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For: Terrin G, Tomaiuolo R, Passariello A, Elce A, Amato F, Di Costanzo M, Castaldo G, Canani RB. Congenital diarrheal disorders: an updated diagnostic approach. Int J Mol Sci. 2012;13:4168-4185. [PMID: 22605972 DOI: 10.3390/ijms13044168] [Cited by in Crossref: 46] [Cited by in F6Publishing: 33] [Article Influence: 5.1] [Reference Citation Analysis]
Number Citing Articles
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2 d'Apolito M, Pisanelli D, Faletra F, Giardino I, Gigante M, Pettoello-Mantovani M, Goulet O, Gasparini P, Campanozzi A. Genetic analysis of Italian patients with congenital tufting enteropathy. World J Pediatr 2016;12:219-24. [PMID: 26684320 DOI: 10.1007/s12519-015-0070-y] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 2.2] [Reference Citation Analysis]
3 Siahanidou T, Koutsounaki E, Skiathitou AV, Stefanaki K, Marinos E, Panajiotou I, Chouliaras G. Extraintestinal manifestations in an infant with microvillus inclusion disease: complications or features of the disease? Eur J Pediatr 2013;172:1271-5. [PMID: 23354788 DOI: 10.1007/s00431-013-1948-0] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 0.9] [Reference Citation Analysis]
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8 Gericke B, Amiri M, Scott CR, Naim HY. Molecular pathogenicity of novel sucrase-isomaltase mutations found in congenital sucrase-isomaltase deficiency patients. Biochim Biophys Acta. 2017;1863:817-826. [PMID: 28062276 DOI: 10.1016/j.bbadis.2016.12.017] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 3.3] [Reference Citation Analysis]
9 Canani RB, Castaldo G, Bacchetta R, Martín MG, Goulet O. Congenital diarrhoeal disorders: advances in this evolving web of inherited enteropathies. Nat Rev Gastroenterol Hepatol 2015;12:293-302. [PMID: 25782092 DOI: 10.1038/nrgastro.2015.44] [Cited by in Crossref: 49] [Cited by in F6Publishing: 37] [Article Influence: 8.2] [Reference Citation Analysis]
10 Guarino A, Lo Vecchio A, Berni Canani R. Chronic diarrhoea in children. Best Pract Res Clin Gastroenterol 2012;26:649-61. [PMID: 23384809 DOI: 10.1016/j.bpg.2012.11.004] [Cited by in Crossref: 25] [Cited by in F6Publishing: 19] [Article Influence: 3.1] [Reference Citation Analysis]
11 Bou Chaaya S, Eason JD, Ofoegbu BN. Syndromic congenital diarrhoea: new SPINT2 mutation identified in the UAE. BMJ Case Rep 2017;2017:bcr-2016-217464. [PMID: 28716867 DOI: 10.1136/bcr-2016-217464] [Reference Citation Analysis]
12 Wilschanski M, Abbasi M, Blanco E, Lindberg I, Yourshaw M, Zangen D, Berger I, Shteyer E, Pappo O, Bar-Oz B, Martín MG, Elpeleg O. A novel familial mutation in the PCSK1 gene that alters the oxyanion hole residue of proprotein convertase 1/3 and impairs its enzymatic activity. PLoS One 2014;9:e108878. [PMID: 25272002 DOI: 10.1371/journal.pone.0108878] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 1.4] [Reference Citation Analysis]
13 Bandyopadhyay T, Deswal S, Maria A, Phulware RH, Das P, Ahuja A. Microvillous inclusion disease as a cause of severe congenital diarrhea in a newborn. J Matern Fetal Neonatal Med 2021;:1-3. [PMID: 33843415 DOI: 10.1080/14767058.2021.1910656] [Reference Citation Analysis]
14 Diamanti A, Calvitti G, Martinelli D, Santariga E, Capriati T, Bolasco G, Iughetti L, Pujia A, Knafelz D, Maggiore G. Etiology and Management of Pediatric Intestinal Failure: Focus on the Non-Digestive Causes. Nutrients 2021;13:786. [PMID: 33673586 DOI: 10.3390/nu13030786] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
15 Jayawardena D, Alrefai WA, Dudeja PK, Gill RK. Recent advances in understanding and managing malabsorption: focus on microvillus inclusion disease. F1000Res. 2019;8 (F1000 Faculty Rev):2061. [PMID: 31824659 DOI: 10.12688/f1000research.20762.1] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
16 Cakir M, Sag E, Guven B, Akbulut UE, Issi F, Cebi AH, Müller T, Aldrian D, Janecke AR. Early onset congenital diarrheas; single center experience. Pediatr Neonatol 2021:S1875-9572(21)00122-4. [PMID: 34330684 DOI: 10.1016/j.pedneo.2021.05.024] [Reference Citation Analysis]
