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Cited by in F6Publishing
For: Räty S, Piironen A, Babu M, Pelli H, Sand J, Uotila S, Nordback I, Herzig K. Screening for human cationic trypsinogen (PRSS1) and trypsinogen inhibitor gene (SPINK1) mutations in a Finnish family with hereditary pancreatitis. Scandinavian Journal of Gastroenterology 2007;42:1000-1005. [DOI: 10.1080/00365520701206738] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.1] [Reference Citation Analysis]
Number Citing Articles
1 Ramalho GX, Dytz MG. Diabetes of the Exocrine Pancreas Related to Hereditary Pancreatitis, an Update. Curr Diab Rep 2020;20:16. [PMID: 32221727 DOI: 10.1007/s11892-020-01299-8] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
2 Mustafa MI, Abdelmoneim AH, Elfadol NM, osman SA, Abdelhameed TA, Hassan MA. Novel mutations within PRSS1 Gene that could potentially cause hereditary pancreatitis: Using Comprehensive in silico Approach.. [DOI: 10.1101/519926] [Reference Citation Analysis]
3 Grzybowska-Chlebowczyk U, Jasielska M, Flak-Wancerz A, Więcek S, Gruszczyńska K, Chlebowczyk W, Woś H. Acute pancreatitis in children. Prz Gastroenterol 2018;13:69-75. [PMID: 29657614 DOI: 10.5114/pg.2017.70470] [Cited by in Crossref: 6] [Cited by in F6Publishing: 10] [Article Influence: 1.2] [Reference Citation Analysis]