George M. Solomon Department of Medicine and the Gregory Fleming James Cystic Fibrosis Center University of Alabama at Birmingham Biography Publications Institution JoVE Articles George M. Solomon has not added a biography. If you are George M. Solomon and would like to personalize this page please email our Author Liaison for assistance. Publications CFTR Modulator Theratyping: Current Status, Gaps and Future Directions Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. Jun, 2018 | Pubmed ID: 29934203 Effectiveness of Ivacaftor in Cystic Fibrosis Patients with Non-G551D Gating Mutations Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. Apr, 2018 | Pubmed ID: 29685811 Seeing Cilia: Imaging Modalities for Ciliary Motion and Clinical Connections American Journal of Physiology. Lung Cellular and Molecular Physiology. Jun, 2018 | Pubmed ID: 29493257 MicroRNA-145 Antagonism Reverses TGF-β Inhibition of F508del CFTR Correction in Airway Epithelia American Journal of Respiratory and Critical Care Medicine. Mar, 2018 | Pubmed ID: 29232160 The Therapeutic Potential of CFTR Modulators for COPD and Other Airway Diseases Current Opinion in Pharmacology. 06, 2017 | Pubmed ID: 29132121 Systematic Computational Identification of Variants That Activate Exonic and Intronic Cryptic Splice Sites American Journal of Human Genetics. May, 2017 | Pubmed ID: 28475858 A Multiple Reader Scoring System for Nasal Potential Difference Parameters Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. Sep, 2017 | Pubmed ID: 28465124 Standardized Treatment of Pulmonary Exacerbations (STOP) Study: Observations at the Initiation of Intravenous Antibiotics for Cystic Fibrosis Pulmonary Exacerbations Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. Sep, 2017 | Pubmed ID: 28460885 Standardized Treatment of Pulmonary Exacerbations (STOP) Study: Physician Treatment Practices and Outcomes for Individuals with Cystic Fibrosis with Pulmonary Exacerbations Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. Sep, 2017 | Pubmed ID: 28457954 Assessment of Ciliary Phenotype in Primary Ciliary Dyskinesia by Micro-optical Coherence Tomography JCI Insight. Mar, 2017 | Pubmed ID: 28289722 Pharmacokinetics and Safety of Cavosonstat (N91115) in Healthy and Cystic Fibrosis Adults Homozygous for F508DEL-CFTR Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. May, 2017 | Pubmed ID: 28209466 Flexible, High-resolution Micro-optical Coherence Tomography Endobronchial Probe Toward in Vivo Imaging of Cilia Optics Letters. Feb, 2017 | Pubmed ID: 28198885 Therapeutic Benefit Observed with the CFTR Potentiator, Ivacaftor, in a CF Patient Homozygous for the W1282X CFTR Nonsense Mutation Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. Jan, 2017 | Pubmed ID: 27707539 In Vivo Imaging of Airway Cilia and Mucus Clearance with Micro-optical Coherence Tomography Biomedical Optics Express. Jul, 2016 | Pubmed ID: 27446685 Dual SMAD Signaling Inhibition Enables Long-Term Expansion of Diverse Epithelial Basal Cells Cell Stem Cell. 08, 2016 | Pubmed ID: 27320041 Pilot Evaluation of Ivacaftor for Chronic Bronchitis The Lancet. Respiratory Medicine. 06, 2016 | Pubmed ID: 27185048 Therapeutic Approaches to Acquired Cystic Fibrosis Transmembrane Conductance Regulator Dysfunction in Chronic Bronchitis Annals of the American Thoracic Society. Apr, 2016 | Pubmed ID: 27115953 Neutrophil Fates in Bronchiectasis and Alpha-1 Antitrypsin Deficiency Annals of the American Thoracic Society. Apr, 2016 | Pubmed ID: 27115946 Combination Therapy with Cystic Fibrosis Transmembrane Conductance Regulator Modulators Augment the Airway Functional Microanatomy American Journal of Physiology. Lung Cellular and Molecular Physiology. 05, 2016 | Pubmed ID: 26968770 Acquired Cystic Fibrosis Transmembrane Conductance Regulator Dysfunction in Chronic Bronchitis and Other Diseases of Mucus Clearance Clinics in Chest Medicine. Mar, 2016 | Pubmed ID: 26857776 Breakthrough Therapies: Cystic Fibrosis (CF) Potentiators and Correctors Pediatric Pulmonology. Oct, 2015 | Pubmed ID: 26097168 Improved Clinical and Radiographic Outcomes After Treatment with Ivacaftor in a Young Adult with Cystic Fibrosis with the P67L CFTR Mutation Chest. Mar, 2015 | Pubmed ID: 25732475 IP-10 is a Potential Biomarker of Cystic Fibrosis Acute Pulmonary Exacerbations PloS One. 2013 | Pubmed ID: 23977293 An International Randomized Multicenter Comparison of Nasal Potential Difference Techniques Chest. Oct, 2010 | Pubmed ID: 20472865 Standardized Measurement of Nasal Membrane Transepithelial Potential Difference (NPD) George M. Solomon1, Inez Bronsveld2, Kathryn Hayes3, Michael Wilschanski4, Paola Melotti5, Steven M. Rowe1, Isabelle Sermet-Gaudelus6,7 1Department of Medicine and the Gregory Fleming James Cystic Fibrosis Center, University of Alabama at Birmingham, 2Department of Pulmonology and Tuberculosis, University Medical Center Utrecht, 3Center for Experimental Medicine, Queens University, Northern Ireland, 4Hadassah Hebrew University Medical Center, Jerusalem, 5Centro Fibrosi Cistica, Azienda Ospedaliera Universitaria Integrata, 6Service de Pneumologie et Allergologie Pédiatriques and Center de Ressources et de Compétence de la Mucoviscidose, Hôpital Necker Enfants Malades, 7INSERM U 1151, Institut Necker Enfants Malades JoVE 57006 Medicine
Standardized Measurement of Nasal Membrane Transepithelial Potential Difference (NPD) George M. Solomon1, Inez Bronsveld2, Kathryn Hayes3, Michael Wilschanski4, Paola Melotti5, Steven M. Rowe1, Isabelle Sermet-Gaudelus6,7 1Department of Medicine and the Gregory Fleming James Cystic Fibrosis Center, University of Alabama at Birmingham, 2Department of Pulmonology and Tuberculosis, University Medical Center Utrecht, 3Center for Experimental Medicine, Queens University, Northern Ireland, 4Hadassah Hebrew University Medical Center, Jerusalem, 5Centro Fibrosi Cistica, Azienda Ospedaliera Universitaria Integrata, 6Service de Pneumologie et Allergologie Pédiatriques and Center de Ressources et de Compétence de la Mucoviscidose, Hôpital Necker Enfants Malades, 7INSERM U 1151, Institut Necker Enfants Malades JoVE 57006 Medicine
