154 related articles for article (PubMed ID: 35748740)
1. Very-Early Onset Chronic Active Colitis with Heterozygous Variants in
He M; Wong A; Sutton K; Gondim MJB; Samson C
Fetal Pediatr Pathol; 2023 Apr; 42(2):297-306. PubMed ID: 35748740
[TBL] [Abstract][Full Text] [Related]
2. Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease.
Kelsen JR; Dawany N; Moran CJ; Petersen BS; Sarmady M; Sasson A; Pauly-Hubbard H; Martinez A; Maurer K; Soong J; Rappaport E; Franke A; Keller A; Winter HS; Mamula P; Piccoli D; Artis D; Sonnenberg GF; Daly M; Sullivan KE; Baldassano RN; Devoto M
Gastroenterology; 2015 Nov; 149(6):1415-24. PubMed ID: 26193622
[TBL] [Abstract][Full Text] [Related]
3. Hematopoietic stem cell transplantation for CYBB heterozygous mutation resulting in very early onset inflammatory bowel disease in children: a case report.
Li Z; Chen H; Feng X; Ruan Y; Yang M
BMC Pediatr; 2023 Jul; 23(1):348. PubMed ID: 37434114
[TBL] [Abstract][Full Text] [Related]
4. Higher Prevalence of Monogenic Cause Among Very Early Onset Inflammatory Bowel Disease in Children: Experience From a Tertiary Care Center From Northern India.
Poddar U; Aggarwal A; Jayalakshmi K; Sarma MS; Srivastava A; Rawat A; Yachha SK
Inflamm Bowel Dis; 2023 Oct; 29(10):1572-1578. PubMed ID: 36594920
[TBL] [Abstract][Full Text] [Related]
5. A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case report.
Kelsen JR; Dawany N; Martinez A; Grochowski CM; Maurer K; Rappaport E; Piccoli DA; Baldassano RN; Mamula P; Sullivan KE; Devoto M
BMC Gastroenterol; 2015 Nov; 15():160. PubMed ID: 26581487
[TBL] [Abstract][Full Text] [Related]
6. Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic disease.
Dorjbal B; Stinson JR; Ma CA; Weinreich MA; Miraghazadeh B; Hartberger JM; Frey-Jakobs S; Weidinger S; Moebus L; Franke A; Schäffer AA; Bulashevska A; Fuchs S; Ehl S; Limaye S; Arkwright PD; Briggs TA; Langley C; Bethune C; Whyte AF; Alachkar H; Nejentsev S; DiMaggio T; Nelson CG; Stone KD; Nason M; Brittain EH; Oler AJ; Veltri DP; Leahy TR; Conlon N; Poli MC; Borzutzky A; Cohen JI; Davis J; Lambert MP; Romberg N; Sullivan KE; Paris K; Freeman AF; Lucas L; Chandrakasan S; Savic S; Hambleton S; Patel SY; Jordan MB; Theos A; Lebensburger J; Atkinson TP; Torgerson TR; Chinn IK; Milner JD; Grimbacher B; Cook MC; Snow AL
J Allergy Clin Immunol; 2019 Apr; 143(4):1482-1495. PubMed ID: 30170123
[TBL] [Abstract][Full Text] [Related]
7. Phenotypic and genotypic characterization of inflammatory bowel disease in children under six years of age in China.
Fang YH; Luo YY; Yu JD; Lou JG; Chen J
World J Gastroenterol; 2018 Mar; 24(9):1035-1045. PubMed ID: 29531467
[TBL] [Abstract][Full Text] [Related]
8. Very early onset inflammatory bowel disease: Spectrum of clinical presentation, diagnostic tools and outcome in children.
Cheema HA; Waheed N; Saeed A; Fayyaz Z; Anjum MN; Alvi MA; Batool SS
J Pak Med Assoc; 2021 Oct; 71(10):2350-2354. PubMed ID: 34974569
[TBL] [Abstract][Full Text] [Related]
9. The Growing Need to Understand Very Early Onset Inflammatory Bowel Disease.
Zheng HB; de la Morena MT; Suskind DL
Front Immunol; 2021; 12():675186. PubMed ID: 34122435
[TBL] [Abstract][Full Text] [Related]
10. Very Early Onset Inflammatory Bowel Disease: A Clinical Approach With a Focus on the Role of Genetics and Underlying Immune Deficiencies.
Ouahed J; Spencer E; Kotlarz D; Shouval DS; Kowalik M; Peng K; Field M; Grushkin-Lerner L; Pai SY; Bousvaros A; Cho J; Argmann C; Schadt E; Mcgovern DPB; Mokry M; Nieuwenhuis E; Clevers H; Powrie F; Uhlig H; Klein C; Muise A; Dubinsky M; Snapper SB
Inflamm Bowel Dis; 2020 May; 26(6):820-842. PubMed ID: 31833544
[TBL] [Abstract][Full Text] [Related]
11. Genetic Sequencing of Pediatric Patients Identifies Mutations in Monogenic Inflammatory Bowel Disease Genes that Translate to Distinct Clinical Phenotypes.
