145 related articles for article (PubMed ID: 33761697)
21. 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]
22. 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]
23. 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]
24. IPEX syndrome from diagnosis to cure, learning along the way.
Bacchetta R; Roncarolo MG
J Allergy Clin Immunol; 2024 Mar; 153(3):595-605. PubMed ID: 38040040
[TBL] [Abstract][Full Text] [Related]
25. Deficiency in Mucosa-associated Lymphoid Tissue Lymphoma Translocation 1: A Novel Cause of IPEX-Like Syndrome.
Charbit-Henrion F; Jeverica AK; Bègue B; Markelj G; Parlato M; Avčin SL; Callebaut I; Bras M; Parisot M; Jazbec J; Homan M; Ihan A; Rieux-Laucat F; Stolzenberg MC; Ruemmele FM; Avčin T; Cerf-Bensussan N;
J Pediatr Gastroenterol Nutr; 2017 Mar; 64(3):378-384. PubMed ID: 27253662
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Opinion and Special Articles: Cerebellar Ataxia and Liver Failure Complicating IPEX Syndrome.
Rim J; Byler M; Soldatos A; Notarangelo L; Leibovitch E; Jacobson S; Gorman M; Lebel RR; Werner K
Neurology; 2021 Feb; 96(6):e956-e959. PubMed ID: 33168705
[No Abstract] [Full Text] [Related]
28. 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]
29. 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]
30. 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]
31. 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]
32. Clinical and immunological characteristics of five patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in China-expanding the atypical phenotypes.
Huang Y; Fang S; Zeng T; Chen J; Yang L; Sun G; Dai R; An Y; Tang X; Dou Y; Zhao X; Zhou L
Front Immunol; 2022; 13():972746. PubMed ID: 36091011
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Long-term disease course in a patient with severe neonatal IPEX syndrome.
Duclaux-Loras R; Collardeau-Frachon S; Nancey S; Fabien N; Kaiserlian D; Lachaux A
Clin Res Hepatol Gastroenterol; 2015 Sep; 39(4):e43-7. PubMed ID: 25977242
[TBL] [Abstract][Full Text] [Related]
35. [Clinical features and genetic analysis of three patients with Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome due to variants of FOXP3 gene].
Zheng C; Meng Y; Deng Z; Liu J; Yan G; Huang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Feb; 41(2):181-186. PubMed ID: 38311556
[TBL] [Abstract][Full Text] [Related]
36. [Girl with IPEX syndrome with low expression of Foxp3].
Horiuchi S; Ishiguro A; Nakagawa T; Shoji K; Nagai A; Arai K; Horikawa R; Kawai T; Watanabe N; Onodera M
Nihon Rinsho Meneki Gakkai Kaishi; 2012; 35(6):526-32. PubMed ID: 23291488
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. 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]
39. 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]
40. 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]
[Previous] [Next] [New Search]