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1 que (1172 [96%]) large (>/=15 cm, 444 [36%]) ulcerative (805 [66%]) lesion of the lower limb (733 [60
2 ients had a history of unique neonatal-onset ulcerative and cutaneous lesions in cold-sensitive regio
4 Hemorrhagic cystitis is an inflammatory and ulcerative bladder condition associated with systemic ch
6 asis (85 232), bullous skin diseases (4284), ulcerative colitis (12 203), Crohn's disease (7628), inf
8 relapse in patients with Crohn's disease or ulcerative colitis (approximately 75% of patients experi
9 s disease (hazard ratio 2.19; 1.44-3.34) and ulcerative colitis (hazard ratio 1.63; 1.18-2.27) was si
10 follow-up, 48 men were newly diagnosed with ulcerative colitis (incidence rate (IR) = 36/100,000 per
11 ADT was associated with a decreased risk of ulcerative colitis (IR = 24/100,000 PY vs. IR = 50/100,0
12 ens from the terminal ileum of patients with ulcerative colitis (n = 20), CD (n = 20), or individuals
13 colon tissues from age-matched patients with ulcerative colitis (n=10) vs without IBD (n=8, controls)
14 strong colonic expression, protects against ulcerative colitis (overall P=6.89 x 10(-7), odds ratio=
15 ated macular degeneration (P=1.4 x 10(-12)), ulcerative colitis (P<1.0 x 10(-20)), type 2 diabetes (P
16 ide genetic correlation (rG) between PSC and ulcerative colitis (UC) (rG = 0.29) was significantly gr
17 was associated with Crohn's disease (CD) and ulcerative colitis (UC) among Moroccan patients, and eva
18 The studies included 67,057 patients with ulcerative colitis (UC) and 75,971 patients with Crohn's
19 tic approaches fail to differentiate between ulcerative colitis (UC) and Crohn's colitis (CC) in one-
21 AIMS: The inflammatory bowel diseases (IBD) ulcerative colitis (UC) and Crohn's disease (CD) cause s
24 to determine LP macrophage phenotypes in CD, ulcerative colitis (UC) and healthy controls (HC), and i
25 ase (PIBD), comprising Crohn's disease (CD), ulcerative colitis (UC) and inflammatory bowel disease u
26 ulate inflammation during the development of ulcerative colitis (UC) and progression to colitis-assoc
27 owel disease (IBD), Crohn's disease (CD) and ulcerative colitis (UC) and to compare the occurrence of
29 the mainstay treatments in the management of ulcerative colitis (UC) but up to a third of patients wi
34 hat affect risk for Crohn's disease (CD) and ulcerative colitis (UC) in a case-only study of patients
41 ospective study with Crohn's disease (CD) or ulcerative colitis (UC) patients initiating anti-integri
43 mmon long-term complication in patients with ulcerative colitis (UC) undergoing proctocolectomy with
44 r role in pediatric Crohn's disease (CD) and ulcerative colitis (UC) we obtained mucosal biopsies of
47 cting the colon such as medically refractory ulcerative colitis (UC), aggressive Crohn's disease (CD)
48 , colorectal cancer (CRC), benign neoplasms, ulcerative colitis (UC), and Crohn's disease (CD) betwee
50 The ST2/IL-33 pathway has been related to ulcerative colitis (UC), and soluble ST2 (sST2), to dise
51 es (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), are complex chronic inflammator
54 transabdominal minimal invasive approach in ulcerative colitis (UC), using the comprehensive complic
55 ype 2 immune response in the pathogenesis of ulcerative colitis (UC)-few data are available from trea
76 0.05 for Crohn's disease (CD), p = 0.03 for Ulcerative Colitis (UC); Odds Ratio 1.09, 95 % Confidenc
77 n disease-subtypes, Crohn's disease (CD) and ulcerative colitis (UC); these subtypes share overlappin
78 nts [123 with Crohn disease (CD) and 94 with ulcerative colitis (UC)] were analyzed; 75 of 150 (50%)
79 om patients with Crohn's disease (n = 61) or ulcerative colitis (UC, n = 74) or from patients without
80 R, $87335-$126541]), and total colectomy for ulcerative colitis (WIQR, $24497; median, $34910 [IQR, $
81 disease +11.1% [95% CI 4.8-17.8] and APC for ulcerative colitis +14.9% [10.4-19.6]) and Taiwan (APC f
83 2 per 100 000 in Germany) and North America (ulcerative colitis 286 per 100 000 in the USA; Crohn's d
84 t reported prevalence values were in Europe (ulcerative colitis 505 per 100 000 in Norway; Crohn's di
86 matory bowel disease (Crohn disease [CD] and ulcerative colitis [UC]) and diabetic nephropathy (macro
87 tory bowel disease (IBD; Crohn disease [CD], ulcerative colitis [UC]) and is inversely related to typ
88 h IBD (43 with Crohn's disease [CD], 23 with ulcerative colitis [UC]), and 30 children without IBD (c
89 535 consecutive patients with IBD (211 with ulcerative colitis [UC], 234 with Crohn's disease [CD];
90 roscopy in 110 consecutive subjects (31 with ulcerative colitis [UC], 57 with Crohn's disease [CD], a
94 were present there in 11 of 13 patients with ulcerative colitis and 14 of 15 with Crohn's disease.
