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M Carballo

Showing results (51-60 of 156) with videos related to

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Clinical Genetics|June 18, 2004
De novo germline mutation in the serine-threonine kinase STK11/LKB1 gene associated with Peutz-Jeghers syndromeI Hernan, I Roig, B Martin, et al.
Medicina Clinica|February 17, 1996
[Identification of Arg-135-Leu mutation in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa]C Reig, J Antich, E Gean, et al.
Human Genetics|September 1, 1994
Identification of a novel rhodopsin mutation (Met-44-Thr) in a simplex case of retinitis pigmentosaC Reig, J Antich, E Gean, et al.
Organic Letters|August 11, 2006
Iron(III)-promoted aza-Prins-cyclization: direct synthesis of six-membered azacyclesRubén M Carballo, Miguel A Ramírez, Matías L Rodríguez, et al.
Acta Crystallographica. Section E, Structure Reports Online|February 15, 2014
4-Methyl-N-(4-methyl-phenyl-sulfon-yl)-N-[4-(4-methyl-phen-yl)-1,3-thia-zol-2-yl]benzene-sulfonamideRubén M Carballo, Simón Hernández-Ortega, Nayely Padilla-Montaño, et al.
Human Mutation|June 1, 2001
Mutations P51U and G122E in retinal transcription factor NRL associated with autosomal dominant and sporadic retinitis pigmentosaM Martinez-Gimeno, M Maseras, M Baiget, et al.
Ecancermedicalscience|July 12, 2026
BCG in the fight against cancer: exploring its applications in diverse tumour types and future directionsP Ignacio A Bianco, O Jeismar M Carballo, P Isaac R Blanca, et al.
BMJ Case Reports|September 16, 2022
Gamma Knife radiosurgery for a recurrent craniocervical junction solitary fibrous tumourOrlando De Jesus, Cesar M Carballo Cuello, Ricardo J Fernández-de Thomas, et al.
Archivos De La Sociedad Espanola De Oftalmologia|September 11, 2002
[Genetic and molecular characterization of 148 patients with autosomal dominant retinitis pigmentosa (ADRP)]E Millá, M Maseras, M Martínez-Gimeno, et al.
Medicina Intensiva|January 7, 2011
[Multi-tissue donor: a reachable option]D Daga Ruiz, C Fernández Aguirre, M A Frutos Sanz, et al.
Pageof 16

Showing results (51-60 of 156) with videos related to

Sort By:
Pageof 16
Clinical Genetics|June 18, 2004
De novo germline mutation in the serine-threonine kinase STK11/LKB1 gene associated with Peutz-Jeghers syndromeI Hernan, I Roig, B Martin, et al.
Medicina Clinica|February 17, 1996
[Identification of Arg-135-Leu mutation in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa]C Reig, J Antich, E Gean, et al.
Human Genetics|September 1, 1994
Identification of a novel rhodopsin mutation (Met-44-Thr) in a simplex case of retinitis pigmentosaC Reig, J Antich, E Gean, et al.
Organic Letters|August 11, 2006
Iron(III)-promoted aza-Prins-cyclization: direct synthesis of six-membered azacyclesRubén M Carballo, Miguel A Ramírez, Matías L Rodríguez, et al.
Acta Crystallographica. Section E, Structure Reports Online|February 15, 2014
4-Methyl-N-(4-methyl-phenyl-sulfon-yl)-N-[4-(4-methyl-phen-yl)-1,3-thia-zol-2-yl]benzene-sulfonamideRubén M Carballo, Simón Hernández-Ortega, Nayely Padilla-Montaño, et al.
Human Mutation|June 1, 2001
Mutations P51U and G122E in retinal transcription factor NRL associated with autosomal dominant and sporadic retinitis pigmentosaM Martinez-Gimeno, M Maseras, M Baiget, et al.
Ecancermedicalscience|July 12, 2026
BCG in the fight against cancer: exploring its applications in diverse tumour types and future directionsP Ignacio A Bianco, O Jeismar M Carballo, P Isaac R Blanca, et al.
BMJ Case Reports|September 16, 2022
Gamma Knife radiosurgery for a recurrent craniocervical junction solitary fibrous tumourOrlando De Jesus, Cesar M Carballo Cuello, Ricardo J Fernández-de Thomas, et al.
Archivos De La Sociedad Espanola De Oftalmologia|September 11, 2002
[Genetic and molecular characterization of 148 patients with autosomal dominant retinitis pigmentosa (ADRP)]E Millá, M Maseras, M Martínez-Gimeno, et al.
Medicina Intensiva|January 7, 2011
[Multi-tissue donor: a reachable option]D Daga Ruiz, C Fernández Aguirre, M A Frutos Sanz, et al.
Pageof 16