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A Munck

Showing results (171-180 of 189) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 1, 1996
[Contribution of endosonography to the diagnosis and follow-up of pediatric gastric neurofibroma revealing von Recklinghausen's disease]S Ategbo, A Munck, Y Aigrain, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|February 14, 2012
A new highly discriminatory multiplex capillary-based MLVA assay as a tool for the epidemiological survey of Pseudomonas aeruginosa in cystic fibrosis patientsD Sobral, P Mariani-Kurkdjian, E Bingen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 25, 2020
Penetrance is a critical parameter for assessing the disease liability of CFTR variantsA Boussaroque, M-P Audrézet, C Raynal, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 22, 2022
Standards of care guidance for sweat testing; phase two of the ECFS quality improvement programmeN Cirilli, K W Southern, J Barben, et al.
Science (New York, N.Y.)|November 6, 1992
Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemiaJ R Wetterau, L P Aggerbeck, M E Bouma, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 26, 2023
Letter to the editor: Risk of false newborn screening after intra-uterine exposure to ETIE De Wachter, J C Davies, N J Simmonds, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 5, 2017
Inhaled dry powder mannitol in children with cystic fibrosis: A randomised efficacy and safety trialK De Boeck, E Haarman, J Hull, et al.
Microorganisms|December 24, 2021
Comparison of Diplodia Tip Blight Pathogens in Spanish and North American Pine EcosystemsAna Aragonés, Tania Manzanos, Glen Stanosz, et al.
Gastroenterology|October 26, 2001
Apolipoprotein B48 glycosylation in abetalipoproteinemia and Anderson's diseaseN Berriot-Varoqueaux, A H Dannoura, A Moreau, et al.
Thorax|March 26, 2009
Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosisC Goubau, M Wilschanski, V Skalická, et al.
Pageof 19

Showing results (171-180 of 189) with videos related to

Sort By:
Pageof 19
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 1, 1996
[Contribution of endosonography to the diagnosis and follow-up of pediatric gastric neurofibroma revealing von Recklinghausen's disease]S Ategbo, A Munck, Y Aigrain, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|February 14, 2012
A new highly discriminatory multiplex capillary-based MLVA assay as a tool for the epidemiological survey of Pseudomonas aeruginosa in cystic fibrosis patientsD Sobral, P Mariani-Kurkdjian, E Bingen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 25, 2020
Penetrance is a critical parameter for assessing the disease liability of CFTR variantsA Boussaroque, M-P Audrézet, C Raynal, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 22, 2022
Standards of care guidance for sweat testing; phase two of the ECFS quality improvement programmeN Cirilli, K W Southern, J Barben, et al.
Science (New York, N.Y.)|November 6, 1992
Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemiaJ R Wetterau, L P Aggerbeck, M E Bouma, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 26, 2023
Letter to the editor: Risk of false newborn screening after intra-uterine exposure to ETIE De Wachter, J C Davies, N J Simmonds, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 5, 2017
Inhaled dry powder mannitol in children with cystic fibrosis: A randomised efficacy and safety trialK De Boeck, E Haarman, J Hull, et al.
Microorganisms|December 24, 2021
Comparison of Diplodia Tip Blight Pathogens in Spanish and North American Pine EcosystemsAna Aragonés, Tania Manzanos, Glen Stanosz, et al.
Gastroenterology|October 26, 2001
Apolipoprotein B48 glycosylation in abetalipoproteinemia and Anderson's diseaseN Berriot-Varoqueaux, A H Dannoura, A Moreau, et al.
Thorax|March 26, 2009
Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosisC Goubau, M Wilschanski, V Skalická, et al.
Pageof 19