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 *

266 related articles for article (PubMed ID: 3063529)

  • 21. 3-HMG Coenzyme A Lyase Deficiency: Macrocephaly and Left Ventricular Noncompaction with a Novel Mutation.
    Köksal T; Gündüz M; Özaydın E; Azak E
    Indian J Pediatr; 2015 Jul; 82(7):645-8. PubMed ID: 25708061
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 3-hydroxy-3-methylglutaryl-CoA lyase deficiency in an infant with macrocephaly and mild metabolic acidosis.
    Leupold D; Bojasch M; Jakobs C
    Eur J Pediatr; 1982 Feb; 138(1):73-6. PubMed ID: 7075630
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Studies on a child suspected of having a dficiency in 3-hydroxy-3-methylglutaryl-Co A lyase.
    Truscott RJ; Halpern B; Wysocki SJ; Hähnel R; Wilcken B
    Clin Chim Acta; 1979 Jul; 95(1):11-16. PubMed ID: 509721
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: Clinical presentation and outcome in a series of 37 patients.
    Grünert SC; Schlatter SM; Schmitt RN; Gemperle-Britschgi C; Mrázová L; Balcı MC; Bischof F; Çoker M; Das AM; Demirkol M; de Vries M; Gökçay G; Häberle J; Uçar SK; Lotz-Havla AS; Lücke T; Roland D; Rutsch F; Santer R; Schlune A; Staufner C; Schwab KO; Mitchell GA; Sass JO
    Mol Genet Metab; 2017 Jul; 121(3):206-215. PubMed ID: 28583327
    [TBL] [Abstract][Full Text] [Related]  

  • 25. MR imaging and proton spectroscopy in 3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency.
    van der Knaap MS; Bakker HD; Valk J
    AJNR Am J Neuroradiol; 1998 Feb; 19(2):378-82. PubMed ID: 9504498
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency.
    Walter JH; Clayton PT; Leonard JV
    J Inherit Metab Dis; 1986; 9(3):287-8. PubMed ID: 3099075
    [No Abstract]   [Full Text] [Related]  

  • 27. 3-Hydroxy-3-methylglutaric aciduria: 3-hydroxy-3-methylglutaryl-coenzyme A lyase levels in leucocytes.
    Wysocki SJ; Hähnel R
    Clin Chim Acta; 1976 Dec; 73(2):373-5. PubMed ID: 1000856
    [No Abstract]   [Full Text] [Related]  

  • 28. 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease - many faces.
    Grünert SC; Sass JO
    Orphanet J Rare Dis; 2020 Feb; 15(1):48. PubMed ID: 32059735
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 3-Hydroxy-3-methylglutaryl coenzyme a lyase deficiency with reversible white matter changes after treatment.
    Zafeiriou DI; Vargiami E; Mayapetek E; Augoustidou-Savvopoulou P; Mitchell GA
    Pediatr Neurol; 2007 Jul; 37(1):47-50. PubMed ID: 17628222
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Clinical and biochemical observations on a child with a deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase.
    Ketel A; Ket JL; Schutgens RB; Duran M; Wadman SK
    J Inherit Metab Dis; 1980; 3(3):89-90. PubMed ID: 6158624
    [No Abstract]   [Full Text] [Related]  

  • 31. The management of pregnancy and delivery in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.
    Pipitone A; Raval DB; Duis J; Vernon H; Martin R; Hamosh A; Valle D; Gunay-Aygun M
    Am J Med Genet A; 2016 Jun; 170(6):1600-2. PubMed ID: 26997609
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Lethal hypoglycemia in a child with a deficiency of 3-hydroxy-3-methylglutarylcoenzyme A lyase.
    Schutgens RB; Heymans H; Ketel A; Veder HA; Duran M; Ketting D; Wadman SK
    J Pediatr; 1979 Jan; 94(1):89-91. PubMed ID: 758433
    [No Abstract]   [Full Text] [Related]  

  • 33. 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]  

  • 34. A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.
    Wilson WG; Cass MB; Søvik O; Gibson KM; Sweetman L
    Eur J Pediatr; 1984 Sep; 142(4):289-91. PubMed ID: 6489380
    [TBL] [Abstract][Full Text] [Related]  

  • 35. First report of type 2 diabetes mellitus in an adult with 3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency.
    Lai V; Shahidi M; Chan A; Jain-Ghai S
    Endocrinol Diabetes Metab Case Rep; 2023 Mar; 2023(1):. PubMed ID: 36988218
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Sudden death of a patient with 3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency].
    Vilaseca Busca MA; Ribes Rubio A; Briones Godino P; Cusi Sánchez V; Baraíbar Castelló R; Gairi Taull JM
    An Esp Pediatr; 1990 Feb; 32(2):149-53. PubMed ID: 1971743
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 3-Hydroxy-3-methylglutaric aciduria: deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase.
    Wysocki SJ; Hähnel R
    Clin Chim Acta; 1976 Sep; 71(2):349-51. PubMed ID: 963901
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Management and long-term evolution of a patient with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency.
    Muñoz-Bonet JI; Ortega-Sánchez MD; León Guijarro JL
    Ital J Pediatr; 2017 Jan; 43(1):12. PubMed ID: 28257639
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Enzymatic diagnosis of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency with high-performance liquid chromatography.
    Kikuchi M; Narisawa K; Tada K; Sweetman L
    Clin Chim Acta; 1990 Aug; 189(3):297-301. PubMed ID: 2225461
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The E37X is a common HMGCL mutation in Portuguese patients with 3-hydroxy-3-methylglutaric CoA lyase deficiency.
    Cardoso ML; Rodrigues MR; Leão E; Martins E; Diogo L; Rodrigues E; Garcia P; Rolland MO; Vilarinho L
    Mol Genet Metab; 2004 Aug; 82(4):334-8. PubMed ID: 15308132
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.