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.
191 related articles for article (PubMed ID: 6223454)
21. Pachyonychia congenita: a clinical study of 12 cases and review of the literature. Su WP; Chun SI; Hammond DE; Gordon H Pediatr Dermatol; 1990 Mar; 7(1):33-8. PubMed ID: 2140447 [TBL] [Abstract][Full Text] [Related]
22. Insights into genotype-phenotype correlation in pachyonychia congenita from the human intermediate filament mutation database. McLean WH; Smith FJ; Cassidy AJ J Investig Dermatol Symp Proc; 2005 Oct; 10(1):31-6. PubMed ID: 16250207 [TBL] [Abstract][Full Text] [Related]
23. Pachyonychia Congenita (Jadassohn-Lewandowsky syndrome): a seventeen-member, four-generation pedigree with unusual respiratory and dental involvement. Stieglitz JB; Centerwall WR Am J Med Genet; 1983 Jan; 14(1):21-8. PubMed ID: 6829608 [TBL] [Abstract][Full Text] [Related]
24. [Familial coexistence of erythrokeratodermia variabilis and keratosis palmoplantaris transgrediens et progrediens]. Wollina U; Knopf B; Schaaschmidt H; Frille I Hautarzt; 1989 Mar; 40(3):169-72. PubMed ID: 2523877 [TBL] [Abstract][Full Text] [Related]
25. A severe case of pachyonychia congenita type I due to a novel proline mutation in keratin 6a. García-Rio I; Peñas PF; García-Díez A; McLean WH; Smith FJ Br J Dermatol; 2005 Apr; 152(4):800-2. PubMed ID: 15840119 [No Abstract] [Full Text] [Related]
27. Keratosis follicularis (Darier-White disease), with an unusual palmoplantar keratoderma. Kim C; Fangman W Dermatol Online J; 2007 Jan; 13(1):7. PubMed ID: 17511940 [TBL] [Abstract][Full Text] [Related]
28. [Pachyonychia congenita with Steatocystoma multiplex: a report of 12 cases in one family [author's transl]]. Aoyagi T; Ohnishi O Nihon Hifuka Gakkai Zasshi; 1976 Sep; 86(11):767-75. PubMed ID: 1034800 [No Abstract] [Full Text] [Related]
29. Erythrokeratodermia congenitalis progressiva symmetrica (Gottron). II. An analysis of kinetics of epidermal cell proliferation. Hopsu-Havu VK; Tuohimaa P Dermatologica; 1971; 142(3):137-44. PubMed ID: 5112612 [No Abstract] [Full Text] [Related]
30. Palmoplantar keratoderma, nail dystrophy, and hereditary motor and sensory neuropathy: an autosomal dominant trait. Tolmie JL; Wilcox DE; McWilliam R; Assindi A; Stephenson JB J Med Genet; 1988 Nov; 25(11):754-7. PubMed ID: 2976839 [TBL] [Abstract][Full Text] [Related]
36. [Hereditary palmo-plantar keratoses and corneal changes]. Schnyder UW; Franceschetti A Ber Zusammenkunft Dtsch Ophthalmol Ges; 1972; 71():106-9. PubMed ID: 4542557 [No Abstract] [Full Text] [Related]
37. [Progressive symmetric erythrokeratodermia of Darier-Gottron]. Ott H; Lehmann S; Poblete-Gutiérrez P; Frank J Hautarzt; 2004 Oct; 55(10):994-6. PubMed ID: 15340705 [TBL] [Abstract][Full Text] [Related]
38. Progressive symmetric erythrokeratodermia. Histological and ultrastructural study of patient before and after treatment with etretinate. Nazzaro V; Blanchet-Bardon C Arch Dermatol; 1986 Apr; 122(4):434-40. PubMed ID: 2937369 [TBL] [Abstract][Full Text] [Related]
39. Palmoplantar orthokeratotic filiform hyperkeratosis in a patient with associated Darier's disease. Classification of filiform hyperkeratosis. Zarour H; Grob JJ; Andrac L; Bonerandi JJ Dermatology; 1992; 185(3):205-9. PubMed ID: 1446087 [TBL] [Abstract][Full Text] [Related]
40. Recurrent mutation in keratin 17 in a large family with pachyonychia congenita type 2. Oh Adib C; Jones B; Liao H; Smith FJ; Solomon R; Egan CA; Leachman S Arch Dermatol Res; 2008 Jun; 300(5):211-4. PubMed ID: 18347808 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]