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 *

100 related articles for article (PubMed ID: 9407766)

  • 1. Sulphite oxidase deficiency--a report of two siblings.
    Goh A; Lim KW
    Singapore Med J; 1997 Sep; 38(9):391-4. PubMed ID: 9407766
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A mild form of infantile isolated sulphite oxidase deficiency.
    Barbot C; Martins E; Vilarinho L; Dorche C; Cardoso ML
    Neuropediatrics; 1995 Dec; 26(6):322-4. PubMed ID: 8719749
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel mutation in neonatal isolated sulphite oxidase deficiency.
    Lee HF; Mak BS; Chi CS; Tsai CR; Chen CH; Shu SG
    Neuropediatrics; 2002 Aug; 33(4):174-9. PubMed ID: 12368985
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Infantile isolated sulphite oxidase deficiency in a Chinese family: a rare neurodegenerative disorder.
    Chan KY; Li CK; Lai CK; Ng SF; Chan AY
    Hong Kong Med J; 2002 Aug; 8(4):279-82. PubMed ID: 12167732
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Isolated sulfite oxidase deficiency: mutation analysis and DNA-based prenatal diagnosis.
    Johnson JL; Rajagopalan KV; Renier WO; Van der Burgt I; Ruitenbeek W
    Prenat Diagn; 2002 May; 22(5):433-6. PubMed ID: 12001203
    [TBL] [Abstract][Full Text] [Related]  

  • 6. New approaches towards laboratory diagnosis of isolated sulphite oxidase deficiency.
    Sass JO; Nakanishi T; Sato T; Shimizu A
    Ann Clin Biochem; 2004 Mar; 41(Pt 2):157-9. PubMed ID: 15025809
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Sulfite oxidase deficiency presenting as Leigh syndrome].
    Amiel J; Gagey V; Rabier D; Dorche C; Bonnefont JP; Dufier JL; Saudubray JM; Rey J; Munnich A
    Arch Pediatr; 1994 Nov; 1(11):1023-7. PubMed ID: 7834040
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Isolated sulfite oxidase deficiency.
    Rupar CA; Gillett J; Gordon BA; Ramsay DA; Johnson JL; Garrett RM; Rajagopalan KV; Jung JH; Bacheyie GS; Sellers AR
    Neuropediatrics; 1996 Dec; 27(6):299-304. PubMed ID: 9050047
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Magnetic resonance imaging and magnetic resonance spectroscopy in isolated sulfite oxidase deficiency.
    Hoffmann C; Ben-Zeev B; Anikster Y; Nissenkorn A; Brand N; Kuint J; Kushnir T
    J Child Neurol; 2007 Oct; 22(10):1214-21. PubMed ID: 17940249
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Isolated sulfite oxidase deficiency: review of two cases in one family.
    Edwards MC; Johnson JL; Marriage B; Graf TN; Coyne KE; Rajagopalan KV; MacDonald IM
    Ophthalmology; 1999 Oct; 106(10):1957-61. PubMed ID: 10519592
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Isolated sulphite oxidase deficiency mimics the features of hypoxic ischaemic encephalopathy.
    Hobson EE; Thomas S; Crofton PM; Murray AD; Dean JC; Lloyd D
    Eur J Pediatr; 2005 Nov; 164(11):655-9. PubMed ID: 16025295
    [TBL] [Abstract][Full Text] [Related]  

  • 12. DNA-based diagnosis of isolated sulfite oxidase deficiency by denaturing high-performance liquid chromatography.
    Lam CW; Li CK; Lai CK; Tong SF; Chan KY; Ng GS; Yuen YP; Cheng AW; Chan YW
    Mol Genet Metab; 2002 Jan; 75(1):91-5. PubMed ID: 11825068
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Report on a new patient with combined deficiencies of sulphite oxidase and xanthine dehydrogenase due to molybdenum cofactor deficiency.
    Endres W; Shin YS; Günther R; Ibel H; Duran M; Wadman SK
    Eur J Pediatr; 1988 Dec; 148(3):246-9. PubMed ID: 3215199
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Absence of hepatic molybdenum cofactor: an inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenase.
    Wadman SK; Duran M; Beemer FA; Cats BP; Johnson JL; Rajagopalan KV; Saudubray JM; Ogier H; Charpentier C; Berger R
    J Inherit Metab Dis; 1983; 6 Suppl 1():78-83. PubMed ID: 6413778
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Combined deficiency of xanthine oxidase and sulphite oxidase: a defect of molybdenum metabolism or transport?
    Duran M; Beemer FA; van de Heiden C; Korteland J; de Bree PK; Brink M; Wadman SK; Lombeck I
    J Inherit Metab Dis; 1978; 1(4):175-8. PubMed ID: 117254
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molybdenum cofactor deficiency: first prenatal genetic analysis.
    Reiss J; Christensen E; Dorche C
    Prenat Diagn; 1999 Apr; 19(4):386-8. PubMed ID: 10327149
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Combined xanthine and sulphite oxidase defect due to a deficiency of molybdenum cofactor.
    Roesel RA; Bowyer F; Blankenship PR; Hommes FA
    J Inherit Metab Dis; 1986; 9(4):343-7. PubMed ID: 3104671
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Combined deficiency of xanthine oxidase and sulfite oxidase; ophthalmological findings in a 3-week-old girl.
    Beemer FA; Delleman JW
    Metab Pediatr Ophthalmol; 1980; 4(1):49-52. PubMed ID: 6969337
    [No Abstract]   [Full Text] [Related]  

  • 19. Infantile isolated sulphite oxidase deficiency: report of a case with negative sulphite test and normal sulphate excretion.
    van der Klei-van Moorsel JM; Smit LM; Brockstedt M; Jakobs C; Dorche C; Duran M
    Eur J Pediatr; 1991 Jan; 150(3):196-7. PubMed ID: 2044591
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis and carrier detection for molybdenum cofactor deficiency type A in northern Israel using polymorphic DNA markers.
    Shalata A; Mandel H; Dorche C; Zabot MT; Shalev S; Hugeirat Y; Arieh D; Ronit Z; Reiss J; Anbinder Y; Cohen N
    Prenat Diagn; 2000 Jan; 20(1):7-11. PubMed ID: 10701843
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.