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 *

135 related articles for article (PubMed ID: 10893736)

  • 1. [Diagnostic error of mental retardation of neurometabolic origin confirmed by mass sequential spectrometry].
    Osorio-Orozco JH; Pourfarzam M
    Rev Neurol; 2000 Apr 16-30; 30(8):728-30. PubMed ID: 10893736
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Tyrosinaemia type II: an easily diagnosed metabolic disorder with a rewarding therapeutic response.
    al-Essa MA; Rashed MS; Ozand PT
    East Mediterr Health J; 1999 Nov; 5(6):1204-7. PubMed ID: 11924112
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Richner-Hanhart syndrome detected by expanded newborn screening.
    Meissner T; Betz RC; Pasternack SM; Eigelshoven S; Ruzicka T; Kruse R; Laitenberger G; Mayatepek E
    Pediatr Dermatol; 2008; 25(3):378-80. PubMed ID: 18577048
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A rapid ultra performance liquid chromatography tandem mass spectrometric method for measuring amino acids associated with maple syrup urine disease, tyrosinaemia and phenylketonuria.
    Freeto S; Mason D; Chen J; Scott RH; Narayan SB; Bennett MJ
    Ann Clin Biochem; 2007 Sep; 44(Pt 5):474-81. PubMed ID: 17761035
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A biochemical perspective on the use of tandem mass spectrometry for newborn screening and clinical testing.
    Chace DH; Kalas TA
    Clin Biochem; 2005 Apr; 38(4):296-309. PubMed ID: 15766731
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Screening of newborns for inborn errors of metabolism by tandem mass spectrometry].
    Simonsen H
    Ugeskr Laeger; 2002 Nov; 164(48):5607-12. PubMed ID: 12523003
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Screening for congenital metabolic diseases in mentally retarded patients in 6 psychiatric institutions of Lower Saxony].
    Byrd DJ; Brötling D; Brodehl J; Hunneman DH
    Klin Padiatr; 1984; 196(5):298-303. PubMed ID: 6492685
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Application of tandem mass spectrometry on the diagnosis of fatty acid oxidation disorders].
    Han LS; Ye J; Qiu WJ; Gao XL; Wang Y; Zhang YJ; Gu XF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):692-5. PubMed ID: 18067086
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Delayed diagnosis of phenylketonuria as the cause of mental retardation in an adolescent].
    Villaverde R; Escribano JB; Salmerón P; Tortosa D; Meca J; Fernández-Barreiro A
    Rev Neurol; 1997 Dec; 25(148):1911-6. PubMed ID: 9528029
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An exceptional Albanian family with seven children presenting with dysmorphic features and mental retardation: maternal phenylketonuria.
    Knerr I; Zschocke J; Schellmoser S; Topf HG; Weigel C; Dötsch J; Rascher W
    BMC Pediatr; 2005 Apr; 5(1):5. PubMed ID: 15811181
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Further results of studies on metabolic disorders in a population of severely retarded children (2)].
    Opałka S; Galewicz A; Pisarska E; Wegrzynowicz Z
    Psychiatr Neurol Med Psychol Beih; 1968; 8-9():126-9. PubMed ID: 5006367
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [A clinico-genealogic analysis of mentally retarded patients with abnormal amino acid metabolism].
    Krasnopol'skaia KD; Marincheva GS; Stonova NS
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1975; 75(10):1539-43. PubMed ID: 1210933
    [No Abstract]   [Full Text] [Related]  

  • 13. The Vodskov project. 3. Thin-layer chromatography of amino acids in urine from mentally retarded patients. Methodology of the investigation.
    Andersen HE; Bang HO
    Dan Med Bull; 1969 Sep; 16(8):235-8. PubMed ID: 5377695
    [No Abstract]   [Full Text] [Related]  

  • 14. Incidence of phenylketonuria and other inborn errors of the amino acid metabolism in the normal and mentally retarded population.
    Hyánek J; Homolka J; Seemanová E
    Rev Czech Med; 1974; 20(1):18-22. PubMed ID: 4815837
    [No Abstract]   [Full Text] [Related]  

  • 15. [Diagnosis of inborn errors of metabolism using tandem mass spectrometry and gas chromatography mass spectrometry].
    Han LS; Ye J; Qiu WJ; Gao XL; Wang Y; Jin J; Gu XF
    Zhonghua Yi Xue Za Zhi; 2008 Aug; 88(30):2122-6. PubMed ID: 19080473
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The use of Guthrie's test to detect phenylketonuria in a population of mentally retarded individuals.
    Krasnopol'skaya KD; Martinson AE
    Sov Genet; 1974 May; 8(4):526-33. PubMed ID: 4213489
    [No Abstract]   [Full Text] [Related]  

  • 17. The results of chromatographic screening for the detection of inborn metabolic errors in normal and mentally retarded population.
    Hyánek J; Homolka J
    Acta Univ Carol Med Monogr; 1973; 56():63-6. PubMed ID: 4791780
    [No Abstract]   [Full Text] [Related]  

  • 18. [Neurometabolic diagnosis of mental retardation].
    García L
    Rev Neurol; 1997 May; 25(141):765-8. PubMed ID: 9206607
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Detection of inborn errors of metabolism in San Pablo, Brazil].
    Schmidt BJ; Diament AJ; Krynski S; Kamei ME; Rodrígues MM; Takata S
    Bol Med Hosp Infant Mex; 1981; 38(2):217-29. PubMed ID: 7259843
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [The frequency of some oligophrenias due to metabolic diseases in the grand-duchy of Luxembourg].
    Kutter D; Metz H
    Schweiz Arch Neurol Neurochir Psychiatr; 1968; 101(2):369-82. PubMed ID: 5705003
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.