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‘If I see a black dot, I shoot it on sight!’: Italian rap between anti- and neo-fascisms

Global Hip Hop Studies, 2020-08, Vol.1 (2), p.293-312

Zammarchi, Enrico

2020

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Timira, romanzo meticcio e stratificato

Forum italicum, 2021-05, Vol.55 (1), p.68-84

2021

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New Strategy for the Screening of Lysosomal Storage Disorders: The Use of the Online Trapping-and-Cleanup Liquid Chromatography/Mass Spectrometry

Analytical chemistry (Washington), 2009-08, Vol.81 (15), p.6113-6121

2009

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Altered Thymidine Metabolism Due to Defects of Thymidine Phosphorylase

The Journal of biological chemistry, 2002-02, Vol.277 (6), p.4128-4133

2002

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Primary and Secondary Elastin-Binding Protein Defect Leads to Impaired Elastogenesis in Fibroblasts from GM1-Gangliosidosis Patients

The American journal of pathology, 2005-12, Vol.167 (6), p.1689-1698

2005

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Implementing tandem mass spectrometry as a routine tool for characterizing the complete purine and pyrimidine metabolic profile in urine samples

Journal of mass spectrometry., 2006-11, Vol.41 (11), p.1442-1452

2006

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The potential action of galactose as a “chemical chaperone”: Increase of beta galactosidase activity in fibroblasts from an adult GM1-gangliosidosis patient

European journal of paediatric neurology, 2009-03, Vol.13 (2), p.160-164

2009

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The Synergistic Activity of Thyroid Transcription Factor 1 and Pax 8 Relies on the Promoter/Enhancer Interplay

Molecular endocrinology (Baltimore, Md.), 2002-04, Vol.16 (4), p.837-846

2002

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Role for p300 in Pax 8 Induction of Thyroperoxidase Gene Expression

The Journal of biological chemistry, 2000-11, Vol.275 (44), p.34100-34105

2000

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Rapid determination of orotic acid in urine by a fast liquid chromatography/tandem mass spectrometric method

Rapid communications in mass spectrometry, 2003-01, Vol.17 (8), p.788-793

2003

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Rapid 2nd-Tier Test for Measurement of 3-OH-Propionic and Methylmalonic Acids on Dried Blood Spots: Reducing the False-Positive Rate for Propionylcarnitine during Expanded Newborn Screening by Liquid Chromatography-Tandem Mass Spectrometry

Clinical chemistry (Baltimore, Md.), 2007-07, Vol.53 (7), p.1364-1369

2007

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The inclusion of succinylacetone as marker for tyrosinemia type I in expanded newborn screening programs

Rapid communications in mass spectrometry, 2008-03, Vol.22 (6), p.812-818

2008

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Hyperinsulinism and Hyperammonemia in Infants with Regulatory Mutations of the Glutamate Dehydrogenase Gene

The New England journal of medicine, 1998-05, Vol.338 (19), p.1352-1357

1998

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Unbalanced GLA mRNAs ratio quantified by real-time PCR in Fabry patients' fibroblasts results in Fabry disease

European journal of human genetics : EJHG, 2008-11, Vol.16 (11), p.1311-1317

2008

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The successful inclusion of succinylacetone as a marker of tyrosinemia type I in Tuscany newborn screening program

Rapid communications in mass spectrometry, 2009-12, Vol.23 (23), p.3891-3893

2009

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Newborn Screening for Tyrosinemia Type I: Further Evidence that Succinylacetone Determination on Blood Spot Is Essential

JIMD Reports - Case and Research Reports, 2011/1, 2011-01, Vol.1, p.107-109

2011

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Genotype/phenotype correlation in glycogen storage disease type 1b : a multicentre study and review of the literature

European journal of pediatrics, 2005-08, Vol.164 (8), p.501-508

2005

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Novel mutations in lysosomal neuraminidase identify functional domains and determine clinical severity in sialidosis

Human molecular genetics, 2000-11, Vol.9 (18), p.2715-2725

2000

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Role of β-galactosidase and elastin binding protein in lysosomal and nonlysosomal complexes of patients with GM1-gangliosidosis

