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 *

222 related articles for article (PubMed ID: 25720200)

  • 1. Newborn screening programme expanded.
    Community Pract; 2015 Feb; 88(2):5. PubMed ID: 25720200
    [No Abstract]   [Full Text] [Related]  

  • 2. Newborn babies will be tested for four more disorders, committee decides.
    Hawkes N
    BMJ; 2014 May; 348():g3267. PubMed ID: 25134132
    [No Abstract]   [Full Text] [Related]  

  • 3. Screening programme. Changes in the pipeline.
    Midwives; 2014; 17(5):10. PubMed ID: 25328969
    [No Abstract]   [Full Text] [Related]  

  • 4. Systematic review and meta-analysis to estimate the birth prevalence of five inherited metabolic diseases.
    Moorthie S; Cameron L; Sagoo GS; Bonham JR; Burton H
    J Inherit Metab Dis; 2014 Nov; 37(6):889-98. PubMed ID: 25022222
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prevention team.
    Hawkes N
    BMJ; 2016 Mar; 352():i1680. PubMed ID: 27012884
    [No Abstract]   [Full Text] [Related]  

  • 6. Extended newborn screening: an update for the general paediatrician.
    Coman D; Bhattacharya K
    J Paediatr Child Health; 2012 Feb; 48(2):E68-72. PubMed ID: 22017206
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Metabolic Serendipities of Expanded Newborn Screening.
    Yahyaoui R; Blasco-Alonso J; Gonzalo-Marín M; Benito C; Serrano-Nieto J; González-Gallego I; Ruiz-Sala P; Pérez B; González-Lamuño D
    Genes (Basel); 2020 Aug; 11(9):. PubMed ID: 32872442
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Decline of acute encephalopathic crises in children with glutaryl-CoA dehydrogenase deficiency identified by newborn screening in Germany.
    Kölker S; Garbade SF; Boy N; Maier EM; Meissner T; Mühlhausen C; Hennermann JB; Lücke T; Häberle J; Baumkötter J; Haller W; Muller E; Zschocke J; Burgard P; Hoffmann GF
    Pediatr Res; 2007 Sep; 62(3):357-63. PubMed ID: 17622945
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Progress of glutaric aciduria type I].
    Gao JZ; Luo XP
    Zhonghua Er Ke Za Zhi; 2012 Dec; 50(12):912-4. PubMed ID: 23324148
    [No Abstract]   [Full Text] [Related]  

  • 10. [Screening newborn infants for phenylketonuria, histadinemia, homocystinuria and maple syrup disease. Results from north rhein-westphalia (1974-1976) (author's transl].
    Menne F; Otte HJ; Krüger M; Winterhoff D
    MMW Munch Med Wochenschr; 1978 May; 120(18):619-22. PubMed ID: 306535
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An Economic Evaluation of Neonatal Screening for Inborn Errors of Metabolism Using Tandem Mass Spectrometry in Thailand.
    Thiboonboon K; Leelahavarong P; Wattanasirichaigoon D; Vatanavicharn N; Wasant P; Shotelersuk V; Pangkanon S; Kuptanon C; Chaisomchit S; Teerawattananon Y
    PLoS One; 2015; 10(8):e0134782. PubMed ID: 26258410
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Next generation sequencing as a follow-up test in an expanded newborn screening programme.
    Smon A; Repic Lampret B; Groselj U; Zerjav Tansek M; Kovac J; Perko D; Bertok S; Battelino T; Trebusak Podkrajsek K
    Clin Biochem; 2018 Feb; 52():48-55. PubMed ID: 29111448
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Expanded newborn screening in New South Wales: missed cases.
    Estrella J; Wilcken B; Carpenter K; Bhattacharya K; Tchan M; Wiley V
    J Inherit Metab Dis; 2014 Nov; 37(6):881-7. PubMed ID: 24970580
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [A screening test for phenylketonuria using a paper chromatography method].
    Halvorsen S; Skjelkvåle L
    Lakartidningen; 1974 Mar; 71(12):1166-7. PubMed ID: 4821497
    [No Abstract]   [Full Text] [Related]  

  • 16. Doctors' knowledge of the acute management of Inborn Errors of Metabolism.
    Hawkes CP; Walsh A; O'Sullivan S; Crushell E
    Acta Paediatr; 2011 Mar; 100(3):461-3. PubMed ID: 21133998
    [No Abstract]   [Full Text] [Related]  

  • 17. [Dystonia, megalencephaly, and seizure].
    Sfaihi L; Maaloul I; Hentati Y; Kamoun F; Kamoun T; Mnif Z; Hachicha M
    Arch Pediatr; 2013 Aug; 20(8):876, 900-2. PubMed ID: 23835096
    [No Abstract]   [Full Text] [Related]  

  • 18. Renal insufficiency mimicking glutaric acidemia type 1 on newborn screening.
    Matsumoto M; Awano H; Bo R; Nagai M; Tomioka K; Nishiyama M; Ninchouji T; Nagase H; Yagi M; Morioka I; Hasegawa Y; Takeshima Y; Iijima K
    Pediatr Int; 2018 Jan; 60(1):67-69. PubMed ID: 29059480
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Glutaric aciduria type 1 presenting as subdural haematoma.
    Carman KB; Aydogdu SD; Yakut A; Yarar C
    J Paediatr Child Health; 2012 Aug; 48(8):712. PubMed ID: 22882417
    [No Abstract]   [Full Text] [Related]  

  • 20. Teaching NeuroImages: Glutaric aciduria type 1 (glutaryl-CoA dehydrogenase deficiency).
    Singh P; Goraya JS; Ahluwalia A; Saggar K
    Neurology; 2011 Jul; 77(1):e6. PubMed ID: 21727264
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.