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Medicinal Research Reviews
|
January 6, 2004
Dihydropteridine reductase deficiency in man: from biology to treatment
Alberto Ponzone, Marco Spada, Silvio Ferraris, et al.
Metabolism: Clinical and Experimental
|
November 17, 2009
Unresponsiveness to tetrahydrobiopterin of phenylalanine hydroxylase deficiency
Alberto 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 phenylketonuria
Alberto Ponzone, Marco Spada, Luca Roasio, et al.
European Journal of Pediatrics
|
April 25, 2003
Hair anomalies as a sign of mitochondrial disease
Margherita 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 syndrome
Michelangelo 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 gene
Silvio Ferraris, Angelo Giovanni Del Monaco, Emanuela Garelli, et al.
Annals of Neurology
|
June 2, 2005
POLG mutations and Alpers syndrome
Guido 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 issue
Silvio 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 mutation
Michelangelo 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 OPA1
Silvio Ferraris, Susanna Clark, Emanuela Garelli, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Medicinal Research Reviews
|
January 6, 2004
Dihydropteridine reductase deficiency in man: from biology to treatment
Alberto Ponzone, Marco Spada, Silvio Ferraris, et al.
Metabolism: Clinical and Experimental
|
November 17, 2009
Unresponsiveness to tetrahydrobiopterin of phenylalanine hydroxylase deficiency
Alberto 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 phenylketonuria
Alberto Ponzone, Marco Spada, Luca Roasio, et al.
European Journal of Pediatrics
|
April 25, 2003
Hair anomalies as a sign of mitochondrial disease
Margherita 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 syndrome
Michelangelo 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 gene
Silvio Ferraris, Angelo Giovanni Del Monaco, Emanuela Garelli, et al.
Annals of Neurology
|
June 2, 2005
POLG mutations and Alpers syndrome
Guido 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 issue
Silvio 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 mutation
Michelangelo 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 OPA1
Silvio Ferraris, Susanna Clark, Emanuela Garelli, et al.
Page
of 2