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For: Thiagarajah JR, Kamin DS, Acra S, Goldsmith JD, Roland JT, Lencer WI, Muise AM, Goldenring JR, Avitzur Y, Martín MG; PediCODE Consortium. Advances in Evaluation of Chronic Diarrhea in Infants. Gastroenterology 2018;154:2045-2059.e6. [PMID: 29654747 DOI: 10.1053/j.gastro.2018.03.067] [Cited by in Crossref: 91] [Cited by in F6Publishing: 93] [Article Influence: 22.8] [Reference Citation Analysis]
Number Citing Articles
1 Babcock SJ, Flores-marin D, Thiagarajah JR. The genetics of monogenic intestinal epithelial disorders. Hum Genet 2022. [DOI: 10.1007/s00439-022-02501-5] [Reference Citation Analysis]
2 Prasad BS, Yachha SK. Congenital Glucose-Galactose Malabsorption in a Child. Indian Pediatr 2022;59:811-812. [DOI: 10.1007/s13312-022-2627-x] [Reference Citation Analysis]
3 Marek-Yagel D, Stenke E, Pode-Shakked B, Dunne C, Crushell E, Bryce-Smith A, McDermott M, O'Sullivan MJ, Veber A, Krishnamurthy M, Wells JM, Anikster Y, Bourke B. Nonsense mutation in the novel PERCC1 gene as a genetic cause of congenital diarrhea and enteropathy. Hum Genet 2022. [PMID: 36076104 DOI: 10.1007/s00439-022-02486-1] [Reference Citation Analysis]
4 Gonzalez-hakspiel LC, Wilches-cuadros MA, Nausa-suárez PA, Fernández F, Patiño-ascencio P, Manrique-guerrero A, Díaz-díaz D, Castro-rojas C. Severe congenital diarrhea secondary to tufting enteropathy. Case report. Case reports 2022;8:41-50. [DOI: 10.15446/cr.v8n1.90883] [Reference Citation Analysis]
5 Ahsan MK, dos Reis DC, Barbieri A, Sumigray KD, Nottoli T, Salas PJ, Ameen NA. Loss of Serum Glucocorticoid-Inducible Kinase 1 SGK1 Worsens Malabsorption and Diarrhea in Microvillus Inclusion Disease (MVID). JCM 2022;11:4179. [DOI: 10.3390/jcm11144179] [Reference Citation Analysis]
6 Bogdanic E, Müller T, Heinz-Erian P, Garczarczyk-Asim D, Janecke AR, Rückel A. Further delineation of SLC9A3-related congenital sodium diarrhea. Mol Genet Genomic Med 2022;:e2000. [PMID: 35775128 DOI: 10.1002/mgg3.2000] [Reference Citation Analysis]
7 Claßen M. Chronische Diarrhö bei Kindern und Jugendlichen. Gastro-News 2022;9:40-45. [DOI: 10.1007/s15036-022-2502-6] [Reference Citation Analysis]
8 Blachier F, Andriamihaja M, Kong X. Fate of undigested proteins in the pig large intestine: What impact on the colon epithelium? Animal Nutrition 2022;9:110-118. [DOI: 10.1016/j.aninu.2021.08.001] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
9 Klee KM, Hess MW, Lohmüller M, Herzog S, Pfaller K, Müller T, Vogel GF, Huber LA. A CRISPR-screen in intestinal epithelial cells identifies novel factors for polarity and apical transport.. [DOI: 10.1101/2022.05.16.492077] [Reference Citation Analysis]
10 Hoşnut FÖ, Sahin GE, Ozyazıcı A, Olgac A, Aksu AU. Congenital Rare Diseases Causing Persistent Diarrhea in the Newborn: A Single Center Experience. Z Geburtshilfe Neonatol 2022. [PMID: 35576965 DOI: 10.1055/a-1774-5005] [Reference Citation Analysis]
11 DeMaria KA, Fink C, Pepper M, Rieger K, Tan SY, Namjoshi SS. Intestinal Failure in Junctional Epidermolysis Bullosa: Mild Skin Disease, Severe Diarrhea. Dig Dis Sci 2022;67:1740-3. [PMID: 35147818 DOI: 10.1007/s10620-022-07410-1] [Reference Citation Analysis]
