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1 aseptic abscesses, including IBDs (primarily Crohn's Disease).
2 1 and Paneth cell lysozymes in patients with Crohn's disease.
3 everity of gut-associated conditions such as Crohn's Disease.
4 evealed an increased amount in patients with Crohn's disease.
5 restore CD39 along with immunohomeostasis in Crohn's disease.
6 ent of inflammation and might be a result of Crohn's disease.
7 n why patients with XLA are prone to develop Crohn's disease.
8 nia, low-density-lipoprotein cholesterol and Crohn's disease.
9 agement scenarios for ulcerative colitis and Crohn's disease.
10 g colonoscopies (controls) and patients with Crohn's disease.
11 ne diseases such as rheumatoid arthritis and Crohn's disease.
12 active inflammation in patients with colonic Crohn's Disease.
13 wel disease including ulcerative colitis and Crohn's disease.
14 y studies of medical management of pediatric Crohn's disease.
15 emperate phage sequences in individuals with Crohn's disease.
16 that might contribute to the development of Crohn's disease.
17 intestinal biopsies that poses diagnosis of Crohn's disease.
18 tribute to the development of or result from Crohn's disease.
19 ion studies as linked with increased risk of Crohn's disease.
20 ease continuum within ulcerative colitis and Crohn's disease.
21 ivity and predicting outcomes in small bowel Crohn's disease.
22 ed mucosa and associated with fibrostenosing Crohn's disease.
23 be a new option for the treatment of active Crohn's disease.
24 splenic nodules as a first manifestation of Crohn's Disease.
25 CT-P13 to infliximab in patients with active Crohn's disease.
26 rography were consistent with a diagnosis of Crohn's disease.
27 disease, hereditary polyposis syndromes and Crohn's disease.
28 g clinical remission in patients with active Crohn's disease.
29 ecrease the risk of relapse in patients with Crohn's disease.
30 19 might be a viable therapeutic approach in Crohn's disease.
31 erosis, rheumatoid arthritis, psoriasis, and Crohn's disease.
32 bnormal biomarkers typically associated with Crohn's disease.
33 ation) in patients with treatment-refractory Crohn's disease.
34 ally and biologically in the pathogenesis of Crohn's disease.
35 us adverse event was worsening of underlying Crohn's disease.
36 matory diet with statistical significance in Crohn's disease.
37 olonized with a microbiota from a donor with Crohn's disease.
38 the MAT contribute to the "creeping fat" of Crohn's disease.
39 ory diseases, such as ulcerative colitis and Crohn's disease.
40 m are involved in three viral infections and Crohn's disease.
41 activation of fetal transcription factors in Crohn's disease.
42 this modification might contribute to PD and Crohn's disease.
43 to cardiovascular and metabolic diseases and Crohn's disease.
44 d with increased risk of future diagnosis of Crohn's disease.
45 PD) and also to autoimmune disorders such as Crohn's disease.
46 rus as well as in the inflammatory condition Crohn's disease.
47 with ulcerative colitis 4.0, 95% CI 3.4-4.7; Crohn's disease 2.3, 95% CI 1.8-3.0; and IBD unclassifie
49 coccus gnavus, a prevalent gut microbe, with Crohn's disease, a major type of inflammatory bowel dise
50 observed in blood samples from patients with Crohn's disease accompany acute inflammation; with treat
51 eted a disease activity questionnaire (short Crohn's Disease Activity (sCDAI) or Patient Simple Clini
52 ed twelve patients (72%) had active disease (Crohn's Disease Activity Index > 150) and 44 patients (2
54 ents with a decrease of 70 points or more in Crohn's Disease Activity Index (CDAI) from baseline to w
55 e Crohn's disease at screening, defined as a Crohn's Disease Activity Index (CDAI) of 220-450, with m
56 were correlated with the following indexes: Crohn's disease activity index (CDAI), fCal, serum C-rea
59 imary outcome, defined as an increase in the Crohn's disease activity index score by 70 points or mor
60 ab biosimilar CT-P13 was approved for use in Crohn's disease after clinical comparison with originato
61 on of acquired generalized lipodystrophy and Crohn's disease (AGLCD) featuring a lack of adipose tiss
62 he autophagy gene ATG16L1 is associated with Crohn's disease, an inflammatory bowel disease (IBD), an
63 8% and 0.3% (odds ratio 2.04; 1.59-2.62) for Crohn's disease and 1.3% and 0.7% (odds ratio 1.75; 1.44
66 sy specimens from patients with IBD (30 with Crohn's disease and 27 with ulcerative colitis) and 30 p
67 hildren with a new diagnosis of IBD (71 with Crohn's disease and 41 with ulcerative colitis) and 19 c
68 okinetics were measured in six patients with Crohn's disease and evidence of target engagement assess
69 immune cells among associations stronger in Crohn's disease and in gut mucosa among associations str
70 y and specificity in patients with suspected Crohn's disease and in the detection of inflammatory act
