264 related articles for article (PubMed ID: 26395338)
1. 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]
2. Recurrent Non Immune Fetal Hydrops Associated With IPEX Syndrome.
Shanes E; Propst L; Ouyang DW; Ernst LM
Pediatr Dev Pathol; 2019 Oct; 22(5):465-471. PubMed ID: 30813833
[TBL] [Abstract][Full Text] [Related]
3. Novel premature termination codon in the FOXP3 gene as the cause of familial hydrops fetalis in males.
Goodhue B; Smith M; Bennett K; Grace M
Prenat Diagn; 2024 Apr; 44(4):519-521. PubMed ID: 38342853
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. A hemizygous mutation in the FOXP3 gene (IPEX syndrome) resulting in recurrent X-linked fetal hydrops: a case report.
Shangaris P; Ho A; Marnerides A; George S; AlAdnani M; Yau S; Jansson M; Hoyle J; Ahn JW; Ellard S; Irving M; Wellesley D; Pasupathy D; Holder-Espinasse M
BMC Med Genomics; 2021 Feb; 14(1):58. PubMed ID: 33637067
[TBL] [Abstract][Full Text] [Related]
6. Whole genome sequencing identifies etiology of recurrent male intrauterine fetal death.
Shehab O; Tester DJ; Ackerman NC; Cowchock FS; Ackerman MJ
Prenat Diagn; 2017 Oct; 37(10):1040-1045. PubMed ID: 28833278
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. Somatic and germline FOXP3 mosaicism in the mother of a boy with IPEX syndrome.
Lin Y; Xu A; Zeng C; Cheng J; Li N; Niu H; Liu L; Li X
Eur J Immunol; 2018 May; 48(5):885-887. PubMed ID: 29400909
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. Treatment with rapamycin can restore regulatory T-cell function in IPEX patients.
Passerini L; Barzaghi F; Curto R; Sartirana C; Barera G; Tucci F; Albarello L; Mariani A; Testoni PA; Bazzigaluppi E; Bosi E; Lampasona V; Neth O; Zama D; Hoenig M; Schulz A; Seidel MG; Rabbone I; Olek S; Roncarolo MG; Cicalese MP; Aiuti A; Bacchetta R
J Allergy Clin Immunol; 2020 Apr; 145(4):1262-1271.e13. PubMed ID: 31874182
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) and IPEX-related disorders: an evolving web of heritable autoimmune diseases.
Verbsky JW; Chatila TA
Curr Opin Pediatr; 2013 Dec; 25(6):708-14. PubMed ID: 24240290
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Unusual and early onset IPEX syndrome: a case report.
Doğruel D; Gürbüz F; Turan İ; Altıntaş DU; Yılmaz M; Yüksel B
Turk J Pediatr; 2019; 61(4):580-584. PubMed ID: 31990476
[TBL] [Abstract][Full Text] [Related]
18. Fetal-onset IPEX: report of two families and review of literature.
Xavier-da-Silva MM; Moreira-Filho CA; Suzuki E; Patricio F; Coutinho A; Carneiro-Sampaio M
Clin Immunol; 2015 Feb; 156(2):131-40. PubMed ID: 25546394
[TBL] [Abstract][Full Text] [Related]
19. FOXP3 mutations causing early-onset insulin-requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
Hwang JL; Park SY; Ye H; Sanyoura M; Pastore AN; Carmody D; Del Gaudio D; Wilson JF; Hanis CL; Liu X; Atzmon G; Glaser B; Philipson LH; Greeley SAW;
Pediatr Diabetes; 2018 May; 19(3):388-392. PubMed ID: 29193502
[TBL] [Abstract][Full Text] [Related]
20. Lentiviral Gene Therapy in HSCs Restores Lineage-Specific Foxp3 Expression and Suppresses Autoimmunity in a Mouse Model of IPEX Syndrome.
Masiuk KE; Laborada J; Roncarolo MG; Hollis RP; Kohn DB
Cell Stem Cell; 2019 Feb; 24(2):309-317.e7. PubMed ID: 30639036
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
