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For: 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: 3.2] [Reference Citation Analysis]
Number Citing Articles
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2 Rao MC. Physiology of Electrolyte Transport in the Gut: Implications for Disease. Compr Physiol 2019;9:947-1023. [PMID: 31187895 DOI: 10.1002/cphy.c180011] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 2.3] [Reference Citation Analysis]
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6 Coman D, Fullston T, Shoubridge C, Leventer R, Wong F, Nazaretian S, Simpson I, Gecz J, McGillivray G. X-Linked Lissencephaly With Absent Corpus Callosum and Abnormal Genitalia: An Evolving Multisystem Syndrome With Severe Congenital Intestinal Diarrhea Disease. Child Neurol Open 2017;4:2329048X17738625. [PMID: 29152528 DOI: 10.1177/2329048X17738625] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.6] [Reference Citation Analysis]
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8 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]
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10 Tavano OL, Berenguer-murcia A, Secundo F, Fernandez-lafuente R. Biotechnological Applications of Proteases in Food Technology: Proteases in food technology…. Comprehensive Reviews in Food Science and Food Safety 2018;17:412-36. [DOI: 10.1111/1541-4337.12326] [Cited by in Crossref: 82] [Cited by in F6Publishing: 46] [Article Influence: 20.5] [Reference Citation Analysis]
11 Dhekne HS, Pylypenko O, Overeem AW, Zibouche M, Ferreira RJ, van der Velde KJ, Rings EHHM, Posovszky C, van der Sluijs P, Swertz MA, Houdusse A, van IJzendoorn SCD. MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update. Hum Mutat 2018;39:333-44. [PMID: 29266534 DOI: 10.1002/humu.23386] [Cited by in Crossref: 22] [Cited by in F6Publishing: 22] [Article Influence: 5.5] [Reference Citation Analysis]
12 Kurolap A, Eshach Adiv O, Konnikova L, Werner L, Gonzaga-Jauregui C, Steinberg M, Mitsialis V, Mory A, Nunberg MY, Wall S, Shaoul R, Overton JD, Shuldiner AR, Zohar Y, Paperna T, Snapper SB, Shouval DS, Baris Feldman H; Regeneron Genetics Center. A Unique Presentation of Infantile-Onset Colitis and Eosinophilic Disease without Recurrent Infections Resulting from a Novel Homozygous CARMIL2 Variant. J Clin Immunol 2019;39:430-9. [PMID: 31079270 DOI: 10.1007/s10875-019-00631-6] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.7] [Reference Citation Analysis]
13 Tesouro Rodríguez L, Lázaro de Lucas C, Magallares García LN, Martínez-Ojinaga Nodal E, Ramos Boluda E. [Management and prognosis of intestinal epithelial dysplasia]. An Pediatr (Engl Ed) 2018;88:48-9. [PMID: 28366696 DOI: 10.1016/j.anpedi.2017.02.001] [Reference Citation Analysis]
14 Sankararaman S, Schindler T, Sferra TJ. Management of Exocrine Pancreatic Insufficiency in Children. Nutrition in Clinical Practice 2019;34:S27-42. [DOI: 10.1002/ncp.10388] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
15 Neves JF, Afonso I, Borrego L, Martins C, Cordeiro AI, Neves C, Lacoste C, Badens C, Fabre A. Missense mutation of TTC7A mimicking tricho-hepato-enteric (SD/THE) syndrome in a patient with very-early onset inflammatory bowel disease. Eur J Med Genet 2018;61:185-8. [PMID: 29174094 DOI: 10.1016/j.ejmg.2017.11.014] [Cited by in Crossref: 12] [Cited by in F6Publishing: 7] [Article Influence: 2.4] [Reference Citation Analysis]
16 Posovszky C, Sirin M, Jacobsen E, Lorenz M, Schwarz K, Schmidt-Choudhury A, Rothoeft T, Schuetz C, Hönig M, Debatin KM, Schulz A, Möller P, Barth TF. Persisting enteropathy and disturbed adaptive mucosal immunity due to MHC class II deficiency. Clin Immunol 2019;203:125-33. [PMID: 31028919 DOI: 10.1016/j.clim.2019.04.012] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
17 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]
18 Posovszky C, Barth TFE. [The gut: center of immunity : Rare inflammatory bowel diseases caused by immunodeficiencies]. Pathologe 2020;41:211-23. [PMID: 32253499 DOI: 10.1007/s00292-020-00775-y] [Reference Citation Analysis]