Hereditary pancreatitis. Afamily with 4 affected members
Jiménez Caballero, R.; Salnas Carmona, M.C.; Campuzano Fernández, M.; Pérez-Briceño, R.; Lisker, R.; Carío, A.
Revista de Investigacion Clinica; Organo del Hospital de Enfermedades de la Nutricion 29(2): 165-169
1977
ISSN/ISBN: 0034-8376 PMID: 897392 Document Number: 120430
Document emailed within 1 workday
Related Documents
Girard, R.M.; Dubé, S.; Archambault, A.P. 1981: Hereditary pancreatitis: report of an affected Canadian kindred and review of the disease Canadian Medical Association Journal 125(6): 576-580Liu, Q-cai.; Gao, F.; Ou, Q-shui.; Zhuang, Z-hao.; Lin, S-rong.; Yang, B.; Cheng, Z-jian. 2008: Novel mutation and polymorphism of PRSS1 gene in the Chinese patients with hereditary pancreatitis and chronic pancreatitis Chinese Medical Journal 121(2): 108-111
Merli, M.; Patriarca, M.; Loudianos, G.; Valente, C.; Riggio, O.; De Felice, G.; Petrucci, F.; Caroli, S.; Attili, A.F. 1998: Use of the stable isotope 65Cu test for the screening of Wilson's disease in a family with two affected members Italian Journal of Gastroenterology and Hepatology 30(3): 270-275
Zdansky, R.; Madl, W.; Rett, A.; Piperger, A. 1971: Hereditary chromosomal mosaicism and its importance for the affected family Wiener Medizinische Wochenschrift 121(4): 59-63
Morales Asin, F.; Mostacero Miguel, E.; García Alvarez, F.; Olascoaga Urtaza, J.; Domínguez Arranz, M.; Morales Asin, J.; López del Val, J. 1980: Clinical study of 8 families with various members affected with myotonic dystrophy of Curshmann Steinert's type. Genetic considerations Revista Clinica Espanola 157(5): 319-323
Judkiewicz, L.; Pawlowska-Krykowska, D.; Polkowska-Kulesza, E.; Pluzańska, A. 1973: 3 generations of a family affected by hereditary microspherocytic anemia treated by splenectomy Polski Tygodnik Lekarski 28(45): 1768-1770
Jørgensen, M.T.; Schaffalitzky de Muckadell, O.B. 2003: Hereditary pancreatitis Ugeskrift for Laeger 165(5): 447-451
Milani, M.Y.; Kotze, M.J. 1999: Molecular diagnosis of hereditary haemochromatosis--identify an affected person and save a family South African Medical Journal 89(3): 263-264
Vorechovský, I.; Cullen, M.; Carrington, M.; Hammarström, L.; Webster, A.D. 2000: Fine mapping of IGAD1 in IgA deficiency and common variable immunodeficiency: identification and characterization of haplotypes shared by affected members of 101 multiple-case families Journal of Immunology 164(8): 4408-4416
Armendares, S.; Carnevale, A.; Del Castillo, V.; Najar Aparicio, A. 1973: Smith-Lemli-Opitz syndrome: description of 2 affected brothers, clinical characterization and hereditary mechanism Revista de Investigacion Clinica; Organo del Hospital de Enfermedades de la Nutricion 25(2): 129-142
Albornoz, P.; Villasmil, A.; Moreno, H.; Sánchez, R. 1988: Hereditary pancreatitis: report of a family G.E.N 42(4): 152-156
Giniès, J.L.; Duverne, C.; Champion, G.; Limal, J.M.; Coupris, L. 1986: Mediastinal pseudocyst in hereditary pancreatitis Archives Francaises de Pediatrie 43(9): 709-710
Beggs, I.; Salmon, P.R. 1984: A case of hereditary pancreatitis and pancreas divisum European Journal of Radiology 4(1): 71-73
García Díaz, J.J.; Simón, M.A.; Blanco, J.R.; Yangüela, J.; Blanco, M. 1990: Chronic hereditary pancreatitis. A report of a new case Medicina Clinica 95(14): 557-558
Ravnik-Glavac, M.; Dean, M.; di Sant'Agnese, P.; Chernick, M.; Kozelj, M.; Krizman, I.; Glavac, D. 2000: Evidence that hereditary pancreatitis is genetically heterogeneous disorder Pflugers Archiv: European Journal of Physiology 439(3 Suppl): R50-R52
Svendsen, I.H.; Steensgaard-Hansen, F.; Nordvåg, B.Y. 1999: Hereditary amyloid cardiomyopathy related to a mutation at transthyretin protein number 111. a clinical, genetic and echocardiographic study of an affected Danish family Ugeskrift for Laeger 161(36): 4995-4999
Schiemann, U.; Papatheodorou, L.; Glasl, S.; Gross, M. 2001: Hereditary non-polyposis colorectal cancer (HNPCC): new germline mutation (190-191 del AA) in the human MLH1 gene and review of clinical guidelines for surveillance of affected families European Journal of Medical Research 6(3): 93-100
Sossenheimer, M.J.; Aston, C.E.; Preston, R.A.; Gates, L.K.; Ulrich, C.D.; Martin, S.P.; Zhang, Y.; Gorry, M.C.; Ehrlich, G.D.; Whitcomb, D.C. 1997: Clinical characteristics of hereditary pancreatitis in a large family, based on high-risk haplotype. the Midwest Multicenter Pancreatic Study Group (MMPSG) American Journal of Gastroenterology 92(7): 1113-1116
Ginter, E.K.; Budagova, K.A.; Revazov, A.A.; Petrin, A.N.; Bugaeva, E.A. 1986: Medico-genetical study of the Uzbekistan population. IX. Variability of hereditary pathology, territorial distribution of hereditary diseases and hereditary disease load in the population of the Urgut district of the Samarkand region Genetika 22(7): 1199-1206
Suda, K.; Mogaki, M.; Oyama, T.; Matsumoto, Y. 1990: Histopathologic and immunohistochemical studies on alcoholic pancreatitis and chronic obstructive pancreatitis: special emphasis on ductal obstruction and genesis of pancreatitis American Journal of Gastroenterology 85(3): 271-276