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1987 2
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1990 3
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1992 4
1993 4
1994 3
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1999 3
2000 5
2001 3
2002 7
2003 6
2004 6
2005 2
2006 3
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2012 5
2013 9
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The following term was not found in PubMed: Hypotrichosis-osteolysis-periodontitis-palmoplantar
Page 1
Cutaneous paraneoplastic syndromes.
Wick MR, Patterson JW. Wick MR, et al. Semin Diagn Pathol. 2019 Jul;36(4):211-228. doi: 10.1053/j.semdp.2019.01.001. Epub 2019 Jan 31. Semin Diagn Pathol. 2019. PMID: 30736994 Review.
Some of the processes show a predominant association with alimentary tract malignancies (acanthosis nigricans, acrodermatitis paraneoplastica, florid cutaneous papillomatosis, necrolytic migratory erythema, palmoplantar keratoderma, pancreatic fat necrosis, and pityriasis …
Some of the processes show a predominant association with alimentary tract malignancies (acanthosis nigricans, acrodermatitis paraneoplastic …
Wilson disease.
Aggarwal A, Bhatt M. Aggarwal A, et al. Curr Opin Neurol. 2020 Aug;33(4):534-542. doi: 10.1097/WCO.0000000000000837. Curr Opin Neurol. 2020. PMID: 32657896 Review.
These disorders include diseases of copper disposition, such as mental retardation, enteropathy, deafness, neuropathy, ichthyosis, keratoderma syndrome, Niemann-Pick type C, and certain congenital disorders of glycosylation, as well as analogous disorders of iron an …
These disorders include diseases of copper disposition, such as mental retardation, enteropathy, deafness, neuropathy, ichthyosis, kerato
[Paraneoplastic skin diseases].
Khoschbin T, Löser C, Dippel E. Khoschbin T, et al. Internist (Berl). 2019 Aug;60(8):775-782. doi: 10.1007/s00108-019-0636-1. Internist (Berl). 2019. PMID: 31273399 Review. German.
Some of the processes predominantly show a link with malignant diseases of the digestive tract, e.g. acanthosis nigricans, florid cutaneous papillomatosis, necrolytic migratory erythema, Leser-Trelat syndrome, palmoplantar keratoderma, panniculitis and pityriasis ru …
Some of the processes predominantly show a link with malignant diseases of the digestive tract, e.g. acanthosis nigricans, florid cutaneous …
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.
Palmoplantar keratodermas are grouped depending on the morphology of the keratoderma into diffuse, focal/striate or papular/punctate. Some palmoplantar keratodermas just affect the skin of the palms and soles and others have associated syndromic featur …
Palmoplantar keratodermas are grouped depending on the morphology of the keratoderma into diffuse, focal/striate or papular/pu …
Non-Classic Signs of Sézary Syndrome: A Review.
Morris L, Tran J, Duvic M. Morris L, et al. Am J Clin Dermatol. 2020 Jun;21(3):383-391. doi: 10.1007/s40257-020-00501-7. Am J Clin Dermatol. 2020. PMID: 31953789 Review.
The majority of patients with Sezary syndrome (SS) present with classic symptoms of erythroderma, lymphadenopathy, and pruritus. ...Of these 505 patients, the most common non-classic signs of SS were keratoderma, onychodystrophy, alopecia, leonine facies, and ectrop …
The majority of patients with Sezary syndrome (SS) present with classic symptoms of erythroderma, lymphadenopathy, and pruritus. ...O …
Palmoplantar keratodermas: clinical and genetic aspects.
Has C, Technau-Hafsi K. Has C, et al. J Dtsch Dermatol Ges. 2016 Feb;14(2):123-39; quiz 140. doi: 10.1111/ddg.12930. J Dtsch Dermatol Ges. 2016. PMID: 26819106 Review.
Palmoplantar keratodermas comprise a diverse group of acquired and hereditary disorders marked by excessive thickening of the epidermis of palms and soles. Early onset and positive family history suggest a genetic cause. While hereditary forms of palmoplantar keratoderm
Palmoplantar keratodermas comprise a diverse group of acquired and hereditary disorders marked by excessive thickening of the epiderm …
[Hands cutaneous exam].
Lorette G, Samimi M. Lorette G, et al. Presse Med. 2013 Dec;42(12):1582-95. doi: 10.1016/j.lpm.2013.06.016. Epub 2013 Oct 21. Presse Med. 2013. PMID: 24157184 Review. French.
SAPHO syndrome (Synovitis - Acne - Pustulosis - Hyperostosis - Osteomyelitis) presents pustules on palms. ...Spontaneous blue finger syndrome can be a benign process that resolves rapidly....
SAPHO syndrome (Synovitis - Acne - Pustulosis - Hyperostosis - Osteomyelitis) presents pustules on palms. ...Spontaneous blue finger …
[Genetics of complex and syndromic palmoplantar keratoderma].
Sperelakis-Beedham B, Lopez M, Girodon E, Hickman G, Bourrat E, Bienvenu T. Sperelakis-Beedham B, et al. Ann Biol Clin (Paris). 2021 Dec 1;79(6):551-565. doi: 10.1684/abc.2021.1688. Ann Biol Clin (Paris). 2021. PMID: 34961738 Review. French.
Hereditary PPKs can be classified into 3 groups: 1) isolated non-syndromic PPKs; 2) complex non-syndromic PPKs associated with other ectodermal defects; and 3) syndromic PPKs associated with extracutaneous manifestations. ...This review describes the differen …
Hereditary PPKs can be classified into 3 groups: 1) isolated non-syndromic PPKs; 2) complex non-syndromic PPKs associated with …
Connexin channels in congenital skin disorders.
Lilly E, Sellitto C, Milstone LM, White TW. Lilly E, et al. Semin Cell Dev Biol. 2016 Feb;50:4-12. doi: 10.1016/j.semcdb.2015.11.018. Epub 2016 Jan 13. Semin Cell Dev Biol. 2016. PMID: 26775130 Free PMC article. Review.
Increasing evidence suggests that the skin diseases produced by connexin mutations result from dominant gains of function. In palmoplantar keratoderma with deafness, the connexin 26 mutations transdominantly alter the function of wild-type connexin 43 and create leaky hete …
Increasing evidence suggests that the skin diseases produced by connexin mutations result from dominant gains of function. In palmoplantar …
Skin and Mucosal Manifestations in NEMO Syndrome: A Case Series and Literature Review.
Kohn LL, Braun M, Cordoro KM, McCalmont TH, Shah SD, Frieden IJ, Mathur AN. Kohn LL, et al. Pediatr Dermatol. 2022 Jan;39(1):84-90. doi: 10.1111/pde.14905. Epub 2022 Jan 5. Pediatr Dermatol. 2022. PMID: 34989033 Review.
OBJECTIVES: To characterize the skin and mucosal findings of NEMO syndrome. METHODS: Retrospective review of clinical characteristics from a cohort of two families with mutations in IKBKG (the NEMO-encoding gene). ...MAIN OUTCOMES AND MEASURES: Skin and mucosal characteris …
OBJECTIVES: To characterize the skin and mucosal findings of NEMO syndrome. METHODS: Retrospective review of clinical characteristics …
162 results