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 *

142 related articles for article (PubMed ID: 2416490)

  • 1. Photodiode array detection for liquid chromatographic profiling of carboxylic acids in physiological fluids: 3-hydroxy-3-methylglutaric aciduria.
    Buchanan DN; Thoene JG
    Clin Chem; 1986 Jan; 32(1 Pt 1):169-71. PubMed ID: 2416490
    [TBL] [Abstract][Full Text] [Related]  

  • 2. First trimester prenatal diagnosis of 3-hydroxy-3-methylglutaric aciduria.
    Chalmers RA; Mistry J; Penketh R; McFadyen IR
    J Inherit Metab Dis; 1989; 12 Suppl 2():283-5. PubMed ID: 2480477
    [No Abstract]   [Full Text] [Related]  

  • 3. 3-Hydroxy-3-methylglutaric aciduria: a possible pitfall in diagnosis.
    Mills GA; Hill MA; Buchanan R; Corina DL; Walker V
    Clin Chim Acta; 1991 Dec; 204(1-3):131-6. PubMed ID: 1726424
    [No Abstract]   [Full Text] [Related]  

  • 4. 3-Hydroxy-3-methylglutaric aciduria: response to carnitine therapy and fat and leucine restriction.
    Dasouki M; Buchanan D; Mercer N; Gibson KM; Thoene J
    J Inherit Metab Dis; 1987; 10(2):142-6. PubMed ID: 2443756
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Positive-ion thermospray liquid chromatography-mass spectrometry: detection of organic acidurias.
    Buchanan DN; Muenzer J; Thoene JG
    J Chromatogr; 1990 Dec; 534():1-11. PubMed ID: 1709942
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 3-Hydroxy-3-methylglutaryl-CoA lyase in human skin fibroblasts: study of its properties and deficient activity in 3-hydroxy-3-methylglutaric aciduria patients using a simple spectrophotometric method.
    Wanders RJ; Schutgens RB; Zoeters PH
    Clin Chim Acta; 1988 Jan; 171(1):95-101. PubMed ID: 2450702
    [TBL] [Abstract][Full Text] [Related]  

  • 7. L-Carnitine insufficiency in disorders of organic acid metabolism: response to L-carnitine by patients with methylmalonic aciduria and 3-hydroxy-3-methylglutaric aciduria.
    Chalmers RA; Stacey TE; Tracey BM; de Sousa C; Roe CR; Millington DS; Hoppel CL
    J Inherit Metab Dis; 1984; 7 Suppl 2():109-10. PubMed ID: 6207380
    [No Abstract]   [Full Text] [Related]  

  • 8. 3-Hydroxy-3-methylglutaric aciduria.
    Greene CL; Cann HM; Robinson BH; Gibson KM; Sweetman L; Holm J; Nyhan WL
    J Neurogenet; 1984 Apr; 1(2):165-73. PubMed ID: 6085636
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A case of organic aciduria--suspected 3-hydroxy-3-methylglutaric aciduria.
    Kulczycka H; Mielniczuk Z; Kamińska H; Lewanowicz W; Pronicka E
    Mater Med Pol; 1991; 23(4):312-4. PubMed ID: 1726825
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 3-hydroxy-3-methylglutaric aciduria: a new assay of 3-hydroxy-3-methylglutaryl-coa lyase using high performance liquid chromatography.
    Gibson KM; Sweetman L; Nyhan WL; Page TM; Greene C; Cann HM
    Clin Chim Acta; 1982 Dec; 126(2):171-81. PubMed ID: 6185253
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Diagnosing 3-hydroxy-3-methylglutaric aciduria.
    Wilkinson SP; Wysocki SJ; Hähnel R
    Clin Chem; 1986 Aug; 32(8):1615-6. PubMed ID: 2426013
    [No Abstract]   [Full Text] [Related]  

  • 12. 3-Hydroxy-3-methylglutaric aciduria in a girl with trisomy 21.
    Ferreira G; Freitas S; Pereira SA; Martins I; Tavares E; Vilarinho L
    Eur J Pediatr; 1996 Dec; 155(12):1068. PubMed ID: 8956952
    [No Abstract]   [Full Text] [Related]  

  • 13. 3-Methylcrotonylglycine excretion in 3-hydroxy-3-methylglutaric aciduria.
    Wysocki SJ; Hähnel R
    Clin Chim Acta; 1978 May; 86(1):101-8. PubMed ID: 657530
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dizygotic twins with 3-hydroxy-3-methylglutaric aciduria; unusual presentation, family studies and dietary management.
    Stacey TE; de Sousa C; Tracey BM; Whitelaw A; Mistry J; Timbrell P; Chalmers RA
    Eur J Pediatr; 1985 Jul; 144(2):177-81. PubMed ID: 2412823
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Deconvolution gas chromatography/mass spectrometry of urinary organic acids--potential for pattern recognition and automated identification of metabolic disorders.
    Halket JM; Przyborowska A; Stein SE; Mallard WG; Down S; Chalmers RA
    Rapid Commun Mass Spectrom; 1999; 13(4):279-84. PubMed ID: 10097403
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of 3-hydroxy-3-methylglutaric aciduria via enzyme activity measurements in chorionic villi, chorionic villous fibroblasts or amniocytes using a simple spectrophotometric method.
    Wanders RJ; Schutgens RB; Zoeters BH
    J Inherit Metab Dis; 1988; 11(4):430. PubMed ID: 2468820
    [No Abstract]   [Full Text] [Related]  

  • 17. [3-hydroxy-3-methylglutaraciduria (case report of a female Turkish sisters with 3-hydroxy-3- methylglutaryl-Coenzyme A lyase deficiency].
    Koling S; Kalhoff H; Schauerte P; Lehnert W; Diekmann L
    Klin Padiatr; 2000; 212(3):113-6. PubMed ID: 10916782
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 3-hydroxy-3-methylglutaric, 3-methylglutaconic and 3-methylglutaric acids can be non-specific indicators of metabolic disease.
    Hammond J; Wilcken B
    J Inherit Metab Dis; 1984; 7 Suppl 2():117-8. PubMed ID: 6207381
    [No Abstract]   [Full Text] [Related]  

  • 19. 3-hydroxy-3-methylglutaric aciduria presenting with Reye like syndrome: report of one case.
    Lee C; Tsai FJ; Wu JY; Peng CT; Tsai CH; Hwu WL; Wang TR; Millington DS
    Acta Paediatr Taiwan; 1999; 40(6):445-7. PubMed ID: 10927963
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A neonatal case of 3-hydroxy-3-methylglutaric-coenzyme A lyase deficiency.
    Santarelli F; Cassanello M; Enea A; Poma F; D'Onofrio V; Guala G; Garrone G; Puccinelli P; Caruso U; Porta F; Spada M
    Ital J Pediatr; 2013 May; 39():33. PubMed ID: 23705938
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.