BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 28960390)

  • 1. Prenatal Bowel Findings in Male Siblings With a Confirmed FOXP3 Mutation.
    Griswold C; Durica AR; Dennis LG; Jewell AF
    J Ultrasound Med; 2018 Apr; 37(4):1033-1037. PubMed ID: 28960390
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A challenging undertaking: Stem cell transplantation for immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome.
    Kucuk ZY; Bleesing JJ; Marsh R; Zhang K; Davies S; Filipovich AH
    J Allergy Clin Immunol; 2016 Mar; 137(3):953-5.e4. PubMed ID: 26559324
    [No Abstract]   [Full Text] [Related]  

  • 3. Novel pathogenic variants in FOXP3 in fetuses with echogenic bowel and skin desquamation identified by ultrasound.
    Louie RJ; Tan QK; Gilner JB; Rogers RC; Younge N; Wechsler SB; McDonald MT; Gordon B; Saski CA; Jones JR; Chapman SJ; Stevenson RE; Sleasman JW; Friez MJ
    Am J Med Genet A; 2017 May; 173(5):1219-1225. PubMed ID: 28317311
    [TBL] [Abstract][Full Text] [Related]  

  • 4. From IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation.
    Bacchetta R; Barzaghi F; Roncarolo MG
    Ann N Y Acad Sci; 2018 Apr; 1417(1):5-22. PubMed ID: 26918796
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Extremely Early Onset IPEX Syndrome Caused by a Novel Small Exonic Deletion in FOXP3.
    Smith E; Greeley SA; Ye H; Torgerson TR; Dimmitt R; Atkinson P; Philips J; Goldman F
    J Pediatr Gastroenterol Nutr; 2016 Nov; 63(5):e119-e120. PubMed ID: 25187107
    [No Abstract]   [Full Text] [Related]  

  • 6. IPEX Syndrome: Genetics and Treatment Options.
    Ben-Skowronek I
    Genes (Basel); 2021 Feb; 12(3):. PubMed ID: 33668198
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial IPEX syndrome: different glomerulopathy in two siblings.
    Park E; Chang HJ; Shin JI; Lim BJ; Jeong HJ; Lee KB; Moon KC; Kang HG; Ha IS; Cheong HI
    Pediatr Int; 2015 Apr; 57(2):e59-61. PubMed ID: 25712815
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Fecal microbiota transplantation before hematopoietic stem cell transplantation in a pediatric case of chronic diarrhea with a FOXP3 mutation.
    Wu W; Shen N; Luo L; Deng Z; Chen J; Tao Y; Mo X; Cao Q
    Pediatr Neonatol; 2021 Mar; 62(2):172-180. PubMed ID: 33358585
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Persistent Enteropathy in a Toddler with a Novel FOXP3 Mutation and Normal FOXP3 Protein Expression.
    Seghezzo S; Bleesing JJ; Kucuk ZY
    J Pediatr; 2017 Jul; 186():183-185. PubMed ID: 28457527
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and structural impact of mutations affecting the residue Phe367 of FOXP3 in patients with IPEX syndrome.
    Colobran R; Álvarez de la Campa E; Soler-Palacín P; Martín-Nalda A; Pujol-Borrell R; de la Cruz X; Martínez-Gallo M
    Clin Immunol; 2016 Feb; 163():60-5. PubMed ID: 26748374
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hematopoietic stem cell transplantation recovers insulin deficiency in type 1 diabetes mellitus associated with IPEX syndrome.
    Yamauchi T; Takasawa K; Kamiya T; Kirino S; Gau M; Inoue K; Hoshino A; Kashimada K; Kanegane H; Morio T
    Pediatr Diabetes; 2019 Nov; 20(7):1035-1040. PubMed ID: 31322807
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of a novel nonsense mutation in the FOXP3 gene in a fetus with hydrops--Expanding the phenotype of IPEX syndrome.
    Reichert SL; McKay EM; Moldenhauer JS
    Am J Med Genet A; 2016 Jan; 170A(1):226-32. PubMed ID: 26395338
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [New mutation in FOXP3 gene identified in an infant with chronic diarrhea as manifestation of autoinmune enteropathy - IPEX syndrome].
    Plata García C; Martín-Marín L; Soler-Ramírez A; Rojas JA; Salazar MP
    Rev Chil Pediatr; 2020 Aug; 91(4):584-590. PubMed ID: 33399737
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [A case of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome with very early onset inflammatory bowel disease-like changes].
    Bao WT; Li ZL; Li J; Shi XY; Zhang J; Wu H
    Zhonghua Er Ke Za Zhi; 2019 Jul; 57(7):559-561. PubMed ID: 31269558
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Anti-voltage-Gated Potassium Channel (VGKC) Antibodies and Acquired Neuromyotonia in Patients with Immune Dysregulation, Polyendocrinopathy, Enteropathy X-Lined (IPEX) Syndrome.
    Moseley N; King J; Van Dort B; Williams S; Rodriguez-Casero V; Ramachandran S; Choo S; Cole T; McLean-Tooke A
    J Clin Immunol; 2021 Nov; 41(8):1972-1974. PubMed ID: 34478044
    [No Abstract]   [Full Text] [Related]  

  • 16. New Findings of Immunodysregulation, Polyendocrinopathy, and Enteropathy X-linked Syndrome (IPEX); Granulomas in Lung and Duodenum.
    Duztas DT; Al-Shadfan L; Ozturk H; Yazan H; Cakir E; Ekinci NUO; Dalgic B; Rohlfs M; Jeske T; Klein C; Kotlarz D; Gurkan OE
    Pediatr Dev Pathol; 2021; 24(3):252-257. PubMed ID: 33683986
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular feature and therapeutic perspectives of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
    Huang Q; Liu X; Zhang Y; Huang J; Li D; Li B
    J Genet Genomics; 2020 Jan; 47(1):17-26. PubMed ID: 32081609
    [TBL] [Abstract][Full Text] [Related]  

  • 18. IPEX due to an exon 7 skipping FOXP3 mutation with autoimmune diabetes mellitus cured by selective T
    Magg T; Wiebking V; Conca R; Krebs S; Arens S; Schmid I; Klein C; Albert MH; Hauck F
    Clin Immunol; 2018 Jun; 191():52-58. PubMed ID: 29567430
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked Syndrome in Two Siblings: Same Mutation But Different Clinical Manifestations at Onset.
    Karagüzel G; Polat R; Abul MH; Cebi AH; Orhan F
    J Clin Res Pediatr Endocrinol; 2022 Aug; 14(3):361-365. PubMed ID: 34044499
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Quantitative analysis of tissue inflammation and responses to treatment in immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome, and review of literature.
    Chen CA; Chung WC; Chiou YY; Yang YJ; Lin YC; Ochs HD; Shieh CC
    J Microbiol Immunol Infect; 2016 Oct; 49(5):775-782. PubMed ID: 26748735
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.