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Cited by in F6Publishing
For: Alsaleem BMR, Ahmed ABM, Fageeh MA. Microvillus Inclusion Disease Variant in an Infant with Intractable Diarrhea. Case Rep Gastroenterol. 2017;11:647-651. [PMID: 29282386 DOI: 10.1159/000479624] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Tang BL. SNAREs and developmental disorders. J Cell Physiol 2021;236:2482-504. [PMID: 32959907 DOI: 10.1002/jcp.30067] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Julia J, Shui V, Mittal N, Heim-hall J, Blanco CL. Microvillus inclusion disease, a diagnosis to consider when abnormal stools and neurological impairments run together due to a rare syntaxin 3 gene mutation. NPM 2019;12:313-9. [DOI: 10.3233/npm-1852] [Cited by in Crossref: 7] [Cited by in F6Publishing: 2] [Article Influence: 3.5] [Reference Citation Analysis]
3 Janecke AR, Liu X, Adam R, Punuru S, Viestenz A, Strauß V, Laass M, Sanchez E, Adachi R, Schatz MP, Saboo US, Mittal N, Rohrschneider K, Escher J, Ganesh A, Al Zuhaibi S, Al Murshedi F, AlSaleem B, Alfadhel M, Al Sinani S, Alkuraya FS, Huber LA, Müller T, Heidelberger R, Janz R. Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset severe retinal dystrophy in microvillus inclusion disease subjects. Hum Genet 2021;140:1143-56. [PMID: 33974130 DOI: 10.1007/s00439-021-02284-1] [Reference Citation Analysis]
4 Sadiq M, Choudry O, Kashyap AK, Velazquez DM. Congenital diarrhea in a newborn infant: A case report. World J Clin Pediatr 2019;8:43-8. [PMID: 31559144 DOI: 10.5409/wjcp.v8.i3.43] [Cited by in CrossRef: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
5 Russo P. Updates in Pediatric Congenital Enteropathies: Differential Diagnosis, Testing, and Genetics. Surg Pathol Clin 2020;13:581-600. [PMID: 33183722 DOI: 10.1016/j.path.2020.08.001] [Reference Citation Analysis]
6 Badawy A, Elfadul M, Aziabi M, Ageel HI, Aqeel A. Challenges of Microvillus Inclusion Disease in the NICU. Neoreviews 2020;21:e600-4. [PMID: 32873653 DOI: 10.1542/neo.21-9-e600] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]