Cargando…

Intestinal current measurement versus nasal potential difference measurements for diagnosis of cystic fibrosis: a case–control study

BACKGROUND: Nasal potential difference (NPD) and intestinal current measurement (ICM) are functional CFTR tests that are used as adjunctive diagnostic tools for cystic fibrosis (CF). Smoking has a systemic negative impact on CFTR function. A diagnostic comparison between NPD and ICM and the impact o...

Descripción completa

Detalles Bibliográficos
Autores principales:	Bagheri-Hanson, Azadeh, Nedwed, Sebastian, Rueckes-Nilges, Claudia, Naehrlich, Lutz
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2014
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199064/ https://www.ncbi.nlm.nih.gov/pubmed/25280757 http://dx.doi.org/10.1186/1471-2466-14-156

Ejemplares similares

Personalized medicine with drugs targeting the underlying protein defect in cystic fibrosis: is monitoring of treatment response necessary?
por: Niedermayr, Katharina, et al.
Publicado: (2022)

The Changing Face of Cystic Fibrosis and Its Implications for Screening
por: Naehrlich, Lutz
Publicado: (2020)

Potential of Intestinal Current Measurement for Personalized Treatment of Patients with Cystic Fibrosis
por: Graeber, Simon Y., et al.
Publicado: (2021)

Diabetes in Cystic Fibrosis: Multicenter Screening Results Based on Current Guidelines
por: Scheuing, Nicole, et al.
Publicado: (2013)

Impact of COVID-19 on people with cystic fibrosis
por: Colombo, Carla, et al.
Publicado: (2020)

Risk factors for respiratory Aspergillus fumigatus in German Cystic Fibrosis patients and impact on lung function
por: Düesberg, Uta, et al.
Publicado: (2020)

Risk factors for forced expiratory volume in 1 s decline in European patients with cystic fibrosis: data from the European Cystic Fibrosis Society Patient Registry
por: Hatziagorou, Elpis, et al.
Publicado: (2023)

Serum Proteome Profiling Identifies Novel and Powerful Markers of Cystic Fibrosis Liver Disease
por: Rath, Timo, et al.
Publicado: (2013)

Measuring cystic fibrosis drug responses in organoids derived from 2D differentiated nasal epithelia
por: Amatngalim, Gimano D, et al.
Publicado: (2022)

Multicentre feasibility of multiple-breath washout in preschool children with cystic fibrosis and other lung diseases
por: Stahl, Mirjam, et al.
Publicado: (2020)

Chronic rhinosinusitis and nasal polyposis in cystic fibrosis: update on diagnosis and treatment
por: Kang, Suzie Hyeona, et al.
Publicado: (2015)

Cystic Fibrosis in Europe - remote measurement of outcome
por: Mehta, Anil, et al.
Publicado: (2010)

Nasal endoscopic evaluation of children and adolescents with cystic fibrosis
por: Paiva Franco, Letícia, et al.
Publicado: (2015)

Correlation of Electrophysiological and Fluorescence-Based Measurements of Modulator Efficacy in Nasal Epithelial Cultures Derived from People with Cystic Fibrosis
por: Gunawardena, Tarini N. A., et al.
Publicado: (2023)

Cytokine profile in subjects with Cystic Fibrosis and nasal polyposis compared to patients with no nasal disorders
por: Nunes, Flávio Barbosa, et al.
Publicado: (2015)

Novel Outcome Measures for Clinical Trials in Cystic Fibrosis
por: Tiddens, Harm AWM, et al.
Publicado: (2015)

Human Nasal Epithelial Organoids for Therapeutic Development in Cystic Fibrosis
por: Liu, Zhongyu, et al.
Publicado: (2020)

Incidence and evolution of nasal polyps in children and adolescents with cystic fibrosis
por: Weber, Silke Anna Thereza, et al.
Publicado: (2015)

Intestinal current measurement and nasal potential difference to make a diagnosis of cases with inconclusive CFTR genetics and sweat test
por: Minso, Rebecca, et al.
Publicado: (2020)

Cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis: current perspectives
por: Schmidt, Béla Z, et al.
Publicado: (2016)

Intestinal Dysbiosis in Young Cystic Fibrosis Rabbits
por: Liang, Xiubin, et al.
Publicado: (2021)

Proteomic Analysis of Nasal Epithelial Cells from Cystic Fibrosis Patients
por: Jeanson, Ludovic, et al.
Publicado: (2014)

Nasal Potential Difference in Cystic Fibrosis considering Severe CFTR Mutations
por: Ng, Ronny Tah Yen, et al.
Publicado: (2015)

Nasal Resistome Development in Infants With Cystic Fibrosis in the First Year of Life
por: Allemann, Aurélie, et al.
Publicado: (2019)

Nasal Epithelial Cell-Based Models for Individualized Study in Cystic Fibrosis
por: Keegan, Duncan E., et al.
Publicado: (2021)

Discordance between clinical, physiological, and radiological measures in cystic fibrosis
por: Barry, Peter J, et al.
Publicado: (2014)

High Variability in Oral Glucose Tolerance among 1,128 Patients with Cystic Fibrosis: A Multicenter Screening Study
por: Scheuing, Nicole, et al.
Publicado: (2014)

Nasal endoscopic and CT scan alterations of the paranasal sinuses as predictors of severity in patients with cystic fibrosis
por: de Freitas, Marcos Rabelo, et al.
Publicado: (2015)

Lubiprostone ameliorates the cystic fibrosis mouse intestinal phenotype
por: De Lisle, Robert C, et al.
Publicado: (2010)

Development of the intestinal microbiome in cystic fibrosis in early life
por: Price, Courtney E., et al.
Publicado: (2023)

Nasal polyposis from cystic fibrosis in children – the experience of a single center
por: Iovănescu, Gheorghe, et al.
Publicado: (2023)

Exploring intrinsic variability between cultured nasal and bronchial epithelia in cystic fibrosis
por: Rodenburg, Lisa W., et al.
Publicado: (2023)

Effect of Ivacaftor on Objective and Subjective Measures of Cough in Patients with Cystic Fibrosis
por: Faruqi, Shoaib, et al.
Publicado: (2016)

Value Assessment in Cystic Fibrosis: ICER’s Rejection of the Axioms of Fundamental Measurement
por: Langley, Paul C
Publicado: (2020)

Novel volumetric capnography indices measure ventilation inhomogeneity in cystic fibrosis
por: Fouzas, Sotirios, et al.
Publicado: (2022)

Home Self-Collection of Nasal Swabs for Diagnosis of Acute Respiratory Virus Infections in Children With Cystic Fibrosis
por: Emerson, Julia, et al.
Publicado: (2013)

Diagnosis of chronic rhinosinusitis in patients with cystic fibrosis: correlation between anamnesis, nasal endoscopy and computed tomography
por: Boari, Letícia, et al.
Publicado: (2015)

High-flow nasal oxygen versus noninvasive ventilation in adult patients with cystic fibrosis: a randomized crossover physiological study
por: Sklar, Michael C., et al.
Publicado: (2018)

Elexacaftor-Tezacaftor-Ivacaftor Treatment Reduces Abdominal Symptoms in Cystic Fibrosis-Early results Obtained With the CF-Specific CFAbd-Score
por: Mainz, Jochen G., et al.
Publicado: (2022)

Corrigendum: Elexacaftor-Tezacaftor-Ivacaftor treatment reduces abdominal symptoms in cystic fibrosis-early results obtained with the CF-specific CFAbd-Score
por: Mainz, Jochen G., et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_vjsus2ro99lm4lbb0sghje1ist