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 *

153 related articles for article (PubMed ID: 37732042)

  • 1. The effect of intravenous trehalose administration in a patient with multiple sulfatase deficiency.
    Radbakhsh S; Mobini M; Gumpricht E; Banach M; Jamialahmadi T; Sahebkar A
    Arch Med Sci; 2023; 19(5):1564-1568. PubMed ID: 37732042
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Impact of Intravenous Trehalose Administration in Patients with Niemann-Pick Disease Types A and B.
    Mobini M; Radbakhsh S; Kubaski F; Eshraghi P; Vakili S; Vakili R; Khalili M; Varesvazirian M; Jamialahmadi T; Alamdaran SA; Sayedi SJ; Rajabi O; Emami SA; Reiner Ž; Sebkar A
    J Clin Med; 2022 Jan; 11(1):. PubMed ID: 35011993
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The Effects of N-Acetyl-L-Leucine on the Improvement of Symptoms in a Patient with Multiple Sulfatase Deficiency.
    Saberi-Karimian M; Houra M; Jamialahmadi T; Sarvghadi P; Nikbaf M; Akhlaghi S; Sahebkar A
    Cerebellum; 2023 Dec; 22(6):1250-1256. PubMed ID: 36482027
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Effects of Trehalose Administration in Patients with Mucopolysaccharidosis Type III.
    Mobini M; Radbakhsh S; Kubaski F; Eshraghi P; Vakili S; Vakili R; Abbasifard M; Jamialahmadi T; Rajabi O; Emami SA; Tayarani-Najaran Z; Rizzo M; Eid AH; Banach M; Sahebkar A
    Curr Med Chem; 2024; 31(20):3033-3042. PubMed ID: 37038706
    [TBL] [Abstract][Full Text] [Related]  

  • 5. New mouse models with hypomorphic SUMF1 variants mimic attenuated forms of multiple sulfatase deficiency.
    Sorrentino NC; Presa M; Attanasio S; Cacace V; Sofia M; Zuberi A; Ryan J; Ray S; Petkovic I; Radhakrishnan K; Schlotawa L; Ballabio A; Lutz C; Brunetti-Pierri N
    J Inherit Metab Dis; 2023 Mar; 46(2):335-347. PubMed ID: 36433920
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A systematic review and meta-analysis of published cases reveals the natural disease history in multiple sulfatase deficiency.
    Schlotawa L; Preiskorn J; Ahrens-Nicklas R; Schiller S; Adang LA; Gärtner J; Friede T
    J Inherit Metab Dis; 2020 Nov; 43(6):1288-1297. PubMed ID: 32621519
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Multiple Sulfatase Deficiency: A Disease Comprising Mucopolysaccharidosis, Sphingolipidosis, and More Caused by a Defect in Posttranslational Modification.
    Schlotawa L; Adang LA; Radhakrishnan K; Ahrens-Nicklas RC
    Int J Mol Sci; 2020 May; 21(10):. PubMed ID: 32414121
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Multiple sulfatase deficiency: catalytically inactive sulfatases are expressed from retrovirally introduced sulfatase cDNAs.
    Rommerskirch W; von Figura K
    Proc Natl Acad Sci U S A; 1992 Apr; 89(7):2561-5. PubMed ID: 1348358
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Drug screening identifies tazarotene and bexarotene as therapeutic agents in multiple sulfatase deficiency.
    Schlotawa L; Tyka K; Kettwig M; Ahrens-Nicklas RC; Baud M; Berulava T; Brunetti-Pierri N; Gagne A; Herbst ZM; Maguire JA; Monfregola J; Pena T; Radhakrishnan K; Schröder S; Waxman EA; Ballabio A; Dierks T; Fischer A; French DL; Gelb MH; Gärtner J
    EMBO Mol Med; 2023 Mar; 15(3):e14837. PubMed ID: 36789546
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Molecular basis of multiple sulfatase deficiency, mucolipidosis II/III and Niemann-Pick C1 disease - Lysosomal storage disorders caused by defects of non-lysosomal proteins.
    Dierks T; Schlotawa L; Frese MA; Radhakrishnan K; von Figura K; Schmidt B
    Biochim Biophys Acta; 2009 Apr; 1793(4):710-25. PubMed ID: 19124046
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Direct comparison of measures of endurance, mobility, and joint function during enzyme-replacement therapy of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): results after 48 weeks in a phase 2 open-label clinical study of recombinant human N-acetylgalactosamine 4-sulfatase.
    Harmatz P; Ketteridge D; Giugliani R; Guffon N; Teles EL; Miranda MC; Yu ZF; Swiedler SJ; Hopwood JJ;
    Pediatrics; 2005 Jun; 115(6):e681-9. PubMed ID: 15930196
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Late infantile form of multiple sulfatase deficiency with a novel missense variant in the SUMF1 gene: case report and review.
    Sheth J; Shah S; Datar C; Bhatt K; Raval P; Nair A; Jain D; Shah J; Sheth F; Sheth H
    BMC Pediatr; 2023 Mar; 23(1):133. PubMed ID: 36959582
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Long-term disease course of two patients with multiple sulfatase deficiency differs from metachromatic leukodystrophy in a broad cohort.
    Beck-Wödl S; Kehrer C; Harzer K; Haack TB; Bürger F; Haas D; Rieß A; Groeschel S; Krägeloh-Mann I; Böhringer J
    JIMD Rep; 2021 Mar; 58(1):80-88. PubMed ID: 33728250
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expanding the genetic cause of multiple sulfatase deficiency: A novel SUMF1 variant in a patient displaying a severe late infantile form of the disease.
    Jaszczuk I; Schlotawa L; Dierks T; Ohlenbusch A; Koppenhöfer D; Babicz M; Lejman M; Radhakrishnan K; Ługowska A
    Mol Genet Metab; 2017 Jul; 121(3):252-258. PubMed ID: 28566233
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Multiple sulfatase deficiency with a novel biochemical presentation.
    Constantopoulos G
    Eur J Pediatr; 1988 Aug; 147(6):634-8. PubMed ID: 2903054
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A homozygous missense variant of SUMF1 in the Bedouin population extends the clinical spectrum in ultrarare neonatal multiple sulfatase deficiency.
    Staretz-Chacham O; Schlotawa L; Wormser O; Golan-Tripto I; Birk OS; Ferreira CR; Dierks T; Radhakrishnan K
    Mol Genet Genomic Med; 2020 Sep; 8(9):e1167. PubMed ID: 32048457
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Difficulty in recognizing multiple sulfatase deficiency in an infant.
    Santos RP; Hoo JJ
    Pediatrics; 2006 Mar; 117(3):955-8. PubMed ID: 16510683
    [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 8.