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Stefano Pensiero

Showing results (21-30 of 30) with videos related to

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Journal of Clinical Medicine|March 28, 2024
Non-Invasive Recording of Ocular-Following Responses in Children: A Promising Tool for Stereo Deficiency EvaluationAleksandar Miladinović, Christian Quaia, Miloš Ajčević, et al.
Ophthalmic Genetics|August 1, 2012
A novel CRYBB2 missense mutation causing congenital autosomal dominant cataract in an Italian familyFlavio Faletra, Adamo Pio d'Adamo, Stefano Pensiero, et al.
Plos One|November 10, 2022
Ocular-following responses in school-age childrenAleksandar Miladinović, Christian Quaia, Miloš Ajčević, et al.
JMIR Pediatrics and Parenting|December 9, 2024
High-Resolution Eye-Tracking System for Accurate Measurement of Short-Latency Ocular Following Responses: Development and Observational StudyAleksandar Miladinović, Christian Quaia, Simone Kresevic, et al.
Menopause (New York, N.Y.)|January 25, 2003
Visual function in menopause: the role of hormone replacement therapySecondo Guaschino, Eva Grimaldi, Andrea Sartore, et al.
Ophthalmic Genetics|April 18, 2009
Ophthalmic features in a dysmorphic boy with chromosome 4q deletion and duplicationFulvio Parentin, Antonella Fabretto, Daniela Gambel Benussi, et al.
Ophthalmic Genetics|April 23, 2011
Horizontal gaze palsy and progressive scoliosis without ROBO3 mutationsKhaled K Abu-Amero, Flavio Faletra, Paolo Gasparini, et al.
Scientific Reports|December 23, 2015
PSIP1/LEDGF: a new gene likely involved in sensorineural progressive hearing lossGiorgia Girotto, Déborah I Scheffer, Anna Morgan, et al.
Biomedicines|August 28, 2025
Hidden in the Genome: The First Italian Family with North Carolina Macular Dystrophy Carrying a Novel <i>PRDM13</i> and <i>CCNC</i> DuplicationBeatrice Spedicati, Domizia Pasquetti, Aurora Santin, et al.
Biomedicines|June 26, 2026
Reply to Small, K.W. Comment on "Spedicati et al. Hidden in the Genome: The First Italian Family with North Carolina Macular Dystrophy Carrying a Novel <i>PRDM13</i> and <i>CCNC</i> Duplication. <i>Biomedicines</i> 2025, <i>13</i>, 1904"Beatrice Spedicati, Domizia Pasquetti, Aurora Santin, et al.
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Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Journal of Clinical Medicine|March 28, 2024
Non-Invasive Recording of Ocular-Following Responses in Children: A Promising Tool for Stereo Deficiency EvaluationAleksandar Miladinović, Christian Quaia, Miloš Ajčević, et al.
Ophthalmic Genetics|August 1, 2012
A novel CRYBB2 missense mutation causing congenital autosomal dominant cataract in an Italian familyFlavio Faletra, Adamo Pio d'Adamo, Stefano Pensiero, et al.
Plos One|November 10, 2022
Ocular-following responses in school-age childrenAleksandar Miladinović, Christian Quaia, Miloš Ajčević, et al.
JMIR Pediatrics and Parenting|December 9, 2024
High-Resolution Eye-Tracking System for Accurate Measurement of Short-Latency Ocular Following Responses: Development and Observational StudyAleksandar Miladinović, Christian Quaia, Simone Kresevic, et al.
Menopause (New York, N.Y.)|January 25, 2003
Visual function in menopause: the role of hormone replacement therapySecondo Guaschino, Eva Grimaldi, Andrea Sartore, et al.
Ophthalmic Genetics|April 18, 2009
Ophthalmic features in a dysmorphic boy with chromosome 4q deletion and duplicationFulvio Parentin, Antonella Fabretto, Daniela Gambel Benussi, et al.
Ophthalmic Genetics|April 23, 2011
Horizontal gaze palsy and progressive scoliosis without ROBO3 mutationsKhaled K Abu-Amero, Flavio Faletra, Paolo Gasparini, et al.
Scientific Reports|December 23, 2015
PSIP1/LEDGF: a new gene likely involved in sensorineural progressive hearing lossGiorgia Girotto, Déborah I Scheffer, Anna Morgan, et al.
Biomedicines|August 28, 2025
Hidden in the Genome: The First Italian Family with North Carolina Macular Dystrophy Carrying a Novel <i>PRDM13</i> and <i>CCNC</i> DuplicationBeatrice Spedicati, Domizia Pasquetti, Aurora Santin, et al.
Biomedicines|June 26, 2026
Reply to Small, K.W. Comment on "Spedicati et al. Hidden in the Genome: The First Italian Family with North Carolina Macular Dystrophy Carrying a Novel <i>PRDM13</i> and <i>CCNC</i> Duplication. <i>Biomedicines</i> 2025, <i>13</i>, 1904"Beatrice Spedicati, Domizia Pasquetti, Aurora Santin, et al.
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