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 *

197 related articles for article (PubMed ID: 26006721)

  • 1. CSF 5-Methyltetrahydrofolate Serial Monitoring to Guide Treatment of Congenital Folate Malabsorption Due to Proton-Coupled Folate Transporter (PCFT) Deficiency.
    Torres A; Newton SA; Crompton B; Borzutzky A; Neufeld EJ; Notarangelo L; Berry GT
    JIMD Rep; 2015; 24():91-6. PubMed ID: 26006721
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The first Chinese case report of hereditary folate malabsorption with a novel mutation on SLC46A1.
    Wang Q; Li X; Ding Y; Liu Y; Qin Y; Yang Y
    Brain Dev; 2015 Jan; 37(1):163-7. PubMed ID: 24534056
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption.
    Zhao R; Aluri S; Goldman ID
    Mol Aspects Med; 2017 Feb; 53():57-72. PubMed ID: 27664775
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorption.
    Diop-Bove N; Jain M; Scaglia F; Goldman ID
    Gene; 2013 Sep; 527(2):673-4. PubMed ID: 23816405
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Role of Intramuscular Levofolinate Administration in the Treatment of Hereditary Folate Malabsorption: Report of Three Cases.
    Manea E; Gissen P; Pope S; Heales SJ; Batzios S
    JIMD Rep; 2018; 39():7-12. PubMed ID: 28685492
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Two cases with generalized intracranial calcification due to hereditary folate malabsorption and literature review].
    Zhang Y; Wang Q; Li DX; Liu YP; Song JQ; Li MQ; Qin YP; Yang YL
    Zhonghua Er Ke Za Zhi; 2016 Dec; 54(12):931-935. PubMed ID: 27938595
    [No Abstract]   [Full Text] [Related]  

  • 7. Successful Treatment of Hereditary Folate Malabsorption With Intramuscular Folinic Acid.
    Lubout CMA; Goorden SMI; van den Hurk K; Jaeger B; Jager NGL; van Koningsbruggen S; Chegary M; van Karnebeek CDM
    Pediatr Neurol; 2020 Jan; 102():62-66. PubMed ID: 31371121
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel localization of folate transport systems in the murine central nervous system.
    Sangha V; Hoque MT; Henderson JT; Bendayan R
    Fluids Barriers CNS; 2022 Nov; 19(1):92. PubMed ID: 36419095
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Neurological improvement following intravenous high-dose folinic acid for cerebral folate transporter deficiency caused by FOLR-1 mutation.
    Delmelle F; Thöny B; Clapuyt P; Blau N; Nassogne MC
    Eur J Paediatr Neurol; 2016 Sep; 20(5):709-13. PubMed ID: 27328863
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Properties of the Arg376 residue of the proton-coupled folate transporter (PCFT-SLC46A1) and a glutamine mutant causing hereditary folate malabsorption.
    Mahadeo K; Diop-Bove N; Shin D; Unal ES; Teo J; Zhao R; Chang MH; Fulterer A; Romero MF; Goldman ID
    Am J Physiol Cell Physiol; 2010 Nov; 299(5):C1153-61. PubMed ID: 20686069
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cerebral folate deficiency.
    Ramaekers VT; Blau N
    Dev Med Child Neurol; 2004 Dec; 46(12):843-51. PubMed ID: 15581159
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutation of the proton-coupled folate transporter gene (PCFT-SLC46A1) in Turkish siblings with hereditary folate malabsorption.
    Atabay B; Turker M; Ozer EA; Mahadeo K; Diop-Bove N; Goldman ID
    Pediatr Hematol Oncol; 2010 Nov; 27(8):614-9. PubMed ID: 20795774
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption.
    Shin DS; Mahadeo K; Min SH; Diop-Bove N; Clayton P; Zhao R; Goldman ID
    Mol Genet Metab; 2011 May; 103(1):33-7. PubMed ID: 21333572
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Treatable Cause of Pancytopenia, Recurrent Infections and Refractory Epilepsy: Secondary to Hereditary Folate Malabsorption (HFM) Due to Novel Pathogenic Variant.
    Gowda VK; Battina M; Shivappa SK; Benakappa N
    Indian J Pediatr; 2021 Jun; 88(6):586-588. PubMed ID: 33146883
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary folate malabsorption due to a mutation in the external gate of the proton-coupled folate transporter SLC46A1.
    Aluri S; Zhao R; Lubout C; Goorden SMI; Fiser A; Goldman ID
    Blood Adv; 2018 Jan; 2(1):61-68. PubMed ID: 29344585
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cerebral folate deficiency: Analytical tests and differential diagnosis.
    Pope S; Artuch R; Heales S; Rahman S
    J Inherit Metab Dis; 2019 Jul; 42(4):655-672. PubMed ID: 30916789
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An infantile case of hereditary folate malabsorption with sudden development of pulmonary hemorrhage: a case report.
    Sakurai Y; Toriumi N; Sarashina T; Ishioka T; Nagata M; Kobayashi H; Azuma H
    J Med Case Rep; 2022 Jun; 16(1):268. PubMed ID: 35773682
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The obligatory intestinal folate transporter PCFT (SLC46A1) is regulated by nuclear respiratory factor 1.
    Gonen N; Assaraf YG
    J Biol Chem; 2010 Oct; 285(44):33602-13. PubMed ID: 20724482
    [TBL] [Abstract][Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

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

    [Next]    [New Search]
    of 10.