داء بطني (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "داء بطني" in Arabic language version.

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about.com

celiacdisease.about.com

archive.org

bcmj.org

  • "Celiac disease: A review". BCMJ. ج. 43 ع. 7: 390–395. سبتمبر 2001. مؤرشف من الأصل في 22 فبراير 2014. اطلع عليه بتاريخ 15 فبراير 2014.

books.google.com

catholic.org

catholicceliacs.org

celiac.org

codexalimentarius.net

coeliac.org.au

columbia.edu

celiacdiseasecenter.columbia.edu

doi.org

doi.org

dx.doi.org

eden.co.uk

espghan.org

  • Husby S، Koletzko S، Korponay-Szabó IR، Mearin ML، Phillips A، Shamir R، Troncone R، Giersiepen K، Branski D، Catassi C، Lelgeman M، Mäki M، Ribes-Koninckx C، Ventura A، Zimmer KP، ESPGHAN Working Group on Coeliac Disease Diagnosis; ESPGHAN Gastroenterology Committee; European Society for Pediatric Gastroenterology, Hepatology, and Nutrition (يناير 2012). "European Society for Pediatric Gastroenterology, Hepatology, and Nutrition guidelines for the diagnosis of coeliac disease" (PDF). J Pediatr Gastroenterol Nutr (Practice Guideline). ج. 54 ع. 1: 136–60. DOI:10.1097/MPG.0b013e31821a23d0. PMID:22197856. S2CID:15029283. مؤرشف من الأصل (PDF) في 2016-04-03. اطلع عليه بتاريخ 2016-03-19. Since 1990, the understanding of the pathological processes of CD has increased enormously, leading to a change in the clinical paradigm of CD from a chronic, gluten-dependent enteropathy of childhood to a systemic disease with chronic immune features affecting different organ systems. (...) atypical symptoms may be considerably more common than classic symptoms

europa.eu

ec.europa.eu

europeanreview.org

fda.gov

  • "What is Gluten-Free? FDA Has an Answer". إدارة الغذاء والدواء. 2 أغسطس 2013. مؤرشف من الأصل في 4 أغسطس 2013. اطلع عليه بتاريخ 2 أغسطس 2013. As one of the criteria for using the claim 'gluten-free,' FDA is setting a gluten limit of less than 20 ppm (parts per million) in foods that carry this label. This is the lowest level that can be consistently detected in foods using valid scientific analytical tools. Also, most people with celiac disease can tolerate foods with very small amounts of gluten. This level is consistent with those set by other countries and international bodies that set food safety standards.

