237 related articles for article (PubMed ID: 26559324)
1. 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]
2. [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]
3. 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]
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. 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]
6. Autoimmune Polyendocrine Syndromes.
Husebye ES; Anderson MS; Kämpe O
N Engl J Med; 2018 Mar; 378(12):1132-1141. PubMed ID: 29562162
[No Abstract] [Full Text] [Related]
7. The immunological and genetic basis of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
Bin Dhuban K; Piccirillo CA
Curr Opin Allergy Clin Immunol; 2015 Dec; 15(6):525-32. PubMed ID: 26485097
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study.
Barzaghi F; Amaya Hernandez LC; Neven B; Ricci S; Kucuk ZY; Bleesing JJ; Nademi Z; Slatter MA; Ulloa ER; Shcherbina A; Roppelt A; Worth A; Silva J; Aiuti A; Murguia-Favela L; Speckmann C; Carneiro-Sampaio M; Fernandes JF; Baris S; Ozen A; Karakoc-Aydiner E; Kiykim A; Schulz A; Steinmann S; Notarangelo LD; Gambineri E; Lionetti P; Shearer WT; Forbes LR; Martinez C; Moshous D; Blanche S; Fisher A; Ruemmele FM; Tissandier C; Ouachee-Chardin M; Rieux-Laucat F; Cavazzana M; Qasim W; Lucarelli B; Albert MH; Kobayashi I; Alonso L; Diaz De Heredia C; Kanegane H; Lawitschka A; Seo JJ; Gonzalez-Vicent M; Diaz MA; Goyal RK; Sauer MG; Yesilipek A; Kim M; Yilmaz-Demirdag Y; Bhatia M; Khlevner J; Richmond Padilla EJ; Martino S; Montin D; Neth O; Molinos-Quintana A; Valverde-Fernandez J; Broides A; Pinsk V; Ballauf A; Haerynck F; Bordon V; Dhooge C; Garcia-Lloret ML; Bredius RG; Kałwak K; Haddad E; Seidel MG; Duckers G; Pai SY; Dvorak CC; Ehl S; Locatelli F; Goldman F; Gennery AR; Cowan MJ; Roncarolo MG; Bacchetta R;
J Allergy Clin Immunol; 2018 Mar; 141(3):1036-1049.e5. PubMed ID: 29241729
[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. 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]
13. 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]
14. 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]
15. Nonclassic Inflammatory Bowel Disease in Young Infants: Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome, and Other Disorders.
Chandrakasan S; Venkateswaran S; Kugathasan S
Pediatr Clin North Am; 2017 Feb; 64(1):139-160. PubMed ID: 27894441
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. IPEX Syndrome: Genetics and Treatment Options.
Ben-Skowronek I
Genes (Basel); 2021 Feb; 12(3):. PubMed ID: 33668198
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
