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1 (IBDs, which include ulcerative colitis and Crohn disease).
2 are now the preferred treatment options for Crohn disease.
3 erum in patients with ulcerative colitis and Crohn disease.
4 ncluding vitiligo, rheumatoid arthritis, and Crohn disease.
5 herapeutic interventions in the treatment of Crohn disease.
6 hisms (SNP) of the NOD2 gene associated with Crohn disease.
7 ociated with the increased susceptibility to Crohn disease.
8 E) alone, in the assessment of patients with Crohn disease.
9 ding of active inflammation in patients with Crohn disease.
10 prominently involved in the pathogenesis of Crohn disease.
11 s, particularly the apthoid lesions of early Crohn disease.
12 ulation leads to increased susceptibility to Crohn disease.
13 the demonstration of early apthous ulcers of Crohn disease.
14 nd imaging features of active terminal ileal Crohn disease.
15 are the most sensitive CT findings of active Crohn disease.
16 biopsy were examined for CT signs of active Crohn disease.
17 iologists examined CT images for findings of Crohn disease.
18 opic and histologic findings of inflammatory Crohn disease.
19 variants have been associated with risk for Crohn disease.
20 t in the overall management of patients with Crohn disease.
21 re highly associated with the development of Crohn disease.
22 and may prevent recurrence of postoperative Crohn disease.
23 other specific nutrient deficiencies seen in Crohn disease.
24 he pathogenesis, treatment, and morbidity of Crohn disease.
25 e inflammatory terminal or neoterminal ileal Crohn disease.
26 hibitor infliximab in surgical patients with Crohn disease.
27 increased T(H)1 responses characteristic of Crohn disease.
28 nal ileum, similar to what is found in human Crohn disease.
29 e, in 23 patients known or suspected to have Crohn disease.
30 ve small bowel inflammation in patients with Crohn disease.
31 rder, Blau syndrome, and also predisposes to Crohn disease.
32 act that manifests as ulcerative colitis and Crohn disease.
33 fistulas occur in up to 43% of patients with Crohn disease.
34 f a gene (IBD5) conferring susceptibility to Crohn disease.
35 ine region in 5q31 confers susceptibility to Crohn disease.
36 s proximal in patients with peptic ulcer and Crohn disease.
37 c stricture, bowel obstruction, fibrosis, or Crohn disease.
38 es were found primarily in the children with Crohn disease.
39 liximab therapy in children with small bowel Crohn disease.
40 ts for quality and diagnostic confidence for Crohn disease.
41 onders among patients with clinically active Crohn disease.
42 RTE can be used to detect fibrosis in human Crohn disease.
43 ead use of HSCT for patients with refractory Crohn disease.
44 ients with no history of immunocompromise or Crohn disease.
45 et for several inflammatory diseases such as Crohn disease.
46 tation (HSCT) may benefit some patients with Crohn disease.
47 nt for the management of complex small bowel Crohn disease.
48 purely CRDD in the context of long-standing Crohn disease.
49 the pathogenetic parallels between CRDD and Crohn disease.
50 rheumatoid arthritis, ulcerative colitis and Crohn disease.
51 , lipid levels, height, body mass index, and Crohn disease.
52 when examining skin lesions in patients with Crohn disease.
53 se of LYG related to azathioprine therapy in Crohn disease.
54 currently the standard for imaging perianal Crohn disease.
55 olymorphism analysis in 160 individuals with Crohn disease, 149 individuals with ulcerative colitis,
58 ity of life (HRQOL) in pediatric small bowel Crohn disease (a) change in response to infliximab thera
59 ary end point comprising clinical remission (Crohn Disease Activity Index (CDAI) <150 [range, 0-600])
60 with severe Crohn disease (CD) defined as a Crohn Disease Activity Index (CDAI) greater than 250, an
61 ents with severe Crohn disease, defined by a Crohn Disease Activity Index (CDAI) higher than 250 desp
62 l remission at week 8, measured by Pediatric Crohn Disease Activity Index (PCDAI) score and reduction
63 ory score <7, and/or a decrease >/=70 in the Crohn disease activity index score compared with baselin
64 onders among patients with clinically active Crohn disease after 6 weeks of pharmacologic treatment.