12 Belza C, Wales PW. MANAGEMENT OF PEDIATRIC INTESTINAL FAILURE RELATED TO SHORT BOWEL SYNDROME. Seminars in Pediatric Surgery 2022. [DOI: 10.1016/j.sempedsurg.2022.151175] [Reference Citation Analysis]
13 Steg Saban O, Pode-shakked B, Abu-libdeh B, Granot M, Barkai G, Haberman Y, Roterman I, Lahad A, Shouval DS, Weiss B, Marek-yagel D, Barel O, Loberman-nachum N, Abraham S, Somech R, Weinstein DA, Anikster Y. Glycogen Storage Disease type IA refractory to cornstarch: Can next generation sequencing offer a solution? European Journal of Medical Genetics 2022. [DOI: 10.1016/j.ejmg.2022.104518] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Kupfer SS. Gastrointestinal and hepatic manifestations of specific genetic disorders. Yamada's Textbook of Gastroenterology 2022. [DOI: 10.1002/9781119600206.ch110] [Reference Citation Analysis]
15 Mou W, Yang S, Guo R, Fu L, Zhang L, Guo W, Du J, He J, Ren Q, Hao C, Gui J, Huang J. A Novel Homozygous TTC7A Missense Mutation Results in Familial Multiple Intestinal Atresia and Combined Immunodeficiency. Front Immunol 2021;12:759308. [PMID: 34975848 DOI: 10.3389/fimmu.2021.759308] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
16 Francis KL, Verma A, Pacheco MC, Wendel D, Vue PM, Hu SJ, Scarlett JM. Neurogenin-3 Enteric Endocrinopathy: A Rare Case of Pediatric Congenital Diarrhea and Diabetes Mellitus. JPGN Reports 2022;3:e173. [DOI: 10.1097/pg9.0000000000000173] [Reference Citation Analysis]
17 Gordon SM, O'Connell AE. Inborn Errors of Immunity in the Premature Infant: Challenges in Recognition and Diagnosis. Front Immunol 2021;12:758373. [PMID: 35003071 DOI: 10.3389/fimmu.2021.758373] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
18 Rundle AL, Baron N, John RM. Care of the Child with a Gastrointestinal Disorder. Pediatric Diagnostic Labs for Primary Care: An Evidence-based Approach 2022. [DOI: 10.1007/978-3-030-90642-9_9] [Reference Citation Analysis]
19 David EE, Yameen MA, Igwenyi IO, David CN, Nwobodo V, Ismail AK. Zinc Deficiency Elevates Fecal Protein, But Not Electrolyte and Short-Chain Fatty Acid, Levels in Enterotoxigenic Escherichia coli-Induced Diarrhea in Rats. Pediatr Gastroenterol Hepatol Nutr 2022;25:79-86. [PMID: 35087736 DOI: 10.5223/pghn.2022.25.1.79] [Reference Citation Analysis]
20 Puertolas M, Sentongo TA. Enteral Nutrition. Textbook of Pediatric Gastroenterology, Hepatology and Nutrition 2022. [DOI: 10.1007/978-3-030-80068-0_45] [Reference Citation Analysis]
21 Sharma SS, Sankaranarayanan S, Kumar VH, Kumar NC, Sundaram CS. Congenital Diarrheal Disorders in Neonates: A Single-Center Experience. Indian Pediatr 2021;58:1096-7. [DOI: 10.1007/s13312-021-2382-4] [Reference Citation Analysis]
22 Yang X, Xiong W, Huang T, He J. Meteorological and social conditions contribute to infectious diarrhea in China. Sci Rep 2021;11:23374. [PMID: 34862400 DOI: 10.1038/s41598-021-00932-0] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
23 Bardet A, Riccardi F, Torrents J, Capasso F, Devooght M, Buffat C, Fabre A, Piercecchi-marti M, Delteil C. Diagnostic d’une maladie inflammatoire rare et sévère de l’intestin chez un nourrisson présentant des ulcérations péri-orificielles. Annales de Pathologie 2021. [DOI: 10.1016/j.annpat.2021.11.007] [Reference Citation Analysis]
