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

Year Number of Results
1909 1
1910 1
1912 1
1916 1
1918 1
1919 1
1921 1
1923 1
1924 2
1928 1
1938 1
1939 2
1944 1
1945 4
1946 19
1947 20
1948 18
1949 14
1950 18
1951 19
1952 16
1953 16
1954 19
1955 10
1956 12
1957 11
1958 12
1959 19
1960 16
1961 14
1962 11
1963 30
1964 30
1965 29
1966 16
1967 25
1968 39
1969 33
1970 36
1971 31
1972 27
1973 27
1974 31
1975 23
1976 23
1977 38
1978 25
1979 36
1980 28
1981 32
1982 34
1983 42
1984 23
1985 26
1986 19
1987 27
1988 26
1989 27
1990 37
1991 22
1992 26
1993 22
1994 35
1995 26
1996 31
1997 24
1998 21
1999 32
2000 34
2001 35
2002 30
2003 29
2004 42
2005 44
2006 40
2007 31
2008 39
2009 55
2010 47
2011 72
2012 38
2013 56
2014 58
2015 69
2016 61
2017 48
2018 67
2019 51
2020 66
2021 76
2022 64
2023 78
2024 66
2025 69
2026 27

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2,574 results

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Page 1
Acrokeratosis verruciformis of Hopf: dermoscopy approach in dark skin patients.
Llamas-Molina JM, De la Torre-Gomar FJ, Carrero-Castaño A, Gil-Villalba A, Prados-Carmona Á, Ruiz-Villaverde R. Llamas-Molina JM, et al. J Eur Acad Dermatol Venereol. 2022 Nov;36(11):e944-e945. doi: 10.1111/jdv.18367. Epub 2022 Jul 13. J Eur Acad Dermatol Venereol. 2022. PMID: 35771037 No abstract available.
Acrokeratosis verruciformis of Hopf is caused by mutation in ATP2A2: evidence that it is allelic to Darier's disease.
Dhitavat J, Macfarlane S, Dode L, Leslie N, Sakuntabhai A, MacSween R, Saihan E, Hovnanian A. Dhitavat J, et al. J Invest Dermatol. 2003 Feb;120(2):229-32. doi: 10.1046/j.1523-1747.2003.t01-1-12045.x. J Invest Dermatol. 2003. PMID: 12542527 Free article.
Acrokeratosis verruciformis of Hopf is a localized disorder of keratinization affecting the distal extremities. ...This result demonstrates loss of function of the sarco(endo)plasmic reticulum Ca2+ ATPase2 mutant in acrokeratosis verruciformi
Acrokeratosis verruciformis of Hopf is a localized disorder of keratinization affecting the distal extremities.
Acrokeratosis verruciformis of Hopf.
Schueller WA. Schueller WA. Arch Dermatol. 1972 Jul;106(1):81-3. Arch Dermatol. 1972. PMID: 5039112 No abstract available.
Genetic heterogeneity in acrokeratosis verruciformis of Hopf.
Wang PG, Gao M, Lin GS, Yang S, Lin D, Liang YH, Zhang GL, Zhu YG, Cui Y, Zhang KY, Huang W, Zhang XJ. Wang PG, et al. Clin Exp Dermatol. 2006 Jul;31(4):558-63. doi: 10.1111/j.1365-2230.2006.02134.x. Clin Exp Dermatol. 2006. PMID: 16716163
BACKGROUND: Acrokeratosis verruciformis of Hopf (AKV) is a rare genodermatosis characterized by multiple flat-topped, flesh-coloured papules on the dorsa of hands and feet, and punctuate keratoses on the palms and soles. A mutation in the ATP2A2 gene h …
BACKGROUND: Acrokeratosis verruciformis of Hopf (AKV) is a rare genodermatosis characterized by multiple flat-to …
Dermoscopy of acrokeratosis verruciformis of Hopf.
Behera B, Prabhakaran N, Naveed S, Kumari R, Thappa DM, Gochhait D. Behera B, et al. J Am Acad Dermatol. 2017 Aug;77(2):e33-e35. doi: 10.1016/j.jaad.2017.01.003. J Am Acad Dermatol. 2017. PMID: 28711099 No abstract available.
Late-onset non-familial acrokeratosis verruciformis of Hopf: a case report.
Faina V, Magri F, Sernicola A, Chello C, Gagliostro N, Grieco T. Faina V, et al. Clin Ter. 2019 Nov-Dec;170(6):e418-e420. doi: 10.7417/CT.2019.2168. Clin Ter. 2019. PMID: 31696902 Free article.
Acrokeratosis verruciformis of Hopf is a rare heritable autosomal dominant genodermatosis and keratinization disorder, first described in 1931 by Hopf. ...AKV is an allelic disorder, associated with heterozygous missense mutation in ATP2A2 gene,
Acrokeratosis verruciformis of Hopf is a rare heritable autosomal dominant genodermatosis and keratinization dis
Coexistence of Darier's disease and acrokeratosis verruciformis of Hopf.
Piskin S, Saygin A, Doganay L, Kircuval D, Gurkan E. Piskin S, et al. Yonsei Med J. 2004 Oct 31;45(5):956-9. doi: 10.3349/ymj.2004.45.5.956. Yonsei Med J. 2004. PMID: 15515213 Free article.
Darier's disease and acrokeratosis verruciformis are inherited with the same pattern and they share similar clinical properties. We present a patient with both Darier's disease and acrokeratosis verruciformis. The patient ha
Darier's disease and acrokeratosis verruciformis are inherited with the same pattern and they share similar clin
2,574 results