65 onfers increased risk for the development of Crohn disease, although the mechanisms by which single d
67 ren with inflammatory bowel disease (12 with Crohn disease and 12 with ulcerative colitis) and in 23
68 nety subjects (45 with active terminal ileal Crohn disease and 45 without Crohn disease) underwent CT
70 n associated with two inflammatory diseases, Crohn disease and Blau syndrome, and are thought to cont
72 ease based on ileocolonoscopy or established Crohn disease and imaging features of active terminal il
73 amiliar with MR imaging features of perianal Crohn disease and knowledgeable about what features may
74 effective therapy for active and fistulizing Crohn disease and may even be helpful in some patients w
75 gestive of neutrophil activity, and those in Crohn disease and mouse sera were suggestive of both mac
78 diated intestinal inflammation, particularly Crohn disease and pouchitis, whereas viral, bacterial, f
79 tional disorders and ulcerative colitis from Crohn disease and predicting complications of disease.
81 sent a categorization of complex small bowel Crohn disease and review its surgical treatment as a pot
91 Inflammatory bowel diseases (IBD), such as Crohn disease and ulcerative colitis, are chronic relaps
92 Inflammatory bowel disease (IBD), including Crohn disease and ulcerative colitis, is characterized b
96 of some patients with previously intractable Crohn disease, and further TNF-alpha directed therapies
97 disease, but not ulcerative colitis or ileal Crohn disease, and may prevent recurrence of postoperati
99 s of obesity, gastrointestinal malignancies, Crohn disease, and perioperative complications including
100 doscopy had the highest diagnostic yield for Crohn disease, and SBFT had the lowest, but these differ
101 modern trends in the surgical management of Crohn disease, and the increasing use of laparoscopy in
104 ed to treat rheumatoid arthritis, psoriasis, Crohns disease, and osteoporosis, with a total market of
106 anti-TNF therapy not only in RA but also in Crohn disease, ankylosing spondylitis, and several other
109 n addition, advances in biologic therapy for Crohn disease are beginning to be formally evaluated in
112 Emerging innovative treatments for perianal Crohn disease are now available and have the promise to
114 ses (IBDs), including ulcerative colitis and Crohn disease, are chronic inflammatory disorders of the
115 -related p47 GTPase Irgm1 has been linked to Crohn disease as well as susceptibility to tuberculosis.
118 patients undergoing intestinal resection for Crohns disease at The Mount Sinai Hospital from 1976 to
119 on and cancer, as well as conditions such as Crohn disease, atherosclerosis, and Alzheimer disease.
120 tive Crohn disease was active terminal ileal Crohn disease based on ileocolonoscopy or established Cr
121 hen flagellin, was elevated in patients with Crohn disease, but not in patients with ulcerative colit
122 and ciprofloxacin selectively treat colonic Crohn disease, but not ulcerative colitis or ileal Crohn
123 with disease chronicity and angiogenesis in Crohn disease, but not with histologic and clinical mark
127 nd uncovered significant association between Crohn Disease (CD) and the IL12/IL23 pathway, harboring
130 e chronic inflammatory bowel diseases (IBDs)-Crohn disease (CD) and ulcerative colitis (UC)-are idiop
140 ansplantation (HSCT) in patients with severe Crohn disease (CD) defined as a Crohn Disease Activity I
151 severity of disease and additional surgery, Crohn disease (CD) may result in intestinal failure (IF)
152 gut microbial community likely contribute to Crohn disease (CD) pathogenesis; however, direct evidenc
154 is useful in patients undergoing surgery for Crohn disease (CD) to avoid wide small-bowel resections.
