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Felipe Moreno

Showing results (11-20 of 41) with videos related to

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Aerospace Medicine and Human Performance|January 20, 2021
Data-Driven Estimation of the Impact of Diversions Due to In-Flight Medical Emergencies on Flight Delay and Aircraft Operating CostsBridget A Lewis, Valerie J Gawron, Ehsan Esmaeilzadeh, et al.
Frontiers in Neural Circuits|October 22, 2021
SynapseJ: An Automated, Synapse Identification Macro for ImageJJuan Felipe Moreno Manrique, Parker R Voit, Kathryn E Windsor, et al.
The New England Journal of Medicine|January 25, 2002
A deletion involving the connexin 30 gene in nonsyndromic hearing impairmentIgnacio del Castillo, Manuela Villamar, Miguel A Moreno-Pelayo, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 20, 2008
Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVAAlejandra Pera, Silvia Dossena, Simona Rodighiero, et al.
Neuromuscular Disorders : NMD|October 28, 2008
A Spanish sporadic case of deafness-dystonia (Mohr-Tranebjaerg) syndrome with a novel mutation in the gene encoding TIMM8a, a component of the mitochondrial protein translocase complexesLuis A Aguirre, Manuel Pérez-Bas, Manuela Villamar, et al.
Medicina Clinica|March 15, 2003
[Non invasive ventilation for acute exacerbation of chronic obstructive pulmonary disease: a meta-analysis]José Fernández Guerra, José Luis López-Campos Bodineau, Emilio Perea-Milla López, et al.
Journal of the Association for Research in Otolaryngology : JARO|May 3, 2008
Characterization of a spontaneous, recessive, missense mutation arising in the Tecta geneMiguel Angel Moreno-Pelayo, Richard J Goodyear, Angeles Mencía, et al.
Human Genetics|December 17, 2002
A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29Silvia Modamio-Høybjør, Miguel Angel Moreno-Pelayo, Angeles Mencía, et al.
American Journal of Medical Genetics. Part A|August 10, 2005
High prevalence of the W24X mutation in the gene encoding connexin-26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive non-syndromic hearing lossAraceli Alvarez, Ignacio del Castillo, Manuela Villamar, et al.
Medicina Clinica|July 11, 2006
[Arterial blood gases study in patients with stable chronic obstructive pulmonary disease in accordance with spirometric values]José Fernández Guerra, José María García Jiménez, Emilio Perea-Milla López, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Aerospace Medicine and Human Performance|January 20, 2021
Data-Driven Estimation of the Impact of Diversions Due to In-Flight Medical Emergencies on Flight Delay and Aircraft Operating CostsBridget A Lewis, Valerie J Gawron, Ehsan Esmaeilzadeh, et al.
Frontiers in Neural Circuits|October 22, 2021
SynapseJ: An Automated, Synapse Identification Macro for ImageJJuan Felipe Moreno Manrique, Parker R Voit, Kathryn E Windsor, et al.
The New England Journal of Medicine|January 25, 2002
A deletion involving the connexin 30 gene in nonsyndromic hearing impairmentIgnacio del Castillo, Manuela Villamar, Miguel A Moreno-Pelayo, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 20, 2008
Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVAAlejandra Pera, Silvia Dossena, Simona Rodighiero, et al.
Neuromuscular Disorders : NMD|October 28, 2008
A Spanish sporadic case of deafness-dystonia (Mohr-Tranebjaerg) syndrome with a novel mutation in the gene encoding TIMM8a, a component of the mitochondrial protein translocase complexesLuis A Aguirre, Manuel Pérez-Bas, Manuela Villamar, et al.
Medicina Clinica|March 15, 2003
[Non invasive ventilation for acute exacerbation of chronic obstructive pulmonary disease: a meta-analysis]José Fernández Guerra, José Luis López-Campos Bodineau, Emilio Perea-Milla López, et al.
Journal of the Association for Research in Otolaryngology : JARO|May 3, 2008
Characterization of a spontaneous, recessive, missense mutation arising in the Tecta geneMiguel Angel Moreno-Pelayo, Richard J Goodyear, Angeles Mencía, et al.
Human Genetics|December 17, 2002
A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29Silvia Modamio-Høybjør, Miguel Angel Moreno-Pelayo, Angeles Mencía, et al.
American Journal of Medical Genetics. Part A|August 10, 2005
High prevalence of the W24X mutation in the gene encoding connexin-26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive non-syndromic hearing lossAraceli Alvarez, Ignacio del Castillo, Manuela Villamar, et al.
Medicina Clinica|July 11, 2006
[Arterial blood gases study in patients with stable chronic obstructive pulmonary disease in accordance with spirometric values]José Fernández Guerra, José María García Jiménez, Emilio Perea-Milla López, et al.
Pageof 5