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harvard.edu

ui.adsabs.harvard.edu

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nice.org.uk

guidance.nice.org.uk

nih.gov

ncbi.nlm.nih.gov

  • Tovoli F، Masi C، Guidetti E، Negrini G، Paterini P، Bolondi L (مارس 2015). "Clinical and diagnostic aspects of gluten related disorders". World Journal of Clinical Cases (Review). ج. 3 ع. 3: 275–84. DOI:10.12998/wjcc.v3.i3.275. PMC:4360499. PMID:25789300.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
  • Ciccocioppo R، Kruzliak P، Cangemi GC، Pohanka M، Betti E، Lauret E، Rodrigo L (22 أكتوبر 2015). "The Spectrum of Differences between Childhood and Adulthood Celiac Disease". Nutrients (Review). ج. 7 ع. 10: 8733–51. DOI:10.3390/nu7105426. PMC:4632446. PMID:26506381. Several additional studies in extensive series of coeliac patients have clearly shown that TG2A sensitivity varies depending on the severity of duodenal damage, and reaches almost 100% in the presence of complete villous atrophy (more common in children under three years), 70% for subtotal atrophy, and up to 30% when only an increase in IELs is present. (IELs: intraepithelial lymphocytes){{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
  • Lebwohl B، Ludvigsson JF، Green PH (أكتوبر 2015). "Celiac disease and non-celiac gluten sensitivity". BMJ (Review). ج. 351: h4347. DOI:10.1136/bmj.h4347. PMC:4596973. PMID:26438584. Celiac disease occurs in about 1% of the population worldwide, although most people with the condition are undiagnosed. It can cause a wide variety of symptoms, both intestinal and extra-intestinal because it is a systemic autoimmune disease that is triggered by dietary gluten. Patients with coeliac disease are at increased risk of cancer, including a twofold to fourfold increased risk of non-Hodgkin's lymphoma and a more than 30-fold increased risk of small intestinal adenocarcinoma, and they have a 1.4-fold increased risk of death.
  • Vivas S، Vaquero L، Rodríguez-Martín L، Caminero A (نوفمبر 2015). "Age-related differences in celiac disease: Specific characteristics of adult presentation". World Journal of Gastrointestinal Pharmacology and Therapeutics (Review). ج. 6 ع. 4: 207–12. DOI:10.4292/wjgpt.v6.i4.207. PMC:4635160. PMID:26558154. In addition, the presence of intraepithelial lymphocytosis and/or villous atrophy and crypt hyperplasia of small-bowel mucosa, and clinical remission after withdrawal of gluten from the diet, are also used for diagnosis antitransglutaminase antibody (tTGA) titers and the degree of histological lesions inversely correlate with age. Thus, as the age of diagnosis increases antibody titers decrease and histological damage is less marked. It is common to find adults without villous atrophy showing only an inflammatory pattern in duodenal mucosa biopsies: Lymphocytic enteritis (Marsh I) or added crypt hyperplasia (Marsh II){{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
  • Penagini F، Dilillo D، Meneghin F، Mameli C، Fabiano V، Zuccotti GV (نوفمبر 2013). "Gluten-free diet in children: an approach to a nutritionally adequate and balanced diet". Nutrients (Review). ج. 5 ع. 11: 4553–65. DOI:10.3390/nu5114553. PMC:3847748. PMID:24253052.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
  • Comino I، Moreno M، Sousa C (نوفمبر 2015). "Role of oats in celiac disease". World Journal of Gastroenterology. ج. 21 ع. 41: 11825–31. DOI:10.3748/wjg.v21.i41.11825. PMC:4631980. PMID:26557006. It is necessary to consider that oats include many varieties, containing various amino acid sequences and showing different immunoreactivities associated with toxic prolamins. As a result, several studies have shown that the immunogenicity of oats varies depending on the cultivar consumed. Thus, it is essential to thoroughly study the variety of oats used in a food ingredient before including it in a gluten-free diet.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
  • Ludvigsson JF، Card T، Ciclitira PJ، Swift GL، Nasr I، Sanders DS، Ciacci C (أبريل 2015). "Support for patients with celiac disease: A literature review". United European Gastroenterology Journal (Review). ج. 3 ع. 2: 146–59. DOI:10.1177/2050640614562599. PMC:4406900. PMID:25922674.
