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Journal Abstract Search

216 related items for PubMed ID: 154319

  • 1. [Tyrosinemia and Richner-Hanhart syndrome (an autosomal recessive hereditary metabolic disease of childhood with bilateral dendritic pseudokeratitis, keratosis palmaris et plantaris and mental deficiency)].
    Jaeger W, Gallasch G, Schnyder UW, Lutz P, Schmidt H.
    Ber Zusammenkunft Dtsch Ophthalmol Ges; 1978; (75):649-54. PubMed ID: 154319
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  • 2. Tyrosinemia type II in two cases previously reported as Richner-Hanhart syndrome.
    Balato N, Cusano F, Lembo G, Santoianni P.
    Dermatologica; 1986; 173(2):66-74. PubMed ID: 2947825
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  • 7. [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
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  • 8. 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
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  • 9. 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 09; 60(5):353-5. PubMed ID: 8546145
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  • 10. Richner-Hanhart syndrome and tyrosinemia type II.
    Hunziker N.
    Dermatologica; 1980 Oct 09; 160(3):180-9. PubMed ID: 6446465
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  • 11. 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 09; 16(11):1069-74. PubMed ID: 6240214
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  • 12. [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 09; 2(1):23-8. PubMed ID: 34642
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  • 13. [Herpetiform bilateral epithelial corneal dystrophy caused by Tyrosinemia (Richner-Hanhart-Syndrome) (author's transl)].
    Jaeger W, Gallasch G, Schnyder UW, Lutz P, Schmidt H.
    Klin Monbl Augenheilkd; 1978 Oct 09; 173(4):506-15. PubMed ID: 153427
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  • 14. Pseudodendritic keratitis and systemic tyrosinemia.
    Charlton KH, Binder PS, Wozniak L, Digby DJ.
    Ophthalmology; 1981 Apr 09; 88(4):355-60. PubMed ID: 6454871
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  • 15. 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 Apr 09; 53(6):692-4. PubMed ID: 22389994
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  • 16. [Palmoplantar keratosis associated with keratitis: hereditary hypertyrosinemia treated by diet].
    Ogier H, Hervé F, Saudubray JM, Dufier JL, Charpentier C, Lemonnier F, Moreno JL, Frezal J.
    Ann Med Interne (Paris); 1986 Apr 09; 137(2):129-32. PubMed ID: 2940955
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  • 17. [Changes in the keratinocytes in oculo-cutaneous tyrosinosis: Richner-Hanhart syndrome (author's transl)].
    Larrègue M, De Giacomoni P, Odièvre P, Prigent F.
    Ann Dermatol Venereol; 1980 Apr 09; 107(11):1023-30. PubMed ID: 7235483
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  • 19. Tyrosinemia type II with incomplete Richner-Hanhart's syndrome.
    Lestringant GG.
    Int J Dermatol; 1988 Apr 09; 27(1):43-4. PubMed ID: 2964425
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