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.
3. Familial Richner-Hanhart syndrome: genetic, clinical, and metabolic studies. Sammartino A; de Crecchio G; Balato N; Lembo G; Federico A; Pallini R Ann Ophthalmol; 1984 Nov; 16(11):1069-74. PubMed ID: 6240214 [TBL] [Abstract][Full Text] [Related]
4. [A case of Richner-Hanhart syndrome (tyrosinosis with ocular, cutaneous and mental manifestations]. Goddé-Jolly D; Larregue M; Roussat B; Van Effenterre G J Fr Ophtalmol; 1979 Jan; 2(1):23-8. PubMed ID: 34642 [TBL] [Abstract][Full Text] [Related]
6. [4 cases of Richner-Hanhart syndrome (tyrosinemia type II) with neurological symptomatology in a Yugoslav family]. Salamon T; Hrnjica M; Schnyder UW; Lazović O; Softić M; Topić B; Stolić V; Popović N; Cerkez A; Basić V Hautarzt; 1988 Mar; 39(3):149-54. PubMed ID: 2967808 [TBL] [Abstract][Full Text] [Related]
7. Richner-Hanhart syndrome (tyrosinemia II): early diagnosis of an incomplete presentation with unusual findings. Viglizzo GM; Occella C; Bleidl D; Rongioletti F Pediatr Dermatol; 2006; 23(3):259-61. PubMed ID: 16780475 [TBL] [Abstract][Full Text] [Related]
8. Richner-Hanhart syndrome (tyrosinemia type II): a case report of delayed diagnosis with pseudodendritic corneal lesion. Iskeleli G; Bilgeç MD; Arici C; Atalay E; Oğreden T; Aydin A Turk J Pediatr; 2011; 53(6):692-4. PubMed ID: 22389994 [TBL] [Abstract][Full Text] [Related]
9. Tyrosinemia without liver or renal damage with plantar and palmar keratosis and keratitis (hypertyrosinemia type II). Pelet B; Antener I; Faggioni R; Spahr A; Gautier E Helv Paediatr Acta; 1979 May; 34(2):177-83. PubMed ID: 156708 [TBL] [Abstract][Full Text] [Related]
10. [Oculocutaneous type II tyrosinosis]. Podglajen-Wecxsteen O; Delaporte E; Piette F; le Flohic X; Bergoend H Ann Dermatol Venereol; 1993; 120(2):139-42. PubMed ID: 8363306 [TBL] [Abstract][Full Text] [Related]
11. [Oculo-cutaneous tyrosinosis (Richner-Hanhart syndrome). Histo-pathological study of a case]. Larregue M; de Giacomoni P; Odievre M; Babin P; Lorette G Ann Anat Pathol (Paris); 1980; 25(3):185-200. PubMed ID: 6112939 [TBL] [Abstract][Full Text] [Related]
13. Acral malignant melanoma and striated palmoplantar keratoderma (Brunauer-Fohs-Siemens syndrome): a fortuitous association? Rubegni P; Poggiali S; Cuccia A; Biagioli M; Fimiani M Dermatol Surg; 2004 Dec; 30(12 Pt 2):1539-42. PubMed ID: 15606835 [TBL] [Abstract][Full Text] [Related]
14. Familial richner-Hanhart syndrome in Kuwait: twelve-year clinical reassessment by a multidisciplinary approach. el-Badramany MH; Fawzy AR; Farag TI Am J Med Genet; 1995 Oct; 60(5):353-5. PubMed ID: 8546145 [No Abstract] [Full Text] [Related]
15. Tyrosinemia type II (Richner-Hanhart syndrome): a new mutation in the TAT gene. Culic V; Betz RC; Refke M; Fumic K; Pavelic J Eur J Med Genet; 2011; 54(3):205-8. PubMed ID: 21145993 [TBL] [Abstract][Full Text] [Related]
16. Richner-Hanhart syndrome: importance of early diagnosis and early intervention. Tallab TM J Am Acad Dermatol; 1996 Nov; 35(5 Pt 2):857-9. PubMed ID: 8912606 [TBL] [Abstract][Full Text] [Related]