BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 38217098)

  • 1. Late-onset 5,10-methylenetetrahydrofolate reductase deficiency with subacute disturbance of consciousness.
    Miura M; Nishijima H; Suzuki C; Tomiyama M
    Pediatr Int; 2024; 66(1):e15720. PubMed ID: 38217098
    [No Abstract]   [Full Text] [Related]  

  • 2. Methylenetetrahydrofolate Reductase Deficiency as a Cause of Treatable Adult-onset Leukoencephalopathy and Myelopathy.
    Senthilvelan S; Kandasamy S; Menon RN; Nampoothiri S; Ramachandran H; Thomas B; Kesavadas C
    Clin Neuroradiol; 2021 Mar; 31(1):277-281. PubMed ID: 32880657
    [No Abstract]   [Full Text] [Related]  

  • 3. Methylenetetrahydrofolate reductase deficiency (homocystinuria type II) as a rare cause of rapidly progressive tetraspasticity and psychosis in a previously healthy adult.
    Birnbaum T; Blom HJ; Prokisch H; Hartig M; Klopstock T
    J Neurol; 2008 Nov; 255(11):1845-6. PubMed ID: 18854913
    [No Abstract]   [Full Text] [Related]  

  • 4. Reversible leukoencephalopathy and cerebral atrophy in homocystinuria due to MTHFR deficiency: A treatable metabolic disorder.
    Padmanabha H; Shekhar R; Mahale R; Annam H; Bhat M; Sangeeth TA; Christopher R; Arunachal G; Mailankody P; Mathuranath PS
    J Inherit Metab Dis; 2021 Nov; 44(6):1505-1506. PubMed ID: 34541688
    [No Abstract]   [Full Text] [Related]  

  • 5. Adult-onset severe methylenetetrahydrofolate reductase deficiency characterized by reversible spastic paraplegia with a novel mutation.
    Lin N; Jiang N; Dai Y; Gao J; Wang L
    Neurol Sci; 2016 Oct; 37(10):1735-7. PubMed ID: 27118298
    [No Abstract]   [Full Text] [Related]  

  • 6. From resveratrol to ISIDE11: how to activate SIRT1 and improve endothelial function? New therapeutic insights for methylenetetrahydrofolate reductase deficiency.
    Jankauskas SS; Mone P; Santulli G
    Cell Mol Life Sci; 2022 Jul; 79(8):451. PubMed ID: 35895130
    [No Abstract]   [Full Text] [Related]  

  • 7. A case of MTHFR deficiency characterized by adult-onset spastic paraplegia.
    Liu L; Sun Q; Yang G
    QJM; 2024 Mar; 117(3):223-225. PubMed ID: 37972026
    [No Abstract]   [Full Text] [Related]  

  • 8. Pearls & oy-sters: familial epileptic encephalopathy due to methylenetetrahydrofolate reductase deficiency.
    Cappuccio G; Cozzolino C; Frisso G; Romanelli R; Parenti G; D'Amico A; Carotenuto B; Salvatore F; Del Giudice E
    Neurology; 2014 Jul; 83(3):e41-4. PubMed ID: 25024447
    [No Abstract]   [Full Text] [Related]  

  • 9. [Methylenetetrahydrofolate Reductase deficiency and anesthesia: importance of a detailed preoperative evaluation].
    Santos CDSE; Grayson BE
    Braz J Anesthesiol; 2019; 69(6):637-638. PubMed ID: 31796301
    [No Abstract]   [Full Text] [Related]  

  • 10. Homocystinuria Due to MTHFR Variant Presenting As Infantile Tremor Syndrome.
    Gowda VK; Srinivasan VM; Shivappa SK
    Indian J Pediatr; 2021 Nov; 88(11):1153. PubMed ID: 34347262
    [No Abstract]   [Full Text] [Related]  

  • 11. Methylene Tetrahydrofolate Reductase Deficiency.
    Kaur R; Correa ARE; Thakur S; Kabra M; Gupta N
    Indian J Pediatr; 2020 Nov; 87(11):951-953. PubMed ID: 32451826
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Posterior-predominant leukoencephalopathy which was caused by methylenetetrahydrofolate reductase deficiency and successfully treated with folic acid].
    Tamura A; Sasaki R; Kagawa K; Nakatani K; Osaka H; Tomimoto H
    Rinsho Shinkeigaku; 2014; 54(3):200-6. PubMed ID: 24705833
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Focal epilepsy as the revealing symptom of 5,10-methylenetetrahydrofolate reductase deficiency in a young adult.
    Mezouar N; Mochel F; An-Gourfinkel I; Baulac M; Gales A
    Rev Neurol (Paris); 2018 Mar; 174(3):173-175. PubMed ID: 29366491
    [No Abstract]   [Full Text] [Related]  

  • 14. Early treatment using betaine and methionine for a neonate with MTHFR deficiency.
    Nishimoto E; Ito Y; Sakakibara T; Nishikubo T
    Pediatr Int; 2019 Dec; 61(12):1265-1266. PubMed ID: 31782227
    [No Abstract]   [Full Text] [Related]  

  • 15. Rapidly progressive psychotic symptoms triggered by infection in a patient with methylenetetrahydrofolate reductase deficiency: a case report.
    Iida S; Nakamura M; Asayama S; Kunieda T; Kaneko S; Osaka H; Kusaka H
    BMC Neurol; 2017 Feb; 17(1):47. PubMed ID: 28241805
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A founder mutation causing a severe methylenetetrahydrofolate reductase (MTHFR) deficiency in Bukharian Jews.
    Ben-Shachar S; Zvi T; Rolfs A; Breda Klobus A; Yaron Y; Bar-Shira A; Orr-Urtreger A
    Mol Genet Metab; 2012 Nov; 107(3):608-10. PubMed ID: 22947400
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Determination and interpretation of MTHFR gene mutations in gynecology and internal medicine.
    Undas A; Chojnowski K; Klukowska A; Łętowska M; Mital A; Młynarski W; Musiał J; Podolak-Dawidziak M; Sąsiadek M; Treliński J; Urasiński T; Windyga J; Zdziarska J; Zawilska K
    Pol Arch Intern Med; 2019 Oct; 129(10):728-732. PubMed ID: 31670725
    [No Abstract]   [Full Text] [Related]  

  • 18. Severe scoliosis in a patient with severe methylenetetrahydrofolate reductase deficiency.
    Munoz T; Patel J; Badilla-Porras R; Kronick J; Mercimek-Mahmutoglu S
    Brain Dev; 2015 Jan; 37(1):168-70. PubMed ID: 24726568
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Acute leukoencephalopathy possibly induced by phenytoin intoxication in an adult patient with methylenetetrahydrofolate reductase deficiency.
    Arai M; Osaka H
    Epilepsia; 2011 Jul; 52(7):e58-61. PubMed ID: 21480888
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation Update and Review of Severe Methylenetetrahydrofolate Reductase Deficiency.
    Froese DS; Huemer M; Suormala T; Burda P; Coelho D; Guéant JL; Landolt MA; Kožich V; Fowler B; Baumgartner MR
    Hum Mutat; 2016 May; 37(5):427-38. PubMed ID: 26872964
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.