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M J Trujillo

Showing results (11-20 of 128) with videos related to

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Human Genetics|March 30, 2004
Gene symbol: CFTR. Disease: Cystic fibrosisM J Trujillo-Tiebas, J Gallego, M García, et al.
Revista Espanola De Anestesiologia Y Reanimacion|November 13, 2007
[Epidural anesthesia for coronary revascularization in the conscious patient]A Ysasi, R Llorens, E Calderón, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: OA1. Disease: albinism, ocularMonica Martinez-Garcia, M J Trujillo-Tiebas, C Villaverde, et al.
Human Genetics|February 14, 2007
Gene symbol: ABCA4. Disease: Stargardt disease 1. Accession #Hm0537R Riveiro-Alvarez, M J Trujillo, D Cantalapiedra, et al.
Human Genetics|November 28, 2006
Gene symbol: ABCA4. Disease: Stargardt disease 1R Riveiro-Alvarez, M J Trujillo, D Cantalapiedra, et al.
Human Genetics|February 14, 2007
Gene symbol: ABCA4. Disease: Stargardt disease 1. Accession #Hs0512R Riveiro-Alvarez, M J Trujillo, D Cantalapiedra, et al.
Journal of Investigational Allergology & Clinical Immunology|October 24, 2018
Deflazacort-Induced Erythema Multiforme Exudativum Successfully Treated With a Single Dose of EtanerceptM J Trujillo-Trujillo, E González-Mancebo, M Gandolfo-Cano, et al.
Ophthalmic Genetics|September 1, 1996
G106R rhodopsin mutation is also present in Spanish ADRP patientsC Ayuso, C Reig, B Garcia-Sandoval, et al.
Human Mutation|January 8, 2000
Three novel RDS-peripherin mutations (689delT, 857del17, G208D) in Spanish families affected with autosomal dominant retinal degenerations. Mutations in brief no. 147. OnlineM J Trujillo, J Bueno, A Osorio, et al.
Leukemia|June 1, 1995
Genetic instability of microsatellites in hematological neoplasmsM Robledo, B Martinez, E Arranz, et al.
Pageof 13

Showing results (11-20 of 128) with videos related to

Sort By:
Pageof 13
Human Genetics|March 30, 2004
Gene symbol: CFTR. Disease: Cystic fibrosisM J Trujillo-Tiebas, J Gallego, M García, et al.
Revista Espanola De Anestesiologia Y Reanimacion|November 13, 2007
[Epidural anesthesia for coronary revascularization in the conscious patient]A Ysasi, R Llorens, E Calderón, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: OA1. Disease: albinism, ocularMonica Martinez-Garcia, M J Trujillo-Tiebas, C Villaverde, et al.
Human Genetics|February 14, 2007
Gene symbol: ABCA4. Disease: Stargardt disease 1. Accession #Hm0537R Riveiro-Alvarez, M J Trujillo, D Cantalapiedra, et al.
Human Genetics|November 28, 2006
Gene symbol: ABCA4. Disease: Stargardt disease 1R Riveiro-Alvarez, M J Trujillo, D Cantalapiedra, et al.
Human Genetics|February 14, 2007
Gene symbol: ABCA4. Disease: Stargardt disease 1. Accession #Hs0512R Riveiro-Alvarez, M J Trujillo, D Cantalapiedra, et al.
Journal of Investigational Allergology & Clinical Immunology|October 24, 2018
Deflazacort-Induced Erythema Multiforme Exudativum Successfully Treated With a Single Dose of EtanerceptM J Trujillo-Trujillo, E González-Mancebo, M Gandolfo-Cano, et al.
Ophthalmic Genetics|September 1, 1996
G106R rhodopsin mutation is also present in Spanish ADRP patientsC Ayuso, C Reig, B Garcia-Sandoval, et al.
Human Mutation|January 8, 2000
Three novel RDS-peripherin mutations (689delT, 857del17, G208D) in Spanish families affected with autosomal dominant retinal degenerations. Mutations in brief no. 147. OnlineM J Trujillo, J Bueno, A Osorio, et al.
Leukemia|June 1, 1995
Genetic instability of microsatellites in hematological neoplasmsM Robledo, B Martinez, E Arranz, et al.
Pageof 13