostly sporadic, but some hereditary diseases like Li-Fraumeni syndrom …
Gorlin Syndrome: Assessing Genotype-Phenotype Correlations and Analysis of Early Clinical Characteristics as Risk Factors for Disease Severity.
Betancourt NJ, Qian MF, Pickford JR, Bailey-Healy I, Tang JY, Teng JMC. Betancourt NJ, et al. J Clin Oncol. 2022 Jul 1;40(19):2119-2127. doi: 10.1200/JCO.21.02385. Epub 2022 Mar 25. J Clin Oncol. 2022. PMID: 35333541
PURPOSE: Gorlin syndrome (GS) is a rare genetic disorder characterized by lifetime risk of basal cell carcinomas (BCCs), skeletal anomalies (SAs), and other extracutaneous neoplasms. ...
PURPOSE: Gorlin syndrome (GS) is a rare genetic disorder characterized by lifetime risk of basal cell carcinomas (BCCs), skele …
Interventions for the treatment of keratocystic odontogenic tumours.
Sharif FN, Oliver R, Sweet C, Sharif MO. Sharif FN, et al. Cochrane Database Syst Rev. 2015 Nov 5;2015(11):CD008464. doi: 10.1002/14651858.CD008464.pub3. Cochrane Database Syst Rev. 2015. PMID: 26545201 Free PMC article. Review.
Adults, over the age of 18 with a validated diagnosis of solitary KCOTs arising in the jaw bones of the maxilla or mandible. Patients with known Gorlin syndrome were to be excluded. DATA COLLECTION AND ANALYSIS: Review authors screened trials for inclusion. ...
Adults, over the age of 18 with a validated diagnosis of solitary KCOTs arising in the jaw bones of the maxilla or mandible. Patients with k …
29 results