β-Adrenergic Sweat Secretion as a Diagnostic Test for Cystic Fibrosis

WS14.6 Beta-adrenergic sweat secretion rate as accurate biomarker for CFTR function

(2012) W. Ip et al.   Journal of Cystic Fibrosis

Recommendations for the classification of diseases as CFTR-related disorders

(2011) C. Bombieri et al.   Journal of Cystic Fibrosis

Time course of acetylcholine-induced activation of sympathetic efferents matches axon reflex sweating in humans

(2011) Roland Schmidt et al.   JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM

Type of CFTR Mutation Determines Risk of Pancreatitis in Patients With Cystic Fibrosis

(2010) Chee Y. Ooi et al.   GASTROENTEROLOGY

Cystic fibrosis newborn screening: using experience to optimize the screening algorithm

(2010) Jaime E. Hale et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Effect of VX-770 in Persons with Cystic Fibrosis and the G551D-CFTRMutation

(2010) Frank J. Accurso et al.   NEW ENGLAND JOURNAL OF MEDICINE

Non-classic cystic fibrosis associated with D1152HCFTRmutation

(2009) P-R Burgel et al.   CLINICAL GENETICS

Correlation of transepidermal water loss with skin barrier propertiesin vitro: comparison of three evaporimeters

(2009) Rania Elkeeb et al.   SKIN RESEARCH AND TECHNOLOGY

Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report

(2008) Philip M. Farrell et al.   JOURNAL OF PEDIATRICS

Effectiveness of PTC124 treatment of cystic fibrosis caused by nonsense mutations: a prospective phase II trial

(2008) Eitan Kerem et al.   LANCET