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

Year Number of Results
1978 1
1981 1
1990 1
1991 3
1992 1
1994 2
1995 2
1996 1
1997 1
1998 4
1999 1
2000 2
2001 5
2002 8
2003 6
2004 13
2005 9
2006 3
2007 4
2008 8
2009 10
2010 12
2011 8
2012 9
2013 2
2014 10
2015 9
2016 3
2017 6
2018 6
2019 9
2020 10
2021 13
2022 7
2023 9
2024 1

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180 results

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Page 1
Update in the Management of Basal Cell Carcinoma.
Basset-Seguin N, Herms F. Basset-Seguin N, et al. Acta Derm Venereol. 2020 Jun 3;100(11):adv00140. doi: 10.2340/00015555-3495. Acta Derm Venereol. 2020. PMID: 32346750 Free PMC article. Review.
Basal cell carcinomas are heterogeneous, from superficial or nodular lesions of good prognosis to very extensive difficult-to-treat lesions that must be discussed in multidisciplinary committees. Recent guidelines have updated the management of basal cell carcinoma. The …
Basal cell carcinomas are heterogeneous, from superficial or nodular lesions of good prognosis to very extensive difficult-to-treat l …
Incontinentia pigmenti: multisistemic genodermatosis.
Martínez-Gayosso A, García-Romero MT. Martínez-Gayosso A, et al. Bol Med Hosp Infant Mex. 2020;77(3):112-118. doi: 10.24875/BMHIM.19000173. Bol Med Hosp Infant Mex. 2020. PMID: 32496467 English.
Incontinentia pigmenti patients with no clinically significant ophthalmic or neurological compromise have a good prognosis and a normal life expectancy. The abnormalities present are permanent, which can be a cause of concern for the patients....
Incontinentia pigmenti patients with no clinically significant ophthalmic or neurological compromise have a good prognosis and a norm …
Neonatal erythroderma.
Fraitag S, Bodemer C. Fraitag S, et al. Curr Opin Pediatr. 2010 Aug;22(4):438-44. doi: 10.1097/MOP.0b013e32833bc396. Curr Opin Pediatr. 2010. PMID: 20616730 Review.
Cutaneous Expression of Familial Cancer Syndromes.
Andersen AJ, Schierbeck J, Bygum A, Puente-Pablo N. Andersen AJ, et al. Acta Derm Venereol. 2021 Jul 30;101(7):adv00505. doi: 10.2340/00015555-3852. Acta Derm Venereol. 2021. PMID: 34159396 Free PMC article. Review.
The dermatologist has an important role in the early detection of these signs and syndromes, as early detection may affect the clinical course of the disease. We report here the characteristic cutaneous findings that dermatologists should be aware of in order to identify a …
The dermatologist has an important role in the early detection of these signs and syndromes, as early detection may affect the clinical c …
European guidelines (S3) on diagnosis and management of mucous membrane pemphigoid, initiated by the European Academy of Dermatology and Venereology - Part I.
Rashid H, Lamberts A, Borradori L, Alberti-Violetti S, Barry RJ, Caproni M, Carey B, Carrozzo M, Caux F, Cianchini G, Corrà A, Diercks GFH, Dikkers FG, Di Zenzo G, Feliciani C, Geerling G, Genovese G, Hertl M, Joly P, Marzano AV, Meijer JM, Mercadante V, Murrell DF, Ormond M, Pas HH, Patsatsi A, Prost C, Rauz S, van Rhijn BD, Roth M, Schmidt E, Setterfield J, Zambruno G, Zillikens D, Horváth B. Rashid H, et al. J Eur Acad Dermatol Venereol. 2021 Sep;35(9):1750-1764. doi: 10.1111/jdv.17397. Epub 2021 Jul 10. J Eur Acad Dermatol Venereol. 2021. PMID: 34245180 Free PMC article.
MMP describes a group of autoimmune skin and mucous membrane blistering diseases, characterized by a chronic course and by predominant involvement of the mucous membranes, such as the oral, ocular, nasal, nasopharyngeal, anogenital, laryngeal and oesophageal mucosa. ...Pat …
