tryptophan and Exocrine Pancreatic Insufficiency

tryptophan has been researched along with Exocrine Pancreatic Insufficiency in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Dapena, J; Estivill, X; Ferrer, J; Giménez, J; Llevadot, R; Nunes, V; Ortigosa, L; Peña, L; Pérez-Frias, J	1
Ambrosioni, A; Bassotti, A; Cantù-Rajnoldi, A; Fiori, S; Giunta, A; Padoan, R; Pizzamiglio, G; Seia, M	1

Other Studies

2 other study(ies) available for tryptophan and Exocrine Pancreatic Insufficiency

Article	Year
Clinical characteristics of 16 cystic fibrosis patients with the missense mutation R334W, a pancreatic insufficiency mutation with variable age of onset and interfamilial clinical differences. Human genetics, 1995, Volume: 95, Issue:3 Topics: Age of Onset; Arginine; Child; Child, Preschool; Cystic Fibrosis; Exocrine Pancreatic Insufficiency; Female; Forced Expiratory Volume; Genotype; Humans; Intestinal Obstruction; Lung; Male; Phenotype; Point Mutation; Tryptophan; Vital Capacity	1995
A novel stop mutation in exon 18 (W1145X) of the CFTR (ABCC7) gene in an adult CF patient. Human mutation, 2000, Volume: 16, Issue:6 Topics: Adolescent; Adult; Amino Acid Substitution; Child, Preschool; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Exocrine Pancreatic Insufficiency; Exons; Humans; Male; Mutation, Missense; Phenotype; Pneumonia, Bacterial; Staphylococcal Infections; Tryptophan	2000

Article

Year

Clinical characteristics of 16 cystic fibrosis patients with the missense mutation R334W, a pancreatic insufficiency mutation with variable age of onset and interfamilial clinical differences.

Human genetics, 1995, Volume: 95, Issue:3

Topics: Age of Onset; Arginine; Child; Child, Preschool; Cystic Fibrosis; Exocrine Pancreatic Insufficiency; Female; Forced Expiratory Volume; Genotype; Humans; Intestinal Obstruction; Lung; Male; Phenotype; Point Mutation; Tryptophan; Vital Capacity

1995

A novel stop mutation in exon 18 (W1145X) of the CFTR (ABCC7) gene in an adult CF patient.

Human mutation, 2000, Volume: 16, Issue:6

Topics: Adolescent; Adult; Amino Acid Substitution; Child, Preschool; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Exocrine Pancreatic Insufficiency; Exons; Humans; Male; Mutation, Missense; Phenotype; Pneumonia, Bacterial; Staphylococcal Infections; Tryptophan

2000