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Roberto Colombo

Showing results (191-200 of 201) with videos related to

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Remote Sensing of Environment|January 8, 2021
Remote sensing of solar-induced chlorophyll fluorescence (SIF) in vegetation: 50 years of progressGina H Mohammed, Roberto Colombo, Elizabeth M Middleton, et al.
Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica|January 19, 2019
Multidisciplinary approach to prostatitisVittorio Magri, Matteo Boltri, Tommaso Cai, et al.
Alimentary Pharmacology & Therapeutics|May 21, 2003
An inter- and intra-laboratory comparison of breath ¹³CO₂analysisF Perri, R M Zagari, J S Uebersax, et al.
Frontiers in Urology|August 8, 2025
Recommendations and optimal approaches to robotic-assisted partial nephrectomy: A consensus of Brazilian expertsEliney Ferreira Faria, Marcio Covas Moschovas, Carlos Vaz, et al.
Journal of Medical Genetics|August 22, 2020
De novo missense variants in <i>LMBRD2</i> are associated with developmental and motor delays, brain structure abnormalities and dysmorphic featuresAlka Malhotra, Alban Ziegler, Li Shu, et al.
The Journal of Clinical Endocrinology and Metabolism|May 2, 2019
Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of DiseaseAngad Jolly, Yavuz Bayram, Serap Turan, et al.
Human Mutation|June 18, 2019
Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenitaSuzanna G M Frints, Friederike Hennig, Roberto Colombo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 30, 2019
De novo and biallelic DEAF1 variants cause a phenotypic spectrumMaria J Nabais Sá, Philip J Jensik, Stacey R McGee, et al.
Annals of Neurology|December 6, 2017
Progressive deafness-dystonia due to SERAC1 mutations: A study of 67 casesRoeltje R Maas, Katarzyna Iwanicka-Pronicka, Sema Kalkan Ucar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2020
Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7Laura Castilla-Vallmanya, Kaja K Selmer, Clémantine Dimartino, et al.
Pageof 21

Showing results (191-200 of 201) with videos related to

Sort By:
Pageof 21
Remote Sensing of Environment|January 8, 2021
Remote sensing of solar-induced chlorophyll fluorescence (SIF) in vegetation: 50 years of progressGina H Mohammed, Roberto Colombo, Elizabeth M Middleton, et al.
Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica|January 19, 2019
Multidisciplinary approach to prostatitisVittorio Magri, Matteo Boltri, Tommaso Cai, et al.
Alimentary Pharmacology & Therapeutics|May 21, 2003
An inter- and intra-laboratory comparison of breath ¹³CO₂analysisF Perri, R M Zagari, J S Uebersax, et al.
Frontiers in Urology|August 8, 2025
Recommendations and optimal approaches to robotic-assisted partial nephrectomy: A consensus of Brazilian expertsEliney Ferreira Faria, Marcio Covas Moschovas, Carlos Vaz, et al.
Journal of Medical Genetics|August 22, 2020
De novo missense variants in <i>LMBRD2</i> are associated with developmental and motor delays, brain structure abnormalities and dysmorphic featuresAlka Malhotra, Alban Ziegler, Li Shu, et al.
The Journal of Clinical Endocrinology and Metabolism|May 2, 2019
Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of DiseaseAngad Jolly, Yavuz Bayram, Serap Turan, et al.
Human Mutation|June 18, 2019
Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenitaSuzanna G M Frints, Friederike Hennig, Roberto Colombo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 30, 2019
De novo and biallelic DEAF1 variants cause a phenotypic spectrumMaria J Nabais Sá, Philip J Jensik, Stacey R McGee, et al.
Annals of Neurology|December 6, 2017
Progressive deafness-dystonia due to SERAC1 mutations: A study of 67 casesRoeltje R Maas, Katarzyna Iwanicka-Pronicka, Sema Kalkan Ucar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2020
Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7Laura Castilla-Vallmanya, Kaja K Selmer, Clémantine Dimartino, et al.
Pageof 21