72 opment of IBD as a time-dependent covariate, Crohn's disease and no IBD (both vs ulcerative colitis)
73 sociation studies genetically linked IRGM to Crohn's disease and other inflammatory disorders in whic
76 has been associated with ulcerative colitis, Crohn's disease and potentially could have links with co
77 ope and Israel, comprising 212 patients with Crohn's disease and treatment-refractory, draining, comp
78 Inflammatory bowel diseases (IBDs) such as Crohn's disease and ulcerative colitis are characterized
85 We aimed to identify serum biomarkers of Crohn's disease and ulcerative colitis that can be detec
86 Inflammatory bowel diseases, which include Crohn's disease and ulcerative colitis, affect several m
87 inflammatory bowel disease (IBD), including Crohn's disease and ulcerative colitis, and in 2,4,6-tri
88 nflammatory bowel diseases (IBDs), including Crohn's disease and ulcerative colitis, are associated w
89 ed with inflammatory bowel disease including Crohn's disease and ulcerative colitis, the arthritis re
92 1), 1854 (54.9%) were male, 1923 (57.0%) had Crohn's disease, and 1451 (43.0%) had ulcerative colitis
93 mean age was 15.1 (SD 1.7) years, 69.9% had Crohn's disease, and 30.1% had ulcerative colitis or IBD
94 arrhea (BAD) is common with ileal resection, Crohn's disease, and diarrhea-predominant irritable bowe
95 lymphoma, gastrointestinal stromal tumours, Crohn's disease, and groove pancreatitis are discussed.
97 that are traditional for clinical trials in Crohn's disease, and identify factors that predict benef
100 uced in the small intestine of patients with Crohn's disease, and this correlated with lower frequenc
102 D), which consists of ulcerative colitis and Crohn's disease, are a significant medical burden-70 000
103 hma, atherosclerosis, pulmonary diseases and Crohn's disease as hubs and thus pointing to common infl
104 mmatory bowel diseases (IBDs), in particular Crohn's Disease, aseptic splenic abscesses have been rep
107 in blood samples of pediatric patients with Crohn's disease at diagnosis and later time points to id
108 ast 3 months, assessed as moderate-to-severe Crohn's disease at screening, defined as a Crohn's Disea
109 atients (aged >=6 years) with active luminal Crohn's disease at the time of first exposure to inflixi
111 164 pediatric patients (1-17 years old) with Crohn's disease (B1 or B2) who participated in a North A
113 asmic antibody (ANCA)-associated vasculitis, Crohn's disease, Behcet's disease, eosinophilic granulom
115 composition of the intestinal microbiota in Crohn's disease, but its role on skin microbiota is unkn
116 (IBD), that includes ulcerative colitis and Crohn's disease, can affect not only the gastrointestina
120 truncation in colon biopsy specimens from 16 Crohn's disease (CD) and 6 ulcerative colitis (UC) patie
121 arker for active ileocolonic inflammation in Crohn's disease (CD) and assess its diagnostic performan
123 e been proposed for patients with refractory Crohn's disease (CD) and fistulizing CD, respectively.
124 LCV is a rare dermatologic manifestation of Crohn's disease (CD) and may occur with the onset of the
125 are a frequent complication in patients with Crohn's Disease (CD) and the presence of fibrosis within
127 d to examine possible symptom profiles among Crohn's disease (CD) and ulcerative colitis (UC) patient
128 Inflammatory bowel diseases (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), are co
129 mmatory bowel diseases (IBDs), which include Crohn's disease (CD) and ulcerative colitis (UC), are mu
130 ing chronic gastrointestinal inflammation in Crohn's disease (CD) and ulcerative colitis (UC), in hum
131 Inflammatory bowel disease (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), is a d
134 small intestinal epithelial cells (IECs) in Crohn's disease (CD) exhibit impaired GPX4 activity and
137 ative colitis (UC) and 108 incident cases of Crohn's disease (CD) in patients with microscopic coliti
143 ctive control of the inflammatory process in Crohn's disease (CD) is reflected in intestinal mucosal
145 etic resonance index of activity (MARIA) for Crohn's disease (CD) is used to assess the activity of l
148 ced by the dramatic therapeutic responses in Crohn's disease (CD) patients induced by chimeric anti-T
152 thin the heterogeneous spectrum of pediatric Crohn's disease (CD) should improve patient management a
153 sitic infestations have a lower incidence of Crohn's disease (CD) than nonendemic countries, and ther
154 ostoperative disease course of patients with Crohn's disease (CD) who have undergone ileocecal resect
155 ned intestinal tissues from 92 patients with Crohn's disease (CD), 48 patients with ulcerative coliti
156 commended for children with mild to moderate Crohn's disease (CD), but implementation is challenging.