24 Otuya DO, Gavgiotaki E, Carlson CJ, Shi SQ, Lee AJ, Krall AA, Chung A, Grant CG, Bhat NM, Choy P, Giddings SL, Gardecki JA, Thiagarajah JR, Rowe SM, Tearney GJ. Minimally Invasive Image-Guided Gut Transport Function Measurement Probe. Front Phys 2021;9. [DOI: 10.3389/fphy.2021.735645] [Reference Citation Analysis]
25 Yan W, Xiao Y, Zhang Y, Tao Y, Cao Y, Liu K, Cai W, Wang Y. Monogenic mutations in four cases of neonatal-onset watery diarrhea and a mutation review in East Asia. Orphanet J Rare Dis 2021;16:383. [PMID: 34503561 DOI: 10.1186/s13023-021-01995-y] [Reference Citation Analysis]
26 Lostao MP, Loo DD, Hernell O, Meeuwisse G, Martin MG, Wright EM. The Molecular Basis of Glucose Galactose Malabsorption in a Large Swedish Pedigree. Function (Oxf) 2021;2:zqab040. [PMID: 34485913 DOI: 10.1093/function/zqab040] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
27 Mantoo MR, Malik R, Das P, Yadav R, Nakra T, Chouhan P. Congenital Diarrhea and Enteropathies in Infants: Approach to Diagnosis. Indian J Pediatr 2021. [PMID: 34292522 DOI: 10.1007/s12098-021-03844-z] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
28 Howard-jones AR, Cristerna-tarrasa GH, Khan R, Stormon M, Arbuckle S, Britton PN. Severe Postnatal Cytomegalovirus Enterocolitis in Immunocompetent Term Infants Requiring Total Parenteral Nutrition. JPGN Reports 2021;2:e110. [DOI: 10.1097/pg9.0000000000000110] [Reference Citation Analysis]
29 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] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
30 M A, M S, L R, T M, N M. A rare cause of neonatal diarrhoea: Microvillositary inclusion disease: about a case report. J Adv Pediatr Child Health 2021;4:053-056. [DOI: 10.29328/journal.japch.1001033] [Reference Citation Analysis]
31 Shankar S, Rosenbaum J. Chronic diarrhoea in children: A practical algorithm-based approach. J Paediatr Child Health 2020;56:1029-38. [PMID: 32725734 DOI: 10.1111/jpc.14986] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
32 Aerts L, Terry NA, Sainath NN, Torres C, Martín MG, Ramos-Molina B, Creemers JW. Novel Homozygous Inactivating Mutation in the PCSK1 Gene in an Infant with Congenital Malabsorptive Diarrhea. Genes (Basel) 2021;12:710. [PMID: 34068683 DOI: 10.3390/genes12050710] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
33 Qian Y, Wu B, Liu R, Lu Y, Zhang P, Shao C, Huang Y, Wang H. Case Report: Complete Maternal Uniparental Isodisomy of Chromosome 5 (iUPD(5)mat) With PCSK1 Nonsense Variant in an Infant With Recurrent Diarrhea. Front Genet 2021;12:668326. [PMID: 34025722 DOI: 10.3389/fgene.2021.668326] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
34 Wolfe RM, Mohsen AW, Walsh Vockley C, Bertrand CA, Nicholls RD, Heiman P, Seibold LM, Vockley J, Ghaloul-Gonzalez L. Novel GUCY2C variant causing familial diarrhea in a Mennonite kindred and a potential therapeutic approach. Am J Med Genet A 2021;185:2046-55. [PMID: 33949097 DOI: 10.1002/ajmg.a.62207] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
