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Mucciolo

Showing results (131-140 of 202) with videos related to

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Photodiagnosis and Photodynamic Therapy|August 21, 2020
Long-term follow-up and "double layer sign" in patients affected by circumscribed choroidal hemangiomaVittoria Murro, Dario Pasquale Mucciolo, Dario Giorgio, et al.
Journal of Endocrinological Investigation|July 13, 2021
Prevalence of copy number variants (CNVs) and rhGH treatment efficacy in an Italian cohort of children born small for gestational age (SGA) with persistent short stature associated with a complex clinical phenotypeE Inzaghi, A Deodati, S Loddo, et al.
Cells|December 24, 2021
Finding Aquaporins in Annelids: An Evolutionary Analysis and a Case StudySerena Mucciolo, Andrea Desiderato, Marika Salonna, et al.
Ophthalmic Genetics|August 29, 2018
Fundus phenotype in retinitis pigmentosa associated with EYS mutationsDario Pasquale Mucciolo, Andrea Sodi, Ilaria Passerini, et al.
Molecular Genetics & Genomic Medicine|March 28, 2019
Uniparental isodisomy of chromosome 1 results in glycogen storage disease type III with profound growth retardationEmanuela Ponzi, Viola Alesi, Francesca R Lepri, et al.
Investigative Ophthalmology & Visual Science|February 14, 2022
Choroidal Caverns in Stargardt DiseaseDario Pasquale Mucciolo, Dario Giorgio, Myrta Lippera, et al.
Plos One|January 6, 2018
EDI OCT evaluation of choroidal thickness in Stargardt diseaseAndrea Sodi, Daniela Bacherini, Chiara Lenzetti, et al.
BMC Ophthalmology|February 26, 2017
Case report of an atypical early onset X-linked retinoschisis in monozygotic twinsVittoria Murro, Roberto Caputo, Giacomo Maria Bacci, et al.
Medicina (Kaunas, Lithuania)|May 25, 2024
Atypic Retinitis Pigmentosa Clinical Features Associated with a Peculiar CRX Gene Mutation in Italian PatientsMarco Piergentili, Vito Spagnuolo, Vittoria Murro, et al.
Ophthalmic Genetics|July 9, 2021
Clinical and molecular findings in patients with pattern dystrophyAndrea Sodi, Dario Pasquale Mucciolo, Dario Giorgio, et al.
Pageof 21

Showing results (131-140 of 202) with videos related to

Sort By:
Pageof 21
Photodiagnosis and Photodynamic Therapy|August 21, 2020
Long-term follow-up and "double layer sign" in patients affected by circumscribed choroidal hemangiomaVittoria Murro, Dario Pasquale Mucciolo, Dario Giorgio, et al.
Journal of Endocrinological Investigation|July 13, 2021
Prevalence of copy number variants (CNVs) and rhGH treatment efficacy in an Italian cohort of children born small for gestational age (SGA) with persistent short stature associated with a complex clinical phenotypeE Inzaghi, A Deodati, S Loddo, et al.
Cells|December 24, 2021
Finding Aquaporins in Annelids: An Evolutionary Analysis and a Case StudySerena Mucciolo, Andrea Desiderato, Marika Salonna, et al.
Ophthalmic Genetics|August 29, 2018
Fundus phenotype in retinitis pigmentosa associated with EYS mutationsDario Pasquale Mucciolo, Andrea Sodi, Ilaria Passerini, et al.
Molecular Genetics & Genomic Medicine|March 28, 2019
Uniparental isodisomy of chromosome 1 results in glycogen storage disease type III with profound growth retardationEmanuela Ponzi, Viola Alesi, Francesca R Lepri, et al.
Investigative Ophthalmology & Visual Science|February 14, 2022
Choroidal Caverns in Stargardt DiseaseDario Pasquale Mucciolo, Dario Giorgio, Myrta Lippera, et al.
Plos One|January 6, 2018
EDI OCT evaluation of choroidal thickness in Stargardt diseaseAndrea Sodi, Daniela Bacherini, Chiara Lenzetti, et al.
BMC Ophthalmology|February 26, 2017
Case report of an atypical early onset X-linked retinoschisis in monozygotic twinsVittoria Murro, Roberto Caputo, Giacomo Maria Bacci, et al.
Medicina (Kaunas, Lithuania)|May 25, 2024
Atypic Retinitis Pigmentosa Clinical Features Associated with a Peculiar CRX Gene Mutation in Italian PatientsMarco Piergentili, Vito Spagnuolo, Vittoria Murro, et al.
Ophthalmic Genetics|July 9, 2021
Clinical and molecular findings in patients with pattern dystrophyAndrea Sodi, Dario Pasquale Mucciolo, Dario Giorgio, et al.
Pageof 21