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 *

155 related articles for article (PubMed ID: 25012580)

  • 21. Newborn screening for inborn errors of metabolism: a systematic review.
    Seymour CA; Thomason MJ; Chalmers RA; Addison GM; Bain MD; Cockburn F; Littlejohns P; Lord J; Wilcox AH
    Health Technol Assess; 1997; 1(11):i-iv, 1-95. PubMed ID: 9483156
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Diagnosis of inborn errors of metabolism using filter paper urine, urease treatment, isotope dilution and gas chromatography-mass spectrometry.
    Kuhara T
    J Chromatogr B Biomed Sci Appl; 2001 Jul; 758(1):3-25. PubMed ID: 11482733
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Present status of expanded newborn screening project for inborn errors of metabolism by tandem mass spectrometry].
    Kuhara T
    Nihon Eiseigaku Zasshi; 2014; 69(1):60-74. PubMed ID: 24476596
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Neonatal screening for biotidinidase deficiency: results of a 1-year pilot study in four cities in central Anatolia.
    Tanzer F; Sancaktar M; Buyukkayhan D
    J Pediatr Endocrinol Metab; 2009 Dec; 22(12):1113-6. PubMed ID: 20333870
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [A pilot study of selective screening for high risk children with inborn error of metabolism using tandem mass spectrometry in China].
    Gu XF; Han LS; Gao XL; Yan YL; Ye J; Qiu WJ
    Zhonghua Er Ke Za Zhi; 2004 Jun; 42(6):401-4. PubMed ID: 15265419
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Diagnostic contribution of metabolic workup for neonatal inherited metabolic disorders in the absence of expanded newborn screening.
    Bower A; Imbard A; Benoist JF; Pichard S; Rigal O; Baud O; Schiff M
    Sci Rep; 2019 Oct; 9(1):14098. PubMed ID: 31575911
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Novel mutations cause biotinidase deficiency in Turkish children.
    Pomponio RJ; Coskun T; Demirkol M; Tokatli A; Ozalp I; Hüner G; Baykal T; Wolf B
    J Inherit Metab Dis; 2000 Mar; 23(2):120-8. PubMed ID: 10801053
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Application of gas chromatography-mass spectrometry analysis on urine filter paper in the high-risk screening and diagnosis of inherited metabolic diseases].
    Luo XP; Wang MT; Wei H; Liang Y; Wang HW; Lin HH; Dong YS; Liu WJ; Fang JM; Ning Q
    Zhonghua Er Ke Za Zhi; 2003 Apr; 41(4):245-8. PubMed ID: 14754523
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Untargeted Metabolomics-Based Screening Method for Inborn Errors of Metabolism using Semi-Automatic Sample Preparation with an UHPLC- Orbitrap-MS Platform.
    Bonte R; Bongaerts M; Demirdas S; Langendonk JG; Huidekoper HH; Williams M; Onkenhout W; Jacobs EH; Blom HJ; Ruijter GJG
    Metabolites; 2019 Nov; 9(12):. PubMed ID: 31779119
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Bloodspot acylcarnitine and amino acid analysis in cord blood samples: efficacy and reference data from a large cohort study.
    Walter JH; Patterson A; Till J; Besley GT; Fleming G; Henderson MJ
    J Inherit Metab Dis; 2009 Feb; 32(1):95-101. PubMed ID: 19191006
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The Urinary Metabolome of Healthy Newborns.
    López-Hernández Y; Oropeza-Valdez JJ; Blanco-Sandate JO; Herrera-Van Oostdam AS; Zheng J; Chi Guo A; Lima-Rogel V; Rajabzadeh R; Salgado-Bustamante M; Adrian-Lopez J; Castillo CG; Robles Arguelles E; Monárrez-Espino J; Mandal R; Wishart DS
    Metabolites; 2020 Apr; 10(4):. PubMed ID: 32340350
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Validation of an ESI-MS/MS screening method for acylcarnitine profiling in urine specimens of neonates, children, adolescents and adults.
    Mueller P; Schulze A; Schindler I; Ethofer T; Buehrdel P; Ceglarek U
    Clin Chim Acta; 2003 Jan; 327(1-2):47-57. PubMed ID: 12482618
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Structural elucidation of novel biomarkers of known metabolic disorders based on multistage fragmentation mass spectra.
    Václavík J; Coene KLM; Vrobel I; Najdekr L; Friedecký D; Karlíková R; Mádrová L; Petsalo A; Engelke UFH; van Wegberg A; Kluijtmans LAJ; Adam T; Wevers RA
    J Inherit Metab Dis; 2018 May; 41(3):407-414. PubMed ID: 29139026
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The national Austrian newborn screening program - eight years experience with mass spectrometry. past, present, and future goals.
    Kasper DC; Ratschmann R; Metz TF; Mechtler TP; Möslinger D; Konstantopoulou V; Item CB; Pollak A; Herkner KR
    Wien Klin Wochenschr; 2010 Nov; 122(21-22):607-13. PubMed ID: 20938748
    [TBL] [Abstract][Full Text] [Related]  

  • 36. LC-MS/MS method for the differential diagnosis of treatable early onset inherited metabolic epilepsies.
    Mathis D; Beese K; Rüegg C; Plecko B; Hersberger M
    J Inherit Metab Dis; 2020 Sep; 43(5):1102-1111. PubMed ID: 32319100
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Incidence of newborn screening disorders among 56632 infants in Central Saudi Arabia. A 6-year study.
    Mohamed S; Elsheikh W; Al-Aqeel AI; Alhashem AM; Alodaib A; Alahaideb L; Almashary M; Alharbi F; AlMalawi H; Ammari A; Almohaimeed S
    Saudi Med J; 2020 Jul; 41(7):703-708. PubMed ID: 32601637
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The first Mongolian cases of phenylketonuria in selective screening of inborn errors of metabolism.
    Purevsuren J; Bolormaa B; Narantsetseg C; Batsolongo R; Enkhchimeg O; Bayalag M; Hasegawa Y; Shintaku H; SeijiYamaguchi
    Mol Genet Metab Rep; 2016 Dec; 9():71-74. PubMed ID: 27830119
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Accurate Identification of Unknown and Known Metabolic Mixture Components by Combining 3D NMR with Fourier Transform Ion Cyclotron Resonance Tandem Mass Spectrometry.
    Wang C; He L; Li DW; Bruschweiler-Li L; Marshall AG; Brüschweiler R
    J Proteome Res; 2017 Oct; 16(10):3774-3786. PubMed ID: 28795575
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Inborn errors of metabolism detectable by tandem mass spectrometry in Egypt: The first newborn screening pilot study.
    Hassan FA; El-Mougy F; Sharaf SA; Mandour I; Morgan MF; Selim LA; Hassan SA; Salem F; Oraby A; Girgis MY; Mahmoud IG; El-Badawy A; El-Nekhely I; Moharam N; Mehaney DA; Elmonem MA
    J Med Screen; 2016 Sep; 23(3):124-9. PubMed ID: 26790708
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.