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

Year Number of Results
1983 1
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1991 1
1992 2
1993 1
1994 2
1996 2
1997 4
1998 4
1999 1
2000 1
2001 2
2002 1
2003 1
2004 2
2005 7
2006 5
2007 3
2008 6
2009 8
2010 9
2011 12
2012 13
2013 12
2014 23
2015 15
2016 15
2017 14
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2020 17
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2023 17
2024 6

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239 results

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Page 1
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.
Long-term follow-up is recommended in patients with high-risk BCC, multiple BCCs, and Gorlin syndrome....
Long-term follow-up is recommended in patients with high-risk BCC, multiple BCCs, and Gorlin syndrome....
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 …
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 …
Tumor Syndromes: Neurosurgical Evaluation and Management.
Ganapathy A, Diaz EJ, Coleman JT, Mackey KA. Ganapathy A, et al. Neurosurg Clin N Am. 2022 Jan;33(1):91-104. doi: 10.1016/j.nec.2021.09.007. Epub 2021 Oct 26. Neurosurg Clin N Am. 2022. PMID: 34801146 Review.
Other syndromes with variable degree of CNS and extra-CNS involvement that the neurosurgeon should be aware of include neurofibromatosis-2; Turcot syndrome; Cowden syndrome; Gorlin syndrome; Li-Fraumeni syndrome; ataxia-telangiectasia; multiple endocrine neoplasia t …
Other syndromes with variable degree of CNS and extra-CNS involvement that the neurosurgeon should be aware of include neurofibromatosis-2; …
Hereditary non-BRCA gynecological tumors.
Vellone VG, Paudice M, Varesco L. Vellone VG, et al. Minerva Ginecol. 2016 Oct;68(5):579-86. Epub 2016 Mar 1. Minerva Ginecol. 2016. PMID: 26930387 Review.
The clinical, genetic and pathological features of hereditary cancer syndromes with gynecological manifestations are reviewed focusing on Lynch Syndrome, also known as hereditary nonpolyposis colorectal carcinoma (HNPCC), Peutz-Jeghers Syndrome (PJS), Cowden Syndrome or multiple …
The clinical, genetic and pathological features of hereditary cancer syndromes with gynecological manifestations are reviewed focusing on Ly …
Genetics of Common Pediatric Brain Tumors.
Malbari F, Lindsay H. Malbari F, et al. Pediatr Neurol. 2020 Mar;104:3-12. doi: 10.1016/j.pediatrneurol.2019.08.004. Epub 2019 Aug 15. Pediatr Neurol. 2020. PMID: 31948735 Review.
This review will include known genetic disorders associated with central nervous system tumors, neurofibromatosis, tuberous sclerosis, Li-Fraumeni syndrome, Gorlin syndrome, and Turcot syndrome, as well as somatic mutations of glioma, medulloblastoma, and ependymoma …
This review will include known genetic disorders associated with central nervous system tumors, neurofibromatosis, tuberous sclerosis, Li-Fr …
Gorlin syndrome.
Hooper JE, Schofield J, Soran H, Whitehouse RW. Hooper JE, et al. BMJ Case Rep. 2013 Oct 30;2013:bcr2013201045. doi: 10.1136/bcr-2013-201045. BMJ Case Rep. 2013. PMID: 24172774 Free PMC article. No abstract available.
Ovarian tumors and genetic predisposition.
Štellmachová Júlia, Vrtěl Petr, Vrtěl Radek, Janíková Mária, Kolaříková Kristýna, Procházka Martin, Vodička Radek. Štellmachová Júlia, et al. Ceska Gynekol. 2022;87(3):211-216. doi: 10.48095/cccg2022211. Ceska Gynekol. 2022. PMID: 35896402 English.
Inherited tumor syndromes include Lynch syndrome, Peutz-Jegers syndrome, Gorlin syndrome, Li-Fraumeni syndrome and others. The indication for genetic examination of germline mutations is given by a clinical geneticist on the basis of the recommendation of the attend …
Inherited tumor syndromes include Lynch syndrome, Peutz-Jegers syndrome, Gorlin syndrome, Li-Fraumeni syndrome and others. The …
Clinical Impact of Cardiac Fibromas.
Covington MK, Young PM, Bois MC, Maleszewski JJ, Anand V, Dearani JA, Klarich KW. Covington MK, et al. Am J Cardiol. 2022 Nov 1;182:95-103. doi: 10.1016/j.amjcard.2022.06.062. Epub 2022 Aug 30. Am J Cardiol. 2022. PMID: 36055811
Symptoms included palpitations (commonly due to ventricular tachycardia, 31%), syncope (15%), angina (15%), heart failure (12%), emboli (4%), and murmur (27%). One patient had Gorlin syndrome. A total of 22 patients were diagnosed through imaging, 15 of whom were bi …
Symptoms included palpitations (commonly due to ventricular tachycardia, 31%), syncope (15%), angina (15%), heart failure (12%), emboli (4%) …
Cancer Surveillance in Gorlin Syndrome and Rhabdoid Tumor Predisposition Syndrome.
Foulkes WD, Kamihara J, Evans DGR, Brugières L, Bourdeaut F, Molenaar JJ, Walsh MF, Brodeur GM, Diller L. Foulkes WD, et al. Clin Cancer Res. 2017 Jun 15;23(12):e62-e67. doi: 10.1158/1078-0432.CCR-17-0595. Clin Cancer Res. 2017. PMID: 28620006 Free PMC article. Review.
Gorlin syndrome and rhabdoid tumor predisposition syndrome (RTPS) are autosomal dominant syndromes associated with an increased risk of childhood-onset brain tumors. Individuals with Gorlin syndrome can manifest a wide range of phenotypic abnormalities …
Gorlin syndrome and rhabdoid tumor predisposition syndrome (RTPS) are autosomal dominant syndromes associated with an increase …
239 results