Add to ORKGinhibitor mutations in hereditary and non-hereditary chronic pancreatitis. Gut 2004;53:723–28
Acute pancreatitis represents an acute nonbacterial inflammation of the pancreas caused by a prematu...
none9noneL. Gullo; L. Laghi; M. Migliori; L. Lucrezio; P. Bianchi; A.E. Randolph; V. Mantovani; L. B...
BackgroundPRSS1 was the first reported chronic pancreatitis (CP) gene. The existence of both gain-of...
Background and aims: Mutations in the cationic trypsinogen (protease, serine, 1 (trypsin 1); PRSS1) ...
Background: Mutations in the PRSS1 gene explain most occurrences of hereditary pancreatitis (HP) but...
Background: Mutations in the PRSS1 gene explain most occurrences of hereditary pancreatitis (HP) but...
Chronic pancreatitis (CP) is a continuing or relapsing inflammatory disease of the pancreas. In appr...
Background/Aims: A relation between some genetic mutations and chronic pancreatitis (CP) has been re...
BackgroundEnvironmental factors and genetic mutations have been increasingly recognized as risk fact...
The N34S mutation of SPINK1 (PSTI) is associated with a familial pattern of idiopathic chronic pancr...
Context Mutations in cystic fibrosis transmembrane conductance regulator (CFTR), in cationic trypsin...
Hereditary pancreatitis (HP) is a rare heterogeneous disease with partial penetrance identified by f...
Chronic pancreatitis (CP) is a clinical situation with persisting inflammation leading to destructio...
International audienceSince the description of the PRSS1 gene encoding the cationic trypsinogen as b...
The aim of this study was to determine whether mutations in SPINK1/PRSS1 genes are associated with b...
Acute pancreatitis represents an acute nonbacterial inflammation of the pancreas caused by a prematu...
none9noneL. Gullo; L. Laghi; M. Migliori; L. Lucrezio; P. Bianchi; A.E. Randolph; V. Mantovani; L. B...
BackgroundPRSS1 was the first reported chronic pancreatitis (CP) gene. The existence of both gain-of...
Background and aims: Mutations in the cationic trypsinogen (protease, serine, 1 (trypsin 1); PRSS1) ...
Background: Mutations in the PRSS1 gene explain most occurrences of hereditary pancreatitis (HP) but...
Background: Mutations in the PRSS1 gene explain most occurrences of hereditary pancreatitis (HP) but...
Chronic pancreatitis (CP) is a continuing or relapsing inflammatory disease of the pancreas. In appr...
Background/Aims: A relation between some genetic mutations and chronic pancreatitis (CP) has been re...
BackgroundEnvironmental factors and genetic mutations have been increasingly recognized as risk fact...
The N34S mutation of SPINK1 (PSTI) is associated with a familial pattern of idiopathic chronic pancr...
Context Mutations in cystic fibrosis transmembrane conductance regulator (CFTR), in cationic trypsin...
Hereditary pancreatitis (HP) is a rare heterogeneous disease with partial penetrance identified by f...
Chronic pancreatitis (CP) is a clinical situation with persisting inflammation leading to destructio...
International audienceSince the description of the PRSS1 gene encoding the cationic trypsinogen as b...
The aim of this study was to determine whether mutations in SPINK1/PRSS1 genes are associated with b...
Acute pancreatitis represents an acute nonbacterial inflammation of the pancreas caused by a prematu...
none9noneL. Gullo; L. Laghi; M. Migliori; L. Lucrezio; P. Bianchi; A.E. Randolph; V. Mantovani; L. B...
BackgroundPRSS1 was the first reported chronic pancreatitis (CP) gene. The existence of both gain-of...