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Journal Abstract Search
206 related items for PubMed ID: 3188604
1. [Dowling-Degos disease--an autosomal dominant genetic dermatosis]. Biltz H, Kiessling M. Z Hautkr; 1988 Aug 15; 63(8):642-4. PubMed ID: 3188604 [Abstract] [Full Text] [Related]
2. [Piebaldism]. Küster W. Hautarzt; 1987 Aug 15; 38(8):481-3. PubMed ID: 3654219 [Abstract] [Full Text] [Related]
3. Hypopigmentation with punctate keratosis of the palms and soles. Cole LA. Arch Dermatol; 1976 Jul 15; 112(7):998-100. PubMed ID: 132904 [Abstract] [Full Text] [Related]
4. Generalized Dowling-Degos disease. Wu YH, Lin YC. J Am Acad Dermatol; 2007 Aug 15; 57(2):327-34. PubMed ID: 17637446 [Abstract] [Full Text] [Related]
5. Dowling-Degos disease with dyschromatosis universalis hereditaria-like pigmentation in a family. Sandhu K, Saraswat A, Kanwar AJ. J Eur Acad Dermatol Venereol; 2004 Nov 15; 18(6):702-4. PubMed ID: 15482301 [Abstract] [Full Text] [Related]
6. Familial comedones. Evidence for autosomal dominant inheritance. Cantú JM, Gómez-Bustamente MO, González-Mendoza A, Sánchez-Corona J. Arch Dermatol; 1978 Dec 15; 114(12):1807-9. PubMed ID: 153732 [Abstract] [Full Text] [Related]
7. Three cases of Dowling Degos disease in two families. Bhagwat PV, Tophakhane RS, Shashikumar BM, Noronha TM, Naidu V. Indian J Dermatol Venereol Leprol; 2009 Dec 15; 75(4):398-400. PubMed ID: 19584468 [Abstract] [Full Text] [Related]
11. [Incontinentia pigmenti. Study of 3 families]. Garcia-Bravo B, Rodriguez-Pichardo A, Camacho-Martinez F. Ann Dermatol Venereol; 1986 May 15; 113(4):301-8. PubMed ID: 3767228 [Abstract] [Full Text] [Related]
12. [Dowling-Degos disease (reticulate pigmentation of the flexures)]. Reymond JL, Beani JC, Pinel-Briquel N, Amblard P. Ann Dermatol Venereol; 1986 May 15; 113(3):249-51. PubMed ID: 3752864 [No Abstract] [Full Text] [Related]
13. [Dowling-Degos disease and Verneuil disease]. Balus L, Fazio M, Amantea A, Menaguale G. Ann Dermatol Venereol; 1993 May 15; 120(10):705-8. PubMed ID: 8161103 [Abstract] [Full Text] [Related]
14. [Branchio-oto-renal dysplasia. A hereditary dominant autosomal syndrome with variable expression]. Stoll C, Roth MP, Hessemann H, Paira M. Arch Fr Pediatr; 1983 Dec 15; 40(10):763-6. PubMed ID: 6673680 [Abstract] [Full Text] [Related]
15. [Hereditary CADASIL cerebral arteriopathy. Report of a family]. Mayer M, Dichgans M, Gasser T, Büttner U, Uttner I, Straube A. Nervenarzt; 1995 Dec 15; 66(12):927-32. PubMed ID: 8584078 [Abstract] [Full Text] [Related]