These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
175 related articles for article (PubMed ID: 18637050)
1. Striate palmoplantar keratoderma in a patient with Rubinstein-Taybi syndrome. Nakai K; Yoneda K; Moriue T; Kubota Y J Eur Acad Dermatol Venereol; 2009 Mar; 23(3):333-5. PubMed ID: 18637050 [No Abstract] [Full Text] [Related]
2. Vohwinkel syndrome (mutilating keratoderma) associated with craniofacial anomalies. Sensi A; Bettoli V; Zampino MR; Gandini E; Calzolari E Am J Med Genet; 1994 Apr; 50(2):201-3. PubMed ID: 8010352 [TBL] [Abstract][Full Text] [Related]
3. [Papillon-Lefévre syndrome. Report of a case with association of campto, clinodactylia and cranial anomalies]. Fonseca Capdevila E; Soto Melo J; Santamaría Solís L; Maza León P Actas Dermosifiliogr; 1980; 71(5-6):237-40. PubMed ID: 6451148 [No Abstract] [Full Text] [Related]
4. [Bureau-Barrière-Thomas-Syndrome. A rare hereditary palmoplantar keratoderma with associated symptoms (author's transl)]. Rauch HJ; Neumayer K Z Hautkr; 1981 Jan; 56(2):102-8. PubMed ID: 6452757 [TBL] [Abstract][Full Text] [Related]
5. Ichthyosis follicularis with congenital atrichia, nail dystrophy and palmoplantar keratoderma. Variant of IFAP syndrome or a new entity? Rai VM; Shenoi SD Dermatol Online J; 2005 Dec; 11(3):36. PubMed ID: 16409932 [TBL] [Abstract][Full Text] [Related]
6. [Genodermatosis with changes in eyes not previously described (author's transl)]. Richard G; Wreesmann P Klin Monbl Augenheilkd; 1980 Dec; 177(6):805-7. PubMed ID: 6451760 [TBL] [Abstract][Full Text] [Related]
8. Case of palmoplantar keratoderma with sensorineural deafness and mental retardation that may be another variant of syndromic palmoplantar keratoderma. Utsumi D; Hanashiro F; Miyagi T; Yamamoto Y; Uezato H; Takahashi K J Dermatol; 2013 Jul; 40(7):579-80. PubMed ID: 23594229 [No Abstract] [Full Text] [Related]
9. [Complex partial seizures in a case of Vohwinkel syndrome (keratoma hereditaria mutilans)]. Martínez Castrillo JC; Medina S; Gobernado Serrano J Neurologia; 1992 Jan; 7(1):39. PubMed ID: 1534485 [No Abstract] [Full Text] [Related]
11. A case with some clinical findings overlapping to Rubinstein-Taybi, Rubinstein-Taybi-like syndrome or multiple pterygium syndrome: coincidental findings or a new entity? Kargi AE; Balci S; Aköz T; Kargi S; Erdoğan B Turk J Pediatr; 2001; 43(2):166-71. PubMed ID: 11432500 [TBL] [Abstract][Full Text] [Related]
20. Olmsted syndrome: a case report and review of literature. Tao J; Huang CZ; Yu NW; Wu Y; Liu YQ; Li Y; Tian J; Yang LY; Zhang J; Li JW; Zhou YW; Tu YT Int J Dermatol; 2008 May; 47(5):432-7. PubMed ID: 18412857 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]