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

Year Number of Results
1939 1
1945 1
1946 1
1947 2
1948 2
1950 3
1951 1
1952 3
1953 1
1954 2
1955 4
1956 4
1957 1
1958 3
1959 4
1960 1
1961 3
1962 2
1964 5
1965 2
1966 1
1967 2
1968 3
1969 2
1970 1
1971 2
1973 2
1975 2
1976 4
1977 9
1978 4
1980 3
1981 6
1982 3
1983 1
1984 5
1985 4
1986 3
1987 5
1988 5
1989 4
1990 8
1991 6
1993 4
1994 4
1995 5
1996 5
1997 4
1998 6
1999 11
2000 7
2001 8
2002 5
2003 8
2004 5
2005 12
2006 8
2007 11
2008 22
2009 21
2010 20
2011 28
2012 22
2013 29
2014 27
2015 30
2016 24
2017 20
2018 22
2019 33
2020 24
2021 19
2022 13
2023 19
2024 16

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553 results

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Page 1
Pachyonychia Congenita.
Smith FJD, Hansen CD, Hull PR, Kaspar RL, McLean WHI, O’Toole E, Sprecher E. Smith FJD, et al. 2006 Jan 27 [updated 2017 Nov 30]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2006 Jan 27 [updated 2017 Nov 30]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301457 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Pachyonychia congenita (PC) is characterized by hypertrophic nail dystrophy, painful palmoplantar keratoderma and blistering, oral leukokeratosis, pilosebaceous cysts (including steatocystoma and vellus hair cysts), palmoplantar hyperhydros …
CLINICAL CHARACTERISTICS: Pachyonychia congenita (PC) is characterized by hypertrophic nail dystrophy, painful palmoplantar ke …
Pachyonychia Congenita.
Tan Y, Ma DL. Tan Y, et al. Indian J Pediatr. 2024 Mar;91(3):300-301. doi: 10.1007/s12098-023-04567-z. Epub 2023 Jun 8. Indian J Pediatr. 2024. PMID: 37289311 No abstract available.
Pachyonychia congenita.
Feinstein A, Friedman J, Schewach-Millet M. Feinstein A, et al. J Am Acad Dermatol. 1988 Oct;19(4):705-11. doi: 10.1016/s0190-9622(88)70226-1. J Am Acad Dermatol. 1988. PMID: 3053803 Review.
Pachyonychia congenita is a rare hereditary disorder characterized mainly by nail hypertrophy and dyskeratoses of skin and mucous membranes. A thorough literature survey since its first description in 1904 up to 1985 revealed 168 cases of pachyonychia cong …
Pachyonychia congenita is a rare hereditary disorder characterized mainly by nail hypertrophy and dyskeratoses of skin and muc …
Pachyonychia Congenita: A Research Agenda Leading to New Therapeutic Approaches.
O'Toole EA, Kelsell DP, Caterina MJ, de Brito M, Hansen D, Hickerson RP, Hovnanian A, Kaspar R, Lane EB, Paller AS, Schwartz J, Shroot B, Teng J, Titeux M, Coulombe PA, Sprecher E. O'Toole EA, et al. J Invest Dermatol. 2024 Apr;144(4):748-754. doi: 10.1016/j.jid.2023.10.030. Epub 2023 Dec 15. J Invest Dermatol. 2024. PMID: 38099888 Review.
Pachyonychia congenita (PC) is a dominantly inherited genetic disorder of cornification. PC stands out among other genodermatoses because despite its rarity, it has been the focus of a very large number of pioneering translational research efforts over the past 2 de …
Pachyonychia congenita (PC) is a dominantly inherited genetic disorder of cornification. PC stands out among other genodermato …
Pachyonychia congenita and botulinum toxin.
Thomas BR, Sahota A. Thomas BR, et al. Br J Dermatol. 2020 Mar;182(3):531-532. doi: 10.1111/bjd.18784. Epub 2019 Dec 25. Br J Dermatol. 2020. PMID: 31875943 No abstract available.
Pachyonychia Congenita: Sporadic Onset with Mutation Analysis.
Athota K, Prabhu SS. Athota K, et al. Indian Dermatol Online J. 2023 Jul 10;14(5):703-705. doi: 10.4103/idoj.idoj_533_22. eCollection 2023 Sep-Oct. Indian Dermatol Online J. 2023. PMID: 37727554 Free PMC article. No abstract available.
Pachyonychia congenita responding favorably to a combination of surgical and medical therapies.
Daroach M, Dogra S, Bhattacharjee R, Tp A, Smith F, Mahajan R. Daroach M, et al. Dermatol Ther. 2019 Sep;32(5):e13045. doi: 10.1111/dth.13045. Epub 2019 Aug 16. Dermatol Ther. 2019. PMID: 31364784 Review.
Pachyonychia congenital (PC) is a rare genetic disorder of cornification and is classified into five types on the basis of keratin gene involved. ...
Pachyonychia congenital (PC) is a rare genetic disorder of cornification and is classified into five types on the basis of keratin ge …
Pachyonychia Congenita: Clinical Features and Future Treatments.
Mccarthy RL, De Brito M, O'toole E. Mccarthy RL, et al. Keio J Med. 2023 Sep 28. doi: 10.2302/kjm.2023-0012-IR. Online ahead of print. Keio J Med. 2023. PMID: 37766547 Free article.
Pachyonychia congenita (PC) is a rare, autosomal dominant inherited disorder of keratinization that is characterized by a triad of focal palmoplantar keratoderma, plantar pain, and hypertrophic nail dystrophy. ...
Pachyonychia congenita (PC) is a rare, autosomal dominant inherited disorder of keratinization that is characterized by a tria …
Pachyonychia Congenita Project: Advancing Research and Drug Development through Collaboration.
Schwartz JN, Evans HA, O'toole EA, Hansen CD. Schwartz JN, et al. Keio J Med. 2023 Dec 8. doi: 10.2302/kjm.2023-0015-IR. Online ahead of print. Keio J Med. 2023. PMID: 38072449 Free article.
Pachyonychia Congenita Project (PC Project) is an international patient advocacy organization dedicated to patients who suffer from pachyonychia congenita (PC). ...Through two primary programs, namely the International Pachyonychia Congenita …
Pachyonychia Congenita Project (PC Project) is an international patient advocacy organization dedicated to patients who suffer …
553 results