154 related articles for article (PubMed ID: 9590041)
1. [Kynureninase deficiency].
Ohura T
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):255-7. PubMed ID: 9590041
[No Abstract] [Full Text] [Related]
2. [Arginase deficiency].
Uchino T; Matsuda I
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):182-4. PubMed ID: 9590022
[No Abstract] [Full Text] [Related]
3. [3-Hydroxyisobutyryl-CoA deacylase deficiency].
Yoshida I
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):314-6. PubMed ID: 9590055
[No Abstract] [Full Text] [Related]
4. On kynureninase activity.
Shibata Y; Takeuchi F; Tsubouchi R; Haneda M; Ohta T; Nakatsuka M; Nisimoto Y; Tamai T; Nomura S; Fujimoto H
Adv Exp Med Biol; 1991; 294():523-6. PubMed ID: 1772086
[TBL] [Abstract][Full Text] [Related]
5. [Tryptophan metabolism and oligophrenia (author's transl)].
Grimm U; Knapp A; Schmitz W; Smetan M; Schmitz KW; Reddemann H; Schulz M; Schlenzka K
Fortschr Neurol Psychiatr Grenzgeb; 1978 Apr; 46(4):178-85. PubMed ID: 147846
[TBL] [Abstract][Full Text] [Related]
6. [Determination of kynureninase activity in oligophrenic children with hereditary taint, before and after vitamin B6 treatment].
Grimm U; Knapp A; Machill G; Schmitz W; Smetan M; Schmitz KW; Reddemann H; Schulz M; Schlenzka K
Acta Biol Med Ger; 1975; 34?710():1659-64. PubMed ID: 1233849
[TBL] [Abstract][Full Text] [Related]
7. The urinary ratio of 3-hydroxykynurenine/3-hydroxyanthranilic acid is an index to predicting the adverse effects of D-tryptophan in rats.
Shibata K; Ohno T; Sano M; Fukuwatari T
J Nutr Sci Vitaminol (Tokyo); 2014; 60(4):261-8. PubMed ID: 25297615
[TBL] [Abstract][Full Text] [Related]
8. [Dihydropyrimidinase deficiency (dihydropyrimidinuria)].
Hamajima N; Wada Y
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):231-4. PubMed ID: 9590033
[No Abstract] [Full Text] [Related]
9. [5-Oxoprolinase deficiency].
Kanno H
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):366-7. PubMed ID: 9590071
[No Abstract] [Full Text] [Related]
10. [Prolidase deficiency].
Tanoue A; Endo F
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):160-2. PubMed ID: 9590016
[No Abstract] [Full Text] [Related]
11. Xanthurenic aciduria due to a mutation in KYNU encoding kynureninase.
Christensen M; Duno M; Lund AM; Skovby F; Christensen E
J Inherit Metab Dis; 2007 Apr; 30(2):248-55. PubMed ID: 17334708
[TBL] [Abstract][Full Text] [Related]
12. [gamma-Glutamyl transpeptidase deficiency].
Kanno H
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):373-5. PubMed ID: 9590074
[No Abstract] [Full Text] [Related]
13. [Argininosuccinate lyase deficiency].
Matsubasa T
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):179-81. PubMed ID: 9590021
[No Abstract] [Full Text] [Related]
14. [Argininosuccinate synthetase deficiency].
Kobayashi K; Saheki T
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):175-8. PubMed ID: 9590020
[No Abstract] [Full Text] [Related]
15. [2-Methylbranched chain acyl-CoA-dehydrogenase deficiency].
Yoshida I
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):325-7. PubMed ID: 9590058
[No Abstract] [Full Text] [Related]
16. [Carbamyl phosphate synthetase I deficiency].
Hoshide R
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):167-9. PubMed ID: 9590018
[No Abstract] [Full Text] [Related]
17. [2-Ketoadipic dehydrogenase deficiency (2-ketoadipic acidemia)].
Hayasaka K
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):336-7. PubMed ID: 9590061
[No Abstract] [Full Text] [Related]
18. [Glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)].
Hayasaka K; Ikeda H
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):332-5. PubMed ID: 9590060
[No Abstract] [Full Text] [Related]
19. [Enzyme deficiency (disorders of amino acid metabolism, disorders of lipid metabolism)].
Tsuchida H; Kitabayashi Y; Yamada C; Yokoyama C; Fukui K
Ryoikibetsu Shokogun Shirizu; 2003; (40):383-6. PubMed ID: 14626144
[No Abstract] [Full Text] [Related]
20. [Hypervalinemia].
Wada Y
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):195-7. PubMed ID: 9590026
[No Abstract] [Full Text] [Related]
[Next] [New Search]
