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 *

246 related articles for article (PubMed ID: 22184735)

  • 1. Newborn screening for inborn errors of metabolism in Beijing, China: 22 years of experience.
    Tu WJ; Cai J; Shi XD
    J Med Screen; 2011; 18(4):213-4. PubMed ID: 22184735
    [No Abstract]   [Full Text] [Related]  

  • 2. Issues in antenatal and neonatal screening and surveillance for hereditary and congenital disorders.
    Holtzman NA; Leonard CO; Farfel MR
    Annu Rev Public Health; 1981; 2():219-51. PubMed ID: 7348552
    [No Abstract]   [Full Text] [Related]  

  • 3. Inherited metabolic disorders: from the newborn to the mother and beyond.
    Levy HL
    Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():119-20. PubMed ID: 11400747
    [No Abstract]   [Full Text] [Related]  

  • 4. Neonatal screening of phenylketonuria and congenital hypothyroidism in China.
    Fan GX; Jun Y; Rui-guan C
    Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():17-9. PubMed ID: 11400761
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Neonatal screening for inborn errors of metabolism: update.
    Seashore MR
    Semin Perinatol; 1990 Dec; 14(6):431-8. PubMed ID: 2077663
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Expanded newborn screening in the Region of Murcia, Spain. Three-years experience].
    Juan-Fita MJ; Egea-Mellado JM; González-Gallego I; Moya-Quiles MR; Fernández-Sánchez A
    Med Clin (Barc); 2012 Dec; 139(13):566-71. PubMed ID: 22137990
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [After PKU and hypothyroidism, what other screening?].
    Frézal J; Briard ML; Saudubray JM
    J Genet Hum; 1981 Mar; 29(1):47-57. PubMed ID: 7334341
    [No Abstract]   [Full Text] [Related]  

  • 8. Detection of other inborn errors of metabolism in hyperphenylalaninemic babies picked up on narrow-spectrum screening programs.
    Unal O; Oztürk-Hişmi B; Coşkun T; Tokatlı A; Dursun A; Sivri HS
    Turk J Pediatr; 2012; 54(4):409-12. PubMed ID: 23692723
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Laboratory examinations for inborn errors of metabolism].
    Kawamura M
    Rinsho Byori; 1986 Feb; 34(2):133-5. PubMed ID: 3702083
    [No Abstract]   [Full Text] [Related]  

  • 10. Neonatal screening for biochemical disorders.
    Holton JB
    Br J Hosp Med; 1988 Apr; 39(4):317-9, 322-4. PubMed ID: 3164641
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Expanded newborn screening using tandem mass spectrometry.
    Fearing MK; Levy HL
    Adv Pediatr; 2003; 50():81-111. PubMed ID: 14626484
    [No Abstract]   [Full Text] [Related]  

  • 12. [Neonatal screening for congenital errors of metabolism by means of Tandem Mass: Italian experience].
    Cerone R; Cassanello M; Caruso U; Schiaffino MC; Lorini R
    Minerva Pediatr; 2007 Oct; 59(5):488-9. PubMed ID: 17947884
    [No Abstract]   [Full Text] [Related]  

  • 13. [History and prospect of the neonatal screening program for inborn errors of metabolism].
    Gu XF
    Zhonghua Er Ke Za Zhi; 2005 May; 43(5):321-4. PubMed ID: 15924741
    [No Abstract]   [Full Text] [Related]  

  • 14. Austria newborn screening programme for inborn errors of metabolism.
    Thalhammer O
    Acta Univ Carol Med Monogr; 1973; 56():79-82. PubMed ID: 4791784
    [No Abstract]   [Full Text] [Related]  

  • 15. Pitfalls in newborn screening.
    Crombez E; Koch R; Cederbaum S
    J Pediatr; 2005 Jul; 147(1):119-20. PubMed ID: 16027710
    [No Abstract]   [Full Text] [Related]  

  • 16. [Screening and group distribute regularity of congenital hypothyroidism of neonatal in Henan province].
    Wang J; Wang BZ; Zhang Z; Hu YL; Zhao DH; Su L; Meng Y
    Zhonghua Liu Xing Bing Xue Za Zhi; 2006 Sep; 27(9):825-6. PubMed ID: 17299975
    [No Abstract]   [Full Text] [Related]  

  • 17. Newborn screening in southeastern Europe.
    Groselj U; Tansek MZ; Smon A; Angelkova N; Anton D; Baric I; Djordjevic M; Grimci L; Ivanova M; Kadam A; Kotori VM; Maksic H; Marginean O; Margineanu O; Milijanovic O; Moldovanu F; Muresan M; Murko S; Nanu M; Lampret BR; Samardzic M; Sarnavka V; Savov A; Stojiljkovic M; Suzic B; Tincheva R; Tahirovic H; Toromanovic A; Usurelu N; Battelino T
    Mol Genet Metab; 2014; 113(1-2):42-5. PubMed ID: 25174966
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Neonatal diagnosis of hereditary metabolic diseases].
    Lambotte C
    Rev Med Liege; 1973 Dec; 28(24):837-51. PubMed ID: 4769974
    [No Abstract]   [Full Text] [Related]  

  • 19. Neonatal screening for metabolic diseases in Missouri.
    Haibach H; Woodruff CW
    Mo Med; 1982 Sep; 79(9):615-20. PubMed ID: 7177101
    [No Abstract]   [Full Text] [Related]  

  • 20. Improvements to the newborn bloodspot screening service are required to meet national standards.
    Bello S; Ferguson C; Wallis R
    J Med Screen; 2010; 17(3):114-20. PubMed ID: 20956720
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.