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46. Type 2 segmental Darier disease. Happle R; Itin PH; Brun AM Eur J Dermatol; 1999 Sep; 9(6):449-51. PubMed ID: 10491500 [TBL] [Abstract][Full Text] [Related]
47. [Cytogenetic investigations in children and adolescents with dystrophic changes of posterior pole of the eyeball (author's transl)]. Rusinowa F; Kaniasta M; Balcer-Boroniowa A; Marcinkowska A; Robińska E Klin Oczna; 1977 Nov; 47(11):477-80. PubMed ID: 592661 [No Abstract] [Full Text] [Related]
48. [Affairs of chromosomal analyses as clinical examination in Department of Pediatrics, Yamaguchi School of Medicine (author's transl)]. Hiraoka K; Yokoyama H; Yanagisawa S; Konishi S Jinrui Idengaku Zasshi; 1974 Jun; 19(1):73-4. PubMed ID: 4476854 [No Abstract] [Full Text] [Related]
49. [On autosomal aberrations in congenital malformations in children]. Dobrzańska A Pol Tyg Lek; 1967 May; 22(21):777-9. PubMed ID: 5342576 [No Abstract] [Full Text] [Related]
50. Darier disease: case report with oral manifestations. Cardoso CL; Freitas P; Taveira LA; Consolaro A Med Oral Patol Oral Cir Bucal; 2006 Aug; 11(5):E404-6. PubMed ID: 16878056 [TBL] [Abstract][Full Text] [Related]
51. [Epidemiology and heredity in otospongiosis]. Wayoff M Acta Otorhinolaryngol Belg; 1981; 35(5-6):431-51. PubMed ID: 7347085 [No Abstract] [Full Text] [Related]
52. [Lutz-Miescher elastosis perforans serpiginosa and osteogenesis imperfecta]. Relias A; Sakellariou G; Tsoitis G; Toubanaki E Ann Dermatol Syphiligr (Paris); 1968; 95(5):491-504. PubMed ID: 5716713 [No Abstract] [Full Text] [Related]
53. [Pedigree analysis of two families with Alport's syndrome]. Wässer S; Theile H; Schöne D; Lemme B Padiatr Grenzgeb; 1980; 19(3):167-71. PubMed ID: 7454376 [No Abstract] [Full Text] [Related]
54. Premenstrual exacerbation in calcium ATPase disorders of the skin. Szigeti R; Chao SC; Szász O; Tészás A; Kosztolányi G; Kellermayer R J Eur Acad Dermatol Venereol; 2007 Mar; 21(3):412-3. PubMed ID: 17309480 [No Abstract] [Full Text] [Related]
55. [Dyskeratosis follicularis Darier. Studies in a family with 11 manifest patients in three from four generations]. Go MJ; Wille KH; Hundeiker M; Wuite J Hautarzt; 1973 Sep; 24(9):393-7. PubMed ID: 4767418 [No Abstract] [Full Text] [Related]
56. Recurrent p.N767S mutation in the ATP2A2 gene in a Japanese family with haemorrhagic Darier disease clinically mimicking epidermolysis bullosa simplex with mottled pigmentation. Hamada T; Yasumoto S; Karashima T; Ishii N; Shimada H; Kawano Y; Imayama S; McGrath JA; Hashimoto T Br J Dermatol; 2007 Sep; 157(3):605-8. PubMed ID: 17635506 [No Abstract] [Full Text] [Related]