  • van Heel DA، West J (يوليو 2006). "Recent advances in coeliac disease". Gut (Review). ج. 55 ع. 7: 1037–46. DOI:10.1136/gut.2005.075119. PMC:1856316. PMID:16766754.
  • Schuppan D, Zimmer KP (December 2013). "The diagnosis and treatment of celiac disease". Deutsches Ärzteblatt International. 110 (49): 835–46. doi:10.3238/arztebl.2013.0835. PMC 3884535. PMID 24355936.
  • Di Sabatino A, Corazza GR (April 2009). "Coeliac disease". Lancet. 373 (9673): 1480–93. doi:10.1016/S0140-6736(09)60254-3. PMID 19394538. S2CID 8415780.
  • Vriezinga SL, Schweizer JJ, Koning F, Mearin ML (September 2015). "Coeliac disease and gluten-related disorders in childhood". Nature Reviews. Gastroenterology & Hepatology (Review). 12 (9): 527–36. doi:10.1038/nrgastro.2015.98. PMID 26100369. S2CID 2023530.
  • van Heel DA, West J (July 2006). "Recent advances in coeliac disease". Gut (Review). 55 (7): 1037–46. doi:10.1136/gut.2005.075119. PMC 1856316. PMID 16766754.
  • Ludvigsson JF, Card T, Ciclitira PJ, Swift GL, Nasr I, Sanders DS, Ciacci C (April 2015). "Support for patients with celiac disease: A literature review". United European Gastroenterology Journal (Review). 3 (2): 146–59. doi:10.1177/2050640614562599. PMC 4406900. PMID 25922674.
  • Lionetti E, Gatti S, Pulvirenti A, Catassi C (June 2015). "Celiac disease from a global perspective". Best Practice & Research. Clinical Gastroenterology (Review). 29 (3): 365–79. doi:10.1016/j.bpg.2015.05.004. PMID 26060103.
  • Ferguson R, Basu MK, Asquith P, Cooke WT (1976). "Jejunal mucosal abnormalities in patients with recurrent aphthous ulceration". Br Med J. 1 (6000): 11–13. doi:10.1136/bmj.1.6000.11. PMC 1638254. PMID 1247715.
  • Irvine, AJ; Chey, WD; Ford, AC (January 2017). "Screening for Celiac Disease in Irritable Bowel Syndrome: An Updated Systematic Review and Meta-analysis" (PDF). The American Journal of Gastroenterology. 112 (1): 65–76. doi:10.1038/ajg.2016.466. PMID 27753436. S2CID 269053.
  • Fasano Alessio, Caio Giacomo; Catassi Carlo, Volta Umberto (July 2019). "Celiac disease: a comprehensive current review". BMC Medicine. Springer Nature. 17 (1): 142. doi:10.1186/s12916-019-1380-z. PMC 6647104. PMID 31331324.
  • Gujral N, Freeman HJ, Thomson AB (November 2012). "Celiac disease: prevalence, diagnosis, pathogenesis and treatment" (PDF). World Journal of Gastroenterology. 18 (42): 6036–59. doi:10.3748/wjg.v18.i42.6036. PMC 3496881. PMID 23155333. Archived from the original (PDF) on 20 March 2014.
  • "American Gastroenterological Association medical position statement: Celiac Sprue". Gastroenterology. 120 (6): 1522–5. 2001. doi:10.1053/gast.2001.24055. PMID 11313323. S2CID 28235994.
  • Presutti RJ, Cangemi JR, Cassidy HD, Hill DA (2007). "Celiac disease". Am Fam Physician. 76 (12): 1795–802. PMID 18217518.
  • Cunningham-Rundles C (September 2001). "Physiology of IgA and IgA deficiency". J. Clin. Immunol. 21 (5): 303–9. doi:10.1023/A:1012241117984. PMID 11720003. S2CID 13285781.
  • Marks J, Shuster S, Watson AJ (1966). "Small-bowel changes in dermatitis herpetiformis". Lancet. 2 (7476): 1280–2. doi:10.1016/S0140-6736(66)91692-8. PMID 4163419.
  • Nicolas ME, Krause PK, Gibson LE, Murray JA (August 2003). "Dermatitis herpetiformis". Int. J. Dermatol. 42 (8): 588–600. doi:10.1046/j.1365-4362.2003.01804.x. PMID 12890100. S2CID 42280769.
  • Di Sabatino A, Corazza GR (April 2009). "Coeliac disease". Lancet. 373 (9673): 1480–93. doi:10.1016/S0140-6736(09)60254-3. PMID 19394538. S2CID 8415780.
  • Tersigni C, Castellani R, de Waure C, Fattorossi A, De Spirito M, Gasbarrini A, Scambia G, Di Simone N (2014). "Celiac disease and reproductive disorders: meta-analysis of epidemiologic associations and potential pathogenic mechanisms". Human Reproduction Update. 20 (4): 582–93. doi:10.1093/humupd/dmu007. PMID 24619876.
  • Ferguson A, Hutton MM, Maxwell JD, Murray D (1970). "Adult coeliac disease in hyposplenic patients". Lancet. 1 (7639): 163–4. doi:10.1016/S0140-6736(70)90405-8. PMID 4189238.
