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Publications by D Dimmock
Cystic Fibrosis Mutations for p.F508del Compound Heterozygotes Predict Sweat Chloride Levels and Pancreatic Sufficiency
Clinical Genetics
Genetics
Related publications
Sweat Gland Function in Cystic Fibrosis.
Journal of Clinical Investigation
Medicine
Cystic Fibrosis Gene Mutation in Two Sisters With Mild Disease and Normal Sweat Electrolyte Levels
New England Journal of Medicine
Medicine
Sweat Testing in Newborns Positive to Neonatal Screening for Cystic Fibrosis
Archives of Disease in Childhood: Fetal and Neonatal Edition
Pediatrics
Gynecology
Perinatology
Obstetrics
Medicine
Child Health
Low Beta-Adrenergic Sweat Responses in Cystic Fibrosis and Cystic Fibrosis Transmembrane Conductance Regulator-Related Metabolic Syndrome Children
Pediatric, Allergy, Immunology, and Pulmonology
Immunology
Pediatrics
Allergy
Perinatology
Child Health
Pulmonary
Respiratory Medicine
Chloride Channels in Cystic Fibrosis Patients
Science
Multidisciplinary
Philosophy of Science
History
Altered Intestinal Chloride Transport in Cystic Fibrosis.
FASEB Journal
Biochemistry
Biotechnology
Genetics
Molecular Biology
Medicine
Comparison of Two Sweat Test Systems for the Diagnosis of Cystic Fibrosis in Newborns
Pediatric Pulmonology
Child Health
Pulmonary
Pediatrics
Perinatology
Respiratory Medicine
Pathology of Pancreatic and Intestinal Disorders in Cystic Fibrosis
Journal of the Royal Society of Medicine
Medicine
Diagnosis of Cystic Fibrosis With Chloride Meter (Sherwood M926s Chloride Analyzer®) and Sweat Test Analysis System (cfΔ Collection System®) Compared to the Gibson Cooke Method
Turkish Journal of Pediatrics
Child Health
Pediatrics
Perinatology