17 Haas JT, Winter HS, Lim E, Kirby A, Blumenstiel B, DeFelice M, Gabriel S, Jalas C, Branski D, Grueter CA, Toporovski MS, Walther TC, Daly MJ, Farese RV Jr. DGAT1 mutation is linked to a congenital diarrheal disorder. J Clin Invest 2012;122:4680-4. [PMID: 23114594 DOI: 10.1172/JCI64873] [Cited by in Crossref: 96] [Cited by in F6Publishing: 50] [Article Influence: 10.7] [Reference Citation Analysis]
18 Posovszky C. Congenital intestinal diarrhoeal diseases: A diagnostic and therapeutic challenge. Best Practice & Research Clinical Gastroenterology 2016;30:187-211. [DOI: 10.1016/j.bpg.2016.03.004] [Cited by in Crossref: 19] [Cited by in F6Publishing: 15] [Article Influence: 3.8] [Reference Citation Analysis]
19 Das B, Sivagnanam M. Congenital Tufting Enteropathy: Biology, Pathogenesis and Mechanisms. J Clin Med 2020;10:E19. [PMID: 33374714 DOI: 10.3390/jcm10010019] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
20 Sala Coromina J, Vinaixa Vergés A, Garcia Puig R. [Congenital lactase deficiency: Identification of a new mutation]. An Pediatr (Barc) 2015;82:365-6. [PMID: 25468453 DOI: 10.1016/j.anpedi.2014.10.017] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.1] [Reference Citation Analysis]
21 Canani RB, Terrin G, Elce A, Pezzella V, Heinz-Erian P, Pedrolli A, Centenari C, Amato F, Tomaiuolo R, Calignano A, Troncone R, Castaldo G. Genotype-dependency of butyrate efficacy in children with congenital chloride diarrhea. Orphanet J Rare Dis 2013;8:194. [PMID: 24350656 DOI: 10.1186/1750-1172-8-194] [Cited by in Crossref: 21] [Cited by in F6Publishing: 13] [Article Influence: 2.6] [Reference Citation Analysis]
22 Fernández Caamaño B, Quiles Blanco MJ, Fernández Tomé L, Burgos Lizáldez E, Sarría Osés J, Molina Arias M, Prieto Bozano G. [Intestinal failure and transplantation in microvillous inclusion disease]. An Pediatr (Barc) 2015;83:160-5. [PMID: 25547668 DOI: 10.1016/j.anpedi.2014.11.013] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 0.4] [Reference Citation Analysis]
23 Griswold C, Durica AR, Dennis LG, Jewell AF. Prenatal Bowel Findings in Male Siblings With a Confirmed FOXP3 Mutation: Prenatal Bowel Findings in FOXP3 Mutation. J Ultrasound Med 2018;37:1033-7. [DOI: 10.1002/jum.14428] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
24 Comegna M, Amato F, Liguori R, Berni Canani R, Spagnuolo MI, Morroni M, Guarino A, Castaldo G. Two cases of microvillous inclusion disease caused by novel mutations in MYO5B gene. Clin Case Rep 2018;6:2451-6. [PMID: 30564347 DOI: 10.1002/ccr3.1879] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
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26 Martin BA, Kerner JA, Hazard FK, Longacre TA. Evaluation of intestinal biopsies for pediatric enteropathy: a proposed immunohistochemical panel approach. Am J Surg Pathol 2014;38:1387-95. [PMID: 25188866 DOI: 10.1097/PAS.0000000000000314] [Cited by in Crossref: 14] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
27 Šuligoj T, Ciclitira PJ, Božič B. Diagnostic and Research Aspects of Small Intestinal Disaccharidases in Coeliac Disease. J Immunol Res 2017;2017:1042606. [PMID: 28512643 DOI: 10.1155/2017/1042606] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
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29 Ensari A, Kelsen J, Russo P. Newcomers in paediatric GI pathology: childhood enteropathies including very early onset monogenic IBD. Virchows Arch 2018;472:111-23. [PMID: 28718031 DOI: 10.1007/s00428-017-2197-9] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
30 Schlegel C, Lapierre LA, Weis VG, Williams JA, Kaji I, Pinzon-Guzman C, Prasad N, Boone B, Jones A, Correa H, Levy SE, Han X, Wang M, Thomsen K, Acra S, Goldenring JR. Reversible deficits in apical transporter trafficking associated with deficiency in diacylglycerol acyltransferase. Traffic 2018;19:879-92. [PMID: 30095213 DOI: 10.1111/tra.12608] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.7] [Reference Citation Analysis]
31 Gupta A, Sanville J, Menz T, Warner N, Muise AM, Fiedler K, Martín MG, Padbury J, Phornphutkul C, Sanchez-Esteban J, Cerezo CS. Application of Whole Exome Sequencing in Congenital Secretory Diarrhea Diagnosis. J Pediatr Gastroenterol Nutr 2019;68:e106-8. [PMID: 30633106 DOI: 10.1097/MPG.0000000000002258] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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