  • Lundin KE, Wijmenga C (September 2015). "Coeliac disease and autoimmune disease-genetic overlap and screening". Nature Reviews. Gastroenterology & Hepatology (Review). 12 (9): 507–15. doi:10.1038/nrgastro.2015.136. PMID 26303674. S2CID 24533103. The abnormal immunological response elicited by gluten-derived proteins can lead to the production of several different autoantibodies, which affect different systems.
  • Jabri B، Kupfer SS ((2012)). [22 (4): 639–60. doi:10.1016/j.giec.2012.07.003. PMC 3872820. PMID 23083984. ""Pathophysiology of celiac disease""]. Gastrointest Endosc Clin N Am (Review). DOI:Gluten comprises two different protein types, gliadins and glutenins, capable of triggering disease. {{استشهاد بدورية محكمة}}: تحقق من التاريخ في: |تاريخ= (مساعدةتأكد من صحة قيمة |doi= (مساعدة)، وتحقق من قيمة |مسار= (مساعدة)
  • Lebwohl B، Ludvigsson JF، Green PH (أكتوبر 2015). "Celiac disease and non-celiac gluten sensitivity". BMJ. ج. 351: h4347. DOI:10.1136/bmj.h4347. PMC:4596973. PMID:26438584.
  • Gujral N، Freeman HJ، Thomson AB (نوفمبر 2012). "Celiac disease: prevalence, diagnosis, pathogenesis and treatment" (PDF). World Journal of Gastroenterology. ج. 18 ع. 42: 6036–59. DOI:10.3748/wjg.v18.i42.6036. PMC:3496881. PMID:23155333. مؤرشف من الأصل (PDF) في 20 مارس 2014.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
  • Kim C، Quarsten H، Bergseng E، Khosla C، Sollid L (2004). "Structural basis for HLA-DQ2-mediated presentation of gluten epitopes in celiac disease". Proc Natl Acad Sci USA. ج. 101 ع. 12: 4175–9. Bibcode:2004PNAS..101.4175K. DOI:10.1073/pnas.0306885101. PMC:384714. PMID:15020763.
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  • Zhernakova A، Elbers CC، Ferwerda B، Romanos J، Trynka G، Dubois PC، de Kovel CG، Franke L، Oosting M، Barisani D، Bardella MT، Joosten LA، Saavalainen P، van Heel DA، Catassi C، Netea MG، Wijmenga C (2010). "Evolutionary and functional analysis of celiac risk loci reveals SH2B3 as a protective factor against bacterial infection". American Journal of Human Genetics. ج. 86 ع. 6: 970–7. DOI:10.1016/j.ajhg.2010.05.004. PMC:3032060. PMID:20560212.
  • Lammers KM، Lu R، Brownley J، Lu B، Gerard C، Thomas K، Rallabhandi P، Shea-Donohue T، Tamiz A، Alkan S، Netzel-Arnett S، Antalis T، Vogel SN، Fasano A (2008). "Gliadin induces an increase in intestinal permeability and zonulin release by binding to the chemokine receptor CXCR3". Gastroenterology. ج. 135 ع. 1: 194–204.e3. DOI:10.1053/j.gastro.2008.03.023. PMC:2653457. PMID:18485912.
  • Qiao SW, Bergseng E, Molberg Ø, et al. (August 2004). "Antigen presentation to celiac lesion-derived T cells of a 33-mer gliadin peptide naturally formed by gastrointestinal digestion". J. Immunol. 173 (3): 1757–62. doi:10.4049/jimmunol.173.3.1757. PMID 15265905. S2CID 24910686.
  • van Heel DA, West J (July 2006). "Recent advances in coeliac disease". Gut (Review). 55 (7): 1037–46. doi:10.1136/gut.2005.075119. PMC 1856316. PMID 16766754.
  • Biesiekierski, Jessica R (2017). "What is gluten?". Journal of Gastroenterology and Hepatology. 32: 78–81. doi:10.1111/jgh.13703. PMID 28244676. S2CID 6493455. Similar proteins to the gliadin found in wheat exist as secalin in rye, hordein in barley, and avenins in oats and are collectively referred to as “gluten.” Derivatives of these grains such as triticale and malt and other ancient wheat varieties such as spelt and kamut also contain gluten. The gluten found in all of these grains has been identified as the component capable of triggering the immune-mediated disorder, coeliac disease.
  • Shan L, Qiao SW, Arentz-Hansen H, Molberg Ø, Gray GM, Sollid LM, Khosla C (2005). "Identification and analysis of multivalent proteolytically resistant peptides from gluten: implications for celiac sprue". J. Proteome Res. 4 (5): 1732–41. doi:10.1021/pr050173t. PMC 1343496. PMID 16212427.
  • Comino I, Moreno M, Sousa C (November 2015). "Role of oats in celiac disease". World Journal of Gastroenterology. 21 (41): 11825–31. doi:10.3748/wjg.v21.i41.11825. PMC 4631980. PMID 26557006. It is necessary to consider that oats include many varieties, containing various amino acid sequences and showing different immunoreactivities associated with toxic prolamins. As a result, several studies have shown that the immunogenicity of oats varies depending on the cultivar consumed. Thus, it is essential to thoroughly study the variety of oats used in a food ingredient before including it in a gluten-free diet.
