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Ana Camacho

Showing results (71-80 of 99) with videos related to

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Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|February 14, 2012
Implementation of a pre-hospital network favoring primary angioplasty in STEMI to reduce mortality: the Algarve ProjectVeloso Gomes, Victor Brandão, Jorge Mimoso, et al.
Revista De Neurologia|November 23, 2013
[Aicardi syndrome: retrospective study of a series of seven case reports]Joaquín Alejandro Fernández-Ramos, Eduardo López-Laso, Rogelio Simón-De Las Heras, et al.
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|December 25, 2010
Female gender: an independent factor in ST-elevation myocardial infarctionJoana Trigo, Jorge Mimoso, Paula Gago, et al.
Journal of Clinical Lipidology|February 22, 2023
Role of lipoprotein lipase activity measurement in the diagnosis of familial chylomicronemia syndromeJosé Rioja, María José Ariza, María José Benítez-Toledo, et al.
Science Signaling|October 28, 2025
Loss of the conserved switch III region in a G protein leads to severe pediatric encephalopathyMikhail Savitsky, Yonika A Larasati, Gonzalo P Solis, et al.
Biomed Research International|October 4, 2013
What is the role of apelin regarding cardiovascular risk and progression of renal disease in type 2 diabetic patients with diabetic nephropathy?Ana Paula Silva, André Fragoso, Claudia Silva, et al.
Journal of Human Genetics|February 15, 2024
Expanding the genetic and phenotypic spectrum of congenital myasthenic syndrome: new homozygous VAMP1 splicing variants in 2 novel individualsFrancisco Javier Cotrina-Vinagre, María Elena Rodríguez-García, Lucía Del Pozo-Filíu, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|November 11, 2021
Impact of COVID-19 in Immunosuppressed Children With Neuroimmunologic DisordersGemma Olivé-Cirera, Elianet Fonseca, Verónica Cantarín-Extremera, et al.
Neurogenetics|September 30, 2016
New ATP8A2 gene mutations associated with a novel syndrome: encephalopathy, intellectual disability, severe hypotonia, chorea and optic atrophyElena Martín-Hernández, María Elena Rodríguez-García, Ana Camacho, et al.
Journal of Clinical Lipidology|August 29, 2018
Molecular basis of the familial chylomicronemia syndrome in patients from the National Dyslipidemia Registry of the Spanish Atherosclerosis SocietyMaría José Ariza, José Rioja, Daiana Ibarretxe, et al.
Pageof 10

Showing results (71-80 of 99) with videos related to

Sort By:
Pageof 10
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|February 14, 2012
Implementation of a pre-hospital network favoring primary angioplasty in STEMI to reduce mortality: the Algarve ProjectVeloso Gomes, Victor Brandão, Jorge Mimoso, et al.
Revista De Neurologia|November 23, 2013
[Aicardi syndrome: retrospective study of a series of seven case reports]Joaquín Alejandro Fernández-Ramos, Eduardo López-Laso, Rogelio Simón-De Las Heras, et al.
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|December 25, 2010
Female gender: an independent factor in ST-elevation myocardial infarctionJoana Trigo, Jorge Mimoso, Paula Gago, et al.
Journal of Clinical Lipidology|February 22, 2023
Role of lipoprotein lipase activity measurement in the diagnosis of familial chylomicronemia syndromeJosé Rioja, María José Ariza, María José Benítez-Toledo, et al.
Science Signaling|October 28, 2025
Loss of the conserved switch III region in a G protein leads to severe pediatric encephalopathyMikhail Savitsky, Yonika A Larasati, Gonzalo P Solis, et al.
Biomed Research International|October 4, 2013
What is the role of apelin regarding cardiovascular risk and progression of renal disease in type 2 diabetic patients with diabetic nephropathy?Ana Paula Silva, André Fragoso, Claudia Silva, et al.
Journal of Human Genetics|February 15, 2024
Expanding the genetic and phenotypic spectrum of congenital myasthenic syndrome: new homozygous VAMP1 splicing variants in 2 novel individualsFrancisco Javier Cotrina-Vinagre, María Elena Rodríguez-García, Lucía Del Pozo-Filíu, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|November 11, 2021
Impact of COVID-19 in Immunosuppressed Children With Neuroimmunologic DisordersGemma Olivé-Cirera, Elianet Fonseca, Verónica Cantarín-Extremera, et al.
Neurogenetics|September 30, 2016
New ATP8A2 gene mutations associated with a novel syndrome: encephalopathy, intellectual disability, severe hypotonia, chorea and optic atrophyElena Martín-Hernández, María Elena Rodríguez-García, Ana Camacho, et al.
Journal of Clinical Lipidology|August 29, 2018
Molecular basis of the familial chylomicronemia syndrome in patients from the National Dyslipidemia Registry of the Spanish Atherosclerosis SocietyMaría José Ariza, José Rioja, Daiana Ibarretxe, et al.
Pageof 10