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Year Number of Results
1980 1
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1986 6
1987 4
1988 5
1989 6
1990 1
1991 6
1992 7
1993 2
1994 4
1995 1
1997 4
1998 2
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62 results

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Page 1
Dysplastic nevus syndrome: a phenotypic association of sporadic cutaneous melanoma.
Elder DE, Goldman LI, Goldman SC, Greene MH, Clark WH Jr. Elder DE, et al. Cancer. 1980 Oct 15;46(8):1787-94. doi: 10.1002/1097-0142(19801015)46:8<1787::aid-cncr2820460816>3.0.co;2-s. Cancer. 1980. PMID: 7427881
It is suggested that these patients represent a distinctive syndrome, the Dysplastic Nevus Syndrome (DNS) and that they are at increased risk for development of primary cutaneous malignant melanoma. The clinically and histologically distinctive …
It is suggested that these patients represent a distinctive syndrome, the Dysplastic Nevus Syndrome (DNS) …
Inheritance of nevus number and size in melanoma and dysplastic nevus syndrome kindreds.
Goldgar DE, Cannon-Albright LA, Meyer LJ, Piepkorn MW, Zone JJ, Skolnick MH. Goldgar DE, et al. J Natl Cancer Inst. 1991 Dec 4;83(23):1726-33. doi: 10.1093/jnci/83.23.1726. J Natl Cancer Inst. 1991. PMID: 1770551
Previous studies of the genetics of melanoma have focused on the dysplastic nevus syndrome (DNS). The variability in clinical and histopathological expression of affected individuals, however, has made definition and diagnosis of the syndrome di …
Previous studies of the genetics of melanoma have focused on the dysplastic nevus syndrome (DNS). The variabilit …
[Dysplastic nevus syndrome].
Niebauer G, Kokoschka EM. Niebauer G, et al. Wien Klin Wochenschr. 1986 Oct 24;98(20):673-8. Wien Klin Wochenschr. 1986. PMID: 3788185 German.
The dysplastic nevus (DN) was first described by Clark in 1976. It was subsequently recognized to be a precursor of melanoma. Dysplastic nevi present with typical clinical and histological criteria. The dysplastic nevus syndrome (DNS
The dysplastic nevus (DN) was first described by Clark in 1976. It was subsequently recognized to be a precursor of melanoma. …
Exclusion of the dysplastic nevus syndrome (DNS) locus from the short arm of chromosome 1 by linkage studies in Dutch families.
van Haeringen A, Bergman W, Nelen MR, van der Kooij-Meijs E, Hendrikse I, Wijnen JT, Khan PM, Klasen EC, Frants RR. van Haeringen A, et al. Genomics. 1989 Jul;5(1):61-4. doi: 10.1016/0888-7543(89)90086-4. Genomics. 1989. PMID: 2504660
Familial dysplastic nevus syndrome (DNS) is an autosomal dominant premalignant condition characterized by multiple large moles of variable size and color and a strongly increased risk for cutaneous malignant melanoma. In order to determine the chromoso …
Familial dysplastic nevus syndrome (DNS) is an autosomal dominant premalignant condition characterized by multip …
Neurofibromatosis type 1 associated with dysplastic nevus syndrome.
Pastar Z, Lipozencić J, Kovacević S, Canović S, Didović-Torbarina A, Vukasović A. Pastar Z, et al. Acta Dermatovenerol Croat. 2009;17(2):118-22. Acta Dermatovenerol Croat. 2009. PMID: 19595268 Review.
It causes tumors to grow on nerves and produces other abnormalities such as skin changes and bone deformities. Dysplastic nevus syndrome (DNS) represents multiple atypical nevi associated with polygenetic inheritance pattern and may rarely occur togeth …
It causes tumors to grow on nerves and produces other abnormalities such as skin changes and bone deformities. Dysplastic nevus
Dysplastic nevi. Occurrence in first- and second-degree relatives of patients with 'sporadic' dysplastic nevus syndrome.
Crijns MB, Vink J, Van Hees CL, Bergman W, Vermeer BJ. Crijns MB, et al. Arch Dermatol. 1991 Sep;127(9):1346-51. doi: 10.1001/archderm.127.9.1346. Arch Dermatol. 1991. PMID: 1892403
In this study a cross-sectional survey was undertaken among 156 living family members of 31 probands originally classified as having sporadic (histologically verified) dysplastic nevus syndrome (DNS). Seven (13.2%) of 53 parents had clinically recogniz …
In this study a cross-sectional survey was undertaken among 156 living family members of 31 probands originally classified as having sporadi …
[Translated article] Survey on the Management of Dysplastic Nevus by Dermatologists in the Center-Spain Section of the Spanish Academy of Dermatology and Venereology (AEDV).
Baeza-Hernández G, Rubio-Aguilera RF, Martínez-Morán C, Álvarez-Garrido H, Garrido-Ríos AA, Borbujo J. Baeza-Hernández G, et al. Actas Dermosifiliogr. 2023 Nov-Dec;114(10):T850-T857. doi: 10.1016/j.ad.2023.09.016. Epub 2023 Sep 19. Actas Dermosifiliogr. 2023. PMID: 37734540 Free article. English, Spanish.
BACKGROUND AND OBJECTIVES: There are no clinical guidelines on the management of dysplastic nevus (DN). The aims of this study were to determine the percentage of dermatologists in the center-Spain section of the Spanish Academy of Dermatology and Venereology (AEDV) …
BACKGROUND AND OBJECTIVES: There are no clinical guidelines on the management of dysplastic nevus (DN). The aims of this study …
Bioreduction of 4-nitroquinoline 1-oxide in dysplastic nevus syndrome fibroblasts.
Mirzayans R, Sabour M, Paterson MC. Mirzayans R, et al. Mutat Res. 1989 Apr;225(4):165-9. doi: 10.1016/0165-7992(89)90114-0. Mutat Res. 1989. PMID: 2494449
Fibroblast strains 3012T and 3072T, derived from normal skin explants of two patients affected with familial dysplastic nevus syndrome (DNS), an hereditary variant of cutaneous malignant melanoma, have been reported to be abnormally sensitive to the cy …
Fibroblast strains 3012T and 3072T, derived from normal skin explants of two patients affected with familial dysplastic nevus
Dysplastic nevus syndrome among Japanese. A case study and review of the Japanese literature.
Hara K, Nitta Y, Ikeya T. Hara K, et al. Am J Dermatopathol. 1992 Feb;14(1):24-31. doi: 10.1097/00000372-199202000-00004. Am J Dermatopathol. 1992. PMID: 1510212 Review.
Three Japanese families with dysplastic nevus syndrome (DNS) are reported. Each family had at least two members with multiple dysplastic nevi (DN). ...Each of two families had one cutaneous malignant melanoma (CMM) patient associated with multip …
Three Japanese families with dysplastic nevus syndrome (DNS) are reported. Each family had at least two members …
62 results