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

Year Number of Results
1884 1
1889 2
1909 1
1938 1
1945 3
1946 3
1947 4
1948 8
1949 12
1950 15
1951 11
1952 16
1953 12
1954 4
1955 11
1956 8
1957 12
1958 7
1959 11
1960 13
1961 20
1962 21
1963 29
1964 22
1965 23
1966 13
1967 16
1968 31
1969 29
1970 38
1971 39
1972 50
1973 47
1974 57
1975 66
1976 60
1977 57
1978 89
1979 69
1980 79
1981 97
1982 94
1983 77
1984 69
1985 77
1986 105
1987 83
1988 69
1989 115
1990 88
1991 91
1992 112
1993 112
1994 140
1995 127
1996 133
1997 108
1998 118
1999 145
2000 167
2001 183
2002 154
2003 143
2004 134
2005 180
2006 182
2007 190
2008 214
2009 192
2010 212
2011 209
2012 225
2013 243
2014 242
2015 219
2016 214
2017 173
2018 189
2019 161
2020 161
2021 161
2022 139
2023 117
2024 117
2025 114
2026 89

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7,187 results

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Page 1
Xeroderma Pigmentosum.
Black JO. Black JO. Head Neck Pathol. 2016 Jun;10(2):139-44. doi: 10.1007/s12105-016-0707-8. Epub 2016 Mar 14. Head Neck Pathol. 2016. PMID: 26975629 Free PMC article. Review.
Xeroderma pigmentosum (XP) is a rare disorder of defective UV-radiation induced damage repair that is characterized by photosensitivity with easy skin burning following minimal sun exposure, early freckling and development of lentiginous pigmentation along with other featu
Xeroderma pigmentosum (XP) is a rare disorder of defective UV-radiation induced damage repair that is characterized by photosensitivi
Xeroderma pigmentosum.
Norgauer J, Idzko M, Panther E, Hellstern O, Herouy Y. Norgauer J, et al. Eur J Dermatol. 2003 Jan-Feb;13(1):4-9. Eur J Dermatol. 2003. PMID: 12609773 Review.
Xeroderma pigmentosum is a rare disorder transmitted in an autosomal recessive manner. Xeroderma pigmentosum is based on a genetic defect in the DNA repair system. ...The majority of patients die before reaching adulthood because of metastases. Genetically, xerod
Xeroderma pigmentosum is a rare disorder transmitted in an autosomal recessive manner. Xeroderma pigmentosum is based on a gen
Xeroderma pigmentosum.
Jung EG. Jung EG. Int J Dermatol. 1986 Dec;25(10):629-33. doi: 10.1111/j.1365-4362.1986.tb04522.x. Int J Dermatol. 1986. PMID: 3542861 Review. No abstract available.
Xeroderma pigmentosum.
Der Kaloustian VM, Kurban AK. Der Kaloustian VM, et al. Br J Dermatol. 1973 May;88(5):513-5. doi: 10.1111/j.1365-2133.1973.tb15461.x. Br J Dermatol. 1973. PMID: 4577062 Review. No abstract available.
Xeroderma.
Gade A, Matin T, Rubenstein R. Gade A, et al. 2023 Oct 29. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–. 2023 Oct 29. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–. PMID: 33351442 Free Books & Documents.
Xeroderma, also known as dry skin, xerosis cutis, or asteatosis, is a prevalent condition resulting from inadequate hydrolipids in the skin. ...The primary treatment approach for xeroderma involves using moisturizers, which effectively repair the epidermal skin barr
Xeroderma, also known as dry skin, xerosis cutis, or asteatosis, is a prevalent condition resulting from inadequate hydrolipids in th
Xeroderma pigmentosum-Cockayne syndrome complex.
Natale V, Raquer H. Natale V, et al. Orphanet J Rare Dis. 2017 Apr 4;12(1):65. doi: 10.1186/s13023-017-0616-2. Orphanet J Rare Dis. 2017. PMID: 28376890 Free PMC article. Review.
Xeroderma pigmentosum-Cockayne syndrome complex is a very rare multisystem degenerative disorder (Orpha: 220295; OMIM: 278730, 278760, 278780, 610651). ...
Xeroderma pigmentosum-Cockayne syndrome complex is a very rare multisystem degenerative disorder (Orpha: 220295; OMIM: 278730, 278760
Xeroderma Pigmentosum.
Lucero R, Horowitz D. Lucero R, et al. 2023 Jul 4. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–. 2023 Jul 4. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–. PMID: 31855390 Free Books & Documents.
Xeroderma pigmentosum (XP) is a rare autosomal recessive genodermatosis that results due to mutations in nucleotide excision repair. ...Further studies over the next several decades highlighted the importance of severe photosensitivity in the pathophysiology of xeroderm
Xeroderma pigmentosum (XP) is a rare autosomal recessive genodermatosis that results due to mutations in nucleotide excision repair.
Therapeutics of xeroderma pigmentosum: A PRISMA-compliant systematic review.
de Andrade FAG, Cavalcanti CEO, Isoldi FC, Ferreira LM. de Andrade FAG, et al. Indian J Dermatol Venereol Leprol. 2021 Mar-Apr;87(2):176-189. doi: 10.25259/IJDVL_431_19. Indian J Dermatol Venereol Leprol. 2021. PMID: 33769755 Free article.
Xeroderma pigmentosum is a rare hereditary autosomal recessive genodermatosis. At present, there are many treatment options for xeroderma pigmentosum, covering medical/procedural, surgical and combined modalities. ...The therapeutic modalities, both clinical and sur
Xeroderma pigmentosum is a rare hereditary autosomal recessive genodermatosis. At present, there are many treatment options for xe
[Xeroderma Pigmentosum].
Nishigori C. Nishigori C. Brain Nerve. 2019 Apr;71(4):394-399. doi: 10.11477/mf.1416201283. Brain Nerve. 2019. PMID: 30988228 Japanese.
Xeroderma pigmentosum is a DNA repair disorder characterized by the occurrence of pigmented freckles and skin cancers on sun-exposed areas. ...
Xeroderma pigmentosum is a DNA repair disorder characterized by the occurrence of pigmented freckles and skin cancers on sun-exposed
[Xeroderma pigmentosum].
Stary A, Sarasin A. Stary A, et al. Presse Med. 1997 Dec 20;26(40):1992-7. Presse Med. 1997. PMID: 9537004 Review. French.
Xeroderma pigmentosum syndrome is associated with an estimated 2000-fold increase in the risk to develop skin cancer (basal cell carcinoma, squamous cell carcinoma and melanoma). ...PATHOPHYSIOLOGY: The Xeroderma pigmentosum complementation groups differ in terms of
Xeroderma pigmentosum syndrome is associated with an estimated 2000-fold increase in the risk to develop skin cancer (basal cell carc
7,187 results