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Lorenzo Monserrat

Showing results (71-80 of 160) with videos related to

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Plos One|November 1, 2018
Next-Generation Sequencing and Quantitative Proteomics of Hutchinson-Gilford progeria syndrome-derived cells point to a role of nucleotide metabolism in premature agingJesús Mateos, Juan Fafián-Labora, Miriam Morente-López, et al.
NPJ Genomic Medicine|March 5, 2021
A cryptic splice-altering KCNQ1 variant in trans with R259L leading to Jervell and Lange-Nielsen syndromeMario Torrado, Germán Fernández, Christian A Ganoza, et al.
The American Journal of Cardiology|June 29, 2004
Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutationsManuel Hermida-Prieto, Lorenzo Monserrat, Alfonso Castro-Beiras, et al.
Heart Rhythm|August 17, 2010
Novel missense mutations in exon 15 of desmoglein-2: role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy?Katja Gehmlich, Angeliki Asimaki, Thomas J Cahill, et al.
Revista Espanola De Cardiologia|November 28, 2006
[Beta-myosin heavy-chain gene mutations in patients with hypertrophic cardiomyopathy]Rafael Laredo, Lorenzo Monserrat, Manuel Hermida-Prieto, et al.
Journal of Cardiology|December 20, 2020
Value of a comprehensive exercise echocardiography assessment for patients with hypertrophic cardiomyopathyJesus Peteiro, Roberto Barriales-Villa, José M Larrañaga-Moreira, et al.
The Canadian Journal of Cardiology|July 26, 2020
A Pathogenic Galactosidase A Mutation Coexisting With an MYBPC3 Mutation in a Female Patient With Hypertrophic CardiomyopathyGiovanni Vitale, Ferdinando Pasquale, Ornella Leone, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophicMaría Isabel Rodriguez-Garcia, Lorenzo Monserrat, Martín Ortiz, et al.
BMC Medical Genetics|May 4, 2010
Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic CardiomyopathyMaría Isabel Rodríguez-García, Lorenzo Monserrat, Martín Ortiz, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophicMaría Isabel Rodriguez-Garcia, Lorenzo Monserrat, Martín Ortiz, et al.
Pageof 16

Showing results (71-80 of 160) with videos related to

Sort By:
Pageof 16
Plos One|November 1, 2018
Next-Generation Sequencing and Quantitative Proteomics of Hutchinson-Gilford progeria syndrome-derived cells point to a role of nucleotide metabolism in premature agingJesús Mateos, Juan Fafián-Labora, Miriam Morente-López, et al.
NPJ Genomic Medicine|March 5, 2021
A cryptic splice-altering KCNQ1 variant in trans with R259L leading to Jervell and Lange-Nielsen syndromeMario Torrado, Germán Fernández, Christian A Ganoza, et al.
The American Journal of Cardiology|June 29, 2004
Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutationsManuel Hermida-Prieto, Lorenzo Monserrat, Alfonso Castro-Beiras, et al.
Heart Rhythm|August 17, 2010
Novel missense mutations in exon 15 of desmoglein-2: role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy?Katja Gehmlich, Angeliki Asimaki, Thomas J Cahill, et al.
Revista Espanola De Cardiologia|November 28, 2006
[Beta-myosin heavy-chain gene mutations in patients with hypertrophic cardiomyopathy]Rafael Laredo, Lorenzo Monserrat, Manuel Hermida-Prieto, et al.
Journal of Cardiology|December 20, 2020
Value of a comprehensive exercise echocardiography assessment for patients with hypertrophic cardiomyopathyJesus Peteiro, Roberto Barriales-Villa, José M Larrañaga-Moreira, et al.
The Canadian Journal of Cardiology|July 26, 2020
A Pathogenic Galactosidase A Mutation Coexisting With an MYBPC3 Mutation in a Female Patient With Hypertrophic CardiomyopathyGiovanni Vitale, Ferdinando Pasquale, Ornella Leone, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophicMaría Isabel Rodriguez-Garcia, Lorenzo Monserrat, Martín Ortiz, et al.
BMC Medical Genetics|May 4, 2010
Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic CardiomyopathyMaría Isabel Rodríguez-García, Lorenzo Monserrat, Martín Ortiz, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophicMaría Isabel Rodriguez-Garcia, Lorenzo Monserrat, Martín Ortiz, et al.
Pageof 16