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 *

122 related articles for article (PubMed ID: 21544987)

  • 1. [Rare causes of hypoglycemia in adults--disorders of gluconeogenesis and fatty acid oxidation disorders].
    Fronczyk A; Romanowska H; Majkowska L
    Pol Merkur Lekarski; 2011 Feb; 30(176):147-9. PubMed ID: 21544987
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Rare causes of hypoglycemia in adults--glycogen storage diseases].
    Fronczyk A; Romanowska H; Majkowska L
    Pol Merkur Lekarski; 2011 Feb; 30(176):143-6. PubMed ID: 21544986
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Inborn Errors of Metabolism with Hypoglycemia: Glycogen Storage Diseases and Inherited Disorders of Gluconeogenesis.
    Weinstein DA; Steuerwald U; De Souza CFM; Derks TGJ
    Pediatr Clin North Am; 2018 Apr; 65(2):247-265. PubMed ID: 29502912
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inborn errors of organic acid metabolism.
    Green A
    Br J Hosp Med; 1989 May; 41(5):426-30, 432, 434. PubMed ID: 2663104
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Myopathies caused by defects of lipid and carbohydrate metabolism].
    Angelini C; Martinuzzi A; Micaglio G; Vergani L
    Riv Neurol; 1988; 58(1):15-25. PubMed ID: 3047844
    [No Abstract]   [Full Text] [Related]  

  • 6. [Hypoglycemias in childhood. Pathophysiologic reflections and examples of hypoglycemias in hereditary disorders of carbohydrate metabolism].
    Baerlocher K
    Monatsschr Kinderheilkd; 1988 Sep; 136(9):597-605. PubMed ID: 3070366
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Studies of metabolic disorders in children with mental retardation].
    Genova R
    Clin Pediatr (Bologna); 1971 Jan; 53(1):3-13. PubMed ID: 5121109
    [No Abstract]   [Full Text] [Related]  

  • 8. [Congenital metabolic disorders with eye manifestations].
    Oura T; Kozaki M
    Ganka; 1969 Nov; 11(11):872-83. PubMed ID: 5391925
    [No Abstract]   [Full Text] [Related]  

  • 9. [Lactic acidosis, hypoglycemia and hepatomegaly due to hereditary defect in hepatic fructose-1, 6-diphosphatase].
    Saudubray JM; Dreyfus JC; Cepanec C; Le Lo'ch H; Trung PH; Mozziconacci P
    Arch Fr Pediatr; 1973; 30(6):609-32. PubMed ID: 4156164
    [No Abstract]   [Full Text] [Related]  

  • 10. Neurometabolic disorders in infancy, childhood and adolescence.
    Hagberg B
    Acta Neurol Scand; 1967; 43(S31):13-19. PubMed ID: 5583240
    [No Abstract]   [Full Text] [Related]  

  • 11. Corneal manifestations of metabolic diseases.
    Vinals AF; Kenyon KR
    Int Ophthalmol Clin; 1998; 38(1):141-53. PubMed ID: 9532478
    [No Abstract]   [Full Text] [Related]  

  • 12. [Neonatal lactic acidosis and hypoglycemia due to a congenital hepatic fructose-1,6-diphosphatase deficiency].
    Retbi JM; Gabilan JC; Marsac C
    Arch Fr Pediatr; 1975 Apr; 32(4):367-80. PubMed ID: 169761
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [New etiologic approach to periodic ketoacidosis in children].
    Boisse J
    Can Med Assoc J; 1971 Aug; 105(3):295-300. PubMed ID: 5001373
    [No Abstract]   [Full Text] [Related]  

  • 14. Hematologic aberrations in metabolic diseases.
    Buehler BA
    Ann Clin Lab Sci; 1980; 10(6):500-7. PubMed ID: 6778367
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Suspected clinical diagnosis of genetic metabolic disorders in prevention and daily practice].
    Grosser V; Knapp A
    Z Arztl Fortbild (Jena); 1973 Dec; 67(24):1233-8. PubMed ID: 4791811
    [No Abstract]   [Full Text] [Related]  

  • 16. [Inborn errors of metabolism, associated with ocular symptoms].
    Oura T
    Nihon Ganka Kiyo; 1969 Aug; 20(8):749-58. PubMed ID: 5391478
    [No Abstract]   [Full Text] [Related]  

  • 17. [Ocular complications of congenital metabolism errors].
    Goux JP; Kallay O
    Bull Soc Belge Ophtalmol; 1971; 157(1):9-322. PubMed ID: 5565533
    [No Abstract]   [Full Text] [Related]  

  • 18. [Intestinal enzyme disorders in children].
    Schreier K
    Minerva Med; 1977 Mar; 68(15):951-9. PubMed ID: 854216
    [No Abstract]   [Full Text] [Related]  

  • 19. Defects in long chain fatty acid oxidation presenting as severe cardiomyopathy and cardiogenic shock in infancy.
    Dereddy NR; Kronn D; Krishnan U
    Cardiol Young; 2009 Sep; 19(5):540-2. PubMed ID: 19691901
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Metabolic and genetic inter-relations between arteriosclerosis and the diabetic syndrome].
    Moncada Lorenzo E
    Rev Clin Esp; 1972 Jan; 124(2):103-8. PubMed ID: 4552522
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.