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R Giugliani

Showing results (61-70 of 164) with videos related to

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Clinical Genetics|April 1, 1997
Evaluation of an aspartame loading test for the detection of heterozygotes for classical phenylketonuriaL C Silva, R F Pires, J C Coelho, et al.
Arquivos De Neuro-Psiquiatria|June 1, 1997
Detection of metabolic disorders in high-risk patients. A pilot study in Salvador, BahiaM B Pereira, G C Da Conceição, J C Coelho, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 1, 1996
Maternal hyperphenylalaninaemia as a cause of microcephaly and mental retardationL B Jardim, R Palma-Dias, L C Silva, et al.
Genetics and Molecular Research : GMR|August 23, 2012
High proportion of mannosidosis and fucosidosis among lysosomal storage diseases in CubaC Menéndez-Sainz, A González-Quevedo, S González-García, et al.
Revista De Neurologia|October 15, 2005
[Neuropathic pain in a young female patient with Fabry's disease: a new mutation of the alpha-galactosidase A gene]J M Politei, M A Pagano, A Dubrovsky, et al.
Clinical Genetics|April 1, 1992
Biochemical investigation of a Brazilian patient with a defect in mitochondrial acetoacetylcoenzyme-A thiolaseM Wajner, M T Sanseverino, R Giugliani, et al.
Acta Paediatrica (Oslo, Norway : 1992)|November 1, 1994
Are fathers prepared to encourage their partners to breast feed? A study about fathers' knowledge of breast feedingE R Giugliani, Y Bronner, W T Caiaffa, et al.
Cell Biology and Toxicology|July 16, 2014
Glycosaminoglycans can be associated with oxidative damage in mucopolysaccharidosis II patients submitted to enzyme replacement therapyG W Negretto, M Deon, G B Biancini, et al.
Prenatal Diagnosis|December 5, 2009
Prenatal diagnosis of mucopolysaccharidosis VI by enzyme assay in a dried spot of fetal blood: a pioneering case reportM G Burin, E Ribeiro, J de Mari, et al.
Gene|May 13, 2015
Genotypic characterization of Brazilian patients with infantile and juvenile forms of metachromatic leukodystrophyM Y F Virgens, M Siebert, H Bock, et al.
Pageof 17

Showing results (61-70 of 164) with videos related to

Sort By:
Pageof 17
Clinical Genetics|April 1, 1997
Evaluation of an aspartame loading test for the detection of heterozygotes for classical phenylketonuriaL C Silva, R F Pires, J C Coelho, et al.
Arquivos De Neuro-Psiquiatria|June 1, 1997
Detection of metabolic disorders in high-risk patients. A pilot study in Salvador, BahiaM B Pereira, G C Da Conceição, J C Coelho, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 1, 1996
Maternal hyperphenylalaninaemia as a cause of microcephaly and mental retardationL B Jardim, R Palma-Dias, L C Silva, et al.
Genetics and Molecular Research : GMR|August 23, 2012
High proportion of mannosidosis and fucosidosis among lysosomal storage diseases in CubaC Menéndez-Sainz, A González-Quevedo, S González-García, et al.
Revista De Neurologia|October 15, 2005
[Neuropathic pain in a young female patient with Fabry's disease: a new mutation of the alpha-galactosidase A gene]J M Politei, M A Pagano, A Dubrovsky, et al.
Clinical Genetics|April 1, 1992
Biochemical investigation of a Brazilian patient with a defect in mitochondrial acetoacetylcoenzyme-A thiolaseM Wajner, M T Sanseverino, R Giugliani, et al.
Acta Paediatrica (Oslo, Norway : 1992)|November 1, 1994
Are fathers prepared to encourage their partners to breast feed? A study about fathers' knowledge of breast feedingE R Giugliani, Y Bronner, W T Caiaffa, et al.
Cell Biology and Toxicology|July 16, 2014
Glycosaminoglycans can be associated with oxidative damage in mucopolysaccharidosis II patients submitted to enzyme replacement therapyG W Negretto, M Deon, G B Biancini, et al.
Prenatal Diagnosis|December 5, 2009
Prenatal diagnosis of mucopolysaccharidosis VI by enzyme assay in a dried spot of fetal blood: a pioneering case reportM G Burin, E Ribeiro, J de Mari, et al.
Gene|May 13, 2015
Genotypic characterization of Brazilian patients with infantile and juvenile forms of metachromatic leukodystrophyM Y F Virgens, M Siebert, H Bock, et al.
Pageof 17