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 *

156 related articles for article (PubMed ID: 38263041)

  • 1. Rheumatological complaints in H syndrome: from inflammatory profiling to target treatment in a case study.
    Tesser A; Valencic E; Boz V; Tornese G; Pastore S; Zanatta M; Tommasini A
    Pediatr Rheumatol Online J; 2024 Jan; 22(1):21. PubMed ID: 38263041
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Case report of H-syndrome with a review from a rheumatological perspective.
    Yadav S; Canchi B
    BMJ Case Rep; 2022 Jun; 15(6):. PubMed ID: 35732361
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An Egyptian family with H syndrome due to a novel mutation in SLC29A3 illustrating overlapping features with pigmented hypertrichotic dermatosis with insulin-dependent diabetes and Faisalabad histiocytosis.
    Elbarbary NS; Tjora E; Molnes J; Lie BA; Habib MA; Salem MA; Njølstad PR
    Pediatr Diabetes; 2013 Sep; 14(6):466-72. PubMed ID: 22989030
    [TBL] [Abstract][Full Text] [Related]  

  • 4. H syndrome: 5 new cases from the United States with novel features and responses to therapy.
    Bloom JL; Lin C; Imundo L; Guthery S; Stepenaskie S; Galambos C; Lowichik A; Bohnsack JF
    Pediatr Rheumatol Online J; 2017 Oct; 15(1):76. PubMed ID: 29041934
    [TBL] [Abstract][Full Text] [Related]  

  • 5. SLC29A3 mutation in a patient with syndromic diabetes with features of pigmented hypertrichotic dermatosis with insulin-dependent diabetes, H syndrome and Faisalabad histiocytosis.
    de Jesus J; Imane Z; Senée V; Romero S; Guillausseau PJ; Balafrej A; Julier C
    Diabetes Metab; 2013 May; 39(3):281-5. PubMed ID: 23623699
    [TBL] [Abstract][Full Text] [Related]  

  • 6. H syndrome treated with Tocilizumab: two case reports and literature review.
    Jacquot R; Jouret M; Valentin MG; Richard M; Jamilloux Y; Rousset F; Emile JF; Haroche J; Steinmüller L; Zekre F; Phan A; Belot A; Seve P
    Front Immunol; 2023; 14():1061182. PubMed ID: 37638031
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Tocilizumab for the Treatment of SLC29A3 Mutation Positive PHID Syndrome.
    Rafiq NK; Hussain K; Brogan PA
    Pediatrics; 2017 Nov; 140(5):. PubMed ID: 29079714
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel homozygous frame-shift mutation in the SLC29A3 gene: a new case report and review of literature.
    Noavar S; Behroozi S; Tatarcheh T; Parvini F; Foroutan M; Fahimi H
    BMC Med Genet; 2019 Aug; 20(1):147. PubMed ID: 31464584
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel start-loss mutation of the SLC29A3 gene in a consanguineous family with H syndrome: clinical characteristics, in silico analysis and literature review.
    Rezaie N; Mansour Samaei N; Ghorbani A; Gholipour N; Vosough S; Rafigh M; Amini A
    BMC Med Genomics; 2024 Jul; 17(1):178. PubMed ID: 38965556
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotypic intrafamilial variability including H syndrome and Rosai-Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 gene.
    Chouk H; Ben Rejeb M; Boussofara L; Elmabrouk H; Ghariani N; Sriha B; Saad A; H'Mida D; Denguezli M
    Hum Genomics; 2021 Oct; 15(1):63. PubMed ID: 34657628
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel homozygous SLC29A3 mutations among two unrelated Egyptian families with spectral features of H-syndrome.
    Al-Haggar M; Salem N; Wahba Y; Ahmad N; Jonard L; Abdel-Hady D; El-Hawary A; El-Sharkawy A; Eid AR; El-Hawary A
    Pediatr Diabetes; 2015 Jun; 16(4):305-16. PubMed ID: 24894595
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Improvement of SLC29A3 spectrum disorder-related sensorineural hearing loss after initiation of IL-6 inhibitor.
    Gunderman LM; Valika T; Carol H; Khojah A
    BMJ Case Rep; 2022 Jun; 15(6):. PubMed ID: 35732371
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Glomerular involvement in children with H syndrome.
    David O; Geylis M; Kristal E; Ling G; Schreiber R
    Pediatr Nephrol; 2021 Mar; 36(3):721-724. PubMed ID: 33387019
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 'H-syndrome': a multisystem genetic disorder with cutaneous clues.
    Mori KS; Balachandran K; Asirvatham AR; Mahadevan S
    BMJ Case Rep; 2021 May; 14(5):. PubMed ID: 33947670
    [TBL] [Abstract][Full Text] [Related]  

  • 15. H syndrome: the first 79 patients.
    Molho-Pessach V; Ramot Y; Camille F; Doviner V; Babay S; Luis SJ; Broshtilova V; Zlotogorski A
    J Am Acad Dermatol; 2014 Jan; 70(1):80-8. PubMed ID: 24172204
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Homozygosity for a novel large deletion in SLC29A3 in a patient with H syndrome.
    Shankar SG; Rangarajan S; Priyadarshini A; Swaminathan A; Sundaram M
    Pediatr Dermatol; 2020 Mar; 37(2):333-336. PubMed ID: 31867772
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical Progression and Manifestations of H Syndrome: A Case Report of Failed Treatment Option.
    Al-Haddab M; Al Muqarrab FJ; Alhumidi A; Alkofide M
    Am J Case Rep; 2024 Jun; 25():e944198. PubMed ID: 38850017
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ophthalmologic Findings in H Syndrome: A Unique Diagnostic Clue.
    Molho-Pessach V; Mechoulam H; Siam R; Babay S; Ramot Y; Zlotogorski A
    Ophthalmic Genet; 2015; 36(4):365-8. PubMed ID: 24547910
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Seropositive Neuromyelitis Optica in a Case of Undiagnosed Ankylosing Spondylitis: A Neuro-Rheumatological Conundrum.
    Ghosh Md R; Roy D; León-Ruiz M; Das S; Dubey S; Benito-León J
    Qatar Med J; 2022; 2022(3):29. PubMed ID: 35864917
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Atypical comorbidities in a child considered to have type 1 diabetes led to the diagnosis of SLC29A3 spectrum disorder.
    Besci Ö; Patel KA; Yıldız G; Tüfekçi Ö; Acinikli KY; Erbaş İM; Abacı A; Böber E; Bayram MT; Yılmaz Ş; Demir K
    Hormones (Athens); 2022 Sep; 21(3):501-506. PubMed ID: 35284993
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.