BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 21298421)

  • 21. Detection of inborn errors of metabolism using GC-MS: over 3 years of experience in southern China.
    Jiang M; Liu L; Mei H; Li X; Cheng J; Cai Y
    J Pediatr Endocrinol Metab; 2015 Mar; 28(3-4):375-80. PubMed ID: 25781538
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Simultaneous LC-MS/MS determination of phenylbutyrate, phenylacetate benzoate and their corresponding metabolites phenylacetylglutamine and hippurate in blood and urine.
    Laryea MD; Herebian D; Meissner T; Mayatepek E
    J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S321-8. PubMed ID: 20694517
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Lysinuric protein intolerance.
    Simell O; Perheentupa J; Rapola J; Visakorpi JK; Eskelin LE
    Am J Med; 1975 Aug; 59(2):229-40. PubMed ID: 1155480
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Urea cycle disorders in Thai infants: a report of 5 cases.
    Wasant P; Srisomsap C; Liammongkolkul S; Svasti J
    J Med Assoc Thai; 2002 Aug; 85 Suppl 2():S720-31. PubMed ID: 12403252
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Diagnosis and monitoring of inborn errors of metabolism using urease-pretreatment of urine, isotope dilution, and gas chromatography-mass spectrometry.
    Kuhara T
    J Chromatogr B Analyt Technol Biomed Life Sci; 2002 Dec; 781(1-2):497-517. PubMed ID: 12450676
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Quantitation of orotic acid in urine using isotope dilution-selected ion gas chromatography-mass spectrometry.
    Chen J; Bennett MJ
    Methods Mol Biol; 2010; 603():445-51. PubMed ID: 20077096
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hyperammonemia in lysinuric protein intolerance.
    Kato T; Mizutani N; Ban M
    Pediatrics; 1984 Apr; 73(4):489-92. PubMed ID: 6424086
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Plasma glutamine concentration: a guide in the management of urea cycle disorders.
    Maestri NE; McGowan KD; Brusilow SW
    J Pediatr; 1992 Aug; 121(2):259-61. PubMed ID: 1640294
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Clinical course of 63 patients with neonatal onset urea cycle disorders in the years 2001-2013.
    Unsinn C; Das A; Valayannopoulos V; Thimm E; Beblo S; Burlina A; Konstantopoulou V; Mayorandan S; de Lonlay P; Rennecke J; Derbinski J; Hoffmann GF; Häberle J
    Orphanet J Rare Dis; 2016 Aug; 11(1):116. PubMed ID: 27538463
    [TBL] [Abstract][Full Text] [Related]  

  • 30. ω-Amidase: an underappreciated, but important enzyme in L-glutamine and L-asparagine metabolism; relevance to sulfur and nitrogen metabolism, tumor biology and hyperammonemic diseases.
    Cooper AJ; Shurubor YI; Dorai T; Pinto JT; Isakova EP; Deryabina YI; Denton TT; Krasnikov BF
    Amino Acids; 2016 Jan; 48(1):1-20. PubMed ID: 26259930
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Decreased plasma l-arginine levels in organic acidurias (MMA and PA) and decreased plasma branched-chain amino acid levels in urea cycle disorders as a potential cause of growth retardation: Options for treatment.
    Molema F; Gleich F; Burgard P; van der Ploeg AT; Summar ML; Chapman KA; Lund AM; Rizopoulos D; Kölker S; Williams M;
    Mol Genet Metab; 2019 Apr; 126(4):397-405. PubMed ID: 30827756
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Assessment of plasma ammonia and glutamine concentrations in urea cycle disorders.
    Serrano M; Ormazábal A; Vilaseca MA; Lambruschini N; Garcia-Romero R; Meavilla S; Perez-Dueñas B; Pineda M; Garcia-Cazorla A; Campistol J; Artuch R
    Clin Biochem; 2011 Jun; 44(8-9):742-4. PubMed ID: 21497589
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Glycerol phenylbutyrate treatment in children with urea cycle disorders: pooled analysis of short and long-term ammonia control and outcomes.
    Berry SA; Lichter-Konecki U; Diaz GA; McCandless SE; Rhead W; Smith W; Lemons C; Nagamani SC; Coakley DF; Mokhtarani M; Scharschmidt BF; Lee B
    Mol Genet Metab; 2014 May; 112(1):17-24. PubMed ID: 24630270
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Gas chromatography/mass spectrometry-based urine metabolome study in children for inborn errors of metabolism: An Indian experience.
    Hampe MH; Panaskar SN; Yadav AA; Ingale PW
    Clin Biochem; 2017 Feb; 50(3):121-126. PubMed ID: 27784639
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Diagnostic challenges of aminoacidopathies and organic acidemias in a developing country: a twelve-year experience.
    Karam PE; Habbal MZ; Mikati MA; Zaatari GE; Cortas NK; Daher RT
    Clin Biochem; 2013 Dec; 46(18):1787-92. PubMed ID: 23994778
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Propionic acidemia and hyperlysinemia in a case with ornithine transcarbamylase (OTC) deficiency.
    Krieger I; Bachmann C; Gronemeyer WH; Cejka J
    J Clin Endocrinol Metab; 1976 Oct; 43(4):796-802. PubMed ID: 977722
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Inherited hyperammonemia].
    Bik-Multanowski M
    Przegl Lek; 1998; 55(6):337-41. PubMed ID: 9857711
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis.
    Brusilow SW
    J Clin Invest; 1984 Dec; 74(6):2144-8. PubMed ID: 6511918
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Survival after treatment with phenylacetate and benzoate for urea-cycle disorders.
    Enns GM; Berry SA; Berry GT; Rhead WJ; Brusilow SW; Hamosh A
    N Engl J Med; 2007 May; 356(22):2282-92. PubMed ID: 17538087
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Hyperammonemia.
    Batshaw ML
    Curr Probl Pediatr; 1984 Nov; 14(11):1-69. PubMed ID: 6510017
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.