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23. Type I hereditary tyrosinaemia: presentation of 11 cases. Coşkun T; Ozalp I; Koçak N; Yüce A; Caglar M; Berger R J Inherit Metab Dis; 1991; 14(5):765-70. PubMed ID: 1664010 [TBL] [Abstract][Full Text] [Related]
24. The effect of diet on the ophthalmological, clinical and biochemical aspects of Richner-Hanhart syndrome: a morphological ultrastructural study of the cornea and the conjunctiva. Sammartino A; Cerbella R; Cecio A; De Crecchio G; Federico A; Fronterre A Int Ophthalmol; 1987 Aug; 10(4):203-12. PubMed ID: 3654059 [TBL] [Abstract][Full Text] [Related]
25. [Incurable keratitis and chronic palmoplantar hyperkeratosis with hypertyrosinemia. Cure using a tyrosine-restricted diet. Type II tyrosinemia]. Hervé F; Moreno JL; Ogier H; Saudubray JM; De Prost Y; Duffier JL; Charpentier C; Lemonnier F; Frézal J Arch Fr Pediatr; 1986 Jan; 43(1):19-22. PubMed ID: 2939812 [TBL] [Abstract][Full Text] [Related]
27. Urinary succinylacetone presence and delta-aminolaevulinic acid excretion in patients with type I tyrosinaemia during treatment. Pronicka E; Mielniczuk Z; Rowińska E; Ksiazyk J; Szczygielska-Kozak M; Wieczorek E; Kulczycka H Mater Med Pol; 1991; 23(2):136-8. PubMed ID: 1842600 [TBL] [Abstract][Full Text] [Related]
28. 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]
29. Successful dietary control of tyrosinemia II. Machino H; Miki Y; Kawatsu T; Kida K; Matsuda H J Am Acad Dermatol; 1983 Oct; 9(4):533-9. PubMed ID: 6195199 [TBL] [Abstract][Full Text] [Related]
30. [Diagnosis and therapy of 6 inherited, metabolic diseases, leading to mental deficiency. 1]. Menne F; Enzenauer J; Matz D Med Klin; 1976 Apr; 71(17):724-8. PubMed ID: 775276 [No Abstract] [Full Text] [Related]
32. Possibilities for treatment and for early prenatal diagnosis of hereditary tyrosinaemia. Holme E; Lindblad B; Lindstedt S Lancet; 1985 Mar; 1(8427):527. PubMed ID: 2857895 [No Abstract] [Full Text] [Related]
33. Prenatal diagnosis of tyrosinaemia type I by use of stable isotope dilution mass spectrometry. Jakobs C; Kvittingen EA; Berger R; Haagen A; Kleijer W; Niermeijer M Eur J Pediatr; 1985 Jul; 144(2):209-10. PubMed ID: 4043138 [No Abstract] [Full Text] [Related]
34. Mental retardation in a family with phenylketonuria and mild hyperphenylalaninemia. Cohen BE; Szeinberg A; Berman W; Aviad Y; Crispin M; Hirshorn N; Goland R Pediatrics; 1969 Nov; 44(5):655-60. PubMed ID: 5374976 [No Abstract] [Full Text] [Related]
39. Effect of dietary treatment on the renal tubular function in a patient with hereditary tyrosinemia. Suzuki Y; Konda M; Imai I; Imamura H; Shimao S; Okaka T Int J Pediatr Nephrol; 1987; 8(3):171-6. PubMed ID: 3429140 [TBL] [Abstract][Full Text] [Related]
40. Hepatic tyrosine aminotransferase in tyrosinaemia type II. Kida K; Takahashi M; Fujisawa Y; Matsuda H; Machino H; Miki Y J Inherit Metab Dis; 1982; 5(4):229-30. PubMed ID: 6133036 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]