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Erik Fransen

Showing results (151-160 of 233) with videos related to

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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|September 23, 2003
Progressive late-onset sensorineural hearing loss and vestibular impairment with vertigo (DFNA9/COCH): longitudinal analyses in a belgian familyFrancois X Lemaire, Louw Feenstra, Patrick L M Huygen, et al.
Plos One|September 2, 2016
Development and Validation of a Histological Method to Measure Microvessel Density in Whole-Slide Images of Cancer TissueKoen M Marien, Valerie Croons, Yannick Waumans, et al.
Human Mutation|July 12, 2002
A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairmentGuy Van Camp, Paul J Coucke, Jiro Akita, et al.
Biomarker Insights|May 20, 2022
Identification of Potential Urinary Metabolite Biomarkers of <i>Pseudomonas aeruginosa</i> Ventilator-Associated PneumoniaBart's Jongers, An Hotterbeekx, Kenny Bielen, et al.
The Journal of ECT|November 26, 2019
Performance of the Psychotic Depression Assessment Scale as a Predictor of ECT OutcomeLinda van Diermen, Pieter Versyck, Seline van den Ameele, et al.
Antioxidants (Basel, Switzerland)|September 28, 2024
A Case-Control Study Supports Genetic Contribution of the <i>PON</i> Gene Family in Obesity and Metabolic Dysfunction Associated Steatotic Liver DiseaseEvelien Van Dijck, Sara Diels, Erik Fransen, et al.
International Journal of Pediatric Otorhinolaryngology|September 20, 2005
Monogenic nonsyndromic otosclerosis: audiological and linkage analysis in a large Greek pedigreeVassiliki Iliadou, Kris Van Den Bogaert, Nikolaos Eleftheriades, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|June 9, 2009
No evidence for association between the renin-angiotensin-aldosterone system and otosclerosis in a large Belgian-Dutch populationIsabelle Schrauwen, Melissa Thys, Kathleen Vanderstraeten, et al.
Human Mutation|March 11, 2014
An FBN1 deep intronic mutation in a familial case of Marfan syndrome: an explanation for genetically unsolved cases?Elisabeth Gillis, Marlies Kempers, Simone Salemink, et al.
BMJ Open|November 21, 2022
Understanding the clinical profile of patients with frozen shoulder: a longitudinal multicentre observational studyMichel Gcam Mertens, Mira Meeus, Suzie Noten, et al.
Pageof 24

Showing results (151-160 of 233) with videos related to

Sort By:
Pageof 24
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|September 23, 2003
Progressive late-onset sensorineural hearing loss and vestibular impairment with vertigo (DFNA9/COCH): longitudinal analyses in a belgian familyFrancois X Lemaire, Louw Feenstra, Patrick L M Huygen, et al.
Plos One|September 2, 2016
Development and Validation of a Histological Method to Measure Microvessel Density in Whole-Slide Images of Cancer TissueKoen M Marien, Valerie Croons, Yannick Waumans, et al.
Human Mutation|July 12, 2002
A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairmentGuy Van Camp, Paul J Coucke, Jiro Akita, et al.
Biomarker Insights|May 20, 2022
Identification of Potential Urinary Metabolite Biomarkers of <i>Pseudomonas aeruginosa</i> Ventilator-Associated PneumoniaBart's Jongers, An Hotterbeekx, Kenny Bielen, et al.
The Journal of ECT|November 26, 2019
Performance of the Psychotic Depression Assessment Scale as a Predictor of ECT OutcomeLinda van Diermen, Pieter Versyck, Seline van den Ameele, et al.
Antioxidants (Basel, Switzerland)|September 28, 2024
A Case-Control Study Supports Genetic Contribution of the <i>PON</i> Gene Family in Obesity and Metabolic Dysfunction Associated Steatotic Liver DiseaseEvelien Van Dijck, Sara Diels, Erik Fransen, et al.
International Journal of Pediatric Otorhinolaryngology|September 20, 2005
Monogenic nonsyndromic otosclerosis: audiological and linkage analysis in a large Greek pedigreeVassiliki Iliadou, Kris Van Den Bogaert, Nikolaos Eleftheriades, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|June 9, 2009
No evidence for association between the renin-angiotensin-aldosterone system and otosclerosis in a large Belgian-Dutch populationIsabelle Schrauwen, Melissa Thys, Kathleen Vanderstraeten, et al.
Human Mutation|March 11, 2014
An FBN1 deep intronic mutation in a familial case of Marfan syndrome: an explanation for genetically unsolved cases?Elisabeth Gillis, Marlies Kempers, Simone Salemink, et al.
BMJ Open|November 21, 2022
Understanding the clinical profile of patients with frozen shoulder: a longitudinal multicentre observational studyMichel Gcam Mertens, Mira Meeus, Suzie Noten, et al.
Pageof 24