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M F De Castro

Showing results (1-10 of 7) with videos related to

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Anticancer Research|January 1, 1982
ATP uptake by mouse lymphoma cellsM F De Castro, S R Ayad
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|January 1, 1989
Cardiovascular change in response to prolonged defense area stimulation in freely moving ratsM F De Castro, L C Schenberg
Acta Anaesthesiologica Scandinavica|May 1, 1992
EDTA-dependent pseudothrombocytopenia in a preoperative patientD Pestaña, C Marcote, M F de Castro
American Journal of Medical Genetics. Part A|December 8, 2006
Unusually severe expression of craniofacial features in Aarskog-Scott syndrome due to a novel truncating mutation of the FGD1 geneA Orrico, L Galli, M G Obregon, et al.
Pediatrics|January 9, 2013
Change in prevalence of congenital defects in children with Prader-Willi syndromeM Torrado, M E Foncuberta, M F de Castro Perez, et al.
Arquivos Brasileiros De Cardiologia|April 1, 1993
[Surgery for Wolff-Parkinson-White syndrome in the first year of life]F A Fantini, E B Sternick, B Gontijo Filho, et al.
Journal of Community Genetics|August 2, 2013
CHACO outreach project: the development of a primary health care-based medical genetic service in an Argentinean provinceC Z Barreiro, M P Bidondo, J A Garrido, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Anticancer Research|January 1, 1982
ATP uptake by mouse lymphoma cellsM F De Castro, S R Ayad
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|January 1, 1989
Cardiovascular change in response to prolonged defense area stimulation in freely moving ratsM F De Castro, L C Schenberg
Acta Anaesthesiologica Scandinavica|May 1, 1992
EDTA-dependent pseudothrombocytopenia in a preoperative patientD Pestaña, C Marcote, M F de Castro
American Journal of Medical Genetics. Part A|December 8, 2006
Unusually severe expression of craniofacial features in Aarskog-Scott syndrome due to a novel truncating mutation of the FGD1 geneA Orrico, L Galli, M G Obregon, et al.
Pediatrics|January 9, 2013
Change in prevalence of congenital defects in children with Prader-Willi syndromeM Torrado, M E Foncuberta, M F de Castro Perez, et al.
Arquivos Brasileiros De Cardiologia|April 1, 1993
[Surgery for Wolff-Parkinson-White syndrome in the first year of life]F A Fantini, E B Sternick, B Gontijo Filho, et al.
Journal of Community Genetics|August 2, 2013
CHACO outreach project: the development of a primary health care-based medical genetic service in an Argentinean provinceC Z Barreiro, M P Bidondo, J A Garrido, et al.
Pageof 1