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 *

120 related articles for article (PubMed ID: 6941627)

  • 41. Relationship between adipic acid concentration and the core symptoms of autism spectrum disorders.
    Puig-Alcaraz C; Fuentes-Albero M; Cauli O
    Psychiatry Res; 2016 Aug; 242():39-45. PubMed ID: 27259135
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Metabolism of dicarboxylic acids in vivo and in the perfused kidney of the rat.
    Bergseth S; Hokland BM; Bremer J
    Biochim Biophys Acta; 1988 Jul; 961(1):103-9. PubMed ID: 3132982
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Clinical and laboratory observations in a child with hepatic phosphorylase kinase deficiency.
    Tuchman M; Brown BI; Burke BA; Ulstrom RA
    Metabolism; 1986 Jul; 35(7):627-33. PubMed ID: 3459948
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Gas chromatography-mass spectrometry of saturated and unsaturated dicarboxylic acids in urine.
    Liebich HM; Pickert A; Stierle U; Wöll J
    J Chromatogr; 1980 Oct; 199():181-9. PubMed ID: 6778884
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Hyperthermia and ketoacidosis during anesthesia in a child with glycogen-storage disease.
    Edelstein G; Hirshman CA
    Anesthesiology; 1980 Jan; 52(1):90-2. PubMed ID: 6928093
    [No Abstract]   [Full Text] [Related]  

  • 46. Azelaic and pimelic acids: metabolic intermediates or artefacts?
    Bennett MJ; Ragni MC; Hood I; Hale DE
    J Inherit Metab Dis; 1992; 15(2):220-3. PubMed ID: 1527989
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels.
    Stanley CA; Hale DE; Coates PM; Hall CL; Corkey BE; Yang W; Kelley RI; Gonzales EL; Williamson JR; Baker L
    Pediatr Res; 1983 Nov; 17(11):877-84. PubMed ID: 6646897
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Urinary excretion of acetylcarnitine during human diabetic and fasting ketosis.
    Hoppel CL; Genuth SM
    Am J Physiol; 1982 Aug; 243(2):E168-72. PubMed ID: 6810706
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Prenatal diagnosis of glutaric aciduria type II by direct chemical analysis of dicarboxylic acids in amniotic fluid.
    Jakobs C; Sweetman L; Wadman SK; Duran M; Saudubray JM; Nyhan WL
    Eur J Pediatr; 1984 Jan; 141(3):153-7. PubMed ID: 6698061
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Some cases of Type III glycogen storage disease.
    Rosenfield EL; Popova IA; Chibisov IV
    Clin Chim Acta; 1976 Mar; 67(2):123-30. PubMed ID: 1061645
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Dicarboxylic acids and the lipid metabolism.
    Mortensen PB
    Dan Med Bull; 1984 Apr; 31(2):121-45. PubMed ID: 6426867
    [No Abstract]   [Full Text] [Related]  

  • 52. Urinary 3-hydroxyadipic acid 3,6-lactone: structural identification and effect of fasting in adults and children.
    Tserng KY; Jin SJ; Hoppel CL; Kerr DS; Genuth SM
    Metabolism; 1989 Jul; 38(7):655-61. PubMed ID: 2739576
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Dicarboxylic Acid Excretion in Normal Formula-Fed and Breastfed Infants.
    Anderson M; Eliot K; Kelly P; Shoemaker J
    Nutr Clin Pract; 2016 Dec; 31(6):819-823. PubMed ID: 27153855
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Ketosis in hepatic glycogenosis.
    Fernandes J; Pikaar NA
    Arch Dis Child; 1972 Feb; 47(251):41-6. PubMed ID: 4336232
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Demonstration of N-dicarboxyl-mono-glycines in dicarboxylic acidurias by mass fragmentography.
    Gregersen N; Kolvraa S; Rasmussen K; Gron I
    Clin Chim Acta; 1977 Jul; 78(2):173-82. PubMed ID: 884855
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Hyperuricemia and dicarboxylicaciduria in glycogen storage disease.
    Dosman JA; Crawhill JC; Klassen GA; Mamer OA
    Adv Exp Med Biol; 1973; 41():361-6. PubMed ID: 4524742
    [No Abstract]   [Full Text] [Related]  

  • 57. [Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II)].
    Liang Y; Liu L; Wei H; Luo XP; Wang MT
    Zhonghua Er Ke Za Zhi; 2003 Dec; 41(12):916-20. PubMed ID: 14723814
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Transient carnitine-responsive medium-chain dicarboxylic aciduria in an infant with cholestasis, hypoglycemia and cardiac failure.
    Matsuo M; Saiki K; Momota T; Ishida A; Kanazawa K; Murakami R; Nakamura H; Matsuo T
    Acta Paediatr Jpn; 1989 Apr; 31(2):211-5. PubMed ID: 2516701
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Structure of some aliphatic dicarboxylic acids found in the urine of an infant with congenital lactic acidosis.
    Lindstedt S; Norberg K; Steen G; Wahl E
    Clin Chem; 1976 Aug; 22(8):1330-8. PubMed ID: 181179
    [TBL] [Abstract][Full Text] [Related]  

  • 60. C6-C10-dicarboxylic acids in liver and kidney tissue in normal, diabetic ketotic and clofibrate-treated rats.
    Mortensen PB
    Biochim Biophys Acta; 1986 Aug; 878(1):14-9. PubMed ID: 3089293
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.