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Items: 1 to 20 of 187

1.

Biochemical observations on so-called hereditary tyrosinemia.

Gaull GE, Rassin DK, Solomon GE, Harris RC, Sturman JA.

Pediatr Res. 1970 Jul;4(4):337-44. No abstract available.

PMID:
4393588
2.

Hereditary tyrosinemia: metabolic studies in a patient with partial p-hydroxyphenylpyruvate hydroxylase activity.

Jagenburg R, Landblad B, De Maré JM, Rödjer S.

J Pediatr. 1972 Jun;80(6):994-1004. No abstract available.

PMID:
5026040
3.

Enzymatic studies in a case of hereditary tyrosinemia with hepatoma.

Gentz J, Heinrich J, Lindblad B, Lindstedt S, Zetterström R.

Acta Paediatr Scand. 1969 Jul;58(4):393-6. No abstract available.

PMID:
4390478
4.

Hereditary tyrosinemia and tyrosyluria in a French Canadian geographic isolate.

Scriver CR, Larochelle J, Silverberg M.

Am J Dis Child. 1967 Jan;113(1):41-6. No abstract available.

PMID:
6016174
5.

Hereditary tyrosinemia. 3. On the differential diagnosis and the lack of effect of early dietary treatment.

Bodegård G, Gentz J, Lindblad B, Lindstedt S, Zetterström R.

Acta Paediatr Scand. 1969 Jan;58(1):37-48. No abstract available.

PMID:
5789740
6.
7.

The enzymatic deficiency in tyrosinemia.

La Du BN.

Am J Dis Child. 1967 Jan;113(1):54-7. No abstract available.

PMID:
4380967
8.
9.

[Tyrosinosis. Primary and secondary biochemical changes].

Nützenadel W, Lutz P, Bickel H.

Z Kinderheilkd. 1972;113(3):193-204. German. No abstract available.

PMID:
4641148
10.

p-hydroxyphenylpyruvate hydroxylase activity in fine-needle aspiration liver biopsies in hereditary tyrosinemia.

Gentz J, Lindblad B.

Scand J Clin Lab Invest. 1972 Feb;29(1):115-26. No abstract available.

PMID:
5014992
11.

[Presentation of a case of chronic type 1 tyrosinemia. Diet therapy and clinical outcome].

Gabrielli O, Maiorana A, Paris D, Zanobini R, Renda B, Montali U, Coppa G.

Minerva Pediatr. 1978 Aug 31;30(16):1329-34. Italian. No abstract available.

PMID:
692506
12.

Persistent tyrosinemia associated with low activity of tyrosine aminotransferase.

Andersson S, Nemeth A, Ohisalo J, Strandvik B.

Pediatr Res. 1984 Jul;18(7):675-8.

PMID:
6147810
13.

[Transitory hypertyrosinemia of young infants and its relation to vitamin C].

Henze H, Bremer HJ.

Monatsschr Kinderheilkd. 1969 Jun;117(6):433-6. Review. German. No abstract available.

PMID:
4393253
14.

[Experimental hyperphenylalanaemic animals and cystathionine contents in brain tissues].

Shoma N.

Nihon Seirigaku Zasshi. 1970;32(4):219-28. Japanese. No abstract available.

PMID:
4987953
15.

Recovery after dietary treatment of an infant with features of tyrosinosis.

Harries JT, Seakins JW, Ersser RS, Lloyd JK.

Arch Dis Child. 1969 Apr;44(234):258-67. No abstract available.

16.

Keratopathy in tyrosinemia.

Burns RP, Gipson IK, Murray MJ.

Birth Defects Orig Artic Ser. 1976;12(3):169-80. Review. No abstract available.

PMID:
8172
17.

Dietary treatment of tyrosinosis.

Halvorsen S.

Am J Dis Child. 1967 Jan;113(1):38-40. No abstract available.

PMID:
6015904
18.

Soluble and mitochondrial forms of tyrosine aminotransferase. Relationship to human tyrosinemia.

Fellman JH, Vanbellinghen PJ, Jones RT, Koler RD.

Biochemistry. 1969 Feb;8(2):615-22. No abstract available.

PMID:
4389443
19.

Enzyme defect in a case of tyrosinemia type I, acute form.

Furukawa N, Kinugasa A, Seo T, Ishii T, Ota T, Machida Y, Inoue F, Imashuku S, Kusunoki T, Takamatsu T.

Pediatr Res. 1984 May;18(5):463-6.

PMID:
6145143
20.

New forms of hereditary tyrosinemia type II in mink: hepatic tyrosine aminotransferase defect.

Christensen K, Henriksen P, Sørensen H.

Hereditas. 1986;104(2):215-22. No abstract available.

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