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Biologicals : Journal of the International Association of Biological Standardization
|
January 31, 2012
Serological profile of buffalo (Bubalus bubalis) female calves vaccinated with standard Brucella abortus strain 19 vaccine using rose bengal, 2-mercaptoethanol and complement fixation tests
G Júnior Nardi, M G Ribeiro, A M Jorge, et al.
Human Gene Therapy
|
September 19, 2001
Retrovirus-mediated transfer and expression of beta-hexosaminidase alpha-chain cDNA in human fibroblasts from G(M2)-gangliosidosis B1 variant
C A Teixeira, M Sena-Esteves, L Lopes, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Biochemical characterization of beta-hexosaminidase in different biological specimens from eleven patients with GM2-gangliosidosis B1 variant
M G Ribeiro, R A Pinto, M R Dos Santos, et al.
Australian Veterinary Journal
|
February 16, 2007
Cutaneous pyogranuloma in a cat caused by virulent Rhodococcus equi containing an 87 kb type I plasmid
M R Farias, S Takai, M G Ribeiro, et al.
American Journal of Human Genetics
|
October 1, 1991
GM2-gangliosidosis B1 variant: analysis of beta-hexosaminidase alpha gene mutations in 11 patients from a defined region in Portugal
M R dos Santos, A Tanaka, M C sá Miranda, et al.
The Veterinary Quarterly
|
October 9, 2014
Exogenous bacterial osteomyelitis in 52 dogs: a retrospective study of etiology and in vitro antimicrobial susceptibility profile (2000-2013)
E G M Siqueira, S C Rahal, M G Ribeiro, et al.
International Journal of Immunogenetics
|
April 14, 2006
Serum IgE levels in neurofibromatosis 1
M Geller, M G Ribeiro, A P de Q C Araújo, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
April 11, 2012
Analysis of acylcarnitine profiles in umbilical cord blood and during the early neonatal period by electrospray ionization tandem mass spectrometry
E Vieira Neto, A A Fonseca, R F Almeida, et al.
Molecular Genetics and Metabolism
|
October 26, 2007
CLN2/TPP1 deficiency: the novel mutation IVS7-10A>G causes intron retention and is associated with a mild disease phenotype
C Bessa, C A Teixeira, A Dias, et al.
Journal of Medical Genetics
|
April 1, 1996
Clinical, enzymatic, and molecular characterisation of a Portuguese family with a chronic form of GM2-gangliosidosis B1 variant
M G Ribeiro, T Sonin, R A Pinto, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 48) with videos related to
Sort By:
Page
of 5
Biologicals : Journal of the International Association of Biological Standardization
|
January 31, 2012
Serological profile of buffalo (Bubalus bubalis) female calves vaccinated with standard Brucella abortus strain 19 vaccine using rose bengal, 2-mercaptoethanol and complement fixation tests
G Júnior Nardi, M G Ribeiro, A M Jorge, et al.
Human Gene Therapy
|
September 19, 2001
Retrovirus-mediated transfer and expression of beta-hexosaminidase alpha-chain cDNA in human fibroblasts from G(M2)-gangliosidosis B1 variant
C A Teixeira, M Sena-Esteves, L Lopes, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Biochemical characterization of beta-hexosaminidase in different biological specimens from eleven patients with GM2-gangliosidosis B1 variant
M G Ribeiro, R A Pinto, M R Dos Santos, et al.
Australian Veterinary Journal
|
February 16, 2007
Cutaneous pyogranuloma in a cat caused by virulent Rhodococcus equi containing an 87 kb type I plasmid
M R Farias, S Takai, M G Ribeiro, et al.
American Journal of Human Genetics
|
October 1, 1991
GM2-gangliosidosis B1 variant: analysis of beta-hexosaminidase alpha gene mutations in 11 patients from a defined region in Portugal
M R dos Santos, A Tanaka, M C sá Miranda, et al.
The Veterinary Quarterly
|
October 9, 2014
Exogenous bacterial osteomyelitis in 52 dogs: a retrospective study of etiology and in vitro antimicrobial susceptibility profile (2000-2013)
E G M Siqueira, S C Rahal, M G Ribeiro, et al.
International Journal of Immunogenetics
|
April 14, 2006
Serum IgE levels in neurofibromatosis 1
M Geller, M G Ribeiro, A P de Q C Araújo, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
April 11, 2012
Analysis of acylcarnitine profiles in umbilical cord blood and during the early neonatal period by electrospray ionization tandem mass spectrometry
E Vieira Neto, A A Fonseca, R F Almeida, et al.
Molecular Genetics and Metabolism
|
October 26, 2007
CLN2/TPP1 deficiency: the novel mutation IVS7-10A>G causes intron retention and is associated with a mild disease phenotype
C Bessa, C A Teixeira, A Dias, et al.
Journal of Medical Genetics
|
April 1, 1996
Clinical, enzymatic, and molecular characterisation of a Portuguese family with a chronic form of GM2-gangliosidosis B1 variant
M G Ribeiro, T Sonin, R A Pinto, et al.
Page
of 5