These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 35491177)

  • 41. 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]  

  • 42. Recombinant Rhodobacter capsulatus xanthine dehydrogenase, a useful model system for the characterization of protein variants leading to xanthinuria I in humans.
    Leimkuhler S; Hodson R; George GN; Rajagopalan KV
    J Biol Chem; 2003 Jun; 278(23):20802-11. PubMed ID: 12670960
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Three cases of xanthinuria identified by gas chromatography/mass spectrometry-based urine metabolomics.
    Kuhara T; Tetsuo M; Ohse M; Shirakawa T; Nakashima Y; Yoshiura KI; Tanaka N; Taya T
    IJU Case Rep; 2023 Nov; 6(6):436-439. PubMed ID: 37928284
    [TBL] [Abstract][Full Text] [Related]  

  • 44. An unusual cause of pink diapers in an infant: Questions and Answers.
    Amin R; Eid L; Edvardsson VO; Fairbanks L; Moudgil A
    Pediatr Nephrol; 2016 Apr; 31(4):575, 577-80. PubMed ID: 25823987
    [No Abstract]   [Full Text] [Related]  

  • 45. Classical xanthinuria: a rare cause of pediatric urolithiasis.
    Akıncı N; Çakıl A; Öner A
    Turk J Urol; 2013 Dec; 39(4):274-6. PubMed ID: 26328123
    [TBL] [Abstract][Full Text] [Related]  

  • 46. 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]  

  • 47. Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the Human Molybdenum Cofactor Sulfurase (HMCS) associated with type II classical xanthinuria.
    Peretz H; Naamati MS; Levartovsky D; Lagziel A; Shani E; Horn I; Shalev H; Landau D
    Mol Genet Metab; 2007 May; 91(1):23-9. PubMed ID: 17368066
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Hypouricaemia in a patient with hereditary xanthinuria type I.
    Maes B; Dedeurwaerdere F
    Lancet; 2024 Apr; 403(10435):1493. PubMed ID: 38614487
    [No Abstract]   [Full Text] [Related]  

  • 49. [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]  

  • 50. 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]  

  • 51. Xanthine urolithiasis: Inhibitors of xanthine crystallization.
    Grases F; Costa-Bauza A; Roig J; Rodriguez A
    PLoS One; 2018; 13(8):e0198881. PubMed ID: 30157195
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Assignment of human xanthine dehydrogenase gene to chromosome 2p22.
    Xu P; Zhu XL; Huecksteadt TP; Brothman AR; Hoidal JR
    Genomics; 1994 Sep; 23(1):289-91. PubMed ID: 7829092
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Hereditary xanthinuria and xanthine urolithiasis: an additional 3 cases.
    Frayha RA; Salti IS; Abu Haidar GI; al-Khalidi U; Hemady K
    J Urol; 1973 May; 109(5):871-3. PubMed ID: 4699688
    [No Abstract]   [Full Text] [Related]  

  • 54. Effect of allopurinol on the xanthinuria in a patient with molybdenum cofactor deficiency.
    van Gennip AH; Mandel H; Stroomer LE; van Cruchten AG
    Adv Exp Med Biol; 1994; 370():375-8. PubMed ID: 7660932
    [No Abstract]   [Full Text] [Related]  

  • 55. The presence of xanthine dehydrogenase is crucial for the maturation of the rat kidneys.
    Dissanayake LV; Kravtsova O; Lowe M; McCrorey MK; Van Beusecum JP; Palygin O; Staruschenko A
    Clin Sci (Lond); 2024 Mar; 138(5):269-288. PubMed ID: 38358003
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Urine concentrations of xanthine, hypoxanthine and uric acid in UK Cavalier King Charles spaniels.
    Jacinto AM; Mellanby RJ; Chandler M; Bommer NX; Carruthers H; Fairbanks LD; Gow AG
    J Small Anim Pract; 2013 Aug; 54(8):395-8. PubMed ID: 23859747
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Kidney failure secondary to hereditary xanthinuria due to a homozygous deletion of the XDH gene, in the absence of overt kidney stone disease.
    Gonçalves PL; Diniz H; Tavares I; Dória S; Dong J; Kyriss M; Fairbanks L; Oliveira JP
    Nephron; 2024 Mar; ():. PubMed ID: 38527446
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Tetrahydrobiopterin loading test in xanthine dehydrogenase and molybdenum cofactor deficiencies.
    Blau N; de Klerk JB; Thöny B; Heizmann CW; Kierat L; Smeitink JA; Duran M
    Biochem Mol Med; 1996 Aug; 58(2):199-203. PubMed ID: 8812740
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Hereditary xanthinuria. A clinical case report].
    Pessano B; Davì S; La Brocca A; Leone L
    Minerva Med; 1989 May; 80(5):507-9. PubMed ID: 2747979
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Hypoxanthine and xanthine concentrations determined by high performance liquid chromatography in biological fluids from patients with xanthinuria.
    Boulieu R; Bory C; Baltassat P; Divry P
    Clin Chim Acta; 1984 Sep; 142(1):83-9. PubMed ID: 6478626
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.