Ashton JJ; Mossotto E; Stafford IS; Haggarty R; Coelho TAF; Batra A; Afzal NA; Mort M; Bunyan D; Beattie RM; Ennis S
Clin Transl Gastroenterol; 2020 Feb; 11(2):e00129. PubMed ID: 32463623
[TBL] [Abstract][Full Text] [Related]
12. Prevalence and Clinical Features of Inflammatory Bowel Diseases Associated With Monogenic Variants, Identified by Whole-Exome Sequencing in 1000 Children at a Single Center.
Crowley E; Warner N; Pan J; Khalouei S; Elkadri A; Fiedler K; Foong J; Turinsky AL; Bronte-Tinkew D; Zhang S; Hu J; Tian D; Li D; Horowitz J; Siddiqui I; Upton J; Roifman CM; Church PC; Wall DA; Ramani AK; Kotlarz D; Klein C; Uhlig H; Snapper SB; Gonzaga-Jauregui C; Paterson AD; McGovern DPB; Brudno M; Walters TD; Griffiths AM; Muise AM
Gastroenterology; 2020 Jun; 158(8):2208-2220. PubMed ID: 32084423
[TBL] [Abstract][Full Text] [Related]
13. Clinical Spectrum of Monogenic Infantile-Onset Inflammatory Bowel Disease.
Ganesh R; Sathiyasekeran M; Srinivas S; Narayanan RK
Indian J Pediatr; 2022 May; 89(5):497-502. PubMed ID: 35246832
[TBL] [Abstract][Full Text] [Related]
14. Identification and Characterization of a Germline Mutation in CARD11 From a Chinese Case of B Cell Expansion With NF-κB and T Cell Anergy.
Zhao P; Meng Q; Huang Y; Zhang L; Luo S; Zhang X; Tan L; Zhou A; Xiong H; He X
Front Immunol; 2021; 12():676386. PubMed ID: 34557185
[TBL] [Abstract][Full Text] [Related]
15. Mechanistic understanding of the combined immunodeficiency in complete human CARD11 deficiency.
Lu HY; Sharma M; Sharma AA; Lacson A; Szpurko A; Luider J; Dharmani-Khan P; Shameli A; Bell PA; Guilcher GMT; Lewis VA; Vasquez MR; Desai S; McGonigle L; Murguia-Favela L; Wright NAM; Sergi C; Wine E; Overall CM; Suresh S; Turvey SE
J Allergy Clin Immunol; 2021 Dec; 148(6):1559-1574.e13. PubMed ID: 33872653
[TBL] [Abstract][Full Text] [Related]
16. Expanding spectrum, intrafamilial diversity, and therapeutic challenges from 15 patients with heterozygous CARD11-associated diseases: A single center experience.
Urdinez L; Erra L; Palma AM; Mercogliano MF; Fernandez JB; Prieto E; Goris V; Bernasconi A; Sanz M; Villa M; Bouso C; Caputi L; Quesada B; Solis D; Aguirre Bruzzo A; Katsicas MM; Galluzzo L; Weyersberg C; Bocian M; Bujan MM; Oleastro M; Almejun MB; Danielian S
Front Immunol; 2022; 13():1020927. PubMed ID: 36405754
[TBL] [Abstract][Full Text] [Related]
17. Genetic profile of patients with early onset inflammatory bowel disease.
Girardelli M; Basaldella F; Paolera SD; Vuch J; Tommasini A; Martelossi S; Crovella S; Bianco AM
Gene; 2018 Mar; 645():18-29. PubMed ID: 29248579
[TBL] [Abstract][Full Text] [Related]
18. Combined immunodeficiency and atopy caused by a dominant negative mutation in caspase activation and recruitment domain family member 11 (CARD11).
Dadi H; Jones TA; Merico D; Sharfe N; Ovadia A; Schejter Y; Reid B; Sun M; Vong L; Atkinson A; Lavi S; Pomerantz JL; Roifman CM
J Allergy Clin Immunol; 2018 May; 141(5):1818-1830.e2. PubMed ID: 28826773
[TBL] [Abstract][Full Text] [Related]
19. A Unique Heterozygous
Desjardins M; Arjunaraja S; Stinson JR; Dorjbal B; Sundaresan J; Niemela J; Raffeld M; Matthews HF; Wang A; Angelus P; Su HC; Mazer BD; Snow AL
Front Immunol; 2018; 9():2944. PubMed ID: 30619304
[TBL] [Abstract][Full Text] [Related]
20. Case Report: A Novel Compound Heterozygous Mutation in
Dong F; Xiao F; Ge T; Li X; Xu W; Wu S; Zhang T; Wang Y
Front Pediatr; 2021; 9():678390. PubMed ID: 34113591
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
