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Ugo Cavallari

Showing results (1-10 of 34) with videos related to

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Prenatal Diagnosis|July 4, 2012
Array CGH in routine prenatal diagnosis practicePietro Cavalli, Ugo Cavallari, Antonio Novelli
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 22, 2011
Caffeine intake and risk of neural tube defectsPietro Cavalli, Ugo Cavallari, Vittorio Unfer, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 9, 2019
Identification of a novel NOTCH3 mutation in an Italian family affected by a mild form of CADASILEnrico Ferrante, Lorena Mosca, Cristina Erminio, et al.
Clinical Dysmorphology|September 8, 2006
Acro-dermato-ungual-lacrimal-tooth-like syndrome: report of a family with variable expressionMaria Francesca Bedeschi, Fabienne Escande, Melissa Bellini, et al.
American Journal of Medical Genetics. Part A|September 13, 2016
Marfan syndrome: Report of a complex phenotype due to a 15q21.1 contiguos gene deletion encompassing FBN1, and literature reviewChiara Dordoni, Claudia Ciaccio, Graziano Santoro, et al.
Cytogenetic and Genome Research|February 5, 2020
Unbalanced X;Autosome Translocations May Lead to Mild Phenotypes and Are Associated with Autoimmune DiseasesClaudia Ciaccio, Serena Redaelli, Angela Bentivegna, et al.
Epigenomics|August 9, 2018
Mitochondrial DNA copy number and D-loop region methylation in carriers of amyotrophic lateral sclerosis gene mutationsAndrea Stoccoro, Lorena Mosca, Vittoria Carnicelli, et al.
Clinical Biochemistry|September 17, 2013
New T530C mutation in the aspartoacylase gene caused Canavan disease with no correlation between severity and N-acetylaspartate excretionValentina Di Pietro, Ugo Cavallari, Angela M Amorini, et al.
European Journal of Human Genetics : EJHG|October 28, 2005
On the association of the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction or coronary artery diseaseElisabetta Trabetti, Michele Biscuola, Ugo Cavallari, et al.
American Journal of Medical Genetics. Part A|February 13, 2008
Germline mosaicism in achondroplasia detected in sperm DNA of the father of three affected sibsFederica Natacci, Maria Baffico, Ugo Cavallari, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Prenatal Diagnosis|July 4, 2012
Array CGH in routine prenatal diagnosis practicePietro Cavalli, Ugo Cavallari, Antonio Novelli
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 22, 2011
Caffeine intake and risk of neural tube defectsPietro Cavalli, Ugo Cavallari, Vittorio Unfer, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 9, 2019
Identification of a novel NOTCH3 mutation in an Italian family affected by a mild form of CADASILEnrico Ferrante, Lorena Mosca, Cristina Erminio, et al.
Clinical Dysmorphology|September 8, 2006
Acro-dermato-ungual-lacrimal-tooth-like syndrome: report of a family with variable expressionMaria Francesca Bedeschi, Fabienne Escande, Melissa Bellini, et al.
American Journal of Medical Genetics. Part A|September 13, 2016
Marfan syndrome: Report of a complex phenotype due to a 15q21.1 contiguos gene deletion encompassing FBN1, and literature reviewChiara Dordoni, Claudia Ciaccio, Graziano Santoro, et al.
Cytogenetic and Genome Research|February 5, 2020
Unbalanced X;Autosome Translocations May Lead to Mild Phenotypes and Are Associated with Autoimmune DiseasesClaudia Ciaccio, Serena Redaelli, Angela Bentivegna, et al.
Epigenomics|August 9, 2018
Mitochondrial DNA copy number and D-loop region methylation in carriers of amyotrophic lateral sclerosis gene mutationsAndrea Stoccoro, Lorena Mosca, Vittoria Carnicelli, et al.
Clinical Biochemistry|September 17, 2013
New T530C mutation in the aspartoacylase gene caused Canavan disease with no correlation between severity and N-acetylaspartate excretionValentina Di Pietro, Ugo Cavallari, Angela M Amorini, et al.
European Journal of Human Genetics : EJHG|October 28, 2005
On the association of the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction or coronary artery diseaseElisabetta Trabetti, Michele Biscuola, Ugo Cavallari, et al.
American Journal of Medical Genetics. Part A|February 13, 2008
Germline mosaicism in achondroplasia detected in sperm DNA of the father of three affected sibsFederica Natacci, Maria Baffico, Ugo Cavallari, et al.
Pageof 4