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Bruno Maranda

Showing results (11-20 of 63) with videos related to

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Bioanalysis|January 26, 2016
Evaluation of urinary keratan sulfate disaccharides in MPS IVA patients using UPLC-MS/MSChristiane Auray-Blais, Pamela Lavoie, Bruno Maranda, et al.
Canadian Respiratory Journal|February 15, 2012
Unusual respiratory manifestations in two young adults with Duchenne muscular dystrophyJulie Lemay, Frédéric Sériès, Mario Sénéchal, et al.
Pediatric Radiology|March 6, 2013
Genetically proven cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in a 3-year-oldYves Benabu, Mathieu Beland, Natasha Ferguson, et al.
Clinical Biochemistry|November 17, 2011
Spinal muscular atrophy: clinical validation of a single-tube multiplex real time PCR assay for determination of SMN1 and SMN2 copy numbersBruno Maranda, Li Fan, Jean-François Soucy, et al.
Orphanet Journal of Rare Diseases|September 30, 2020
Clinical characteristics of patients from Quebec, Canada, with Morquio A syndrome: a longitudinal observational studyLina Moisan, David Iannuzzi, Bruno Maranda, et al.
The Annals of Thoracic Surgery|February 27, 2013
Idiopathic subglottic stenosis: a familial predispositionElaine Dumoulin, David R Stather, Gary Gelfand, et al.
Journal of Medical Genetics|October 4, 2011
Clinical validity of karyotyping for the diagnosis of chromosomal imbalance following array comparative genomic hybridisationJean Gekas, Maud Vallée, Lysanne Castonguay, et al.
American Journal of Medical Genetics. Part A|January 30, 2016
Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestationsSeemi Ayub, Macoura Gadji, Kada Krabchi, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 10, 2007
Clinical and cellular manifestations of OSTM1-related infantile osteopetrosisBruno Maranda, Gilles Chabot, Jean-Claude Décarie, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 23, 2019
Tandem mass spectrometry analysis of urinary podocalyxin and podocin in the investigation of podocyturia in women with preeclampsia and Fabry disease patientsTristan Martineau, Michel Boutin, Anne-Marie Côté, et al.
Pageof 7

Showing results (11-20 of 63) with videos related to

Sort By:
Pageof 7
Bioanalysis|January 26, 2016
Evaluation of urinary keratan sulfate disaccharides in MPS IVA patients using UPLC-MS/MSChristiane Auray-Blais, Pamela Lavoie, Bruno Maranda, et al.
Canadian Respiratory Journal|February 15, 2012
Unusual respiratory manifestations in two young adults with Duchenne muscular dystrophyJulie Lemay, Frédéric Sériès, Mario Sénéchal, et al.
Pediatric Radiology|March 6, 2013
Genetically proven cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in a 3-year-oldYves Benabu, Mathieu Beland, Natasha Ferguson, et al.
Clinical Biochemistry|November 17, 2011
Spinal muscular atrophy: clinical validation of a single-tube multiplex real time PCR assay for determination of SMN1 and SMN2 copy numbersBruno Maranda, Li Fan, Jean-François Soucy, et al.
Orphanet Journal of Rare Diseases|September 30, 2020
Clinical characteristics of patients from Quebec, Canada, with Morquio A syndrome: a longitudinal observational studyLina Moisan, David Iannuzzi, Bruno Maranda, et al.
The Annals of Thoracic Surgery|February 27, 2013
Idiopathic subglottic stenosis: a familial predispositionElaine Dumoulin, David R Stather, Gary Gelfand, et al.
Journal of Medical Genetics|October 4, 2011
Clinical validity of karyotyping for the diagnosis of chromosomal imbalance following array comparative genomic hybridisationJean Gekas, Maud Vallée, Lysanne Castonguay, et al.
American Journal of Medical Genetics. Part A|January 30, 2016
Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestationsSeemi Ayub, Macoura Gadji, Kada Krabchi, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 10, 2007
Clinical and cellular manifestations of OSTM1-related infantile osteopetrosisBruno Maranda, Gilles Chabot, Jean-Claude Décarie, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 23, 2019
Tandem mass spectrometry analysis of urinary podocalyxin and podocin in the investigation of podocyturia in women with preeclampsia and Fabry disease patientsTristan Martineau, Michel Boutin, Anne-Marie Côté, et al.
Pageof 7