35 Prasad H, Visweswariah SS. Impaired Intestinal Sodium Transport in Inflammatory Bowel Disease: From the Passenger to the Driver's Seat. Cell Mol Gastroenterol Hepatol 2021;12:277-92. [PMID: 33744482 DOI: 10.1016/j.jcmgh.2021.03.005] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 7.0] [Reference Citation Analysis]
36 Yin J, Sunuwar L, Kasendra M, Yu H, Tse CM, Talbot CC Jr, Boronina T, Cole R, Karalis K, Donowitz M. Fluid shear stress enhances differentiation of jejunal human enteroids in Intestine-Chip. Am J Physiol Gastrointest Liver Physiol 2021;320:G258-71. [PMID: 33074011 DOI: 10.1152/ajpgi.00282.2020] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 9.0] [Reference Citation Analysis]
37 Eldredge JA, Couper MR, Barnett CP, Rawlings L, Couper RTL. New Pathogenic Mutations Associated with Diacylglycerol O-Acyltransferase 1 Deficiency. J Pediatr 2021;233:268-72. [PMID: 33607125 DOI: 10.1016/j.jpeds.2021.02.028] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
38 Kumar M, Saurabh V, Tomar M, Hasan M, Changan S, Sasi M, Maheshwari C, Prajapati U, Singh S, Prajapat RK, Dhumal S, Punia S, Amarowicz R, Mekhemar M. Mango (Mangifera indica L.) Leaves: Nutritional Composition, Phytochemical Profile, and Health-Promoting Bioactivities. Antioxidants (Basel) 2021;10:299. [PMID: 33669341 DOI: 10.3390/antiox10020299] [Cited by in Crossref: 17] [Cited by in F6Publishing: 19] [Article Influence: 17.0] [Reference Citation Analysis]
39 Parfenov AI, Akhmadullina OV, Belostotsky NI, Sabelnikova EA, Novikov AA, Bykova SV, Dbar SR. Enteropathy with impaired membrane digestion and the prospects for cytoprotective therapy. Terapevticheskii arkhiv 2021;93:129-37. [DOI: 10.26442/00403660.2021.02.200602] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
40 Esposito MV, Comegna M, Cernera G, Gelzo M, Paparo L, Berni Canani R, Castaldo G. NGS Gene Panel Analysis Revealed Novel Mutations in Patients with Rare Congenital Diarrheal Disorders. Diagnostics (Basel) 2021;11:262. [PMID: 33567694 DOI: 10.3390/diagnostics11020262] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
41 Zhang YJ, Jimenez L, Azova S, Kremen J, Chan YM, Elhusseiny AM, Saeed H, Goldsmith J, Al-Ibraheemi A, O'Connell AE, Kovbasnjuk O, Rodan L, Agrawal PB, Thiagarajah JR. Novel variants in the stem cell niche factor WNT2B define the disease phenotype as a congenital enteropathy with ocular dysgenesis. Eur J Hum Genet 2021;29:998-1007. [PMID: 33526876 DOI: 10.1038/s41431-021-00812-1] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
42 Aldrian D, Vogel GF, Frey TK, Ayyıldız Civan H, Aksu AÜ, Avitzur Y, Ramos Boluda E, Çakır M, Demir AM, Deppisch C, Duba HC, Düker G, Gerner P, Hertecant J, Hornová J, Kathemann S, Koeglmeier J, Koutroumpa A, Lanzersdorfer R, Lev-Tzion R, Lima R, Mansour S, Meissl M, Melek J, Miqdady M, Montoya JH, Posovszky C, Rachman Y, Siahanidou T, Tabbers M, Uhlig HH, Ünal S, Wirth S, Ruemmele FM, Hess MW, Huber LA, Müller T, Sturm E, Janecke AR. Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations. J Clin Med 2021;10:481. [PMID: 33525641 DOI: 10.3390/jcm10030481] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 11.0] [Reference Citation Analysis]
