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Silvio Ferraris

Showing results (1-10 of 12) with videos related to

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Medicinal Research Reviews|January 6, 2004
Dihydropteridine reductase deficiency in man: from biology to treatmentAlberto Ponzone, Marco Spada, Silvio Ferraris, et al.
Metabolism: Clinical and Experimental|November 17, 2009
Unresponsiveness to tetrahydrobiopterin of phenylalanine hydroxylase deficiencyAlberto Ponzone, Francesco Porta, Alessandro Mussa, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 22, 2008
Impact of neonatal protein metabolism and nutrition on screening for phenylketonuriaAlberto Ponzone, Marco Spada, Luca Roasio, et al.
European Journal of Pediatrics|April 25, 2003
Hair anomalies as a sign of mitochondrial diseaseMargherita Silengo, Mariella Valenzise, Marco Spada, et al.
Archives of Neurology|May 11, 2005
New DGK gene mutations in the hepatocerebral form of mitochondrial DNA depletion syndromeMichelangelo Mancuso, Silvio Ferraris, Jacklyn Pancrudo, et al.
American Journal of Medical Genetics. Part A|February 28, 2009
HDR syndrome: a novel "de novo" mutation in GATA3 geneSilvio Ferraris, Angelo Giovanni Del Monaco, Emanuela Garelli, et al.
Annals of Neurology|June 2, 2005
POLG mutations and Alpers syndromeGuido Davidzon, Michelangelo Mancuso, Silvio Ferraris, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 28, 2004
Malformations following methimazole exposure in utero: an open issueSilvio Ferraris, Mariella Valenzise, Margherita Lerone, et al.
Journal of the Neurological Sciences|December 21, 2004
Congenital or late-onset myopathy in patients with the T14709C mtDNA mutationMichelangelo Mancuso, Silvio Ferraris, Yutaka Nishigaki, et al.
Archives of Neurology|January 16, 2008
Progressive external ophthalmoplegia and vision and hearing loss in a patient with mutations in POLG2 and OPA1Silvio Ferraris, Susanna Clark, Emanuela Garelli, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Medicinal Research Reviews|January 6, 2004
Dihydropteridine reductase deficiency in man: from biology to treatmentAlberto Ponzone, Marco Spada, Silvio Ferraris, et al.
Metabolism: Clinical and Experimental|November 17, 2009
Unresponsiveness to tetrahydrobiopterin of phenylalanine hydroxylase deficiencyAlberto Ponzone, Francesco Porta, Alessandro Mussa, et al.
Journal of Pediatric Gastroenterology and Nutrition|May 22, 2008
Impact of neonatal protein metabolism and nutrition on screening for phenylketonuriaAlberto Ponzone, Marco Spada, Luca Roasio, et al.
European Journal of Pediatrics|April 25, 2003
Hair anomalies as a sign of mitochondrial diseaseMargherita Silengo, Mariella Valenzise, Marco Spada, et al.
Archives of Neurology|May 11, 2005
New DGK gene mutations in the hepatocerebral form of mitochondrial DNA depletion syndromeMichelangelo Mancuso, Silvio Ferraris, Jacklyn Pancrudo, et al.
American Journal of Medical Genetics. Part A|February 28, 2009
HDR syndrome: a novel "de novo" mutation in GATA3 geneSilvio Ferraris, Angelo Giovanni Del Monaco, Emanuela Garelli, et al.
Annals of Neurology|June 2, 2005
POLG mutations and Alpers syndromeGuido Davidzon, Michelangelo Mancuso, Silvio Ferraris, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 28, 2004
Malformations following methimazole exposure in utero: an open issueSilvio Ferraris, Mariella Valenzise, Margherita Lerone, et al.
Journal of the Neurological Sciences|December 21, 2004
Congenital or late-onset myopathy in patients with the T14709C mtDNA mutationMichelangelo Mancuso, Silvio Ferraris, Yutaka Nishigaki, et al.
Archives of Neurology|January 16, 2008
Progressive external ophthalmoplegia and vision and hearing loss in a patient with mutations in POLG2 and OPA1Silvio Ferraris, Susanna Clark, Emanuela Garelli, et al.
Pageof 2