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 *

145 related articles for article (PubMed ID: 9590056)

  • 1. [3-Hydroxyisobutyric aciduria (3-hydroxyisobutyric acid dehydrogenase deficiency)].
    Yoshida I
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):317-9. PubMed ID: 9590056
    [No Abstract]   [Full Text] [Related]  

  • 2. 3-Hydroxyisobutyric aciduria: an inborn error of valine metabolism.
    Ko FJ; Nyhan WL; Wolff J; Barshop B; Sweetman L
    Pediatr Res; 1991 Oct; 30(4):322-6. PubMed ID: 1956714
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical, biochemical, and molecular findings in three patients with 3-hydroxyisobutyric aciduria.
    Loupatty FJ; van der Steen A; Ijlst L; Ruiter JP; Ofman R; Baumgartner MR; Ballhausen D; Yamaguchi S; Duran M; Wanders RJ
    Mol Genet Metab; 2006 Mar; 87(3):243-8. PubMed ID: 16466957
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 3-Hydroxyisobutyrate dehydrogenase (HIBADH) deficiency-A novel disorder of valine metabolism.
    Meyer M; Hollenbeck JC; Reunert J; Seelhöfer A; Rust S; Fobker M; Biskup S; Och U; Linden M; Sass JO; Marquardt T
    J Inherit Metab Dis; 2021 Nov; 44(6):1323-1329. PubMed ID: 34176136
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 3-Hydroxyisobutyric acid dehydrogenase deficiency: Expanding the clinical spectrum and quantitation of D- and L-3-Hydroxyisobutyric acid by an LC-MS/MS method.
    Sasarman F; Ferdinandusse S; Sinasac DS; Fung E; Sparkes R; Reeves M; Rombough C; Sass JO; Voit R; Ruiter JPN; Koster J; Waterham HR; Pasquini E; Donati MA; Marquardt T; Wanders RJA; Al-Hertani W
    J Inherit Metab Dis; 2022 May; 45(3):445-455. PubMed ID: 35174513
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hypermethioninaemia and 3-hydroxyisobutyric aciduria in an apparently healthy baby.
    Congdon PJ; Haigh D; Smith R; Green A; Pollitt RJ
    J Inherit Metab Dis; 1981; 4(2):79-80. PubMed ID: 6790857
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 3-Hydroxyisobutyrate aciduria and mutations in the ALDH6A1 gene coding for methylmalonate semialdehyde dehydrogenase.
    Sass JO; Walter M; Shield JP; Atherton AM; Garg U; Scott D; Woods CG; Smith LD
    J Inherit Metab Dis; 2012 May; 35(3):437-42. PubMed ID: 21863277
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Methylmalonic semialdehyde dehydrogenase deficiency].
    Yoshida I
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):320-2. PubMed ID: 9590057
    [No Abstract]   [Full Text] [Related]  

  • 9. Succinic semialdehyde dehydrogenase (SSADH) deficiency: Molecular analysis in a South American family.
    Lemes A; Blasi P; Gonzales G; Russi ME; Quadrelli R; Novelletto A; Malaspina P
    J Inherit Metab Dis; 2006 Aug; 29(4):587. PubMed ID: 16788854
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Succinic semialdehyde dehydrogenase deficiency (SSADH) (4-hydroxybutyric aciduria, gamma-hydroxybutyric aciduria).
    Gordon N
    Eur J Paediatr Neurol; 2004; 8(5):261-5. PubMed ID: 15341910
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. [Urocanic aciduria (urocanase deficiency)].
    Imaeda M; Wada Y
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):150-1. PubMed ID: 9590012
    [No Abstract]   [Full Text] [Related]  

  • 13. A new patient with 4-hydroxybutyric aciduria, a possible defect of 4-aminobutyrate metabolism.
    Divry P; Baltassat P; Rolland MO; Cotte J; Hermier M; Duran M; Wadman SK
    Clin Chim Acta; 1983 Apr; 129(3):303-9. PubMed ID: 6133657
    [No Abstract]   [Full Text] [Related]  

  • 14. Brain dysgenesis and congenital intracerebral calcification associated with 3-hydroxyisobutyric aciduria.
    Chitayat D; Meagher-Villemure K; Mamer OA; O'Gorman A; Hoar DI; Silver K; Scriver CR
    J Pediatr; 1992 Jul; 121(1):86-9. PubMed ID: 1625099
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 4-Hydroxybutyric aciduria associated with catheter usage: a diagnostic pitfall in the identification of SSADH deficiency.
    Wamelink MM; Roos B; Jansen EE; Mulder MF; Gibson KM; Jakobs C
    Mol Genet Metab; 2011 Feb; 102(2):216-7. PubMed ID: 20965758
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [3-Methylcrotonyl-CoA carboxylase deficiency].
    Yoshida I
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):284-7. PubMed ID: 9590048
    [No Abstract]   [Full Text] [Related]  

  • 17. Basal ganglia lesions in a patient with 3-hydroxyisobutyric aciduria.
    Sasaki M; Yamada N; Fukumizu M; Sugai K
    Brain Dev; 2006 Oct; 28(9):600-3. PubMed ID: 16713161
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [3-Hydroxyisobutyryl-CoA deacylase deficiency].
    Yoshida I
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):314-6. PubMed ID: 9590055
    [No Abstract]   [Full Text] [Related]  

  • 19. [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]  

  • 20. [Methylglutaconic aciduria (normal hydratase, unspecified)].
    Yoshida I
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):295-8. PubMed ID: 9590051
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.