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V Fernandez

Showing results (421-430 of 597) with videos related to

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Pain|December 2, 2021
Long-term alterations in somatosensory functioning in survivors of childhood cancerPerri R Tutelman, Christine T Chambers, Laura Cornelissen, et al.
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|October 20, 2015
Returning a Research Participant's Genomic Results to Relatives: Analysis and RecommendationsSusan M Wolf, Rebecca Branum, Barbara A Koenig, et al.
Cancer|November 7, 2023
Treatment of children with favorable histology Wilms tumor with extrapulmonary metastases: A report from the COG studies AREN0533 and AREN03B2 and NWTSG study NWTS-5Daniel J Benedetti, Carly R Varela, Lindsay A Renfro, et al.
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|July 17, 2018
Pragmatic Tools for Sharing Genomic Research Results with the Relatives of Living and Deceased Research ParticipantsSusan M Wolf, Emily Scholtes, Barbara A Koenig, et al.
Pediatric Blood & Cancer|May 6, 2006
Disease progression in recently diagnosed patients with inherited marrow failure syndromes: a Canadian Inherited Marrow Failure Registry (CIMFR) reportJ M Steele, L Sung, R Klaassen, et al.
Cancer|February 24, 2024
Treatment and outcomes of clear cell sarcoma of the kidney: A report from the Children's Oncology Group studies AREN0321 and AREN03B2Daniel J Benedetti, Lindsay A Renfro, Ian Tfirn, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 2014
The choice of normative pediatric reference database changes spine bone mineral density Z-scores but not the relationship between bone mineral density and prevalent vertebral fracturesJinhui Ma, Kerry Siminoski, Nathalie Alos, et al.
JAMA Ophthalmology|August 16, 2014
Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutationsJohane M Robitaille, Roxanne M Gillett, Marissa A LeBlanc, et al.
Translational Psychiatry|March 30, 2016
Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathwaysC Cappi, H Brentani, L Lima, et al.
Nature Genetics|May 5, 2009
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemiaDuane L Guernsey, Haiyan Jiang, Dean R Campagna, et al.
Pageof 60

Showing results (421-430 of 597) with videos related to

Sort By:
Pageof 60
Pain|December 2, 2021
Long-term alterations in somatosensory functioning in survivors of childhood cancerPerri R Tutelman, Christine T Chambers, Laura Cornelissen, et al.
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|October 20, 2015
Returning a Research Participant's Genomic Results to Relatives: Analysis and RecommendationsSusan M Wolf, Rebecca Branum, Barbara A Koenig, et al.
Cancer|November 7, 2023
Treatment of children with favorable histology Wilms tumor with extrapulmonary metastases: A report from the COG studies AREN0533 and AREN03B2 and NWTSG study NWTS-5Daniel J Benedetti, Carly R Varela, Lindsay A Renfro, et al.
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|July 17, 2018
Pragmatic Tools for Sharing Genomic Research Results with the Relatives of Living and Deceased Research ParticipantsSusan M Wolf, Emily Scholtes, Barbara A Koenig, et al.
Pediatric Blood & Cancer|May 6, 2006
Disease progression in recently diagnosed patients with inherited marrow failure syndromes: a Canadian Inherited Marrow Failure Registry (CIMFR) reportJ M Steele, L Sung, R Klaassen, et al.
Cancer|February 24, 2024
Treatment and outcomes of clear cell sarcoma of the kidney: A report from the Children's Oncology Group studies AREN0321 and AREN03B2Daniel J Benedetti, Lindsay A Renfro, Ian Tfirn, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 2014
The choice of normative pediatric reference database changes spine bone mineral density Z-scores but not the relationship between bone mineral density and prevalent vertebral fracturesJinhui Ma, Kerry Siminoski, Nathalie Alos, et al.
JAMA Ophthalmology|August 16, 2014
Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutationsJohane M Robitaille, Roxanne M Gillett, Marissa A LeBlanc, et al.
Translational Psychiatry|March 30, 2016
Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathwaysC Cappi, H Brentani, L Lima, et al.
Nature Genetics|May 5, 2009
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemiaDuane L Guernsey, Haiyan Jiang, Dean R Campagna, et al.
Pageof 60