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Laura Bernardini

Showing results (41-50 of 157) with videos related to

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American Journal of Medical Genetics. Part A|October 19, 2021
Koolen-de Vries syndrome in a 63-year-old woman: Report of the oldest patient and a review of the adult phenotypeMarianna Farnè, Laura Bernardini, Anna Capalbo, et al.
Virchows Archiv : an International Journal of Pathology|August 12, 2022
Correction to: Systemic ALK-negative anaplastic large cell lymphoma with distinctive myxoid change and DUSP22 rearrangementStefano Fratoni, Malgorzata Monika Trawinska, Anna Capalbo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 13, 2020
Further delineation of the neurodevelopmental phenotypic spectrum associated to 14q11.2 microduplicationGiulia Pascolini, Emanuele Agolini, Nicole Fleischer, et al.
Respiratory Care|April 8, 2026
Carbon Dioxide Levels in Extremely Preterm Neonates Ventilated With High Frequency Jet VentilationDimitrios Rallis, Danielle Ben-David, Kendra Woo, et al.
Cancer Genetics and Cytogenetics|April 7, 2004
Fluorescence in situ hybridization analysis of allelic losses involving the long arm of chromosome 17 in NF1-associated neurofibromasAlessandro De Luca, Laura Bernardini, Caterina Ceccarini, et al.
Frontiers in Genetics|August 1, 2022
Case Report: A Novel Homozygous Missense Variant of <i>FBN3</i> Supporting It Is a New Candidate Gene Causative of a Bardet-Biedl Syndrome-Like PhenotypeMaria Luce Genovesi, Barbara Torres, Marina Goldoni, et al.
Journal of Migration and Health|March 27, 2023
Unaccompanied foreign minors and mental health: Implementation and evaluation of the RHS-15 screening procedure for unaccompanied foreign minorsMarco Fontana, Francesco Fattori, Sofia Trezzi, et al.
Frontiers in Pediatrics|January 19, 2024
Single center experience with first-intention high-frequency jet vs. volume-targeted ventilation in extremely preterm neonatesDimitrios Rallis, Danielle Ben-David, Kendra Woo, et al.
Diagnostics (Basel, Switzerland)|June 24, 2022
Chromosomal Microarray Analysis in Fetuses Detected with Isolated Cardiovascular Malformation: A Multicenter Study, Systematic Review of the Literature and Meta-AnalysisGioia Mastromoro, Nader Khaleghi Hashemian, Daniele Guadagnolo, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|April 11, 2023
Prenatal <i>CFAP53</i>-related laterality defect: case report and review of the literatureGioia Mastromoro, Daniele Guadagnolo, Antonio Novelli, et al.
Pageof 16

Showing results (41-50 of 157) with videos related to

Sort By:
Pageof 16
American Journal of Medical Genetics. Part A|October 19, 2021
Koolen-de Vries syndrome in a 63-year-old woman: Report of the oldest patient and a review of the adult phenotypeMarianna Farnè, Laura Bernardini, Anna Capalbo, et al.
Virchows Archiv : an International Journal of Pathology|August 12, 2022
Correction to: Systemic ALK-negative anaplastic large cell lymphoma with distinctive myxoid change and DUSP22 rearrangementStefano Fratoni, Malgorzata Monika Trawinska, Anna Capalbo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 13, 2020
Further delineation of the neurodevelopmental phenotypic spectrum associated to 14q11.2 microduplicationGiulia Pascolini, Emanuele Agolini, Nicole Fleischer, et al.
Respiratory Care|April 8, 2026
Carbon Dioxide Levels in Extremely Preterm Neonates Ventilated With High Frequency Jet VentilationDimitrios Rallis, Danielle Ben-David, Kendra Woo, et al.
Cancer Genetics and Cytogenetics|April 7, 2004
Fluorescence in situ hybridization analysis of allelic losses involving the long arm of chromosome 17 in NF1-associated neurofibromasAlessandro De Luca, Laura Bernardini, Caterina Ceccarini, et al.
Frontiers in Genetics|August 1, 2022
Case Report: A Novel Homozygous Missense Variant of <i>FBN3</i> Supporting It Is a New Candidate Gene Causative of a Bardet-Biedl Syndrome-Like PhenotypeMaria Luce Genovesi, Barbara Torres, Marina Goldoni, et al.
Journal of Migration and Health|March 27, 2023
Unaccompanied foreign minors and mental health: Implementation and evaluation of the RHS-15 screening procedure for unaccompanied foreign minorsMarco Fontana, Francesco Fattori, Sofia Trezzi, et al.
Frontiers in Pediatrics|January 19, 2024
Single center experience with first-intention high-frequency jet vs. volume-targeted ventilation in extremely preterm neonatesDimitrios Rallis, Danielle Ben-David, Kendra Woo, et al.
Diagnostics (Basel, Switzerland)|June 24, 2022
Chromosomal Microarray Analysis in Fetuses Detected with Isolated Cardiovascular Malformation: A Multicenter Study, Systematic Review of the Literature and Meta-AnalysisGioia Mastromoro, Nader Khaleghi Hashemian, Daniele Guadagnolo, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|April 11, 2023
Prenatal <i>CFAP53</i>-related laterality defect: case report and review of the literatureGioia Mastromoro, Daniele Guadagnolo, Antonio Novelli, et al.
Pageof 16