155 he odds of having ulcerative colitis (UC) or Crohn disease (CD) were elevated in carriers of the SLC2
157 n genetic risk factor in the pathogenesis of Crohn disease (CD), a chronic relapsing inflammatory dis
160 inflamed intestinal mucosa of patients with Crohn disease (CD), but not in patients with ulcerative
161 testinal fibrosis is a major complication of Crohn disease (CD), but the precise mechanism by which i
162 e associated with rheumatoid arthritis (RA), Crohn disease (CD), type 1 diabetes (T1D), or type 2 dia
163 ole in chronic inflammatory diseases such as Crohn disease (CD), ulcerative colitis, psoriasis, and t
167 e clinically and histologically from that of Crohn disease (CD); however, mucocutaneous granulomatous
169 types related to inflammatory bowel disease (Crohn disease [CD] and ulcerative colitis [UC]) and diab
170 ergence of inflammatory bowel diseases (IBD: Crohn disease [CD] and ulcerative colitis [UC]) where in
171 is (RA) and inflammatory bowel disease (IBD; Crohn disease [CD], ulcerative colitis [UC]) and is inve
172 ation in enterocytes have been documented in Crohn disease, celiac disease, surgical stress, and inte
174 7 levels were decreased in actively inflamed Crohn disease colonic tissues, where CD98 expression was
175 a sensitivity of 90% (18 of 20) for definite Crohn disease (compared with a sensitivity of 80% [16 of
176 cidences of pediatric ulcerative colitis and Crohn disease continue to evolve with geographic variati
177 e presentation of eating disorders including Crohn disease (CrD), celiac disease, gastroesophageal re
182 P = 5.73 x 10-6 for AD, and 6.57 x 10-5 for Crohn disease) demonstrated the same direction of alleli
183 ed clinical trial of 56 children with active Crohn disease despite immunosuppressive treatment, condu
184 raphy for active inflammatory terminal ileal Crohn disease, despite an inferior subjective image qual
185 infectious (HIV) and noninfectious (CGD and Crohn disease) diseases that have been associated with i
187 in responders (those with a decrease in the Crohn disease endoscopic index of severity score of 25-4
190 nd affected gut segments in 10 patients with Crohn disease (four women, six men; median age, 49 years
193 s study provides evidence that children with Crohn disease have alterations in circulating antioxidan
194 e principles of modern surgical treatment of Crohn disease have evolved to bowel conservation such as
195 rich repeat domain, which is associated with Crohn disease, impairs the interaction with FRMPD2, and
196 Seventy-nine patients presented RVF due to Crohn disease in 34 (43%), postoperative in 25 (32%), ob
198 s, 80%) for enabling the detection of active Crohn disease in comparison with CT enteroclysis with na
200 hese results have important implications for Crohn disease in particular and LD mapping in general.
202 is distinguished from granulomatous colitis (Crohn disease) in terms of location of involvement, exte
203 at it occurs in polygenic disorders, such as Crohn disease, in which its mechanism cannot be explaine
204 ly our approach to a genome-wide analysis of Crohn disease, in which we replicate association with 17
205 d CTE images were each visually assessed for Crohn disease involvement in 54 bowel segments with path
210 Malnutrition, which can be present even when Crohn disease is in remission, can affect growth, cellul
215 conditions such as rheumatoid arthritis and Crohn disease, is in part driven by discordant productio
216 ory bowel disease , particularly small bowel Crohn disease, it has also proven useful in assessing th
217 reover, NOD2 deficiency or the presence of a Crohn disease-like Card15 mutation increased Toll-like r
219 on is also implicated in the pathogenesis of Crohn disease, linking these otherwise unrelated entitie
220 enesis of chronic inflammatory diseases like Crohn disease, might thus be considered as a major actor
222 associated with autoimmune diseases such as Crohn disease, multiple sclerosis, and ulcerative coliti
223 ariants predisposing to atrial fibrillation, Crohn disease, multiple sclerosis, rheumatoid arthritis,
224 (n = 16), tubo-ovarian inflammation (n = 5), Crohn disease (n = 10), and internal bowel fistula due t
225 may contribute to the clinical phenotype of Crohn disease, necrotizing enterocolitis, and, perhaps,
227 ith impaired quality of life from refractory Crohn disease not amenable to surgery despite treatment
232 ty-six year old Caucasian woman with colonic Crohn disease on maintenance azathioprine therapy presen
233 categorized as either ulcerative colitis or Crohn disease on the basis of clinical, radiologic, and
234 d, the level of HIV control, and the risk of Crohn disease only among those carrying an intact miR-14
235 had a secondary ICD-9-CM diagnosis code for Crohn disease or if the patient was not continuously enr
236 e of each of these cell types in fibrosis in Crohn disease or other inflammatory bowel diseases is de
237 e), juvenile RA, inflammatory bowel disease (Crohn disease or ulcerative colitis), psoriasis, and pri
238 ents with inflammatory bowel disease, either Crohn disease or ulcerative colitis, are at an increased
239 h colonic levels of CCDC88b in patients with Crohn disease or ulcerative colitis, identifying that ex
241 ease (OR 0.85 [95% CI 0.74-0.98]; p < 0.03), Crohn disease (OR 0.81 [95% CI 0.70-0.94]; p < 0.005), p
242 egulated or excessive T helper cell (T(H))1 (Crohn disease) or T(H)2 (ulcerative colitis) responses.