96 livered by acute CS had an increased risk of ulcerative colitis and celiac disease, whereas children
98 nflammatory bowel diseases (IBDs), including ulcerative colitis and Crohn disease, are chronic inflam
103 To be included in the systematic review, ulcerative colitis and Crohn's disease needed to be repo
104 lammatory bowel diseases (IBD, which include ulcerative colitis and Crohn's disease) are abdominal pa
105 hitecture of the inflammatory bowel diseases ulcerative colitis and Crohn's disease, we sequenced the
107 had been admitted, unscheduled, with severe ulcerative colitis and failed to respond to intravenous
109 ch as Crohn disease, multiple sclerosis, and ulcerative colitis and hereby elucidate the molecular me
110 strongest associations were observed between ulcerative colitis and HLA rs9271366 (P = 7.5 x 10(-6)),
111 in human ileal tissues from individuals with ulcerative colitis and intestinal carcinomas, also have
113 Ps in IL23R, IL12B, and C2orf43; and between ulcerative colitis and SNPs near HDAC11 and near LINC009
114 reased compared with patients with quiescent ulcerative colitis and that colitis was attenuated in IL
116 at will be available include vedolizumab for ulcerative colitis and ustekinumab for Crohn's disease,
117 Crohn's disease, ileal Crohn's disease, and ulcerative colitis are all genetically distinct from eac
123 tients undergoing colonoscopic screening for ulcerative colitis at the Leicester General Hospital, Le
124 tiating profiles between Crohn's disease and ulcerative colitis by means of (orthogonal) partial leas
125 T cells serves an important role in driving ulcerative colitis by regulating intestinal epithelial c
127 ively, who had moderately to severely active ulcerative colitis despite previous conventional therapy
128 Mayo Clinic endoscopic subscores (MCSe) and ulcerative colitis endoscopic index of severity (UCEIS)
131 ries, with a history (>/=3 months) of active ulcerative colitis extending more than 15 cm beyond the
137 from patients with CD and from patients with ulcerative colitis had distinct changes in DNA methylati
138 Previous retrospective studies of paediatric ulcerative colitis have had limited ability to describe
139 d risk of surgery, while former smokers with ulcerative colitis have increased risk of colectomy.
141 surgery in patients with Crohn's disease and ulcerative colitis have reached inconsistent conclusions
142 diseases (IBD) known as Crohn's disease and ulcerative colitis have shown strong evidence of associa
151 nditions in patients with Crohn's disease or ulcerative colitis is necessary for their total care and
154 dian age 14.1 years; Crohn's disease n = 22, ulcerative colitis n = 26, unclassified colitis n = 11)
155 solated from fecal samples of a patient with ulcerative colitis on the basis of their ability to caus
156 onic tissues from human subjects with active ulcerative colitis or Crohn's disease, implicating the l
157 ith CD, whereas 12 patients had a history of ulcerative colitis or were strongly suspected of CD base
158 nt (rs36095412, p.R179X, genotyped in 11,148 ulcerative colitis patients and 295,446 controls, MAF=up
162 ct from gut microbiota collected from either ulcerative colitis patients or healthy controls, with di
164 ll-characterized large-duct PSC patients, 96 ulcerative colitis patients, and 100 healthy controls.
166 e curve (AUC) of scores from the Crohn's and Ulcerative Colitis Questionnaire (CUCQ) completed by par
167 outcomes of patients with moderate to severe ulcerative colitis receiving tofacitinib, although at an
170 hn's disease and 15 (83.3%) of 18 studies on ulcerative colitis reported stable or decreasing inciden
171 ls, models of neurodegenerative diseases and ulcerative colitis suggest the likelihood of this scenar
174 soriasis, primary sclerosing cholangitis and ulcerative colitis to investigate pleiotropy and the rel
175 he response of children newly diagnosed with ulcerative colitis to standardised initial therapy and i
176 We analyzed data collected during the Active Ulcerative Colitis Trials (ACT-1 and ACT-2) to assess re
180 of IL19 in biopsies of patients with active ulcerative colitis was increased compared with patients
181 of colorectal cancer in Asian patients with ulcerative colitis was similar to recent estimates in Eu
183 e genes were also activated in patients with ulcerative colitis where chronic inflammation predispose
184 "future" cancer progression in patients with ulcerative colitis who did and did not develop colon can
185 patients with moderately-to-severely active ulcerative colitis who had not responded to conventional
186 patients with moderately-to-severely active ulcerative colitis who participated in ACT-1 or ACT-2; e
187 Crohn's disease and 33 patients with active ulcerative colitis who were candidates to receive inflix
189 sis included a total of 31 287 patients with ulcerative colitis with a total of 293 reported colorect
192 bowel disease (IBD; i.e. Crohn's disease or ulcerative colitis) and typically developing children wi
193 ts (19,713 with Crohn's disease, 14,683 with ulcerative colitis) genotyped on the Immunochip array.
