165 related articles for article (PubMed ID: 33661338)
1. [Cancer-associated genodermatoses].
Frommherz LH; Steinlein OK; French LE; Sattler EC
Hautarzt; 2021 Apr; 72(4):288-294. PubMed ID: 33661338
[TBL] [Abstract][Full Text] [Related]
2. Cancer-associated genodermatoses: skin neoplasms as clues to hereditary tumor syndromes.
Ponti G; Pellacani G; Seidenari S; Pollio A; Muscatello U; Tomasi A
Crit Rev Oncol Hematol; 2013 Mar; 85(3):239-56. PubMed ID: 22823951
[TBL] [Abstract][Full Text] [Related]
3. Hereditary renal cell carcinoma syndromes: diagnosis, surveillance and management.
Maher ER
World J Urol; 2018 Dec; 36(12):1891-1898. PubMed ID: 29680948
[TBL] [Abstract][Full Text] [Related]
4. Genodermatoses with malignant potential.
Ladd R; Davis M; Dyer JA
Clin Dermatol; 2020; 38(4):432-454. PubMed ID: 32972602
[TBL] [Abstract][Full Text] [Related]
5. Cancer-associated genodermatoses: a personal history.
Burgdorf WH
Exp Dermatol; 2006 Sep; 15(9):653-66. PubMed ID: 16881962
[TBL] [Abstract][Full Text] [Related]
6. Genetics of skin appendage neoplasms and related syndromes.
Lee DA; Grossman ME; Schneiderman P; Celebi JT
J Med Genet; 2005 Nov; 42(11):811-9. PubMed ID: 16272260
[TBL] [Abstract][Full Text] [Related]
7. [Skin tumors as marker lesions for tumor syndromes].
Mentzel T; Kutzner H; Requena L; Hartmann A
Pathologe; 2010 Oct; 31(6):489-96. PubMed ID: 20960199
[TBL] [Abstract][Full Text] [Related]
8. Genitourinary tumors in men with the Muir-Torre syndrome.
Davis DA; Cohen PR
J Am Acad Dermatol; 1995 Nov; 33(5 Pt 2):909-12. PubMed ID: 7593809
[TBL] [Abstract][Full Text] [Related]
9. Birt-Hogg-Dubé syndrome and multinodular goitre.
Drummond C; Grigoris I; Dutta B
Australas J Dermatol; 2002 Nov; 43(4):301-4. PubMed ID: 12423440
[TBL] [Abstract][Full Text] [Related]
10. [Two patients with Muir-Torre syndrome].
Vermeer MH; Neering H; Menko FH
Ned Tijdschr Geneeskd; 1999 Sep; 143(39):1980. PubMed ID: 10610483
[No Abstract] [Full Text] [Related]
11. Inherited skin tumour syndromes.
Brown S; Brennan P; Rajan N
Clin Med (Lond); 2017 Dec; 17(6):562-567. PubMed ID: 29196359
[TBL] [Abstract][Full Text] [Related]
12. [Muir-Torre syndrome and familial colorectal cancer: 2 families with molecular genetic analysis].
Doré MX; Dieumegard B; Grandjouan S; Avril MF; Martinet C; Ducreux M; Lasser P; Bressac-de Paillerets B
Ann Dermatol Venereol; 1999; 126(8-9):582-6. PubMed ID: 10530344
[TBL] [Abstract][Full Text] [Related]
13. Treatment Strategies for Hereditary Kidney Cancer: Current Recommendations and Updates.
Singh S; Chaurasia A; Gopal N; Malayeri A; Ball MW
Discov Med; 2022; 34(173):205-220. PubMed ID: 36602871
[TBL] [Abstract][Full Text] [Related]
14. [Differential diagnostics of sebaceous tumors].
Böer-Auer A
Pathologe; 2014 Sep; 35(5):443-55. PubMed ID: 25103328
[TBL] [Abstract][Full Text] [Related]
15. The genetic basis of Muir-Torre syndrome includes the hMLH1 locus.
Bapat B; Xia L; Madlensky L; Mitri A; Tonin P; Narod SA; Gallinger S
Am J Hum Genet; 1996 Sep; 59(3):736-9. PubMed ID: 8751876
[No Abstract] [Full Text] [Related]
16. Muir-Torre syndrome.
Cohen PR; Kohn SR; Davis DA; Kurzrock R
Dermatol Clin; 1995 Jan; 13(1):79-89. PubMed ID: 7712655
[TBL] [Abstract][Full Text] [Related]
17. Skin lesions of Birt-Hogg-Dubé syndrome: Clinical and histopathological findings in 31 Japanese patients who presented with pneumothorax and/or multiple lung cysts.
Iwabuchi C; Ebana H; Ishiko A; Negishi A; Mizobuchi T; Kumasaka T; Kurihara M; Seyama K
J Dermatol Sci; 2018 Jan; 89(1):77-84. PubMed ID: 29157599
[TBL] [Abstract][Full Text] [Related]
18. Multiple facial angiofibromas: a cutaneous manifestation of Birt-Hogg-Dubé syndrome.
Schaffer JV; Gohara MA; McNiff JM; Aasi SZ; Dvoretzky I
J Am Acad Dermatol; 2005 Aug; 53(2 Suppl 1):S108-11. PubMed ID: 16021156
[TBL] [Abstract][Full Text] [Related]
19. Ophthalmic presentation of the Muir Torre syndrome.
Tay E; Schofield JB; Rowell NP; Jones CA
Ophthalmic Plast Reconstr Surg; 2003 Sep; 19(5):402-4. PubMed ID: 14506428
[TBL] [Abstract][Full Text] [Related]
20. Delayed diagnosis of Birt-Hogg-Dubé syndrome due to marked intrafamilial clinical variability: a case report.
Sattler EC; Steinlein OK
BMC Med Genet; 2018 Mar; 19(1):45. PubMed ID: 29548312
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]