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V Cornejo

Showing results (1-10 of 21) with videos related to

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Revista Chilena De Pediatria|November 1, 1990
[Program of neonatal screening for phenylketonuria]V Cornejo, E Raimann, M Moraga, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Propionic acidaemia: two cases in ChileE Raimann, V Cornejo, C G Perales, et al.
Revista Medica De Chile|September 1, 1992
[Early diagnosis of phenylketonuria. Follow up of 2 cases]E Raimann, V Cornejo, C G Perales, et al.
Human Mutation|July 17, 1999
Molecular characterization of phenylalanine hydroxylase deficiency in Chile. Mutations in brief no. 243. OnlineB Pérez, L R Desviat, M De Lucca, et al.
American Journal of Human Genetics|August 1, 1995
Evidence in Latin America of recurrence of V388M, a phenylketonuria mutation with high in vitro residual activityL R Desviat, B Pérez, M De Lucca, et al.
Revista Chilena De Pediatria|July 1, 1988
[Diagnosis of phenylketonuria in Chile]M Colombo, L Troncoso, E Raimann, et al.
BMJ Case Reports|November 26, 2025
Appendiceal endometriosis: an uncommon manifestation of deep infiltrating endometriosisEsteban A Vásquez Carpio, Lía F Rodriguez Navas, Javiera V Cornejo Peña, et al.
Journal of Inherited Metabolic Disease|August 5, 2010
Past, present and future of newborn screening in ChileV Cornejo, E Raimann, J F Cabello, et al.
Children and Youth Services Review|October 16, 2023
Urban Latinx parents' attitudes towards mental health: Mental health literacy and service useLouise E Dixon De Silva, Carolyn Ponting, Giovanni Ramos, et al.
Human Molecular Genetics|August 1, 1993
Presence of the Mediterranean PKU mutation IVS10 in Latin AmericaB Pérez, L R Desviat, M Díe, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Revista Chilena De Pediatria|November 1, 1990
[Program of neonatal screening for phenylketonuria]V Cornejo, E Raimann, M Moraga, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Propionic acidaemia: two cases in ChileE Raimann, V Cornejo, C G Perales, et al.
Revista Medica De Chile|September 1, 1992
[Early diagnosis of phenylketonuria. Follow up of 2 cases]E Raimann, V Cornejo, C G Perales, et al.
Human Mutation|July 17, 1999
Molecular characterization of phenylalanine hydroxylase deficiency in Chile. Mutations in brief no. 243. OnlineB Pérez, L R Desviat, M De Lucca, et al.
American Journal of Human Genetics|August 1, 1995
Evidence in Latin America of recurrence of V388M, a phenylketonuria mutation with high in vitro residual activityL R Desviat, B Pérez, M De Lucca, et al.
Revista Chilena De Pediatria|July 1, 1988
[Diagnosis of phenylketonuria in Chile]M Colombo, L Troncoso, E Raimann, et al.
BMJ Case Reports|November 26, 2025
Appendiceal endometriosis: an uncommon manifestation of deep infiltrating endometriosisEsteban A Vásquez Carpio, Lía F Rodriguez Navas, Javiera V Cornejo Peña, et al.
Journal of Inherited Metabolic Disease|August 5, 2010
Past, present and future of newborn screening in ChileV Cornejo, E Raimann, J F Cabello, et al.
Children and Youth Services Review|October 16, 2023
Urban Latinx parents' attitudes towards mental health: Mental health literacy and service useLouise E Dixon De Silva, Carolyn Ponting, Giovanni Ramos, et al.
Human Molecular Genetics|August 1, 1993
Presence of the Mediterranean PKU mutation IVS10 in Latin AmericaB Pérez, L R Desviat, M Díe, et al.
Pageof 3