195 rohn's disease, colonic Crohn's disease, and ulcerative colitis) than by Crohn's disease and ulcerati
196 variate, Crohn's disease and no IBD (both vs ulcerative colitis) were associated with a lower risk of
197 liac disease, multiple sclerosis, lupus, and ulcerative colitis), the GWAS association arises from mu
200 ents with IBD and colorectal cancer (15 with ulcerative colitis, 14 with Crohn's disease, and 2 with
201 1088 patients with Crohn's disease, 361 with ulcerative colitis, 62 with IBD type unknown, and 1797 c
202 ected in intestinal samples of patients with ulcerative colitis, a condition associated with increase
203 nd their metabolism is often dysregulated in ulcerative colitis, a major category of inflammatory bow
204 als with Crohn disease, 149 individuals with ulcerative colitis, and 142 healthy control subjects to
205 Crohn's disease, 19/100,000 person-years for ulcerative colitis, and 5/100,000 person-years for IBD u
206 probiotic activity used in the treatment of ulcerative colitis, and a carcinogenic activity under ho
208 nts with Crohn's disease and 8 patients with ulcerative colitis, and from normal colon of 8 healthy i
211 ue therapeutic approach for the treatment of ulcerative colitis, and phase 3 studies have been planne
213 arthritis and significantly least similar to ulcerative colitis, and provided support for three addit
214 el diseases (IBD), such as Crohn disease and ulcerative colitis, are chronic relapsing conditions tha
215 tor cells, including pathogenic TH2 cells in ulcerative colitis, but is expressed poorly or not at al
216 of similar efficacy in treating acute severe ulcerative colitis, but there has been no comparative ev
217 ative regulator of innate immunity) in human ulcerative colitis, by comparing monozygotic twins and o
218 atures for different IBD subtypes, including ulcerative colitis, colonic Crohn's disease and ileal Cr
220 g obesity, atherosclerosis, Crohn's disease, ulcerative colitis, drug toxicity, and even autism.
221 on carcinogenesis and in human patients with ulcerative colitis, even in tissue that appears histolog
222 of CCDC88b in patients with Crohn disease or ulcerative colitis, identifying that expression correlat
223 l disease (IBD), including Crohn disease and ulcerative colitis, is characterized by chronic intestin
224 anti-tumor necrosis factor (TNF) therapy in ulcerative colitis, its effects on postoperative outcome
225 ents were allocated to three disease groups (ulcerative colitis, n=37; dysplasia, n=2; colitis-associ
226 rhea (ICD) in rhesus macaques also resembles ulcerative colitis, one form of human inflammatory bowel
228 ears old or younger and had Crohn's disease, ulcerative colitis, or IBD-unclassified with 24,543.0 pa
229 Defined as a diagnosis of Crohn's disease, ulcerative colitis, or inflammatory bowel disease unclas
230 tissues from healthy subjects, patients with ulcerative colitis, patients with celiac disease, and pa
231 mmatory diseases such as Crohn disease (CD), ulcerative colitis, psoriasis, and type 1 diabetes.
232 tween PD and type 1 diabetes, Crohn disease, ulcerative colitis, rheumatoid arthritis, celiac disease
233 heimer's Project stage 1) and Crohn disease, ulcerative colitis, rheumatoid arthritis, type 1 diabete
235 iants and heterozygous advantage observed in ulcerative colitis, suggesting an important role of the
236 estigated to delineate mechanisms regulating ulcerative colitis, the role of acid ceramidase (AC) in
238 the risk of relapse, to discriminate CD from ulcerative colitis, to select candidates to anti-tumor n
239 patients with moderately to severely active ulcerative colitis, tofacitinib was more effective as in
240 This case report presents a patient with ulcerative colitis, with thrombotic complication of the
241 ne patients out of 100 (Crohn's disease- 67, ulcerative colitis- 23 and IBDU-10) had known TPMT mutat
277 icular disease, benign colonic neoplasm, and ulcerative colitis/regional enteritis were included.
278 efficacy in patients with moderate-to-severe ulcerative colitis; however, complex factors determine t
279 Australia (23 with Crohn's colitis, 29 with ulcerative colitis; median age, 45.0 y; 60% male; mean I
284 t is to describe the first pediatric case of ulcerative jejunitis in celiac disease, diagnosed by cap
285 ion of a gluten free diet, also suggest that ulcerative jejunitis is not always associated with refra
289 bited a significantly larger and more severe ulcerative lesion than mice infected with the wild type.
292 n, presented a spontaneous healing after the ulcerative phase despite stable bacterial load, and myco
293 remission in patients with mild to moderate ulcerative proctitis and ulcerative proctosigmoiditis.
294 ission in 546 patients with mild to moderate ulcerative proctitis or ulcerative proctosigmoiditis who
295 colon, to induce remission in patients with ulcerative proctitis or ulcerative proctosigmoiditis.
296 ith mild to moderate ulcerative proctitis or ulcerative proctosigmoiditis who received budesonide foa
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