Human mutation, 2005-03, Vol.25 (3), p.285-292

2005

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Novel mutations in lysosomal neuraminidase identify functional domains and determine clinical severity in sialidosis

Human molecular genetics, 2000-11, Vol.9 (18), p.2715-2725

2000

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Different genotypes in a large Italian family with recurrent hereditary fructose intolerance

European journal of gastroenterology & hepatology, 2008-02, Vol.20 (2), p.118-121

2008

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GM1 gangliosidosis: molecular analysis of nine patients and development of an RT-PCR assay for GLB1 gene expression profiling

Human mutation, 2007-02, Vol.28 (2), p.204-204

2007

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Cryptogenic Hepatitis Masking the Diagnosis of Ornithine Transcarbamylase Deficiency

Journal of pediatric gastroenterology and nutrition, 1996-05, Vol.22 (4), p.380-383

1996

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The X-Linked Gene G4.5 Is Responsible for Different Infantile Dilated Cardiomyopathies

American journal of human genetics, 1997-10, Vol.61 (4), p.862-867

1997

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Falsely elevated C4-carnitine as expression of glutamate formiminotransferase deficiency in tandem mass spectrometry newborn screening

Journal of mass spectrometry., 2006-02, Vol.41 (2), p.263-265

2006

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‘If I see a black dot, I shoot it on sight!’: Italian rap between anti- and neo-fascisms

Timira, romanzo meticcio e stratificato

New Strategy for the Screening of Lysosomal Storage Disorders: The Use of the Online Trapping-and-Cleanup Liquid Chromatography/Mass Spectrometry

Altered Thymidine Metabolism Due to Defects of Thymidine Phosphorylase

Primary and Secondary Elastin-Binding Protein Defect Leads to Impaired Elastogenesis in Fibroblasts from GM1-Gangliosidosis Patients

Implementing tandem mass spectrometry as a routine tool for characterizing the complete purine and pyrimidine metabolic profile in urine samples

The potential action of galactose as a “chemical chaperone”: Increase of beta galactosidase activity in fibroblasts from an adult GM1-gangliosidosis patient

The Synergistic Activity of Thyroid Transcription Factor 1 and Pax 8 Relies on the Promoter/Enhancer Interplay

Role for p300 in Pax 8 Induction of Thyroperoxidase Gene Expression

Rapid determination of orotic acid in urine by a fast liquid chromatography/tandem mass spectrometric method

Rapid 2nd-Tier Test for Measurement of 3-OH-Propionic and Methylmalonic Acids on Dried Blood Spots: Reducing the False-Positive Rate for Propionylcarnitine during Expanded Newborn Screening by Liquid Chromatography-Tandem Mass Spectrometry

The inclusion of succinylacetone as marker for tyrosinemia type I in expanded newborn screening programs

Hyperinsulinism and Hyperammonemia in Infants with Regulatory Mutations of the Glutamate Dehydrogenase Gene

Unbalanced GLA mRNAs ratio quantified by real-time PCR in Fabry patients' fibroblasts results in Fabry disease

The successful inclusion of succinylacetone as a marker of tyrosinemia type I in Tuscany newborn screening program

Newborn Screening for Tyrosinemia Type I: Further Evidence that Succinylacetone Determination on Blood Spot Is Essential

Genotype/phenotype correlation in glycogen storage disease type 1b : a multicentre study and review of the literature

Novel mutations in lysosomal neuraminidase identify functional domains and determine clinical severity in sialidosis

Role of β-galactosidase and elastin binding protein in lysosomal and nonlysosomal complexes of patients with GM1-gangliosidosis

Novel mutations in lysosomal neuraminidase identify functional domains and determine clinical severity in sialidosis

Different genotypes in a large Italian family with recurrent hereditary fructose intolerance

GM1 gangliosidosis: molecular analysis of nine patients and development of an RT-PCR assay for GLB1 gene expression profiling

Cryptogenic Hepatitis Masking the Diagnosis of Ornithine Transcarbamylase Deficiency

The X-Linked Gene G4.5 Is Responsible for Different Infantile Dilated Cardiomyopathies

Falsely elevated C4-carnitine as expression of glutamate formiminotransferase deficiency in tandem mass spectrometry newborn screening

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