BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

181 related articles for article (PubMed ID: 29391032)

  • 1. Adolescence/adult onset MTHFR deficiency may manifest as isolated and treatable distinct neuro-psychiatric syndromes.
    Gales A; Masingue M; Millecamps S; Giraudier S; Grosliere L; Adam C; Salim C; Navarro V; Nadjar Y
    Orphanet J Rare Dis; 2018 Feb; 13(1):29. PubMed ID: 29391032
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and molecular characterization of adult patients with late-onset MTHFR deficiency.
    Marelli C; Lavigne C; Stepien KM; Janssen MCH; Feillet F; Kožich V; Jesina P; Schule R; Kessler C; Redonnet-Vernhet I; Regnier A; Burda P; Baumgartner M; Benoist JF; Huemer M; Mochel F;
    J Inherit Metab Dis; 2021 May; 44(3):777-786. PubMed ID: 33089527
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Severe 5,10-methylenetetrahydrofolate reductase deficiency: a rare, treatable cause of complicated hereditary spastic paraplegia.
    Perna A; Masciullo M; Modoni A; Cellini E; Parrini E; Ricci E; Donati AM; Silvestri G
    Eur J Neurol; 2018 Mar; 25(3):602-605. PubMed ID: 29284203
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Severe 5,10-methylenetetrahydrofolate reductase deficiency and two MTHFR variants in an adolescent with progressive myoclonic epilepsy.
    D'Aco KE; Bearden D; Watkins D; Hyland K; Rosenblatt DS; Ficicioglu C
    Pediatr Neurol; 2014 Aug; 51(2):266-70. PubMed ID: 25079578
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Adult-onset methylenetetrahydrofolate reductase deficiency.
    Vieira D; Florindo C; Tavares de Almeida I; Macário MC
    BMJ Case Rep; 2020 Mar; 13(3):. PubMed ID: 32161077
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Homocysteinemia due to MTHFR deficiency in a young adult presenting with bilateral lens subluxations.
    Couser NL; McClure J; Evans MW; Haines NR; Burden SK; Muenzer J
    Ophthalmic Genet; 2017; 38(1):91-94. PubMed ID: 27046515
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Severe methylenetetrahydrofolate reductase deficiency: clinical clues to a potentially treatable cause of adult-onset hereditary spastic paraplegia.
    Lossos A; Teltsh O; Milman T; Meiner V; Rozen R; Leclerc D; Schwahn BC; Karp N; Rosenblatt DS; Watkins D; Shaag A; Korman SH; Heyman SN; Gal A; Newman JP; Steiner-Birmanns B; Abramsky O; Kohn Y
    JAMA Neurol; 2014 Jul; 71(7):901-4. PubMed ID: 24797679
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Methylenetetrahydrofolate reductase (MTHFR) deficiency and infantile epilepsy.
    Prasad AN; Rupar CA; Prasad C
    Brain Dev; 2011 Oct; 33(9):758-69. PubMed ID: 21778025
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Adolescent/Adult-Onset Leukodystrophy with MTHFR Deficiency - A Treatable Cause.
    Kumar NH; Mounika KJ; Sundarachary NV
    Neurol India; 2023; 71(2):326-328. PubMed ID: 37148062
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. [Analysis of 9 patients with adolescence-onset methylenetetrahydrofolate reductase deficiency].
    Zhang HT; Ma X; Jin Y; Li MQ; Song JQ; Chen ZH; Liu Y; Lu XP; Zheng H; Yang YL
    Zhonghua Er Ke Za Zhi; 2024 Mar; 62(4):357-362. PubMed ID: 38527507
    [No Abstract]   [Full Text] [Related]  

  • 14. [Methylenetetrahydrofolate reductase deficiency-induced schizophrenia in a school-age boy].
    Wang Q; Liu J; Liu YP; Li XY; Ma YY; Wu TF; Ding Y; Song JQ; Wang YJ; Yang YL
    Zhongguo Dang Dai Er Ke Za Zhi; 2014 Jan; 16(1):62-6. PubMed ID: 24461181
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. The 1316T>C missenses mutation in MTHFR contributes to MTHFR deficiency by targeting MTHFR to proteasome degradation.
    Liu X; Li Y; Wang M; Wang X; Zhang L; Peng T; Liang W; Wang Z; Lu H
    Aging (Albany NY); 2020 Dec; 13(1):1176-1185. PubMed ID: 33290257
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Manifestations of neurological symptoms and thromboembolism in adults with MTHFR-deficiency.
    Rommer PS; Zschocke J; Fowler B; Födinger M; Konstantopoulou V; Möslinger D; Stögmann E; Suess E; Baumgartner M; Auff E; Sunder-Plassmann G
    J Neurol Sci; 2017 Dec; 383():123-127. PubMed ID: 29246599
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Severe methylenetetrahydrofolate reductase deficiency in mice results in behavioral anomalies with morphological and biochemical changes in hippocampus.
    Jadavji NM; Deng L; Leclerc D; Malysheva O; Bedell BJ; Caudill MA; Rozen R
    Mol Genet Metab; 2012 Jun; 106(2):149-59. PubMed ID: 22521626
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Variable neurological phenotypes of homocystinuria caused by biallelic methylenetetrahydrofolate reductase variants.
    Moirangthem A; Saxena D; Masih S; Shambhavi A; Nilay M; Phadke SR
    Clin Dysmorphol; 2022 Apr; 31(2):59-65. PubMed ID: 34845156
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.