245 ion false discovery rate P = .009 for AD and Crohn disease, P = 5.73 x 10-6 for AD, and 6.57 x 10-5 f
246 evaluation of both experimental colitis and Crohn disease patients and thereby offers promising tran
247 In addition, (18)F-FDG PET/CT scans of 25 Crohn disease patients were analyzed, and colonic (18)F-
248 hy may effectively be used to follow up both Crohn disease patients without jejunal disease and in pe
249 an Th17 cells, including those isolated from Crohn disease patients, and it is linked to disease, as
251 prebiotics can potentially prevent and treat Crohn disease, pouchitis, and possibly ulcerative coliti
253 as previously reported to be associated with Crohn disease, psoriasis, alopecia areata, and leprosy.
255 ix children with newly diagnosed small bowel Crohn disease receiving infliximab therapy were prospect
257 f the CARD15/NOD2 protein as contributing to Crohn disease represents a major advance in defining dis
259 housands of control subjects from studies of Crohn disease, showing how it controls false positives,
261 Numerous case reports of angioectasias, Crohn disease, small bowel tumors, and other small bowel
262 with a specific role in the investigation of Crohn disease, small-bowel obstruction, and unexplained
264 In children and adolescents with refractory Crohn disease, thalidomide compared with placebo resulte
265 vern, PA) for the treatment of children with Crohn disease that does not respond to conventional mana
266 gh mesalamines are still often used to treat Crohn disease, the evidence for their efficacy is lackin
268 effective in the treatment of patients with Crohn disease, their use should continue to be restricte
269 the inflamed intestine has revealed that in Crohn disease there is predominantly a T helper cell typ
270 ects, whereas in patients with HIV, CGD, and Crohn disease, there was a significant increase in the p
274 ies of the distal gut microbiome, such as in Crohn disease, ulcerative colitis, and infectious coliti
276 Genomics of Alzheimer's Project stage 1) and Crohn disease, ulcerative colitis, rheumatoid arthritis,
277 d pleiotropy between PD and type 1 diabetes, Crohn disease, ulcerative colitis, rheumatoid arthritis,
278 itis, Graves disease, Hashimoto thyroiditis, Crohn disease, ulcerative colitis, systemic lupus erythe
280 terminal ileal Crohn disease and 45 without Crohn disease) underwent CT enterography with a dual-sou
281 eference standard for confirmation of active Crohn disease was active terminal ileal Crohn disease ba
284 which all included patients were at risk for Crohn disease was equal and that all patients had develo
289 nd CT enterography may depict nonobstructive Crohn disease when techniques such as ileoscopy and SBFT
290 associated with a higher susceptibility for Crohn disease, which highlights the physiological import
291 Mutations in NOD2 are highly associated with Crohn disease, which is characterized by dysregulated in
292 is an effective treatment for patients with Crohn disease who are naive to the chimeric TNF antagoni
293 equently than placebo in adult patients with Crohn disease who cannot tolerate infliximab or have sym
294 een evaluated prospectively in patients with Crohn disease who had responded to another anti-TNF agen
295 hy images were evaluated in 19 patients with Crohn disease who had strictures that underwent surgical
298 ars +/- 9) with a proved diagnosis of active Crohn disease who were scheduled to begin therapy with b
300 reviews each category of complex small bowel Crohn disease, with special emphasis on appropriate surg
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