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6. Congenital Diarrhea and Enteropathies in Infants: Approach to Diagnosis. Mantoo MR; Malik R; Das P; Yadav R; Nakra T; Chouhan P Indian J Pediatr; 2021 Nov; 88(11):1135-1138. PubMed ID: 34292522 [TBL] [Abstract][Full Text] [Related]
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9. Approach to Congenital Diarrhea and Enteropathies (CODEs). Kijmassuwan T; Balouch F Indian J Pediatr; 2024 Jun; 91(6):598-605. PubMed ID: 38105403 [TBL] [Abstract][Full Text] [Related]
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13. Evaluation of intestinal biopsies for pediatric enteropathy: a proposed immunohistochemical panel approach. Martin BA; Kerner JA; Hazard FK; Longacre TA Am J Surg Pathol; 2014 Oct; 38(10):1387-95. PubMed ID: 25188866 [TBL] [Abstract][Full Text] [Related]
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16. A Case Study of Intractable Diarrhea Due to Neonatal Microvillous Inclusion Disease. Bulut O; Ahishali B; Gulluoglu M; Arslanoglu S Fetal Pediatr Pathol; 2017 Aug; 36(4):340-343. PubMed ID: 28707991 [TBL] [Abstract][Full Text] [Related]
17. Microvillus inclusion disease, a diagnosis to consider when abnormal stools and neurological impairments run together due to a rare syntaxin 3 gene mutation. Julia J; Shui V; Mittal N; Heim-Hall J; Blanco CL J Neonatal Perinatal Med; 2019; 12(3):313-319. PubMed ID: 30909251 [TBL] [Abstract][Full Text] [Related]
18. Loss of syntaxin 3 causes variant microvillus inclusion disease. Wiegerinck CL; Janecke AR; Schneeberger K; Vogel GF; van Haaften-Visser DY; Escher JC; Adam R; Thöni CE; Pfaller K; Jordan AJ; Weis CA; Nijman IJ; Monroe GR; van Hasselt PM; Cutz E; Klumperman J; Clevers H; Nieuwenhuis EE; Houwen RH; van Haaften G; Hess MW; Huber LA; Stapelbroek JM; Müller T; Middendorp S Gastroenterology; 2014 Jul; 147(1):65-68.e10. PubMed ID: 24726755 [TBL] [Abstract][Full Text] [Related]