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R Knowles

Showing results (821-830 of 950) with videos related to

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Human Genome Variation|July 5, 2017
Corrigendum: Novel variation at chr11p13 associated with cystic fibrosis lung disease severityHong Dang, Paul J Gallins, Rhonda G Pace, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|September 5, 2018
High-resolution FLAIR MRI at 7 Tesla for treatment planning in glioblastoma patientsSebastian Regnery, Benjamin R Knowles, Daniel Paech, et al.
Human Genome Variation|July 14, 2016
Novel variation at chr11p13 associated with cystic fibrosis lung disease severityHong Dang, Paul J Gallins, Rhonda G Pace, et al.
Trials|September 11, 2016
The Mental Health in Diabetes Service (MINDS) to enhance psychosocial health: study protocol for a randomized controlled trialCasey L O'Brien, Chantal F Ski, David R Thompson, et al.
Psycho-Oncology|December 18, 2024
Scanxiety and Fear of Recurrence in Young Adult Female Breast and Gynaecological Cancer Survivors: Investigating Shared MechanismsDiya S Patel, Sarah N Webster, Emily J Dowling, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|October 27, 2010
Realtime fusion of cardiac magnetic resonance imaging and computed tomography venography with X-ray fluoroscopy to aid cardiac resynchronisation therapy implantation in patients with persistent left superior vena cavaSimon G Duckett, Matthew Ginks, Anoop K Shetty, et al.
Human Mutation|January 1, 1997
Identification of a splice site mutation (2789 +5 G > A) associated with small amounts of normal CFTR mRNA and mild cystic fibrosisW E Highsmith, L H Burch, Z Zhou, et al.
Molecular Genetics & Genomic Medicine|July 5, 2019
Recurring large deletion in DRC1 (CCDC164) identified as causing primary ciliary dyskinesia in two Asian patientsKozo Morimoto, Minako Hijikata, Maimoona A Zariwala, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Basic protocol for transepithelial nasal potential difference measurementsDaniel Schüler, Isabelle Sermet-Gaudelus, Michael Wilschanski, et al.
Human Mutation|June 26, 2013
Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesiaM Leigh Anne Daniels, Margaret W Leigh, Stephanie D Davis, et al.
Pageof 95

Showing results (821-830 of 950) with videos related to

Sort By:
Pageof 95
Human Genome Variation|July 5, 2017
Corrigendum: Novel variation at chr11p13 associated with cystic fibrosis lung disease severityHong Dang, Paul J Gallins, Rhonda G Pace, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|September 5, 2018
High-resolution FLAIR MRI at 7 Tesla for treatment planning in glioblastoma patientsSebastian Regnery, Benjamin R Knowles, Daniel Paech, et al.
Human Genome Variation|July 14, 2016
Novel variation at chr11p13 associated with cystic fibrosis lung disease severityHong Dang, Paul J Gallins, Rhonda G Pace, et al.
Trials|September 11, 2016
The Mental Health in Diabetes Service (MINDS) to enhance psychosocial health: study protocol for a randomized controlled trialCasey L O'Brien, Chantal F Ski, David R Thompson, et al.
Psycho-Oncology|December 18, 2024
Scanxiety and Fear of Recurrence in Young Adult Female Breast and Gynaecological Cancer Survivors: Investigating Shared MechanismsDiya S Patel, Sarah N Webster, Emily J Dowling, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|October 27, 2010
Realtime fusion of cardiac magnetic resonance imaging and computed tomography venography with X-ray fluoroscopy to aid cardiac resynchronisation therapy implantation in patients with persistent left superior vena cavaSimon G Duckett, Matthew Ginks, Anoop K Shetty, et al.
Human Mutation|January 1, 1997
Identification of a splice site mutation (2789 +5 G > A) associated with small amounts of normal CFTR mRNA and mild cystic fibrosisW E Highsmith, L H Burch, Z Zhou, et al.
Molecular Genetics & Genomic Medicine|July 5, 2019
Recurring large deletion in DRC1 (CCDC164) identified as causing primary ciliary dyskinesia in two Asian patientsKozo Morimoto, Minako Hijikata, Maimoona A Zariwala, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Basic protocol for transepithelial nasal potential difference measurementsDaniel Schüler, Isabelle Sermet-Gaudelus, Michael Wilschanski, et al.
Human Mutation|June 26, 2013
Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesiaM Leigh Anne Daniels, Margaret W Leigh, Stephanie D Davis, et al.
Pageof 95