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G La Marca

Showing results (11-20 of 20) with videos related to

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Journal of Inherited Metabolic Disease|July 10, 2009
Insulin-resistant hyperglycaemia complicating neonatal onset of methylmalonic and propionic acidaemiasL Filippi, E Gozzini, C Cavicchi, et al.
Journal of Mass Spectrometry : JMS|February 25, 2006
Pre- and post-dialysis quantitative dosage of thymidine in urine and plasma of a MNGIE patient by using HPLC-ESI-MS/MSG la Marca, S Malvagia, B Casetta, et al.
Clinical Genetics|October 15, 2013
Aminoacylase I deficiency due to ACY1 mRNA exon skippingL Ferri, S Funghini, A Fioravanti, et al.
Journal of Pharmaceutical and Biomedical Analysis|April 11, 2009
Hypocitrullinemia in expanded newborn screening by LC-MS/MS is not a reliable marker for ornithine transcarbamylase deficiencyC Cavicchi, S Malvagia, G la Marca, et al.
Surgical and Radiologic Anatomy : SRA|November 23, 2006
Kinking, coiling, and tortuosity of extracranial internal carotid artery: is it the effect of a metaplasia?G La Barbera, G La Marca, A Martino, et al.
Annals of Human Genetics|May 31, 2007
Fatal malonyl CoA decarboxylase deficiency due to maternal uniparental isodisomy of the telomeric end of chromosome 16S Malvagia, L Papi, A Morrone, et al.
Clinical Genetics|February 3, 2006
Genetic and biochemical approach to early prenatal diagnosis in a family with mut methylmalonic aciduriaC Cavicchi, M A Donati, S Funghini, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|December 5, 2012
Propranolol concentrations after oral administration in term and preterm neonatesL Filippi, G Cavallaro, P Fiorini, et al.
Clinical Genetics|April 27, 2011
Fabry disease: polymorphic haplotypes and a novel missense mutation in the GLA geneL Ferri, C Guido, G la Marca, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 19, 2015
LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk populationO Musumeci, G la Marca, M Spada, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Journal of Inherited Metabolic Disease|July 10, 2009
Insulin-resistant hyperglycaemia complicating neonatal onset of methylmalonic and propionic acidaemiasL Filippi, E Gozzini, C Cavicchi, et al.
Journal of Mass Spectrometry : JMS|February 25, 2006
Pre- and post-dialysis quantitative dosage of thymidine in urine and plasma of a MNGIE patient by using HPLC-ESI-MS/MSG la Marca, S Malvagia, B Casetta, et al.
Clinical Genetics|October 15, 2013
Aminoacylase I deficiency due to ACY1 mRNA exon skippingL Ferri, S Funghini, A Fioravanti, et al.
Journal of Pharmaceutical and Biomedical Analysis|April 11, 2009
Hypocitrullinemia in expanded newborn screening by LC-MS/MS is not a reliable marker for ornithine transcarbamylase deficiencyC Cavicchi, S Malvagia, G la Marca, et al.
Surgical and Radiologic Anatomy : SRA|November 23, 2006
Kinking, coiling, and tortuosity of extracranial internal carotid artery: is it the effect of a metaplasia?G La Barbera, G La Marca, A Martino, et al.
Annals of Human Genetics|May 31, 2007
Fatal malonyl CoA decarboxylase deficiency due to maternal uniparental isodisomy of the telomeric end of chromosome 16S Malvagia, L Papi, A Morrone, et al.
Clinical Genetics|February 3, 2006
Genetic and biochemical approach to early prenatal diagnosis in a family with mut methylmalonic aciduriaC Cavicchi, M A Donati, S Funghini, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|December 5, 2012
Propranolol concentrations after oral administration in term and preterm neonatesL Filippi, G Cavallaro, P Fiorini, et al.
Clinical Genetics|April 27, 2011
Fabry disease: polymorphic haplotypes and a novel missense mutation in the GLA geneL Ferri, C Guido, G la Marca, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 19, 2015
LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk populationO Musumeci, G la Marca, M Spada, et al.
Pageof 2