43 Rytting HB, Yin H. Gastrointestinal Disorders in the Infant and Child. Practical Gastrointestinal Pathology 2021. [DOI: 10.1007/978-3-030-51268-2_1] [Reference Citation Analysis]
44 Albenberg L, Terry NA. Protracted Diarrhea. Pediatric Gastrointestinal and Liver Disease 2021. [DOI: 10.1016/b978-0-323-67293-1.00032-3] [Reference Citation Analysis]
45 Girlanda R, Fujiki M, Osman M, Costa G, Radhakrishnan K, Abu-elmagd K. Intestinal and Multivisceral Transplantation: Recent Advances. Pediatric Gastrointestinal and Liver Disease 2021. [DOI: 10.1016/b978-0-323-67293-1.00036-0] [Reference Citation Analysis]
46 Ediger TR, Erdman SH. Maldigestion and Malabsorption. Pediatric Gastrointestinal and Liver Disease 2021. [DOI: 10.1016/b978-0-323-67293-1.00031-1] [Reference Citation Analysis]
47 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: 8] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
48 Raja TW, Veeramuthu D, Savarimuthu I, Al-Dhabi NA. Current Trends in the Treatment of Systemic Lupus Erythematosus. Curr Pharm Des 2020;26:2602-9. [PMID: 32066358 DOI: 10.2174/1381612826666200211122633] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
49 Xu L, Gu W, Luo Y, Lou J, Chen J. DGAT1 mutations leading to delayed chronic diarrhoea: a case report. BMC Med Genet 2020;21:239. [PMID: 33261563 DOI: 10.1186/s12881-020-01164-1] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
50 Kaji I, Roland JT, Watanabe M, Engevik AC, Goldstein AE, Hodges CA, Goldenring JR. Lysophosphatidic Acid Increases Maturation of Brush Borders and SGLT1 Activity in MYO5B-deficient Mice, a Model of Microvillus Inclusion Disease. Gastroenterology 2020;159:1390-1405.e20. [PMID: 32534933 DOI: 10.1053/j.gastro.2020.06.008] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 7.5] [Reference Citation Analysis]
51 Abtahi S, Turner JR. Exploiting Alternative Brush Border Trafficking Routes to Treat Microvillous Inclusion Disease. Gastroenterology 2020;159:1233-5. [PMID: 32777279 DOI: 10.1053/j.gastro.2020.08.006] [Reference Citation Analysis]
52 Pournami F, Mk AK, Panackal AV, Nandakumar A, Prabhakar J, Jain N. Microvillus Inclusion Disease: A Rare Mutation of STX3 in Exon 9 Causing Fatal Congenital Diarrheal Disease. J Pediatr Genet. [DOI: 10.1055/s-0040-1716401] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
53 Xue J, Thomas L, Tahmasbi M, Valdez A, Dominguez Rieg JA, Fenton RA, Rieg T. An inducible intestinal epithelial cell-specific NHE3 knockout mouse model mimicking congenital sodium diarrhea. Clin Sci (Lond) 2020;134:941-53. [PMID: 32227118 DOI: 10.1042/CS20200065] [Cited by in Crossref: 20] [Cited by in F6Publishing: 20] [Article Influence: 10.0] [Reference Citation Analysis]
54 Azab B, Dardas Z, Rabab'h O, Srour L, Telfah H, Hatmal MM, Mustafa L, Rashdan L, Altamimi E. Enteric anendocrinosis attributable to a novel Neurogenin-3 variant. Eur J Med Genet 2020;63:103981. [PMID: 32574610 DOI: 10.1016/j.ejmg.2020.103981] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
