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 *

358 related articles for article (PubMed ID: 32703178)

  • 21. Neonatal screening for congenital hypothyroidism and phenylketonuria in China.
    Zhan JY; Qin YF; Zhao ZY
    World J Pediatr; 2009 May; 5(2):136-9. PubMed ID: 19718537
    [TBL] [Abstract][Full Text] [Related]  

  • 22. HPLC for confirmatory diagnosis and biochemical monitoring of Cuban patients with hyperphenylalaninemias.
    Contreras J; Alonso E; Fuentes LE
    MEDICC Rev; 2015 Jan; 17(1):23-8. PubMed ID: 25725765
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prevalence of gram-negative bacteria and their antibiotic resistance in neonatal sepsis in Iran: a systematic review and meta-analysis.
    Moftian N; Rezaei-Hachesu P; Arab-Zozani M; Samad-Soltani T; Esfandiari A; Tabib MS; Mirnia K
    BMC Infect Dis; 2023 Aug; 23(1):534. PubMed ID: 37582726
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The Effects of Breastfeeding in Infants With Phenylketonuria.
    Kose E; Aksoy B; Kuyum P; Tuncer N; Arslan N; Ozturk Y
    J Pediatr Nurs; 2018; 38():27-32. PubMed ID: 29167077
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A survey for the incidence of phenylketonuria in Guangdong, China.
    Jiang J; Ma X; Huang X; Pei X; Liu H; Tan Z; Zhu L
    Southeast Asian J Trop Med Public Health; 2003; 34 Suppl 3():185. PubMed ID: 15906732
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Epidemiology of multiple sclerosis in Iran: A systematic review and meta-analysis.
    Azami M; YektaKooshali MH; Shohani M; Khorshidi A; Mahmudi L
    PLoS One; 2019; 14(4):e0214738. PubMed ID: 30964886
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prevalence of classical phenylketonuria in mentally retarded individuals in Iran.
    Ghiasvand NM; Aledavood A; Ghiasvand R; Seyedin Borojeny F; Aledavood AR; Seyed S; Miner W; Saeb Taheri GR
    J Inherit Metab Dis; 2009 Dec; 32 Suppl 1():S283-7. PubMed ID: 19768570
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prevalence of comorbid conditions among adult patients diagnosed with phenylketonuria.
    Burton BK; Jones KB; Cederbaum S; Rohr F; Waisbren S; Irwin DE; Kim G; Lilienstein J; Alvarez I; Jurecki E; Levy H
    Mol Genet Metab; 2018 Nov; 125(3):228-234. PubMed ID: 30266197
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Neonatal screening and long-term follow-up of phenylketonuria: the French database.
    Abadie V; Berthelot J; Feillet F; Maurin N; Mercier A; de Baulny HO; de Parscau L
    Early Hum Dev; 2001 Dec; 65(2):149-58. PubMed ID: 11641035
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A policy analysis of the national phenylketonuria screening program in Iran.
    Heidari A; Arab M; Damari B
    BMC Health Serv Res; 2021 Feb; 21(1):120. PubMed ID: 33546689
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Development of the phenylketonuria screening programme in Estonia.
    Ounap K; Lilleväli H; Metspalu A; Lipping-Sitska M
    J Med Screen; 1998; 5(1):22-3. PubMed ID: 9575455
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Potential role of tetrahydrobiopterin in the treatment of maternal phenylketonuria.
    Trefz FK; Blau N
    Pediatrics; 2003 Dec; 112(6 Pt 2):1566-9. PubMed ID: 14654666
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Phenylketonuria: screening, treatment and maternal PKU.
    Matalon R; Michals K
    Clin Biochem; 1991 Aug; 24(4):337-42. PubMed ID: 1959225
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mutations in the phenylalanine hydroxylase gene: genetic determinants for the phenotypic variability of hyperphenylalaninemia.
    Güttler F; Guldberg P
    Acta Paediatr Suppl; 1994 Dec; 407():49-56. PubMed ID: 7766959
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Hyperphenylalaninemia in the Philippines.
    Capistrano-Estrada S; Padilla CD
    Southeast Asian J Trop Med Public Health; 2003; 34 Suppl 3():182-4. PubMed ID: 15906731
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Phenylketonuria.
    van Spronsen FJ; Blau N; Harding C; Burlina A; Longo N; Bosch AM
    Nat Rev Dis Primers; 2021 May; 7(1):36. PubMed ID: 34017006
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A comprehensive study of phenylalanine hydroxylase gene mutations in the Iranian phenylketonuria patients.
    Esfahani MS; Vallian S
    Eur J Med Genet; 2019 Sep; 62(9):103559. PubMed ID: 30389586
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Detection of phenylketonuria by the newborn screening program in Thailand.
    Pangkanon S; Charoensiriwatana W; Janejai N; Boonwanich W; Chaisomchit S
    Southeast Asian J Trop Med Public Health; 2009 May; 40(3):525-9. PubMed ID: 19842439
    [TBL] [Abstract][Full Text] [Related]  

  • 39. "Mild" hyperphenylalaninemia? A case series of seven treated patients following newborn screening.
    Viall S; Ayyub O; Rasberry M; Lyons K; Ah Mew N
    Mol Genet Metab; 2017 Dec; 122(4):153-155. PubMed ID: 29102225
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cuban neonatal screening of phenylketonuria using an ultramicro-fluorometric test.
    González EC; Frómeta A; del Río L; Castells E; Robaina MS; García SM; Licourt T; Arteaga AL; Martínez L
    Clin Chim Acta; 2009 Apr; 402(1-2):129-32. PubMed ID: 19168043
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.