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Showing results (181-190 of 235) with videos related to

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The European Respiratory Journal|November 16, 2023
Inhaled recombinant GM-CSF reduces the need for whole lung lavage and improves gas exchange in autoimmune pulmonary alveolar proteinosis patientsIlaria Campo, Brenna C Carey, Elena Paracchini, et al.
Conflict and Health|December 7, 2025
Setting research priorities for sexual and reproductive health in humanitarian settings: a global, stakeholder-informed agendaSara L Nam, Arantza Abril, Gillian McKay, et al.
Archives of Gynecology and Obstetrics|April 7, 2019
Comparison of two "a priori" risk assessment algorithms for preeclampsia in Italy: a prospective multicenter studyDaniela Di Martino, Bianca Masturzo, Sara Paracchini, et al.
Journal of Neurodevelopmental Disorders|June 17, 2016
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypesKerry A Pettigrew, Emily Frinton, Ron Nudel, et al.
International Journal of Cancer|June 12, 2014
Antiangiogenic activity of trabectedin in myxoid liposarcoma: involvement of host TIMP-1 and TIMP-2 and tumor thrombospondin-1Romina Dossi, Roberta Frapolli, Silvana Di Giandomenico, et al.
Genes, Brain, and Behavior|February 28, 2014
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairmentR Nudel, N H Simpson, G Baird, et al.
Molecular Psychiatry|October 13, 2006
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexiaD Harold, S Paracchini, T Scerri, et al.
Neurobiology of Disease|December 13, 2016
Blockade of the IL-1R1/TLR4 pathway mediates disease-modification therapeutic effects in a model of acquired epilepsyValentina Iori, Anand M Iyer, Teresa Ravizza, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 18, 2019
A novel mutation in <i>SPART</i> gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolismChiara Diquigiovanni, Christian Bergamini, Rebeca Diaz, et al.
European Journal of Pediatrics|October 27, 2015
Epidemiology of haemolytic uremic syndrome in children. Data from the North Italian HUS networkGianluigi Ardissino, Stefania Salardi, Elisa Colombo, et al.
Pageof 24

Showing results (181-190 of 235) with videos related to

Sort By:
Pageof 24
The European Respiratory Journal|November 16, 2023
Inhaled recombinant GM-CSF reduces the need for whole lung lavage and improves gas exchange in autoimmune pulmonary alveolar proteinosis patientsIlaria Campo, Brenna C Carey, Elena Paracchini, et al.
Conflict and Health|December 7, 2025
Setting research priorities for sexual and reproductive health in humanitarian settings: a global, stakeholder-informed agendaSara L Nam, Arantza Abril, Gillian McKay, et al.
Archives of Gynecology and Obstetrics|April 7, 2019
Comparison of two "a priori" risk assessment algorithms for preeclampsia in Italy: a prospective multicenter studyDaniela Di Martino, Bianca Masturzo, Sara Paracchini, et al.
Journal of Neurodevelopmental Disorders|June 17, 2016
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypesKerry A Pettigrew, Emily Frinton, Ron Nudel, et al.
International Journal of Cancer|June 12, 2014
Antiangiogenic activity of trabectedin in myxoid liposarcoma: involvement of host TIMP-1 and TIMP-2 and tumor thrombospondin-1Romina Dossi, Roberta Frapolli, Silvana Di Giandomenico, et al.
Genes, Brain, and Behavior|February 28, 2014
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairmentR Nudel, N H Simpson, G Baird, et al.
Molecular Psychiatry|October 13, 2006
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexiaD Harold, S Paracchini, T Scerri, et al.
Neurobiology of Disease|December 13, 2016
Blockade of the IL-1R1/TLR4 pathway mediates disease-modification therapeutic effects in a model of acquired epilepsyValentina Iori, Anand M Iyer, Teresa Ravizza, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 18, 2019
A novel mutation in <i>SPART</i> gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolismChiara Diquigiovanni, Christian Bergamini, Rebeca Diaz, et al.
European Journal of Pediatrics|October 27, 2015
Epidemiology of haemolytic uremic syndrome in children. Data from the North Italian HUS networkGianluigi Ardissino, Stefania Salardi, Elisa Colombo, et al.
Pageof 24