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Page 1
Advances in counselling and surveillance of patients at risk for pancreatic cancer.
Brand RE, Lerch MM, Rubinstein WS, Neoptolemos JP, Whitcomb DC, Hruban RH, Brentnall TA, Lynch HT, Canto MI; Participants of the Fourth International Symposium of Inherited Diseases of the Pancreas. Brand RE, et al. Among authors: lerch mm. Gut. 2007 Oct;56(10):1460-9. doi: 10.1136/gut.2006.108456. Gut. 2007. PMID: 17872573 Free PMC article.
The N34S mutation of SPINK1 (PSTI) is associated with a familial pattern of idiopathic chronic pancreatitis but does not cause the disease.
Threadgold J, Greenhalf W, Ellis I, Howes N, Lerch MM, Simon P, Jansen J, Charnley R, Laugier R, Frulloni L, Oláh A, Delhaye M, Ihse I, Schaffalitzky de Muckadell OB, Andrén-Sandberg A, Imrie CW, Martinek J, Gress TM, Mountford R, Whitcomb D, Neoptolemos JP. Threadgold J, et al. Among authors: lerch mm. Gut. 2002 May;50(5):675-81. doi: 10.1136/gut.50.5.675. Gut. 2002. PMID: 11950815 Free PMC article.
Genetic testing for hereditary pancreatitis: guidelines for indications, counselling, consent and privacy issues.
Ellis I, Lerch MM, Whitcomb DC; Consensus Committees of the European Registry of Hereditary Pancreatic Diseases, Midwest Multi-Center Pancreatic Study Group, International Association of Pancreatology. Ellis I, et al. Among authors: lerch mm. Pancreatology. 2001;1(5):405-15. doi: 10.1159/000055840. Pancreatology. 2001. PMID: 12120217 Review. No abstract available.
Third International Symposium on Inherited Diseases of the Pancreas.
Whitcomb DC, Ulrich CD, Lerch MM, Durie P, Neoptolemos JP, Maisonneuve P, Lowenfels AB. Whitcomb DC, et al. Among authors: lerch mm. Pancreatology. 2001;1(5):423-31. doi: 10.1159/000055842. Pancreatology. 2001. PMID: 12120219 No abstract available.
Clinical and genetic characteristics of hereditary pancreatitis in Europe.
Howes N, Lerch MM, Greenhalf W, Stocken DD, Ellis I, Simon P, Truninger K, Ammann R, Cavallini G, Charnley RM, Uomo G, Delhaye M, Spicak J, Drumm B, Jansen J, Mountford R, Whitcomb DC, Neoptolemos JP; European Registry of Hereditary Pancreatitis and Pancreatic Cancer (EUROPAC). Howes N, et al. Among authors: lerch mm. Clin Gastroenterol Hepatol. 2004 Mar;2(3):252-61. doi: 10.1016/s1542-3565(04)00013-8. Clin Gastroenterol Hepatol. 2004. PMID: 15017610
The variable phenotype of the p.A16V mutation of cationic trypsinogen (PRSS1) in pancreatitis families.
Grocock CJ, Rebours V, Delhaye MN, Andrén-Sandberg A, Weiss FU, Mountford R, Harcus MJ, Niemczyck E, Vitone LJ, Dodd S, Jørgensen MT, Ammann RW, Schaffalitzky de Muckadell O, Butler JV, Burgess P, Kerr B, Charnley R, Sutton R, Raraty MG, Devière J, Whitcomb DC, Neoptolemos JP, Lévy P, Lerch MM, Greenhalf W; European Registry of Hereditary Pancreatitis and Pancreatic Cancer. Grocock CJ, et al. Among authors: lerch mm. Gut. 2010 Mar;59(3):357-63. doi: 10.1136/gut.2009.186817. Epub 2009 Dec 1. Gut. 2010. PMID: 19951905
569 results