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Chiara Baroni

Showing results (11-20 of 21) with videos related to

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Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|January 2, 2022
Increased intracranial arterial tortuosity is associated with worse cardiovascular outcome in patients with Loeys-Dietz syndromeGianfranco Vornetti, Luca Spinardi, Elisabetta Mariucci, et al.
RSC Medicinal Chemistry|February 12, 2025
X-ray crystallographic and kinetic studies of biguanide containing aryl sulfonamides as carbonic anhydrase inhibitorsChiara Baroni, Murat Bozdag, Gioele Renzi, et al.
ACS Medicinal Chemistry Letters|October 16, 2024
Lasamide, a Potent Human Carbonic Anhydrase Inhibitor from the Market: Inhibition Profiling and Crystallographic StudiesChiara Baroni, Ilaria D'Agostino, Gioele Renzi, et al.
European Stroke Journal|May 26, 2023
Prevalence of unruptured intracranial aneurysms in patients with Marfan syndrome: A cross-sectional study and meta-analysisGianfranco Vornetti, Sara Rosa Maria De Martino, Maria Chiara Baroni, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|April 14, 2024
Quantitative measurement of dural ectasia: associations with clinical and genetic characteristics in Marfan syndromeGianfranco Vornetti, Giulio Vara, Maria Chiara Baroni, et al.
Genes|September 28, 2023
Diprosopus: A Rare Case of Craniofacial Duplication and a Systematic Review of the LiteratureViola Trevisani, Eleonora Balestri, Manuela Napoli, et al.
Clinical Genetics|July 30, 2020
Whole-exome sequencing in adult patients with developmental and epileptic encephalopathy: It is never too lateRaffaella Minardi, Laura Licchetta, Maria Chiara Baroni, et al.
Genes|August 26, 2023
Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the <i>DLX5/6</i> GenesIrene Ambrosetti, Laura Bernardini, Marzia Pollazzon, et al.
European Journal of Medicinal Chemistry|April 3, 2025
O-derivatization of natural tropolone and β-thujaplicin leading to effective inhibitors of human carbonic anhydrases IX and XIIFrancesco Melfi, Ilaria D'Agostino, Simone Carradori, et al.
European Journal of Human Genetics : EJHG|February 26, 2025
Expanding the mutational spectrum of ReNU syndrome: insights into 5' Stem-loop variantsAlessandro Bruselles, Cecilia Mancini, Luigi Chiriatti, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|January 2, 2022
Increased intracranial arterial tortuosity is associated with worse cardiovascular outcome in patients with Loeys-Dietz syndromeGianfranco Vornetti, Luca Spinardi, Elisabetta Mariucci, et al.
RSC Medicinal Chemistry|February 12, 2025
X-ray crystallographic and kinetic studies of biguanide containing aryl sulfonamides as carbonic anhydrase inhibitorsChiara Baroni, Murat Bozdag, Gioele Renzi, et al.
ACS Medicinal Chemistry Letters|October 16, 2024
Lasamide, a Potent Human Carbonic Anhydrase Inhibitor from the Market: Inhibition Profiling and Crystallographic StudiesChiara Baroni, Ilaria D'Agostino, Gioele Renzi, et al.
European Stroke Journal|May 26, 2023
Prevalence of unruptured intracranial aneurysms in patients with Marfan syndrome: A cross-sectional study and meta-analysisGianfranco Vornetti, Sara Rosa Maria De Martino, Maria Chiara Baroni, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|April 14, 2024
Quantitative measurement of dural ectasia: associations with clinical and genetic characteristics in Marfan syndromeGianfranco Vornetti, Giulio Vara, Maria Chiara Baroni, et al.
Genes|September 28, 2023
Diprosopus: A Rare Case of Craniofacial Duplication and a Systematic Review of the LiteratureViola Trevisani, Eleonora Balestri, Manuela Napoli, et al.
Clinical Genetics|July 30, 2020
Whole-exome sequencing in adult patients with developmental and epileptic encephalopathy: It is never too lateRaffaella Minardi, Laura Licchetta, Maria Chiara Baroni, et al.
Genes|August 26, 2023
Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the <i>DLX5/6</i> GenesIrene Ambrosetti, Laura Bernardini, Marzia Pollazzon, et al.
European Journal of Medicinal Chemistry|April 3, 2025
O-derivatization of natural tropolone and β-thujaplicin leading to effective inhibitors of human carbonic anhydrases IX and XIIFrancesco Melfi, Ilaria D'Agostino, Simone Carradori, et al.
European Journal of Human Genetics : EJHG|February 26, 2025
Expanding the mutational spectrum of ReNU syndrome: insights into 5' Stem-loop variantsAlessandro Bruselles, Cecilia Mancini, Luigi Chiriatti, et al.
Pageof 3