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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1963 1
1964 1
1971 4
1974 1
1975 1
1976 2
1977 3
1980 4
1982 3
1983 2
1984 2
1985 1
1986 3
1987 5
1988 8
1989 6
1990 6
1991 10
1992 3
1993 5
1994 16
1995 12
1996 8
1997 12
1998 6
1999 11
2000 7
2001 13
2002 9
2003 6
2004 16
2005 19
2006 8
2007 10
2008 12
2009 11
2010 11
2011 19
2012 14
2013 17
2014 20
2015 27
2016 17
2017 15
2018 11
2019 9
2020 11
2021 13
2022 16
2023 11
2024 1

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421 results

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Page 1
The odontogenic keratocyst revisited.
Stoelinga PJW. Stoelinga PJW. Int J Oral Maxillofac Surg. 2022 Nov;51(11):1420-1423. doi: 10.1016/j.ijom.2022.02.005. Epub 2022 Mar 8. Int J Oral Maxillofac Surg. 2022. PMID: 35277291 Free article. Review.
The role of the dental lamina and submucosal hamartias, as frequently seen in nevoid basal cell carcinoma syndrome, is discussed, and the implications for treatment are emphasized....
The role of the dental lamina and submucosal hamartias, as frequently seen in nevoid basal cell carcinoma syndrome, is …
Nevoid Basal Cell Carcinoma Syndrome (Gorlin Syndrome).
Bresler SC, Padwa BL, Granter SR. Bresler SC, et al. Head Neck Pathol. 2016 Jun;10(2):119-24. doi: 10.1007/s12105-016-0706-9. Epub 2016 Mar 14. Head Neck Pathol. 2016. PMID: 26971503 Free PMC article. Review.
Nevoid basal cell carcinoma syndrome, or basal cell nevus syndrome (Gorlin syndrome), is a rare autosomal dominantly inherited disorder that is characterized by development of basal cell carcinomas from …
Nevoid basal cell carcinoma syndrome, or basal cell nevus syndrome (Gorlin syndro …
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.
Basal cell carcinoma (BCC) is the most common malignant tumour in white populations. ...Long-term follow-up is recommended in patients with high-risk BCC, multiple BCCs, and Gorlin syndrome....
Basal cell carcinoma (BCC) is the most common malignant tumour in white populations. ...Long-term follow-up is recommended in …
Skin Cancer Associated Genodermatoses: A Literature Review.
Schierbeck J, Vestergaard T, Bygum A. Schierbeck J, et al. Acta Derm Venereol. 2019 Apr 1;99(4):360-369. doi: 10.2340/00015555-3123. Acta Derm Venereol. 2019. PMID: 30653245 Free article. Review.
The disorders are described with clinical characteristics, genetics and management. The most common syndromes associated with basal cell carcinoma are: Gorlin-Goltz syndrome, Rombo syndrome, and Bazex-Dupre-Christol syndrome. Multiple squ …
The disorders are described with clinical characteristics, genetics and management. The most common syndromes associated with basal …
Gorlin Syndrome.
Palacios-Álvarez I, González-Sarmiento R, Fernández-López E. Palacios-Álvarez I, et al. Actas Dermosifiliogr (Engl Ed). 2018 Apr;109(3):207-217. doi: 10.1016/j.ad.2017.07.018. Epub 2018 Jan 17. Actas Dermosifiliogr (Engl Ed). 2018. PMID: 29373110 Review. English, Spanish.
Gorlin syndrome is a rare autosomal dominant disease caused by mutations in the sonic hedgehog signaling pathway. ...Although these agents appear promising options for patients with Gorlin syndrome, their efficacy is limited by adverse effects and the …
Gorlin syndrome is a rare autosomal dominant disease caused by mutations in the sonic hedgehog signaling pathway. ...Although …
The role of the Hedgehog signaling pathway in cancer: A comprehensive review.
Skoda AM, Simovic D, Karin V, Kardum V, Vranic S, Serman L. Skoda AM, et al. Bosn J Basic Med Sci. 2018 Feb 20;18(1):8-20. doi: 10.17305/bjbms.2018.2756. Bosn J Basic Med Sci. 2018. PMID: 29274272 Free PMC article. Review.
It is a highly conserved evolutionary pathway of signal transmission from the cell membrane to the nucleus. The Hh signaling pathway plays an important role in the embryonic development. ...Deregulation of the Hh signaling pathway is associated with developmental anomalies …
It is a highly conserved evolutionary pathway of signal transmission from the cell membrane to the nucleus. The Hh signaling pathway …
Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: Familial Tumor Syndromes.
Nosé V, Lazar AJ. Nosé V, et al. Head Neck Pathol. 2022 Mar;16(1):143-157. doi: 10.1007/s12105-022-01414-z. Epub 2022 Mar 21. Head Neck Pathol. 2022. PMID: 35312981 Free PMC article. Review.
This review highlights the important findings within these syndromes, especially on the update on syndromes with tumors involving the head and neck region, as Gorlin syndrome/nevoid basal cell carcinoma syndrome associated with odontogenic kerat …
This review highlights the important findings within these syndromes, especially on the update on syndromes with tumors involving the head a …
Meier-Gorlin syndrome.
de Munnik SA, Hoefsloot EH, Roukema J, Schoots J, Knoers NV, Brunner HG, Jackson AP, Bongers EM. de Munnik SA, et al. Orphanet J Rare Dis. 2015 Sep 17;10:114. doi: 10.1186/s13023-015-0322-x. Orphanet J Rare Dis. 2015. PMID: 26381604 Free PMC article. Review.
Meier-Gorlin syndrome (MGS) is a rare autosomal recessive primordial dwarfism disorder, characterized by microtia, patellar applasia/hypoplasia, and a proportionate short stature. ...
Meier-Gorlin syndrome (MGS) is a rare autosomal recessive primordial dwarfism disorder, characterized by microtia, patellar ap …
Gorlin syndrome (nevoid basal cell carcinoma syndrome): update and literature review.
Fujii K, Miyashita T. Fujii K, et al. Pediatr Int. 2014 Oct;56(5):667-74. doi: 10.1111/ped.12461. Pediatr Int. 2014. PMID: 25131638 Review.
Gorlin syndrome, also called nevoid basal cell carcinoma syndrome, is an autosomal dominant neurocutaneous disease characterized by developmental anomalies such as palmar pits and rib anomaly, and tumorigenesis such as medulloblastoma and bas …
Gorlin syndrome, also called nevoid basal cell carcinoma syndrome, is an autosomal dominant neurocutaneou …
The expanding genetic and clinical landscape associated with Meier-Gorlin syndrome.
Nielsen-Dandoroff E, Ruegg MSG, Bicknell LS. Nielsen-Dandoroff E, et al. Eur J Hum Genet. 2023 Aug;31(8):859-868. doi: 10.1038/s41431-023-01359-z. Epub 2023 Apr 14. Eur J Hum Genet. 2023. PMID: 37059840 Free PMC article. Review.
Consequently, this hypothesis-free testing manner has revealed the true breadth of clinical features for many established genetic disorders, including Meier-Gorlin syndrome (MGORS). Previously known as ear-patella short stature syndrome, MGORS is characterize …
Consequently, this hypothesis-free testing manner has revealed the true breadth of clinical features for many established genetic disorders, …
421 results