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 *

219 related articles for article (PubMed ID: 34082800)

  • 1. Birth prevalence of phenylalanine hydroxylase deficiency: a systematic literature review and meta-analysis.
    Foreman PK; Margulis AV; Alexander K; Shediac R; Calingaert B; Harding A; Pladevall-Vila M; Landis S
    Orphanet J Rare Dis; 2021 Jun; 16(1):253. PubMed ID: 34082800
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.
    Crider K; Williams J; Qi YP; Gutman J; Yeung L; Mai C; Finkelstain J; Mehta S; Pons-Duran C; Menéndez C; Moraleda C; Rogers L; Daniels K; Green P
    Cochrane Database Syst Rev; 2022 Feb; 2(2022):. PubMed ID: 36321557
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Nutritional management of phenylalanine hydroxylase (PAH) deficiency in pediatric patients in Canada: a survey of dietitians' current practices.
    Yuskiv N; Potter BK; Stockler S; Ueda K; Giezen A; Cheng B; Langley E; Ratko S; Austin V; Chapman M; Chakraborty P; Collet JP; Pender A;
    Orphanet J Rare Dis; 2019 Jan; 14(1):7. PubMed ID: 30621767
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phenylketonuria screening in Iranian newborns: a systematic review and meta-analysis.
    Shokri M; Karimi P; Zamanifar H; Kazemi F; Badfar G; Azami M
    BMC Pediatr; 2020 Jul; 20(1):352. PubMed ID: 32703178
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Impact of neonatal protein metabolism and nutrition on screening for phenylketonuria.
    Ponzone A; Spada M; Roasio L; Porta F; Mussa A; Ferraris S
    J Pediatr Gastroenterol Nutr; 2008 May; 46(5):561-9. PubMed ID: 18493213
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Phenylalanine hydroxylase deficiency treatment and management: A systematic evidence review of the American College of Medical Genetics and Genomics (ACMG).
    Adams AD; Fiesco-Roa MÓ; Wong L; Jenkins GP; Malinowski J; Demarest OM; Rothberg PG; Hobert JA;
    Genet Med; 2023 Sep; 25(9):100358. PubMed ID: 37470789
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Tetrahydrobiopterin (BH4) responsiveness in neonates with hyperphenylalaninemia: a semi-mechanistically-based, nonlinear mixed-effect modeling.
    Trefz F; Lichtenberger O; Blau N; Muntau AC; Feillet F; Bélanger-Quintana A; van Spronsen F; Munafo A
    Mol Genet Metab; 2015 Apr; 114(4):564-9. PubMed ID: 25726095
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Clinical study of tetrahydrobiopterin responsive phenylalanine hydroxylase deficiency in southern and northern Chinese patients].
    Yang L; Zhang ZX; Ye J; Zhou ZS; Shen M; Han LS; Qiu W; Yu WM; Gu XF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):310-3. PubMed ID: 17557244
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 5-year retrospective analysis of patients with phenylketonuria (PKU) and hyperphenylalaninemia treated at two specialized clinics.
    Levy H; Lamppu D; Anastosoaie V; Baker JL; DiBona K; Hawthorne S; Lindenberger J; Kinch D; Seymour A; McIlduff M; Watling S; Vockley J
    Mol Genet Metab; 2020 Mar; 129(3):177-185. PubMed ID: 31883647
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Quantification of derivatized phenylalanine and tyrosine in dried blood spots using liquid chromatography with tandem spectrometry for newborn screening of phenylketonuria.
    Duh TH; Liang YC; Shen PT; Ke YW; Nian YT; Liang SS
    Eur J Mass Spectrom (Chichester); 2024 Apr; 30(2):133-140. PubMed ID: 38321764
    [TBL] [Abstract][Full Text] [Related]  

  • 11. DNA methylated alleles of the phenylalanine hydroxylase promoter remodeled at elevated phenylalanine levels in newborns with hyperphenylalaninemia.
    Item CB; Farhadi S; Schanzer A; Greber-Platzer S
    Clin Biochem; 2017 Aug; 50(12):729-732. PubMed ID: 28389235
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Use of phenylalanine-to-tyrosine ratio determined by tandem mass spectrometry to improve newborn screening for phenylketonuria of early discharge specimens collected in the first 24 hours.
    Chace DH; Sherwin JE; Hillman SL; Lorey F; Cunningham GC
    Clin Chem; 1998 Dec; 44(12):2405-9. PubMed ID: 9836704
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Evaluation of 6-year application of the enzymatic colorimetric phenylalanine assay in the setting of neonatal screening for phenylketonuria.
    Schulze A; Mayatepek E; Hoffmann GF
    Clin Chim Acta; 2002 Mar; 317(1-2):27-37. PubMed ID: 11814455
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic etiology and clinical challenges of phenylketonuria.
    Elhawary NA; AlJahdali IA; Abumansour IS; Elhawary EN; Gaboon N; Dandini M; Madkhali A; Alosaimi W; Alzahrani A; Aljohani F; Melibary EM; Kensara OA
    Hum Genomics; 2022 Jul; 16(1):22. PubMed ID: 35854334
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Evaluation of neonatal BH4 loading test in neonates screened for hyperphenylalaninemia.
    Feillet F; Chery C; Namour F; Kimmoun A; Favre E; Lorentz E; Battaglia-Hsu SF; Guéant JL
    Early Hum Dev; 2008 Sep; 84(9):561-7. PubMed ID: 18321666
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Phenylalanine hydroxylase deficiency.
    Mitchell JJ; Trakadis YJ; Scriver CR
    Genet Med; 2011 Aug; 13(8):697-707. PubMed ID: 21555948
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Analysis of gene variation and long-term follow-up in children with phenylalanine hydroxylase deficiency diagnosed by newborn screening.
    Sun M; Li Y; Li P; Li G; Yan Y; Zou H
    Zhejiang Da Xue Xue Bao Yi Xue Ban; 2023 Dec; 52(6):701-706. PubMed ID: 38105703
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Management of Women With Phenylalanine Hydroxylase Deficiency (Phenylketonuria): ACOG Committee Opinion, Number 802.
    Obstet Gynecol; 2020 Apr; 135(4):e167-e170. PubMed ID: 32217978
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.