55 Crowley E, Warner N, Pan J, Khalouei S, Elkadri A, Fiedler K, Foong J, Turinsky AL, Bronte-Tinkew D, Zhang S, Hu J, Tian D, Li D, Horowitz J, Siddiqui I, Upton J, Roifman CM, Church PC, Wall DA, Ramani AK, Kotlarz D, Klein C, Uhlig H, Snapper SB, Gonzaga-Jauregui C, Paterson AD, McGovern DPB, Brudno M, Walters TD, Griffiths AM, Muise AM. Prevalence and Clinical Features of Inflammatory Bowel Diseases Associated With Monogenic Variants, Identified by Whole-Exome Sequencing in 1000 Children at a Single Center. Gastroenterology 2020;158:2208-20. [PMID: 32084423 DOI: 10.1053/j.gastro.2020.02.023] [Cited by in Crossref: 45] [Cited by in F6Publishing: 46] [Article Influence: 22.5] [Reference Citation Analysis]
56 Ouahed J, Spencer E, Kotlarz D, Shouval DS, Kowalik M, Peng K, Field M, Grushkin-Lerner L, Pai SY, Bousvaros A, Cho J, Argmann C, Schadt E, Mcgovern DPB, Mokry M, Nieuwenhuis E, Clevers H, Powrie F, Uhlig H, Klein C, Muise A, Dubinsky M, Snapper SB. Very Early Onset Inflammatory Bowel Disease: A Clinical Approach With a Focus on the Role of Genetics and Underlying Immune Deficiencies. Inflamm Bowel Dis 2020;26:820-42. [PMID: 31833544 DOI: 10.1093/ibd/izz259] [Cited by in Crossref: 53] [Cited by in F6Publishing: 46] [Article Influence: 26.5] [Reference Citation Analysis]
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58 Klee KMC, Janecke AR, Civan HA, Rosipal Š, Heinz-Erian P, Huber LA, Müller T, Vogel GF. AP1S1 missense mutations cause a congenital enteropathy via an epithelial barrier defect. Hum Genet 2020;139:1247-59. [PMID: 32306098 DOI: 10.1007/s00439-020-02168-w] [Cited by in Crossref: 15] [Cited by in F6Publishing: 11] [Article Influence: 7.5] [Reference Citation Analysis]
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60 Uhlig HH. Congenital abnormalities of the gastrointestinal tract. Oxford Textbook of Medicine 2020. [DOI: 10.1093/med/9780198746690.003.0310] [Reference Citation Analysis]
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62 Lodoso-torrecilla B, Perez de Nanclares G, Garin I, Calvo-saez A, Martinez-fernandez de Pinedo I. Malabsorción de glucosa y galactosa. Nuevo caso en España. Anales de Pediatría 2020;92:104-105. [DOI: 10.1016/j.anpedi.2018.12.006] [Reference Citation Analysis]
63 Lodoso-torrecilla B, Perez de Nanclares G, Garin I, Calvo-saez A, Martinez-fernandez de Pinedo I. Glucose and galactose malabsorption: A new case in Spain. Anales de Pediatría (English Edition) 2020;92:104-105. [DOI: 10.1016/j.anpede.2018.12.011] [Reference Citation Analysis]
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65 Zayede D, Mulaw T, Kahaliw W. Antidiarrheal Activity of Hydromethanolic Root Extract and Solvent Fractions of Clutia abyssinica Jaub. & Spach. (Euphorbiaceae) in Mice. Evid Based Complement Alternat Med 2020;2020:5416749. [PMID: 32419812 DOI: 10.1155/2020/5416749] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
66 Solorzano-Vargas RS, Bjerknes M, Wang J, Wu SV, Garcia-Careaga MG, Pitukcheewanont P, Cheng H, German MS, Georgia S, Martín MG. Null mutations of NEUROG3 are associated with delayed-onset diabetes mellitus. JCI Insight 2020;5:127657. [PMID: 31805014 DOI: 10.1172/jci.insight.127657] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
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