157 stinal permeability has been associated with Crohn's disease (CD), but it is not clear whether it is
158 s the only established dietary treatment for Crohn's disease (CD), but its acceptability is limited.
159 had little impact on intestinal fibrosis in Crohn's disease (CD), increased understanding of the pat
160 ts were grouped based on ultimate diagnosis: Crohn's disease (CD), Irritable bowel syndrome (IBS), NS
161 an effective therapy for moderate to severe Crohn's disease (CD), its effects on the microscopic man
162 hronic inflammatory diseases like psoriasis, Crohn's disease (CD), multiple sclerosis (MS), rheumatoi
163 associated with systemic sclerosis (SSc) and Crohn's disease (CD), some of which confer susceptibilit
164 ated the common genetic basis between CC and Crohn's disease (CD), ulcerative colitis (UC), and celia
165 rs influencing intestinal ACE2 expression in Crohn's disease (CD), ulcerative colitis (UC), and non-i
166 patients with UC compared with patients with Crohn's disease (CD)-associated colitis or without infla
186 inflamed and non-inflamed colonic mucosa [50 Crohn's disease (CD); 80 ulcerative colitis (UC); 31 con
189 (211 with ulcerative colitis [UC], 234 with Crohn's disease [CD]; 236 male), enrolled in Germany fro
190 inflammatory bowel disease(IBD) particularly Crohn's disease(CD), where associations with high and lo
191 barrier are associated with diseases such as Crohn's disease, colitis, and colon cancer, but mechanis
192 rofiles of CD8(+) T cells from children with Crohn's disease correlated with age but not with disease
193 uggest that the inflammatory milieu found in Crohn's disease could lead to or result from deregulatio
194 Most CpG methylation changes associated with Crohn's disease disappeared with treatment of inflammati
195 ulcers in the ileum or colon, or both, and a Crohn's Disease Endoscopic Index of Severity (CDEIS) of
196 ctivity on colonoscopy was measured with the Crohn's Disease Endoscopic Index of Severity (CDEIS).
197 we compare scRNA-seq profiles from pediatric Crohn's disease epithelium alongside matched healthy con
200 s were aged 18-75 years, with a diagnosis of Crohn's disease for at least 3 months, assessed as moder
201 genetic risk scores (GRSs) in distinguishing Crohn's disease from healthy samples, but also serve to
202 atients with ulcerative colitis and inactive Crohn's disease have lower levels of CRT, which might co
203 ease progression compared with patients with Crohn's disease (HR, 1.56; P < .001) or no IBD (HR, 1.15
204 nical benefits of cytokine blockade in ileal Crohn's disease (iCD) are limited to a subset of patient
205 the analyses of microbiomes of patients with Crohn's disease identifies 52 host and 136 microbial pro
206 n subjects with active ulcerative colitis or Crohn's disease, implicating the loss of this barrier-pr
207 we provide a physician-oriented overview of Crohn's disease in adults, ranging from epidemiology and
211 egy designed to predict the future course of Crohn's disease in patients with quiescent disease.
