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Giovanni Neri

Showing results (191-200 of 273) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|July 10, 2012
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutationAmelia Conte, Serena Lattante, Marco Luigetti, et al.
American Journal of Medical Genetics. Part A|September 15, 2005
Clinical and molecular studies on two further families with Simpson-Golabi-Behmel syndromeGermán Rodríguez-Criado, Luis Magano, Mabel Segovia, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 25, 2026
Review of emerging imaging findings to reveal a broader spectrum of lesions in AMDEnrico Borrelli, Giovanni Neri, Alessandro Berni, et al.
Journal of Neurology|December 25, 2012
Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansionsMassimo Santoro, Marcella Masciullo, Roberta Pietrobono, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 20, 2016
Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defectsFrancesca La Carpia, Claudia Rendeli, Clelia Molinario, et al.
Nanomaterials (Basel, Switzerland)|August 7, 2021
Ultrathin Silicon Nanowires for Optical and Electrical Nitrogen Dioxide DetectionDario Morganti, Antonio Alessio Leonardi, Maria José Lo Faro, et al.
European Journal of Human Genetics : EJHG|July 9, 2004
A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndromeMarcella Zollino, Rosetta Lecce, Angelo Selicorni, et al.
Medicina (Kaunas, Lithuania)|June 27, 2024
Deep Learning in Neovascular Age-Related Macular DegenerationEnrico Borrelli, Sonia Serafino, Federico Ricardi, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 11, 2003
Immunoscintigraphic detection of the ED-B domain of fibronectin, a marker of angiogenesis, in patients with cancerMonica Santimaria, Giovanni Moscatelli, Giuseppe L Viale, et al.
European Journal of Human Genetics : EJHG|March 21, 2013
Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11pFiorella Gurrieri, Marcella Zollino, Antonio Oliva, et al.
Pageof 28

Showing results (191-200 of 273) with videos related to

Sort By:
Pageof 28
Journal of Neurology, Neurosurgery, and Psychiatry|July 10, 2012
Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutationAmelia Conte, Serena Lattante, Marco Luigetti, et al.
American Journal of Medical Genetics. Part A|September 15, 2005
Clinical and molecular studies on two further families with Simpson-Golabi-Behmel syndromeGermán Rodríguez-Criado, Luis Magano, Mabel Segovia, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 25, 2026
Review of emerging imaging findings to reveal a broader spectrum of lesions in AMDEnrico Borrelli, Giovanni Neri, Alessandro Berni, et al.
Journal of Neurology|December 25, 2012
Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansionsMassimo Santoro, Marcella Masciullo, Roberta Pietrobono, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 20, 2016
Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defectsFrancesca La Carpia, Claudia Rendeli, Clelia Molinario, et al.
Nanomaterials (Basel, Switzerland)|August 7, 2021
Ultrathin Silicon Nanowires for Optical and Electrical Nitrogen Dioxide DetectionDario Morganti, Antonio Alessio Leonardi, Maria José Lo Faro, et al.
European Journal of Human Genetics : EJHG|July 9, 2004
A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndromeMarcella Zollino, Rosetta Lecce, Angelo Selicorni, et al.
Medicina (Kaunas, Lithuania)|June 27, 2024
Deep Learning in Neovascular Age-Related Macular DegenerationEnrico Borrelli, Sonia Serafino, Federico Ricardi, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 11, 2003
Immunoscintigraphic detection of the ED-B domain of fibronectin, a marker of angiogenesis, in patients with cancerMonica Santimaria, Giovanni Moscatelli, Giuseppe L Viale, et al.
European Journal of Human Genetics : EJHG|March 21, 2013
Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11pFiorella Gurrieri, Marcella Zollino, Antonio Oliva, et al.
Pageof 28