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M Fortuna

Showing results (41-50 of 64) with videos related to

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European Journal of Epidemiology|June 26, 2001
Environmental and serological evidence for the presence of toxocariasis in the urban area of Ancona, ItalyA Giacometti, O Cirioni, M Fortuna, et al.
Biochemistry. Biokhimiia|November 27, 2018
Hydrophobic Derivatives of Glycopeptide Antibiotics as Inhibitors of Protein KinasesG Cozza, M Fortuna, F Meggio, et al.
Phytochemistry|October 4, 2011
Antimicrobial activities of sesquiterpene lactones and inositol derivatives from Hymenoxys robustaAntonio M Fortuna, Zaida N Juárez, Horacio Bach, et al.
European Journal of Medical Genetics|September 21, 2022
Expanding the pre- and postnatal phenotype of WASHC5 and CCDC22 -related Ritscher-Schinzel syndromesSabrina Neri, Nuno Maia, Ana M Fortuna, et al.
Molecular Syndromology|February 20, 2018
Two Novel Pathogenic <i>MID1</i> Variants and Genotype-Phenotype Correlation Reanalysis in X-Linked Opitz G/BBB SyndromeNuno Maia, Maria J Nabais Sá, Nataliya Tkachenko, et al.
Phytotherapy Research : PTR|November 25, 2014
Anti-leishmanial, anti-inflammatory and antimicrobial activities of phenolic derivatives from Tibouchina paratropicaMaría I Tracanna, Antonio M Fortuna, Angel V Contreras Cárdenas, et al.
Behavioral and Brain Functions : BBF|June 7, 2011
FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypesAna I Seixas, José Vale, Paula Jorge, et al.
Frontiers in Medicine|September 28, 2020
Pulmonary Thrombosis or Embolism in a Large Cohort of Hospitalized Patients With Covid-19Natividad Benito, David Filella, Jose Mateo, et al.
Nature Genetics|March 4, 2000
Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type BM Oldridge, A M Fortuna, M Maringa, et al.
Clinical Genetics|December 16, 2010
Clinical and molecular characterization of Diastrophic Dysplasia in the Portuguese populationM Barbosa, A B Sousa, A Medeira, et al.
Pageof 7

Showing results (41-50 of 64) with videos related to

Sort By:
Pageof 7
European Journal of Epidemiology|June 26, 2001
Environmental and serological evidence for the presence of toxocariasis in the urban area of Ancona, ItalyA Giacometti, O Cirioni, M Fortuna, et al.
Biochemistry. Biokhimiia|November 27, 2018
Hydrophobic Derivatives of Glycopeptide Antibiotics as Inhibitors of Protein KinasesG Cozza, M Fortuna, F Meggio, et al.
Phytochemistry|October 4, 2011
Antimicrobial activities of sesquiterpene lactones and inositol derivatives from Hymenoxys robustaAntonio M Fortuna, Zaida N Juárez, Horacio Bach, et al.
European Journal of Medical Genetics|September 21, 2022
Expanding the pre- and postnatal phenotype of WASHC5 and CCDC22 -related Ritscher-Schinzel syndromesSabrina Neri, Nuno Maia, Ana M Fortuna, et al.
Molecular Syndromology|February 20, 2018
Two Novel Pathogenic <i>MID1</i> Variants and Genotype-Phenotype Correlation Reanalysis in X-Linked Opitz G/BBB SyndromeNuno Maia, Maria J Nabais Sá, Nataliya Tkachenko, et al.
Phytotherapy Research : PTR|November 25, 2014
Anti-leishmanial, anti-inflammatory and antimicrobial activities of phenolic derivatives from Tibouchina paratropicaMaría I Tracanna, Antonio M Fortuna, Angel V Contreras Cárdenas, et al.
Behavioral and Brain Functions : BBF|June 7, 2011
FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypesAna I Seixas, José Vale, Paula Jorge, et al.
Frontiers in Medicine|September 28, 2020
Pulmonary Thrombosis or Embolism in a Large Cohort of Hospitalized Patients With Covid-19Natividad Benito, David Filella, Jose Mateo, et al.
Nature Genetics|March 4, 2000
Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type BM Oldridge, A M Fortuna, M Maringa, et al.
Clinical Genetics|December 16, 2010
Clinical and molecular characterization of Diastrophic Dysplasia in the Portuguese populationM Barbosa, A B Sousa, A Medeira, et al.
Pageof 7