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Felipe Moreno

Showing results (1-10 of 41) with videos related to

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Biochimie|November 9, 2002
The regulation of microcin B, C and J operonsFelipe Moreno, José Eduardo Gónzalez-Pastor, Maria Rosario Baquero, et al.
Acta Ortopedica Mexicana|April 10, 2010
[Conservative surgery as an alternative treatment of a knee osteosarcoma in the presence of a pathological fracture]Alejandro G Pérez Serna, Luis Felipe Moreno Hoyos, Salvador Ramírrez Valdivia
Methodsx|March 10, 2023
A methodology to implement a closed-loop feedback-feedforward level control in a laboratory-scale flotation bank using peristaltic pumpsPaulina Quintanilla, Daniel Navia, Felipe Moreno, et al.
The Annals of Thoracic Surgery|February 21, 2006
Persistent sinus venosus valve mimicking pulmonary stenosis and atrial tumorFelipe Moreno, Carmen Castro, Daniel Borches, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and DFNB4 hearing lossAlejandra Pera, Manuela Villamar, Antonio Viñuela, et al.
Revista Espanola De Cardiologia|September 28, 2005
[Balloon angioplasty for native coarctation in children: immediate and medium-term results]María J del Cerro, Aurora Fernández-Ruiz, Fernando Benito, et al.
Medicina Clinica|July 29, 2003
[Familial susceptibility to aminoglycoside ototoxicity due to the A1555G mutation in the mitochondrial DNA]Jaime Gallo-Terán, Carmelo Morales-Angulo, Ignacio del Castillo, et al.
Revista Espanola De Cardiologia|October 18, 2002
[Transcatheter closure of patent ductus arteriosus using the Amplatzer duct occluder: initial results and mid-term follow-up]Aurora Fernández Ruiz, M Jesús del Cerro Marín, Dolores Rubio Vidal, et al.
International Journal of Pediatric Otorhinolaryngology|March 21, 2012
Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndromeMariem Ben Said, Houria Dhouib, Zeineb BenZina, et al.
American Journal of Human Genetics|May 16, 2007
A mutation in CCDC50, a gene encoding an effector of epidermal growth factor-mediated cell signaling, causes progressive hearing lossSilvia Modamio-Hoybjor, Angeles Mencia, Richard Goodyear, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Biochimie|November 9, 2002
The regulation of microcin B, C and J operonsFelipe Moreno, José Eduardo Gónzalez-Pastor, Maria Rosario Baquero, et al.
Acta Ortopedica Mexicana|April 10, 2010
[Conservative surgery as an alternative treatment of a knee osteosarcoma in the presence of a pathological fracture]Alejandro G Pérez Serna, Luis Felipe Moreno Hoyos, Salvador Ramírrez Valdivia
Methodsx|March 10, 2023
A methodology to implement a closed-loop feedback-feedforward level control in a laboratory-scale flotation bank using peristaltic pumpsPaulina Quintanilla, Daniel Navia, Felipe Moreno, et al.
The Annals of Thoracic Surgery|February 21, 2006
Persistent sinus venosus valve mimicking pulmonary stenosis and atrial tumorFelipe Moreno, Carmen Castro, Daniel Borches, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and DFNB4 hearing lossAlejandra Pera, Manuela Villamar, Antonio Viñuela, et al.
Revista Espanola De Cardiologia|September 28, 2005
[Balloon angioplasty for native coarctation in children: immediate and medium-term results]María J del Cerro, Aurora Fernández-Ruiz, Fernando Benito, et al.
Medicina Clinica|July 29, 2003
[Familial susceptibility to aminoglycoside ototoxicity due to the A1555G mutation in the mitochondrial DNA]Jaime Gallo-Terán, Carmelo Morales-Angulo, Ignacio del Castillo, et al.
Revista Espanola De Cardiologia|October 18, 2002
[Transcatheter closure of patent ductus arteriosus using the Amplatzer duct occluder: initial results and mid-term follow-up]Aurora Fernández Ruiz, M Jesús del Cerro Marín, Dolores Rubio Vidal, et al.
International Journal of Pediatric Otorhinolaryngology|March 21, 2012
Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndromeMariem Ben Said, Houria Dhouib, Zeineb BenZina, et al.
American Journal of Human Genetics|May 16, 2007
A mutation in CCDC50, a gene encoding an effector of epidermal growth factor-mediated cell signaling, causes progressive hearing lossSilvia Modamio-Hoybjor, Angeles Mencia, Richard Goodyear, et al.
Pageof 5