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

Year Number of Results
1958 1
1972 1
1974 2
1977 1
1978 2
1982 3
1986 1
1987 2
1988 2
1990 2
1991 1
1993 2
1999 1
2001 1
2002 1
2003 1
2005 2
2006 1
2008 2
2009 2
2010 2
2011 2
2012 3
2013 1
2014 2
2015 3
2016 2
2017 1
2018 3
2019 1
2020 4
2021 7
2022 6
2023 3
2024 1

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64 results

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Page 1
Aquagenic Keratoderma: Treatment Update.
Carbonell Pradas M, Grimalt Santacana R. Carbonell Pradas M, et al. Actas Dermosifiliogr. 2022 Mar;113(3):254-260. doi: 10.1016/j.ad.2021.05.016. Epub 2021 Jun 12. Actas Dermosifiliogr. 2022. PMID: 34126071 Free article. Review. English, Spanish.
Aquagenic keratoderma associated with hyperhidrosis can be treated effectively. ...Topical salicylic acid and aluminum salts are effective, but of little value as maintenance therapy. Oral oxybutynin 5 mg/d is probably the best option for treating aquagenic kerat …
Aquagenic keratoderma associated with hyperhidrosis can be treated effectively. ...Topical salicylic acid and aluminum salts are effe …
Nagashima-Type Palmoplantar Keratosis: Clinical Characteristics, Genetic Characterization, and Clinical Management.
Huang C, Yang Y, Huang X, Zhou Z. Huang C, et al. Biomed Res Int. 2021 Jan 27;2021:8841994. doi: 10.1155/2021/8841994. eCollection 2021. Biomed Res Int. 2021. PMID: 33575348 Free PMC article. Review.
Nagashima-type palmoplantar keratosis (NPPK) is the most prevalent palmoplantar keratoderma (PPK) in East Asia. ...A better understanding of the clinical characteristics and pathogenic gene characterization of NPPK will enhance the diagnosis of NPPK, identify …
Nagashima-type palmoplantar keratosis (NPPK) is the most prevalent palmoplantar keratoderma (PPK) in East Asia. ...A be …
Hereditary palmoplantar keratoderma "clinical and genetic differential diagnosis".
Sakiyama T, Kubo A. Sakiyama T, et al. J Dermatol. 2016 Mar;43(3):264-74. doi: 10.1111/1346-8138.13219. J Dermatol. 2016. PMID: 26945534 Review.
Hereditary palmoplantar keratoderma (PPK) is a heterogeneous group of disorders characterized by hyperkeratosis of the palm and the sole skin. ...
Hereditary palmoplantar keratoderma (PPK) is a heterogeneous group of disorders characterized by hyperkeratosis of the palm an …
Diagnosis and Management of Inherited Palmoplantar Keratodermas.
Thomas BR, O'Toole EA. Thomas BR, et al. Acta Derm Venereol. 2020 Mar 25;100(7):adv00094. doi: 10.2340/00015555-3430. Acta Derm Venereol. 2020. PMID: 32147745 Free PMC article. Review.
Inherited monogenic palmoplantar keratodermas are a heterogeneous group of conditions characterised by persistent epidermal thickening of the palmoplantar skin. Palmoplantar keratodermas are grouped depending on the morphology of the keratoderma into d …
Inherited monogenic palmoplantar keratodermas are a heterogeneous group of conditions characterised by persistent epidermal thickenin …
Papillon-Lefevre syndrome: Oral aspects and treatment.
Giannetti L, Apponi R, Dello Diago AM, Jafferany M, Goldust M, Sadoughifar R. Giannetti L, et al. Dermatol Ther. 2020 May;33(3):e13336. doi: 10.1111/dth.13336. Epub 2020 Apr 9. Dermatol Ther. 2020. PMID: 32222110 Free article. Review.
Papillon-Lefevre syndrome (PLS) is a rare disorder characterized by diffuse palmoplantar erythematous, fissured hyperkeratosis, and aggressive periodontal disease that starts in the early periods of childhood. ...Management could be a conventional periodontal treatment and …
Papillon-Lefevre syndrome (PLS) is a rare disorder characterized by diffuse palmoplantar erythematous, fissured hyperkeratosis, and a …
Tylosis with oesophageal cancer: Diagnosis, management and molecular mechanisms.
Ellis A, Risk JM, Maruthappu T, Kelsell DP. Ellis A, et al. Orphanet J Rare Dis. 2015 Sep 29;10:126. doi: 10.1186/s13023-015-0346-2. Orphanet J Rare Dis. 2015. PMID: 26419362 Free PMC article. Review.
This is coupled with dietary and lifestyle modification advice and symptom education. Symptomatic management of the palmoplantar keratoderma includes regular application of emollients, specialist footwear and early treatment of fissures and super-added infection, pa …
This is coupled with dietary and lifestyle modification advice and symptom education. Symptomatic management of the palmoplantar k …
Management of Plantar Keratodermas(Lessons from Pachyonychia Congenita).
Porter RM, Bravo AA, Smith FJD. Porter RM, et al. J Am Podiatr Med Assoc. 2017 Sep;107(5):428-435. doi: 10.7547/16-043. J Am Podiatr Med Assoc. 2017. PMID: 29077501 Review.
Diagnosis can be aided by observation of other clinical manifestations, such as palmar keratoderma, more widespread hyperkeratosis of the epidermis, hair and nail dystrophies, or erythroderma. However, there are frequent cases of plantar keratoderma that occur in is …
Diagnosis can be aided by observation of other clinical manifestations, such as palmar keratoderma, more widespread hyperkeratosis of …
Keratosis lichenoides chronica: Case-based review of treatment options.
Pistoni F, Peroni A, Colato C, Schena D, Girolomoni G. Pistoni F, et al. J Dermatolog Treat. 2016 Aug;27(4):383-8. doi: 10.3109/09546634.2015.1115818. Epub 2015 Dec 10. J Dermatolog Treat. 2016. PMID: 26652284 Review.
Keratosis lichenoides chronica (KLC) is a rare dermatological condition characterized by keratotic papules arranged in a parallel linear or reticular pattern and facial lesions resembling seborrheic dermatitis or rosacea. The clinical, histological and therapeutic informat …
Keratosis lichenoides chronica (KLC) is a rare dermatological condition characterized by keratotic papules arranged in a parallel linear or …
Treatment of pachyonychia congenita.
Milstone LM, Fleckman P, Leachman SA, Leigh IM, Paller AS, van Steensel MA, Swartling C. Milstone LM, et al. J Investig Dermatol Symp Proc. 2005 Oct;10(1):18-20. doi: 10.1111/j.1087-0024.2005.10203.x. J Investig Dermatol Symp Proc. 2005. PMID: 16250205 Free article. Review.
Ichthyosis with confetti: clinics, molecular genetics and management.
Guerra L, Diociaiuti A, El Hachem M, Castiglia D, Zambruno G. Guerra L, et al. Orphanet J Rare Dis. 2015 Sep 17;10:115. doi: 10.1186/s13023-015-0336-4. Orphanet J Rare Dis. 2015. PMID: 26381864 Free PMC article. Review.
The most important associated clinical features include ear deformities, mammillae hypoplasia, palmoplantar keratoderma, hypertrichosis and ectropion. IWC is due to dominant negative mutations in the KRT10 and KRT1 genes, encoding for keratins 10 and keratin 1, resp …
The most important associated clinical features include ear deformities, mammillae hypoplasia, palmoplantar keratoderma, hyper …
64 results