  • Salmi TT، Collin P، Korponay-Szabó IR، Laurila K، Partanen J، Huhtala H، Király R، Lorand L، Reunala T، Mäki M، Kaukinen K (2006). "Endomysial antibody-negative coeliac disease: clinical characteristics and intestinal autoantibody deposits". Gut. ج. 55 ع. 12: 1746–53. DOI:10.1136/gut.2005.071514. PMC:1856451. PMID:16571636.
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  • Cichewicz AB, Mearns ES, Taylor A, Boulanger T, Gerber M, Leffler DA, et al. (1 March 2019). "Diagnosis and Treatment Patterns in Celiac Disease". Dig Dis Sci(Review). 64 (8): 2095–2106. doi:10.1007/s10620-019-05528-3. PMID 30820708. S2CID 71143826.
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  • Skovbjerg H, Norén O, Anthonsen D, Moller J, Sjöström H (2002). "Gliadin is a good substrate of several transglutaminases: possible implication in the pathogenesis of coeliac disease". Scand J Gastroenterol. 37 (7): 812–7. doi:10.1080/713786534. PMID 12190095
  • Sblattero D, Berti I, Trevisiol C, Marzari R, Tommasini A, Bradbury A, Fasano A, Ventura A, Not T (2000). "Human recombinant tissue transglutaminase ELISA: an innovative diagnostic assay for celiac disease". Am. J. Gastroenterol.95 (5): 1253–57. PMID 10811336.
  • Korponay-Szabó IR, Dahlbom I, Laurila K, Koskinen S, Woolley N, Partanen J, Kovács JB, Mäki M, Hansson T (2003). "Elevation of IgG antibodies against tissue transglutaminase as a diagnostic tool for coeliac disease in selective IgA deficiency". Gut. 52 (11): 1567–71. doi:10.1136/gut.52.11.1567. PMC 1773847. PMID 14570724.
  • Husby S, Koletzko S, Korponay-Szabó IR, Mearin ML, Phillips A, Shamir R, Troncone R, Giersiepen K, Branski D, Catassi C, Lelgeman M, Mäki M, Ribes-Koninckx C, Ventura A, Zimmer KP, ESPGHAN Working Group on Coeliac Disease Diagnosis; ESPGHAN Gastroenterology Committee; European Society for Pediatric Gastroenterology, Hepatology, and Nutrition (January 2012). "European Society for Pediatric Gastroenterology, Hepatology, and Nutrition guidelines for the diagnosis of coeliac disease" (PDF). J Pediatr Gastroenterol Nutr(Practice Guideline). 54 (1): 136–60. doi:10.1097/MPG.0b013e31821a23d0. PMID 22197856. S2CID 15029283. Archived from the original (PDF) on 3 April 2016. Retrieved 19 March2016. Since 1990, the understanding of the pathological processes of CD has increased enormously, leading to a change in the clinical paradigm of CD from a chronic, gluten-dependent enteropathy of childhood to a systemic disease with chronic immune features affecting different organ systems. (...) atypical symptoms may be considerably more common than classic symptoms
  • "American Gastroenterological Association medical position statement: Celiac Sprue". Gastroenterology. 120 (6): 1522–5. 2001. doi:10.1053/gast.2001.24055. PMID 11313323. S2CID 28235994.
  • Hill ID, Dirks MH, Liptak GS, Colletti RB, Fasano A, Guandalini S, Hoffenberg EJ, Horvath K, Murray JA, Pivor M, Seidman EG (2005). "Guideline for the diagnosis and treatment of celiac disease in children: recommendations of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition". J. Pediatr. Gastroenterol. Nutr.40 (1): 1–19. doi:10.1097/00005176-200501000-00001. PMID 15625418. S2CID 14805217.
  • Hill ID (April 2005). "What are the sensitivity and specificity of serologic tests for celiac disease? Do sensitivity and specificity vary in different populations?" (PDF). Gastroenterology. 128 (4 Suppl 1): S25–32. doi:10.1053/j.gastro.2005.02.012. PMID 15825123. Archived (PDF) from the original on 14 April 2007.
  • Nandiwada SL, Tebo AE (April 2013). "Testing for antireticulin antibodies in patients with celiac disease is obsolete: a review of recommendations for serologic screening and the literature". Clin. Vaccine Immunol. 20(4): 447–51. doi:10.1128/CVI.00568-12. PMC 3623418. PMID 23365209.
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