MMP describes a group of autoimmune skin and mucous membrane blistering diseases, characterized by a chronic course and by predominan …
Gardner's syndrome.
Perniciaro C. Perniciaro C. Dermatol Clin. 1995 Jan;13(1):51-6. Dermatol Clin. 1995. PMID: 7712650 Review.
Germline intergenic duplications at Xq26.1 underlie Bazex-Dupré-Christol basal cell carcinoma susceptibility syndrome.
Liu Y, Banka S, Huang Y, Hardman-Smart J, Pye D, Torrelo A, Beaman GM, Kazanietz MG, Baker MJ, Ferrazzano C, Shi C, Orozco G, Eyre S, van Geel M, Bygum A, Fischer J, Miedzybrodzka Z, Abuzahra F, Rübben A, Cuvertino S, Ellingford JM, Smith MJ, Evans DG, Weppner-Parren LJMT, van Steensel MAM, Chaudhary IH, Mangham DC, Lear JT, Paus R, Frank J, Newman WG, Zhang X. Liu Y, et al. Br J Dermatol. 2022 Dec;187(6):948-961. doi: 10.1111/bjd.21842. Epub 2022 Sep 12. Br J Dermatol. 2022. PMID: 35986704
ARHGAP36 was also detected in sporadic BCCs from individuals without BDCS. Our modelling showed the predicted maximum tolerated minor allele frequency of ACTRT1 variants in control populations to be orders of magnitude higher than expected for a high-penetrant ultra-rare d …
ARHGAP36 was also detected in sporadic BCCs from individuals without BDCS. Our modelling showed the predicted maximum tolerated minor …
Muir-Torre syndrome.
Lachiewicz AM, Wilkinson TM, Groben P, Ollila DW, Thomas NE. Lachiewicz AM, et al. Am J Clin Dermatol. 2007;8(5):315-9. doi: 10.2165/00128071-200708050-00008. Am J Clin Dermatol. 2007. PMID: 17902735
While the sebaceous and internal neoplasms of MTS are thought to follow a more indolent course than sporadic malignancies, patients with this disorder should be treated with standard therapies and carefully followed. ...
While the sebaceous and internal neoplasms of MTS are thought to follow a more indolent course than sporadic malignancies, patients w …
Proposal for a 6-step approach for differential diagnosis of neonatal erythroderma.
Cuperus E, Bygum A, Boeckmann L, Bodemer C, Bolling MC, Caproni M, Diociaiuti A, Emmert S, Fischer J, Gostynski A, Guez S, van Gijn ME, Hannulla-Jouppi K, Has C, Hernández-Martín A, Martinez AE, Mazereeuw-Hautier J, Medvecz M, Neri I, Sigurdsson V, Suessmuth K, Traupe H, Oji V, Pasmans SGMA. Cuperus E, et al. J Eur Acad Dermatol Venereol. 2022 Jul;36(7):973-986. doi: 10.1111/jdv.18043. Epub 2022 Mar 15. J Eur Acad Dermatol Venereol. 2022. PMID: 35238435 Free PMC article. Review.
Early correct recognition of the underlying cause leads to better treatment and prognosis. Currently, neonatal erythroderma is approached on a case-by-case basis. ...
Early correct recognition of the underlying cause leads to better treatment and prognosis. Currently, neonatal erythroderma is approa …
Syndrome in question.
Pousa CM, Lavorato FG, Rehfeldt FV, Mann D, Alves Mde F. Pousa CM, et al. An Bras Dermatol. 2015 Sep-Oct;90(5):759-61. doi: 10.1590/abd1806-4841.20153193. An Bras Dermatol. 2015. PMID: 26560227 Free PMC article.
As it is regarded as a subtype of nonpolyposis hereditary colorectal cancer, it is important to evaluate the patient's first-degree relatives. The clinical course of the neoplasm is usually more indolent and the syndrome has a good prognosis. ...
As it is regarded as a subtype of nonpolyposis hereditary colorectal cancer, it is important to evaluate the patient's first-degree relative …
180 results