148 related articles for article (PubMed ID: 10365419)
1. [Unmeasurable uric acid in blood and urine; xanthine dehydrogenase deficiency (or hereditary xanthinuria)].
Mayaudon H; Bauduceau B; Dupuy O; Ceppa F; Roul G; Burnat P
Rev Med Interne; 1999 May; 20(5):445. PubMed ID: 10365419
[No Abstract] [Full Text] [Related]
2. [Hereditary xanthinuria and molybdenum cofactor deficiency].
Ichida K
Nihon Rinsho; 2003 Jan; 61 Suppl 1():377-82. PubMed ID: 12629751
[No Abstract] [Full Text] [Related]
3. Hereditary xanthinuria is not so rare disorder of purine metabolism.
Sebesta I; Stiburkova B; Krijt J
Nucleosides Nucleotides Nucleic Acids; 2018; 37(6):324-328. PubMed ID: 29723117
[TBL] [Abstract][Full Text] [Related]
4. Mutations in xanthine dehydrogenase gene in subjects with hereditary xanthinuria.
Ichida K; Kamatani N; Nishino T; Saji M; Okabe H; Hosoya T
Adv Exp Med Biol; 1998; 431():327-30. PubMed ID: 9598085
[No Abstract] [Full Text] [Related]
5. Beware of the Uric Acid: Severe Azathioprine Myelosuppression in a Patient With Juvenile Idiopathic Arthritis and Hereditary Xanthinuria.
Tanev D; Peteva P; Fairbanks L; Marinaki A; Ivanova M; Alaikov T; Shivarov V
J Clin Rheumatol; 2020 Mar; 26(2):e49-e52. PubMed ID: 32073534
[No Abstract] [Full Text] [Related]
6. Two siblings with classical xanthinuria type 1: significance of allopurinol loading test.
Ichida K; Yoshida M; Sakuma R; Hosoya T
Intern Med; 1998 Jan; 37(1):77-82. PubMed ID: 9510406
[TBL] [Abstract][Full Text] [Related]
7. Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria.
Ichida K; Amaya Y; Kamatani N; Nishino T; Hosoya T; Sakai O
J Clin Invest; 1997 May; 99(10):2391-7. PubMed ID: 9153281
[TBL] [Abstract][Full Text] [Related]
8. Thiopurine-induced toxicity is associated with dysfunction variant of the human molybdenum cofactor sulfurase gene (xanthinuria type II).
Stiburkova B; Pavelcova K; Petru L; Krijt J
Toxicol Appl Pharmacol; 2018 Aug; 353():102-108. PubMed ID: 29935280
[TBL] [Abstract][Full Text] [Related]
9. [A case of Xanthinuria in a patient with marked hypouricemia].
Martella V; Sozzo E; Montagna E; Stefanizzi S; Cito A; Marinello E; Terzuoli L; Micheli V; Napoli M
G Ital Nefrol; 2011; 28(6):648-53. PubMed ID: 22167616
[TBL] [Abstract][Full Text] [Related]
10. Using Next-Generation Sequencing to Identify a Mutation in Human MCSU that is Responsible for Type II Xanthinuria.
Zhou Y; Zhang X; Ding R; Li Z; Hong Q; Wang Y; Zheng W; Geng X; Fan M; Cai G; Chen X; Wu D
Cell Physiol Biochem; 2015; 35(6):2412-21. PubMed ID: 25967871
[TBL] [Abstract][Full Text] [Related]
11. Mutations associated with functional disorder of xanthine oxidoreductase and hereditary xanthinuria in humans.
Ichida K; Amaya Y; Okamoto K; Nishino T
Int J Mol Sci; 2012 Nov; 13(11):15475-95. PubMed ID: 23203137
[TBL] [Abstract][Full Text] [Related]
12. [Xanthinuria (author's transl)].
Cartier P; Perignon JL
Nouv Presse Med; 1978 Apr; 7(16):1381-90. PubMed ID: 673672
[TBL] [Abstract][Full Text] [Related]
13. Identification of a new point mutation in the human xanthine dehydrogenase gene responsible for a case of classical type I xanthinuria.
Sakamoto N; Yamamoto T; Moriwaki Y; Teranishi T; Toyoda M; Onishi Y; Kuroda S; Sakaguchi K; Fujisawa T; Maeda M; Hada T
Hum Genet; 2001 Apr; 108(4):279-83. PubMed ID: 11379872
[TBL] [Abstract][Full Text] [Related]
14. [Classical xanthinuria (type I and II)].
Ichida K; Hosoya T
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):470-3. PubMed ID: 9590104
[No Abstract] [Full Text] [Related]
15. [Xanthine oxidase deficiency (hereditary xanthinuria), molybdenum cofactor deficiency].
Sumi S; Wada Y
Nihon Rinsho; 1996 Dec; 54(12):3333-6. PubMed ID: 8976115
[TBL] [Abstract][Full Text] [Related]
16. Decreased xanthine oxidase activities and increased urinary oxypurines in heterozygotes for hereditary xanthinuria.
Kawachi M; Kono N; Mineo I; Yamada Y; Tarui S
Clin Chim Acta; 1990 Apr; 188(2):137-46. PubMed ID: 2379312
[TBL] [Abstract][Full Text] [Related]
17. A new case with hereditary xanthinuria: response to exercise.
Landaas S; Borch K; Aagaard E
Clin Chim Acta; 1989 May; 181(2):119-24. PubMed ID: 2736776
[TBL] [Abstract][Full Text] [Related]
18. The human gene for xanthine dehydrogenase (XDH) is localized on chromosome band 2q22.
Rytkönen EM; Halila R; Laan M; Saksela M; Kallioniemi OP; Palotie A; Raivio KO
Cytogenet Cell Genet; 1995; 68(1-2):61-3. PubMed ID: 7956361
[TBL] [Abstract][Full Text] [Related]
19. Xanthine dehydrogenase deficiency with novel sequence variations presenting as rheumatoid arthritis in a 78-year-old patient.
Jurecka A; Stiburkova B; Krijt J; Gradowska W; Tylki-Szymanska A
J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S21-4. PubMed ID: 20077140
[TBL] [Abstract][Full Text] [Related]
20. Two successive pregnancies in a woman with xanthinuria: unexpected increase in serum uric acid levels.
Uzan S; Beaufils M; Ragot J; Brault D; Donsimoni R
J Perinat Med; 1980; 8(6):284-7. PubMed ID: 7452437
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
