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 *

121 related articles for article (PubMed ID: 37702680)

  • 21. [Evaluations of newborn screening program performance and enzymatic diagnosis of glucose-6-phosphate dehydrogenase deficiency in Guangzhou].
    Tang F; Huang YL; Jiang X; Jia XF; Li B; Feng Y; Chen QY; Tang CF
    Zhonghua Er Ke Za Zhi; 2018 May; 56(5):359-363. PubMed ID: 29783822
    [No Abstract]   [Full Text] [Related]  

  • 22. Selective screening for inborn errors of metabolism on clinical patients using tandem mass spectrometry in China: a four-year report.
    Han LS; Ye J; Qiu WJ; Gao XL; Wang Y; Gu XF
    J Inherit Metab Dis; 2007 Aug; 30(4):507-14. PubMed ID: 17347912
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Evaluating a Novel Newborn Screening Methodology: Combined Genetic and Biochemical Screenings.
    Yu B; Yang Y; Zhou L; Wang Q
    Arch Med Res; 2024 Feb; 55(2):102959. PubMed ID: 38295467
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Newborn Screening for Five Conditions in a Tertiary Care Government Hospital in Bengaluru, South India-Three Years Experience.
    Kommalur A; Devadas S; Kariyappa M; Sabapathy S; Benakappa A; Gagandeep V; Veranna Sajjan S; Krishnapura Lakshminarayana S; Dakshayani B; Devi Chinnappa G
    J Trop Pediatr; 2020 Jun; 66(3):284-289. PubMed ID: 31821472
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Diagnostic challenges of aminoacidopathies and organic acidemias in a developing country: a twelve-year experience.
    Karam PE; Habbal MZ; Mikati MA; Zaatari GE; Cortas NK; Daher RT
    Clin Biochem; 2013 Dec; 46(18):1787-92. PubMed ID: 23994778
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Newborn screening in China: phenylketonuria, congenital hypothyroidism and expanded screening.
    Gu X; Wang Z; Ye J; Han L; Qiu W
    Ann Acad Med Singap; 2008 Dec; 37(12 Suppl):107-4. PubMed ID: 19904469
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Neonatal screening program in Rajavithi Hospital, Thailand.
    Ratrisawadi V; Horpaopan S; Chotigeat U; Sangtawesin V; Kanjanapattanakul W; Ningsanond V; Sunthornthepvarakul T; Khooarmompatana S; Charoensiriwatana W
    Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():28-32. PubMed ID: 11400773
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Screening and follow-up results of fatty acid oxidative metabolism disorders in 608 818 newborns in Jining, Shandong province.
    Yang C; Shi C; Zhou C; Wan Q; Zhou Y; Chen X; Jin X; Huang C; Xu P
    Zhejiang Da Xue Xue Bao Yi Xue Ban; 2021 Aug; 50(4):472-480. PubMed ID: 34704412
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Newborn screening for primary carnitine deficiency and variant spectrum of SLC22A5 gene in Guangzhou].
    Huang YL; Tang CF; Liu SC; Sheng HY; Tang F; Jiang X; Zheng RD; Mei HF; Liu L
    Zhonghua Er Ke Za Zhi; 2020 Jun; 58(6):476-481. PubMed ID: 32521959
    [No Abstract]   [Full Text] [Related]  

  • 31. Newborn screening.
    Wilcken B; Wiley V
    Pathology; 2008 Feb; 40(2):104-15. PubMed ID: 18203033
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Application of a next-generation sequencing (NGS) panel in newborn screening efficiently identifies inborn disorders of neonates.
    Huang X; Wu D; Zhu L; Wang W; Yang R; Yang J; He Q; Zhu B; You Y; Xiao R; Zhao Z
    Orphanet J Rare Dis; 2022 Feb; 17(1):66. PubMed ID: 35193651
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A multicenter prospective study of next-generation sequencing-based newborn screening for monogenic genetic diseases in China.
    Yang RL; Qian GL; Wu DW; Miao JK; Yang X; Wu BQ; Yan YQ; Li HB; Mao XM; He J; Shen H; Zou H; Xue SY; Li XZ; Niu TT; Xiao R; Zhao ZY
    World J Pediatr; 2023 Jul; 19(7):663-673. PubMed ID: 36847978
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [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]  

  • 35. Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: a two-year summary from the New England Newborn Screening Program.
    Zytkovicz TH; Fitzgerald EF; Marsden D; Larson CA; Shih VE; Johnson DM; Strauss AW; Comeau AM; Eaton RB; Grady GF
    Clin Chem; 2001 Nov; 47(11):1945-55. PubMed ID: 11673361
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Newborn screening.
    Sahai I; Marsden D
    Crit Rev Clin Lab Sci; 2009; 46(2):55-82. PubMed ID: 19255915
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Newborn screening: the role of the obstetrician.
    Larsson A; Therrell BL
    Clin Obstet Gynecol; 2002 Sep; 45(3):697-710; discussion 730-2. PubMed ID: 12370609
    [No Abstract]   [Full Text] [Related]  

  • 38. [Analysis of clinical features, biochemical indices and genetic variants among children with Short/branched-chain acyl-CoA dehydrogenase deficiency detected by neonatal screening].
    Zhao H; Zhou D; Miao H; Chen C; Yang J; Yang R; Huang X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Feb; 40(2):155-160. PubMed ID: 36709932
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Is Expanded Newborn Screening Adequate to Detect Indian Biochemical Low Excretor Phenotype Patients of Glutaric Aciduria Type I?
    Shaik M; T P KV; Kamate M; A B V
    Indian J Pediatr; 2019 Nov; 86(11):995-1001. PubMed ID: 31302874
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Molecular analysis using targeted next generation DNA sequencing and clinical spectrum of Mexican patients with isovaleric acidemia.
    Ibarra-González I; Fernández-Lainez C; Guillén-López S; López-Mejía L; Belmont-Matínez L; Sokolsky TD; Amin VR; Kitchener RL; Vela-Amieva M; Naylor EW; Bhattacharjee A
    Clin Chim Acta; 2020 Feb; 501():216-221. PubMed ID: 31707166
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.