212 nduction of TNFalpha, ultimately aggravating Crohn's disease in the AGLCD patient, which can be rever
214 factors have been implicated in the cause of Crohn's disease, including a dysregulated immune system,
215 ceptibility variants for ulcerative colitis, Crohn's disease, inflammatory bowel disease, celiac dise
216 an 18 years with quiescent (for 3-24 months) Crohn's disease involving the small bowel with confirmed
222 ophagy in intestinal defense and suggest why Crohn's disease is associated with genetic mutations tha
224 r1 displayed mucosal dysfunction and induced Crohn's disease-like ileitis following transfer into Rag
226 analysis included 329 participants; 168 with Crohn's disease (median sCDAI score 93 [IQR 47-156]), an
228 We assessed the ability of the different Crohn's disease monitoring methods used to predict the o
229 ylation profiles at the time of diagnosis of Crohn's disease more closely resembled patterns observed
230 th numerous immunological diseases including Crohn's disease, multiple sclerosis, chronic lymphocytic
231 = 147), rheumatoid arthritis (RA, n = 229), Crohn's disease (n = 148), or ulcerative colitis (n = 36
232 from patients archived before a diagnosis of Crohn's disease (n = 200) or ulcerative colitis (n = 199
233 patients with ulcerative colitis (n = 4671), Crohn's disease (n = 3780), and IBD unclassified (n = 99
234 analyses of colon tissues from patients with Crohn's disease (n = 61) or ulcerative colitis (UC, n =
240 le-blind trial of 52 patients with quiescent Crohn's disease or ulcerative colitis and persistent gut
241 ed from control individuals vs patients with Crohn's disease or ulcerative colitis did not differ sig
243 and colon biopsy samples from patients with Crohn's disease or ulcerative colitis or healthy individ
244 d from healthy individuals and patients with Crohn's disease or ulcerative colitis secreted IL22, whi
247 in patients with gastrointestinal bleeding, Crohn's disease, or celiac disease, who have had negativ
248 hepatitis C, psoriasis, psoriatic arthritis, Crohn's disease, or ulcerative colitis and who were in c
249 uding asthma, breast cancer, celiac disease, Crohn's disease, Parkinson's disease and type 2 diabetes
250 arnelian's effectiveness on type 2 diabetes, Crohn's disease, Parkinson's disease, and industrialized
253 ulcerative colitis patients when compared to Crohn's disease patients (27% vs. 5%, P < 0.001) within
254 ApoA1 expression, which is downregulated in Crohn's disease patients and causally linked to colitis
255 the intestinal mucosa in healthy people and Crohn's disease patients and identified fungi specifical
256 ebsiella strains isolated from the saliva of Crohn's disease patients can induce Th1 cell responses t
259 ient was compared to healthy individuals and Crohn's disease patients regarding immune cell compositi
260 nal CD14(+)CD11c(+) macrophages and mucus of Crohn's disease patients were separated into different c
265 to address severe and extensive small bowel Crohn's disease presenting with 3 severely fibrotic and
267 vious medical and drug history, and previous Crohn's disease-related surgeries were recorded at basel
270 f these findings, our study of patients with Crohn's disease revealed significantly reduced frequenci
272 sease (rg = 0.12 +/- 0.03, P = 2.49 x 10-4), Crohn's disease (rg = 0.097 +/- 0.06, P = 3.27 x 10-3),
275 cohort of 1240 biologic-naive patients with Crohn's disease starting infliximab or adalimumab therap
277 be critical for signaling downstream of the Crohn's disease susceptibility protein nucleotide-bindin
278 lonality in systemic lupus erythematosus and Crohn's disease that was dominated by the IgA isotype, t
281 of developing the inflammatory bowel disease Crohn's disease, thus suggesting that the loss of the im
282 asuring plasma thymidine levels in suspected Crohn's disease to rule out MNGIE, particularly if white
283 edictions from genes known to be involved in Crohn's disease, to genes that are not known to have an
284 umans, gut microbiota density was reduced in Crohn's disease, ulcerative colitis, and ileal pouch-ana
285 atients were 17 years old or younger and had Crohn's disease, ulcerative colitis, or IBD-unclassified
287 s1734907 modulates risk of schizophrenia and Crohn's disease via altered methylation and expression o
288 on profiles of DNA collected at diagnosis of Crohn's disease vs during the follow-up period showed th
290 matory bowel diseases ulcerative colitis and Crohn's disease, we sequenced the whole genomes of 4,280
291 E mediated gastrointestinal food allergy and Crohn's disease, we tested whether therapeutic feeds eff
292 ere up-regulated in serum from patients with Crohn's disease were identified based on changes in prot
293 articipants with irritable bowel syndrome or Crohn's disease were more likely to have continued sympt
294 A total of 193 patients (57% female and 64% Crohn's disease) were included, with a median daily TG d
295 rity study, we enrolled patients with active Crohn's disease who had not responded to, or were intole
296 outcomes in patients with moderate to severe Crohn's disease who were managed with a tight control al
297 non-inferior to infliximab in patients with Crohn's disease who were naive to biological therapy.
299 1 protein biomarkers that were predictive of Crohn's disease within 5 years with an AUROC of 0.76 and