BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

294 related articles for article (PubMed ID: 16602100)

  • 1. Glutaric acidemia type 1.
    Hedlund GL; Longo N; Pasquali M
    Am J Med Genet C Semin Med Genet; 2006 May; 142C(2):86-94. PubMed ID: 16602100
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Inherited Disorders of Lysine Metabolism: A Review.
    Bouchereau J; Schiff M
    J Nutr; 2020 Oct; 150(Suppl 1):2556S-2560S. PubMed ID: 33000154
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Glutaric acidemia type 1: outcomes before and after expanded newborn screening.
    Viau K; Ernst SL; Vanzo RJ; Botto LD; Pasquali M; Longo N
    Mol Genet Metab; 2012 Aug; 106(4):430-8. PubMed ID: 22728054
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision.
    Boy N; Mühlhausen C; Maier EM; Heringer J; Assmann B; Burgard P; Dixon M; Fleissner S; Greenberg CR; Harting I; Hoffmann GF; Karall D; Koeller DM; Krawinkel MB; Okun JG; Opladen T; Posset R; Sahm K; Zschocke J; Kölker S;
    J Inherit Metab Dis; 2017 Jan; 40(1):75-101. PubMed ID: 27853989
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Therapeutic modulation of cerebral L-lysine metabolism in a mouse model for glutaric aciduria type I.
    Sauer SW; Opp S; Hoffmann GF; Koeller DM; Okun JG; Kölker S
    Brain; 2011 Jan; 134(Pt 1):157-70. PubMed ID: 20923787
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Subependymal mass lesions and peripheral polyneuropathy in adult-onset glutaric aciduria type I.
    Herskovitz M; Goldsher D; Sela BA; Mandel H
    Neurology; 2013 Aug; 81(9):849-50. PubMed ID: 23884036
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Biochemistry and bioenergetics of glutaryl-CoA dehydrogenase deficiency.
    Sauer SW
    J Inherit Metab Dis; 2007 Oct; 30(5):673-80. PubMed ID: 17879145
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Glutaric acidemia type 1: Treatment and outcome of 168 patients over three decades.
    Strauss KA; Williams KB; Carson VJ; Poskitt L; Bowser LE; Young M; Robinson DL; Hendrickson C; Beiler K; Taylor CM; Haas-Givler B; Hailey J; Chopko S; Puffenberger EG; Brigatti KW; Miller F; Morton DH
    Mol Genet Metab; 2020 Nov; 131(3):325-340. PubMed ID: 33069577
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pathomechanisms of neurodegeneration in glutaryl-CoA dehydrogenase deficiency.
    Kölker S; Koeller DM; Okun JG; Hoffmann GF
    Ann Neurol; 2004 Jan; 55(1):7-12. PubMed ID: 14705106
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dynamic changes of striatal and extrastriatal abnormalities in glutaric aciduria type I.
    Harting I; Neumaier-Probst E; Seitz A; Maier EM; Assmann B; Baric I; Troncoso M; Mühlhausen C; Zschocke J; Boy NP; Hoffmann GF; Garbade SF; Kölker S
    Brain; 2009 Jul; 132(Pt 7):1764-82. PubMed ID: 19433437
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Maternal glutaric acidemia, type I identified by newborn screening.
    Crombez EA; Cederbaum SD; Spector E; Chan E; Salazar D; Neidich J; Goodman S
    Mol Genet Metab; 2008 May; 94(1):132-4. PubMed ID: 18304851
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Protective effects of L-carnitine on behavioral alterations and neuroinflammation in striatum of glutaryl-COA dehydrogenase deficient mice.
    Guerreiro G; Faverzani J; Moura AP; Volfart V; Gome Dos Reis B; Sitta A; Gonzalez EA; de Lima Rosa G; Coitinho AS; Baldo G; Wajner M; Vargas CR
    Arch Biochem Biophys; 2021 Sep; 709():108970. PubMed ID: 34181873
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Acute renal proximal tubule alterations during induced metabolic crises in a mouse model of glutaric aciduria type 1.
    Thies B; Meyer-Schwesinger C; Lamp J; Schweizer M; Koeller DM; Ullrich K; Braulke T; Mühlhausen C
    Biochim Biophys Acta; 2013 Oct; 1832(10):1463-72. PubMed ID: 23623985
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Is Expanded Newborn Screening Adequate to Detect Indian Biochemical Low Excretor Phenotype Patients of Glutaric Aciduria Type I?
    Shaik M; T P KV; Kamate M; A B V
    Indian J Pediatr; 2019 Nov; 86(11):995-1001. PubMed ID: 31302874
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Toxic synergism between quinolinic acid and organic acids accumulating in glutaric acidemia type I and in disorders of propionate metabolism in rat brain synaptosomes: Relevance for metabolic acidemias.
    Colín-González AL; Paz-Loyola AL; Serratos I; Seminotti B; Ribeiro CA; Leipnitz G; Souza DO; Wajner M; Santamaría A
    Neuroscience; 2015 Nov; 308():64-74. PubMed ID: 26343296
    [TBL] [Abstract][Full Text] [Related]  

  • 16. GAI - distinct genotype and phenotype characteristics in reported Slovak patients.
    Lisyova J; Petrovic R; Jurickova K; Brennerova K; Urbanova D; Behulova D; Bzduch V; Chandoga J
    Bratisl Lek Listy; 2016; 117(11):631-638. PubMed ID: 28125888
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Elevated glutaric acid levels in Dhtkd1-/Gcdh- double knockout mice challenge our current understanding of lysine metabolism.
    Biagosch C; Ediga RD; Hensler SV; Faerberboeck M; Kuehn R; Wurst W; Meitinger T; Kölker S; Sauer S; Prokisch H
    Biochim Biophys Acta Mol Basis Dis; 2017 Sep; 1863(9):2220-2228. PubMed ID: 28545977
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mechanism of age-dependent susceptibility and novel treatment strategy in glutaric acidemia type I.
    Zinnanti WJ; Lazovic J; Housman C; LaNoue K; O'Callaghan JP; Simpson I; Woontner M; Goodman SI; Connor JR; Jacobs RE; Cheng KC
    J Clin Invest; 2007 Nov; 117(11):3258-70. PubMed ID: 17932566
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Induction of S100B secretion in C6 astroglial cells by the major metabolites accumulating in glutaric acidemia type I.
    Quincozes-Santos A; Rosa RB; Leipnitz G; de Souza DF; Seminotti B; Wajner M; Gonçalves CA
    Metab Brain Dis; 2010 Jun; 25(2):191-8. PubMed ID: 20437086
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Selective Screening of Fatty Acids Oxidation Defects and Organic Acidemias by Liquid Chromatography/tandem Mass Spectrometry Acylcarnitine Analysis in Brazilian Patients.
    Vargas CR; Ribas GS; da Silva JM; Sitta A; Deon M; de Moura Coelho D; Wajner M
    Arch Med Res; 2018 Apr; 49(3):205-212. PubMed ID: 30119976
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.