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The Journal of Pediatrics
|
May 1, 1989
Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileus
E Kerem, M Corey, B Kerem, et al.
Pathology
|
October 1, 1990
Xanthogranulomatous cholecystitis and cholecystoduodenal fistula formation associated with total parenteral nutrition in a six year old child
R W Byard, P S Thorner, E Cutz, et al.
Current Medical Research and Opinion
|
October 8, 2017
Diagnosis and management of pancreatic exocrine insufficiency (PEI) in primary care: consensus guidance of a Canadian expert panel
P Durie, J-D Baillargeon, S Bouchard, et al.
The Journal of Pediatrics
|
April 1, 1990
Renal calcium handling in cystic fibrosis: lack of evidence for a primary renal defect
L Bentur, E Kerem, R Couper, et al.
Cancer Journal (Sudbury, Mass.)
|
August 6, 2025
Modulating Redox Biology to Improve Radiation Responses
Jacky K Leung, Ryan Panchal, Selvakumar Anbalagan, et al.
American Journal of Human Genetics
|
June 1, 1992
Genetic determination of exocrine pancreatic function in cystic fibrosis
P Kristidis, D Bozon, M Corey, et al.
Thorax
|
September 8, 2009
Sweat gland bioelectrics differ in cystic fibrosis: a new concept for potential diagnosis and assessment of CFTR function in cystic fibrosis
T Gonska, W Ip, D Turner, et al.
Genomics
|
May 1, 1991
Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene
J Zielenski, D Bozon, B Kerem, et al.
Archives of Disease in Childhood
|
June 23, 2005
The prevalence and clinical characteristics of cystic fibrosis in South Asian Canadian immigrants
M Mei-Zahav, P Durie, J Zielenski, et al.
The American Journal of Clinical Nutrition
|
September 9, 1999
Prevalence of vitamin K deficiency in cystic fibrosis
M Rashid, P Durie, M Andrew, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 51) with videos related to
Sort By:
Page
of 6
The Journal of Pediatrics
|
May 1, 1989
Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileus
E Kerem, M Corey, B Kerem, et al.
Pathology
|
October 1, 1990
Xanthogranulomatous cholecystitis and cholecystoduodenal fistula formation associated with total parenteral nutrition in a six year old child
R W Byard, P S Thorner, E Cutz, et al.
Current Medical Research and Opinion
|
October 8, 2017
Diagnosis and management of pancreatic exocrine insufficiency (PEI) in primary care: consensus guidance of a Canadian expert panel
P Durie, J-D Baillargeon, S Bouchard, et al.
The Journal of Pediatrics
|
April 1, 1990
Renal calcium handling in cystic fibrosis: lack of evidence for a primary renal defect
L Bentur, E Kerem, R Couper, et al.
Cancer Journal (Sudbury, Mass.)
|
August 6, 2025
Modulating Redox Biology to Improve Radiation Responses
Jacky K Leung, Ryan Panchal, Selvakumar Anbalagan, et al.
American Journal of Human Genetics
|
June 1, 1992
Genetic determination of exocrine pancreatic function in cystic fibrosis
P Kristidis, D Bozon, M Corey, et al.
Thorax
|
September 8, 2009
Sweat gland bioelectrics differ in cystic fibrosis: a new concept for potential diagnosis and assessment of CFTR function in cystic fibrosis
T Gonska, W Ip, D Turner, et al.
Genomics
|
May 1, 1991
Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene
J Zielenski, D Bozon, B Kerem, et al.
Archives of Disease in Childhood
|
June 23, 2005
The prevalence and clinical characteristics of cystic fibrosis in South Asian Canadian immigrants
M Mei-Zahav, P Durie, J Zielenski, et al.
The American Journal of Clinical Nutrition
|
September 9, 1999
Prevalence of vitamin K deficiency in cystic fibrosis
M Rashid, P Durie, M Andrew, et al.
Page
of 6