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 *

178 related articles for article (PubMed ID: 29899783)

  • 21. Oxidative stress in plasma from maple syrup urine disease patients during treatment.
    Barschak AG; Sitta A; Deon M; Barden AT; Dutra-Filho CS; Wajner M; Vargas CR
    Metab Brain Dis; 2008 Mar; 23(1):71-80. PubMed ID: 18026828
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Branched-chain amino acids (BCAA) administration increases autophagy and the autophagic pathway in brain tissue of rats submitted to a Maple Syrup Urine Disease (MSUD) protocol.
    Fermo KT; da Silva Lemos I; Farias HR; Rosso MP; Effting PS; Leipnitz G; Streck EL
    Metab Brain Dis; 2023 Jan; 38(1):287-293. PubMed ID: 36305998
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Maple syrup urine disease: diffusion-weighted MRI findings during acute metabolic encephalopathic crisis.
    Kilicarslan R; Alkan A; Demirkol D; Toprak H; Sharifov R
    Jpn J Radiol; 2012 Jul; 30(6):522-5. PubMed ID: 22476847
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Antioxidant administration prevents memory impairment in an animal model of maple syrup urine disease.
    Scaini G; Teodorak BP; Jeremias IC; Morais MO; Mina F; Dominguini D; Pescador B; Comim CM; Schuck PF; Ferreira GC; Quevedo J; Streck EL
    Behav Brain Res; 2012 May; 231(1):92-6. PubMed ID: 22433584
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Definition of the mutation responsible for maple syrup urine disease in Poll Shorthorns and genotyping Poll Shorthorns and Poll Herefords for maple syrup urine disease alleles.
    Dennis JA; Healy PJ
    Res Vet Sci; 1999 Aug; 67(1):1-6. PubMed ID: 10425233
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Lipid changes in the metabolome of a single case study with maple syrup urine disease (MSUD) after five days of improved diet adherence of controlled branched-chain amino acids (BCAA).
    Douglas TD; Newby LK; Eckstrand J; Wixted D; Singh RH
    Mol Genet Metab Rep; 2020 Dec; 25():100651. PubMed ID: 33088714
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Maple syrup urine disease: diffusion-weighted and diffusion-tensor magnetic resonance imaging findings.
    Parmar H; Sitoh YY; Ho L
    J Comput Assist Tomogr; 2004; 28(1):93-7. PubMed ID: 14716239
    [TBL] [Abstract][Full Text] [Related]  

  • 28. L-carnitine Prevents Oxidative Stress in the Brains of Rats Subjected to a Chemically Induced Chronic Model of MSUD.
    Mescka CP; Rosa AP; Schirmbeck G; da Rosa TH; Catarino F; de Souza LO; Guerreiro G; Sitta A; Vargas CR; Dutra-Filho CS
    Mol Neurobiol; 2016 Nov; 53(9):6007-6017. PubMed ID: 26526843
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Acrodermatitis dysmetabolica in an infant with maple syrup urine disease.
    Flores K; Chikowski R; Morrell DS
    Clin Exp Dermatol; 2016 Aug; 41(6):651-4. PubMed ID: 27334242
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Dysmyelination in the brain of adolescents and young adults with maple syrup urine disease.
    Schönberger S; Schweiger B; Schwahn B; Schwarz M; Wendel U
    Mol Genet Metab; 2004 May; 82(1):69-75. PubMed ID: 15110325
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Case report: Aqueous and Vitreous amino-acid concentrations in a patient with maple syrup urine disease operated on rhegmatogenous retinal detachment.
    Kanakis MG; Michelakakis H; Petrou P; Koutsandrea C; Georgalas I
    BMC Ophthalmol; 2016 Oct; 16(1):170. PubMed ID: 27716111
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prevention of DNA damage by L-carnitine induced by metabolites accumulated in maple syrup urine disease in human peripheral leukocytes in vitro.
    Mescka CP; Wayhs CA; Guerreiro G; Manfredini V; Dutra-Filho CS; Vargas CR
    Gene; 2014 Sep; 548(2):294-8. PubMed ID: 25046137
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Atypical phenotype in a boy with a maple syrup urine disease.
    Ben-Omran TI; Blaser S; Phillips H; Callahan J; Feigenbaum A
    J Inherit Metab Dis; 2006 Feb; 29(1):195-200. PubMed ID: 16601891
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Creatine kinase activity from rat brain is inhibited by branched-chain amino acids in vitro.
    Pilla C; Cardozo RF; Dutra-Filho CS; Wyse AT; Wajner M; Wannmacher CM
    Neurochem Res; 2003 May; 28(5):675-9. PubMed ID: 12716015
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Branched-Chain Amino Acids and Brain Metabolism.
    Sperringer JE; Addington A; Hutson SM
    Neurochem Res; 2017 Jun; 42(6):1697-1709. PubMed ID: 28417264
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Expression of mitochondrial branched-chain aminotransferase and α-keto-acid dehydrogenase in rat brain: implications for neurotransmitter metabolism.
    Cole JT; Sweatt AJ; Hutson SM
    Front Neuroanat; 2012; 6():18. PubMed ID: 22654736
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Plasma amino acid analyses in two cases of maple syrup urine disease.
    Surarit R; Srisomsap C; Wasant P; Svasti J; Suthatvoravut U; Chokchaichamnankit D; Liammongkolkul S
    Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():138-9. PubMed ID: 11400750
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Administration of branched-chain amino acids increases the susceptibility to lipopolysaccharide-induced inflammation in young Wistar rats.
    Wessler LB; de Miranda Ramos V; Bittencourt Pasquali MA; Fonseca Moreira JC; de Oliveira J; Scaini G; Streck EL
    Int J Dev Neurosci; 2019 Nov; 78():210-214. PubMed ID: 31330240
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Second-tier test for quantification of alloisoleucine and branched-chain amino acids in dried blood spots to improve newborn screening for maple syrup urine disease (MSUD).
    Oglesbee D; Sanders KA; Lacey JM; Magera MJ; Casetta B; Strauss KA; Tortorelli S; Rinaldo P; Matern D
    Clin Chem; 2008 Mar; 54(3):542-9. PubMed ID: 18178665
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Expanding the genetic and phenotypic spectrum of branched-chain amino acid transferase 2 deficiency.
    Knerr I; Colombo R; Urquhart J; Morais A; Merinero B; Oyarzabal A; Pérez B; Jones SA; Perveen R; Preece MA; Rogers Y; Treacy EP; Mayne P; Zampino G; MacKinnon S; Wassmer E; Yue WW; Robinson I; Rodríguez-Pombo P; Olpin SE; Banka S
    J Inherit Metab Dis; 2019 Sep; 42(5):809-817. PubMed ID: 31177572
    [TBL] [Abstract][Full Text] [Related]  

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