165 related articles for article (PubMed ID: 8782050)
21. [Bazex, Dupré and Christol syndrome. Apropos of a case with prolymphocytic leukemia].
Colomb D; Ducros B; Boussuge N
Ann Dermatol Venereol; 1989; 116(5):381-7. PubMed ID: 2675736
[TBL] [Abstract][Full Text] [Related]
22. The Bazex syndrome: follicular atrophoderma with multiple basal cell carcinomas, hypotrichosis and hypohidrosis.
Plosila M; Kiistala R; Niemi KM
Clin Exp Dermatol; 1981 Jan; 6(1):31-41. PubMed ID: 7273474
[No Abstract] [Full Text] [Related]
23. The Rombo syndrome: a familial disorder with vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, basal cell carcinomas and peripheral vasodilation with cyanosis.
Michaëlsson G; Olsson E; Westermark P
Acta Derm Venereol; 1981; 61(6):497-503. PubMed ID: 6177160
[TBL] [Abstract][Full Text] [Related]
24. Bazex-Dupré-Christol syndrome: a possible diagnosis for basal cell carcinomas, coarse sparse hair, and milia.
Vabres P; de Prost Y
Am J Med Genet; 1993 Mar; 45(6):786. PubMed ID: 8456866
[No Abstract] [Full Text] [Related]
25. Follicular atrophoderma with multiple basal cell carcinomas (Bazex).
Gould DJ; Barker DJ
Br J Dermatol; 1978 Oct; 99(4):431-5. PubMed ID: 708616
[TBL] [Abstract][Full Text] [Related]
26. Bazex-Dupré-Christol syndrome: First report in an Indian family.
Chauhan P; Meena D; Dhanta A; Kansal NK; Durgapal P
Indian J Dermatol Venereol Leprol; 2018; 84(4):451-456. PubMed ID: 29855454
[No Abstract] [Full Text] [Related]
27. Linkage refinement of Bazex-Dupré-Christol syndrome to an 11·4-Mb interval on chromosome Xq25-27.1.
Parren LJ; Abuzahra F; Wagenvoort T; Koene F; Van Steensel MA; Steijlen PM; Van Geel M; Frank J
Br J Dermatol; 2011 Jul; 165(1):201-3. PubMed ID: 21219295
[No Abstract] [Full Text] [Related]
28. What syndrome is this? Bazex-Dupre-Christol syndrome.
Torrelo A; Sprecher E; Mediero IG; Bergman R; Zambrano A
Pediatr Dermatol; 2006; 23(3):286-90. PubMed ID: 16780482
[No Abstract] [Full Text] [Related]
29. Bazex syndrome. Follicular atrophoderma and basal cell epitheliomas.
Mehta VR; Potdar R
Int J Dermatol; 1985 Sep; 24(7):444-6. PubMed ID: 4055198
[TBL] [Abstract][Full Text] [Related]
30. Novel p.Glu519Gln missense mutation in ST14 in a patient with ichthyosis, follicular atrophoderma and hypotrichosis and review of the literature.
Neri I; Virdi A; Tortora G; Baldassari S; Seri M; Patrizi A
J Dermatol Sci; 2016 Jan; 81(1):63-6. PubMed ID: 26596219
[No Abstract] [Full Text] [Related]
31. Clinical and dermatoscopic findings in Bazex-Dupré-Christol and Gorlin-Goltz syndromes.
Tiodorovic-Zivkovic D; Zalaudek I; Ferrara G; Giorgio CM; Di Nola K; Procaccini EM; Argenziano G
J Am Acad Dermatol; 2010 Oct; 63(4):722-4. PubMed ID: 20846576
[No Abstract] [Full Text] [Related]
32. A case of Bazex-Dupré-Christol syndrome associated with multiple genital trichoepitheliomas.
Yung A; Newton-Bishop JA
Br J Dermatol; 2005 Sep; 153(3):682-4. PubMed ID: 16120174
[No Abstract] [Full Text] [Related]
33. Overlap between the Bazex syndrome and congenital hypotrichosis and milia.
Lacombe D; Taïeb A
Am J Med Genet; 1995 May; 56(4):423-4. PubMed ID: 7677860
[No Abstract] [Full Text] [Related]
34. [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
Spiegl B; Hundeiker M
Fortschr Med; 1979 Nov; 97(44):2018-22. PubMed ID: 511082
[TBL] [Abstract][Full Text] [Related]
35. Multiple follicular hamartomas with sweat gland and sebaceous differentiation, vermiculate atrophoderma, milia, hypotrichosis, and late development of multiple basal cell carcinomas.
Pujol RM; Nadal C; Matias-Guiu X; Peyrí J; Ferrándiz C; Palou J; de Moragas JM
J Am Acad Dermatol; 1998 Nov; 39(5 Pt 2):853-7. PubMed ID: 9810915
[TBL] [Abstract][Full Text] [Related]
36. Hereditary hypotrichosis. A previously undescribed syndrome.
Bentley-Phillips B; Grace HJ
Br J Dermatol; 1979 Sep; 101(3):331-9. PubMed ID: 508598
[TBL] [Abstract][Full Text] [Related]
37. Genetic syndrome with ichthyosis: congenital ichthyosis, follicular atrophoderma, hypotrichosis, and woolly hair; second report.
Tursen U; Kaya TI; Ikizoglu G; Aktekin M; Aras N
Br J Dermatol; 2002 Sep; 147(3):604-6. PubMed ID: 12207612
[No Abstract] [Full Text] [Related]
38. A case of sporadic Bazex-Dupré-Christol syndrome presenting with scarring folliculitis of the scalp.
Gambichler T; Hoffjan S; Altmeyer P; Bechara FG
Br J Dermatol; 2007 Jan; 156(1):184-6. PubMed ID: 17199596
[No Abstract] [Full Text] [Related]
39. A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome.
Youssefian L; Touati A; Saeidian AH; Zargari O; Zeinali S; Vahidnezhad H; Uitto J
Orphanet J Rare Dis; 2017 Dec; 12(1):176. PubMed ID: 29208051
[TBL] [Abstract][Full Text] [Related]
40. Marie Unna congenital hypotrichosis: clinical description, histopathology, scanning electron microscopy of a previously unreported large pedigree.
Roberts JL; Whiting DA; Henry D; Basler G; Woolf L
J Investig Dermatol Symp Proc; 1999 Dec; 4(3):261-7. PubMed ID: 10674378
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
