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Massimo Carella

Showing results (51-60 of 207) with videos related to

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Blood Cells, Molecules & Diseases|April 2, 2003
Congenital dyserythropoietic anemia type II: exclusion of seven candidate genesCarmela Lanzara, Romina Ficarella, Angela Totaro, et al.
European Journal of Medical Genetics|December 29, 2011
Thrombocytopenia-absent-radius syndrome in a child showing a larger 1q21.1 deletion than the one in his healthy mother, and a significant downregulation of the commonly deleted genesMaria Corsignano Guastadisegni, Roberta Roberto, Alberto L'Abbate, et al.
Genes|April 5, 2020
Compound Phenotype Due to Recessive Variants in <i>LARP7</i> and <i>OTOG</i> Genes Disclosed by an Integrated Approach of SNP-Array and Whole Exome SequencingPietro Palumbo, Orazio Palumbo, Maria Pia Leone, et al.
European Journal of Medical Genetics|December 24, 2017
Refinement of the critical 7p22.1 deletion region: Haploinsufficiency of ACTB is the cause of the 7p22.1 microdeletion-related developmental disordersOrazio Palumbo, Maria Accadia, Pietro Palumbo, et al.
American Journal of Medical Genetics. Part A|September 4, 2015
Paternal uniparental disomy chromosome 14-like syndrome due a maternal de novo 160 kb deletion at the 14q32.2 region not encompassing the IG- and the MEG3-DMRs: Patient report and genotype-phenotype correlationGiovanni Corsello, Emanuela Salzano, Davide Vecchio, et al.
Human Genetics|January 11, 2003
Genetic heterogeneity of FG syndrome: a fourth locus (FGS4) maps to Xp11.4-p11.3 in an Italian familyGiulio Piluso, Massimo Carella, Michele D'Avanzo, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|May 17, 2005
Audiometric evaluation of carriers of the connexin 26 mutation 35delGAnnamaria Franzé, Antonella Caravelli, Francesca Di Leva, et al.
FEMS Microbiology Ecology|March 4, 2014
Rhodobacter sphaeroides adaptation to high concentrations of cobalt ions requires energetic metabolism changesMariateresa Volpicella, Alessandra Costanza, Orazio Palumbo, et al.
Frontiers in Pharmacology|July 25, 2025
Adverse effects of antiseizure medications: a review of the impact of pharmacogenetics and drugs interactions in clinical practiceMichela De Bellis, Giuseppe d'Orsi, Egidio Maria Rubino, et al.
BMC Genomics|August 25, 2009
Mitochondrial dysregulation and oxidative stress in patients with chronic kidney diseaseSimona Granata, Gianluigi Zaza, Simona Simone, et al.
Pageof 21

Showing results (51-60 of 207) with videos related to

Sort By:
Pageof 21
Blood Cells, Molecules & Diseases|April 2, 2003
Congenital dyserythropoietic anemia type II: exclusion of seven candidate genesCarmela Lanzara, Romina Ficarella, Angela Totaro, et al.
European Journal of Medical Genetics|December 29, 2011
Thrombocytopenia-absent-radius syndrome in a child showing a larger 1q21.1 deletion than the one in his healthy mother, and a significant downregulation of the commonly deleted genesMaria Corsignano Guastadisegni, Roberta Roberto, Alberto L'Abbate, et al.
Genes|April 5, 2020
Compound Phenotype Due to Recessive Variants in <i>LARP7</i> and <i>OTOG</i> Genes Disclosed by an Integrated Approach of SNP-Array and Whole Exome SequencingPietro Palumbo, Orazio Palumbo, Maria Pia Leone, et al.
European Journal of Medical Genetics|December 24, 2017
Refinement of the critical 7p22.1 deletion region: Haploinsufficiency of ACTB is the cause of the 7p22.1 microdeletion-related developmental disordersOrazio Palumbo, Maria Accadia, Pietro Palumbo, et al.
American Journal of Medical Genetics. Part A|September 4, 2015
Paternal uniparental disomy chromosome 14-like syndrome due a maternal de novo 160 kb deletion at the 14q32.2 region not encompassing the IG- and the MEG3-DMRs: Patient report and genotype-phenotype correlationGiovanni Corsello, Emanuela Salzano, Davide Vecchio, et al.
Human Genetics|January 11, 2003
Genetic heterogeneity of FG syndrome: a fourth locus (FGS4) maps to Xp11.4-p11.3 in an Italian familyGiulio Piluso, Massimo Carella, Michele D'Avanzo, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|May 17, 2005
Audiometric evaluation of carriers of the connexin 26 mutation 35delGAnnamaria Franzé, Antonella Caravelli, Francesca Di Leva, et al.
FEMS Microbiology Ecology|March 4, 2014
Rhodobacter sphaeroides adaptation to high concentrations of cobalt ions requires energetic metabolism changesMariateresa Volpicella, Alessandra Costanza, Orazio Palumbo, et al.
Frontiers in Pharmacology|July 25, 2025
Adverse effects of antiseizure medications: a review of the impact of pharmacogenetics and drugs interactions in clinical practiceMichela De Bellis, Giuseppe d'Orsi, Egidio Maria Rubino, et al.
BMC Genomics|August 25, 2009
Mitochondrial dysregulation and oxidative stress in patients with chronic kidney diseaseSimona Granata, Gianluigi Zaza, Simona Simone, et al.
Pageof 21