541 related articles for article (PubMed ID: 16497624)
41. Screening of R122H and N29I mutations in the PRSS1 gene and N34S mutation in the SPINK1 gene in Mexican pediatric patients with acute and recurrent pancreatitis.
Sánchez-Ramírez CA; Flores-Martínez SE; García-Zapién AG; Montero-Cruz SA; Larrosa-Haro A; Sánchez-Corona J
Pancreas; 2012 Jul; 41(5):707-11. PubMed ID: 22699143
[TBL] [Abstract][Full Text] [Related]
42. [Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism caused by inactivating mutations of calcium-sensing receptor].
Watanabe S; Fukumoto S
Nihon Rinsho; 2002 Feb; 60(2):325-30. PubMed ID: 11857921
[TBL] [Abstract][Full Text] [Related]
43. The prevalence of cationic trypsinogen (PRSS1) and serine protease inhibitor, Kazal type 1 (SPINK1) gene mutations in Polish patients with alcoholic and idiopathic chronic pancreatitis.
Gasiorowska A; Talar-Wojnarowska R; Czupryniak L; Smolarz B; Romanowicz-Makowska H; Kulig A; Malecka-Panas E
Dig Dis Sci; 2011 Mar; 56(3):894-901. PubMed ID: 20676769
[TBL] [Abstract][Full Text] [Related]
44. The SPINK1 N34S mutation is not associated with Type 2 diabetes mellitus in a population of the USA.
Schneider A; Lawrence EC; Barmada MM; Norris JM; Hamman RF; Marshall JA; Ferrell RE; Whitcomb DC
Diabet Med; 2005 Jun; 22(6):744-8. PubMed ID: 15910626
[TBL] [Abstract][Full Text] [Related]
45. Differential roles of the SPINK1 gene mutations in alcoholic and nonalcoholic chronic pancreatitis.
Masamune A; Kume K; Shimosegawa T
J Gastroenterol; 2007 Jan; 42 Suppl 17():135-40. PubMed ID: 17238043
[TBL] [Abstract][Full Text] [Related]
46. Mutations of the calcium-sensing receptor (CASR) in familial hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia.
Hendy GN; D'Souza-Li L; Yang B; Canaff L; Cole DE
Hum Mutat; 2000 Oct; 16(4):281-96. PubMed ID: 11013439
[TBL] [Abstract][Full Text] [Related]
47. Mutation analysis of the cystic fibrosis transmembrane conductance regulator (CFTR) gene, the cationic trypsinogen (PRSS1) gene, and the serine protease inhibitor, Kazal type 1 (SPINK1) gene in patients with alcoholic chronic pancreatitis.
Perri F; Piepoli A; Stanziale P; Merla A; Zelante L; Andriulli A
Eur J Hum Genet; 2003 Sep; 11(9):687-92. PubMed ID: 12939655
[TBL] [Abstract][Full Text] [Related]
48. Novel mutation and polymorphism of PRSS1 gene in the Chinese patients with hereditary pancreatitis and chronic pancreatitis.
Liu QC; Gao F; Ou QS; Zhuang ZH; Lin SR; Yang B; Cheng ZJ
Chin Med J (Engl); 2008 Jan; 121(2):108-11. PubMed ID: 18272034
[TBL] [Abstract][Full Text] [Related]
49. Genetic basis of chronic pancreatitis in Asia Pacific region.
Reddy DN; Prasad SS
J Gastroenterol Hepatol; 2011 Mar; 26 Suppl 2():2-5. PubMed ID: 21323990
[TBL] [Abstract][Full Text] [Related]
50. Calcium-sensing-related gene mutations in hypercalcaemic hypocalciuric patients as differential diagnosis from primary hyperparathyroidism: detection of two novel inactivating mutations in an Italian population.
Stratta P; Merlotti G; Musetti C; Quaglia M; Pagani A; Izzo C; Radin E; Airoldi A; Baorda F; Palladino T; Leone MP; Guarnieri V
Nephrol Dial Transplant; 2014 Oct; 29(10):1902-9. PubMed ID: 25104082
[TBL] [Abstract][Full Text] [Related]
51. PRSS1 and SPINK1 mutations in idiopathic chronic and recurrent acute pancreatitis.
Pelaez-Luna M; Robles-Diaz G; Canizales-Quinteros S; Tusié-Luna MT
World J Gastroenterol; 2014 Sep; 20(33):11788-92. PubMed ID: 25206283
[TBL] [Abstract][Full Text] [Related]
52. The course of genetically determined chronic pancreatitis.
Keim V; Witt H; Bauer N; Bodeker H; Rosendahl J; Teich N; Mossner J
JOP; 2003 Jul; 4(4):146-54. PubMed ID: 12853682
[TBL] [Abstract][Full Text] [Related]
53. The SPINK1 N34S variant is associated with acute pancreatitis.
O'Reilly DA; Witt H; Rahman SH; Schulz HU; Sargen K; Kage A; Cartmell MT; Landt O; Larvin M; Demaine AG; McMahon MJ; Becker M; Kingsnorth AN
Eur J Gastroenterol Hepatol; 2008 Aug; 20(8):726-31. PubMed ID: 18617776
[TBL] [Abstract][Full Text] [Related]
54. Calcium-sensing receptor (CASR) mutations in hypercalcemic states: studies from a single endocrine clinic over three years.
Guarnieri V; Canaff L; Yun FH; Scillitani A; Battista C; Muscarella LA; Wong BY; Notarangelo A; D'Agruma L; Sacco M; Cole DE; Hendy GN
J Clin Endocrinol Metab; 2010 Apr; 95(4):1819-29. PubMed ID: 20164288
[TBL] [Abstract][Full Text] [Related]
55. Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism associated with mutations in the human Ca2+-sensing receptor gene in three Danish families.
Schwarz P; Larsen NE; Lønborg Friis IM; Lillquist K; Brown EM; Gammeltoft S
Scand J Clin Lab Invest; 2000 May; 60(3):221-7. PubMed ID: 10885494
[TBL] [Abstract][Full Text] [Related]
56. Gene mutations in children with chronic pancreatitis.
Witt H
Pancreatology; 2001; 1(5):432-8. PubMed ID: 12120220
[TBL] [Abstract][Full Text] [Related]
57. Multisite mutations of the PRSS1 gene in a Chinese patient with chronic pancreatitis.
Liu QC; Gao F; Cheng ZJ; Ou QS
Hepatobiliary Pancreat Dis Int; 2008 Jun; 7(3):331-2. PubMed ID: 18522894
[TBL] [Abstract][Full Text] [Related]
58. Comprehensive screening of chymotrypsin C (CTRC) gene in tropical calcific pancreatitis identifies novel variants.
Paliwal S; Bhaskar S; Mani KR; Reddy DN; Rao GV; Singh SP; Thomas V; Chandak GR
Gut; 2013 Nov; 62(11):1602-6. PubMed ID: 22580415
[TBL] [Abstract][Full Text] [Related]
59. SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitis.
Pfützer RH; Barmada MM; Brunskill AP; Finch R; Hart PS; Neoptolemos J; Furey WF; Whitcomb DC
Gastroenterology; 2000 Sep; 119(3):615-23. PubMed ID: 10982753
[TBL] [Abstract][Full Text] [Related]
60. Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism.
Pearce SH; Trump D; Wooding C; Besser GM; Chew SL; Grant DB; Heath DA; Hughes IA; Paterson CR; Whyte MP
J Clin Invest; 1995 Dec; 96(6):2683-92. PubMed ID: 8675635
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
