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Social and Material Vulnerability of the Italian Municipalities: Comparing Alternative Approaches

Social indicators research, 2022-06, Vol.161 (2-3), p.523-540

2022

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Targeting Policies for Multidimensional Poverty and Social Fragility Relief Among Migrants in Italy, Using F-FOD Analysis

Social indicators research, 2021-08, Vol.157 (1), p.57-75

2021

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Multidimensional Analysis of Deprivation and Fragility Patterns of Migrants in Lombardy, Using Partially Ordered Sets and Self‑Organizing Maps

Social indicators research, 2019-01, Vol.141 (2), p.551-579

2019

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Self-Organized Amphiphiles Are Poor Hydroxyl Radical Scavengers in Fast Photochemical Oxidation of Proteins Experiments

Journal of the American Society for Mass Spectrometry, 2021-05, Vol.32 (5), p.1155-1161

2021

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Clinical, biochemical and neuroradiological findings in L-2-hydroxyglutaric aciduria

Neurological sciences, 2000-06, Vol.21 (2), p.103-108

2000

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Fulminant Leigh syndrome and sudden unexpected death in a family with the T9176C mutation of the mitochondrial ATPase 6 gene

Journal of inherited metabolic disease, 1998-02, Vol.21 (1), p.2-8

1998

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A convenient tubulin-based quantitative assay for paclitaxel (Taxol) derivatives more effective in inducing assembly than the parent compound

Cancer chemotherapy and pharmacology, 1996, Vol.38 (2), p.136-140

1996

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Acute, severe cardiomyopathy as main symptom of late-onset very long-chain acyl-coenzyme A dehydrogenase deficiency

European journal of pediatrics, 1998-12, Vol.157 (12), p.992-995

1998

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Medium‐chain triglyceride loading test in carnitine–acylcarnitine translocase deficiency: Insights on treatment

Journal of inherited metabolic disease, 1999-08, Vol.22 (6), p.733-739

1999

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Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families

Neurological sciences, 2004-07, Vol.25 (3), p.130-137

2004

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Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families

Neurological sciences, 2004-07, Vol.25 (3), p.130-137

2004

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Utility of multimodal evoked potential study and electroencephalography in mitochondrial encephalomyopathy

Italian journal of neurological sciences, 1998-10, Vol.19 (5), p.291-300

1998

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Muscle cytochrome c oxidase deficiency in two Italian patients with ethylmalonic aciduria and peculiar clinical phenotype

Journal of inherited metabolic disease, 1994-05, Vol.17 (3), p.301-303

1994

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4‐Hydroxybutyric aciduria: Clinical findings and vigabatrin therapy

Journal of inherited metabolic disease, 1993-05, Vol.16 (3), p.520-522

1993

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X-linked adrenoleukodystrophy: first report of the Italian Study Group

Italian journal of neurological sciences, 1998-10, Vol.19 (5), p.315-319

1998

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A new stable‐isotope dilution method for measurement of orotic acid utilizing solvent‐extracted urine

Journal of inherited metabolic disease, 1994-03, Vol.17 (2), p.243-244

1994

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Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency

European journal of pediatrics, 1992-02, Vol.151 (2), p.121-126

1992

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4-Hydroxybutyric aciduria: clinical findings and vigabatrin therapy

Journal of inherited metabolic disease, 1993, Vol.16 (3), p.520-522

1993

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Antiemetic activity of the new 5-HT3 antagonist DAU 6215 in animal models of cancer chemotherapy and radiation

Cancer chemotherapy and pharmacology, 1991-01, Vol.28 (6), p.470-474

1991

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Debrancher deficiency neuromuscular disorder with pseudohypertrophy in two brothers

Journal of neurology, 1989-10, Vol.236 (7), p.418-420

1989

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Transcorneal Permeation of L-and D-Aspartate Ester Prodrugs of Acyclovir : Delineation of Passive Diffusion Versus Transporter Involvement : Role of transporters in ocular drug delivery system

Pharmaceutical research, 2009, Vol.26 (5), p.1261-1269

2009

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Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA

Journal of neurology, 1995-05, Vol.242 (5), p.304-312

1995

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Recessive carnitine palmityl transferase deficiency: biochemical studies in tissue cultures and platelets

Journal of neurology, 1987-01, Vol.235 (2), p.74-79

1987

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Cytochrome-C-oxidase deficiency in muscles of a floppy infant without mitochondrial myopathy

Journal of neurology, 1982-01, Vol.227 (4), p.201-207

1982

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A new therapeutic approach for X-linked adrenoleukodystrophy

European journal of pediatrics, 1990-05, Vol.149 (8), p.595-596

1990

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Social and Material Vulnerability of the Italian Municipalities: Comparing Alternative Approaches

Targeting Policies for Multidimensional Poverty and Social Fragility Relief Among Migrants in Italy, Using F-FOD Analysis

Multidimensional Analysis of Deprivation and Fragility Patterns of Migrants in Lombardy, Using Partially Ordered Sets and Self‑Organizing Maps

Self-Organized Amphiphiles Are Poor Hydroxyl Radical Scavengers in Fast Photochemical Oxidation of Proteins Experiments

Clinical, biochemical and neuroradiological findings in L-2-hydroxyglutaric aciduria

Fulminant Leigh syndrome and sudden unexpected death in a family with the T9176C mutation of the mitochondrial ATPase 6 gene

A convenient tubulin-based quantitative assay for paclitaxel (Taxol) derivatives more effective in inducing assembly than the parent compound

Acute, severe cardiomyopathy as main symptom of late-onset very long-chain acyl-coenzyme A dehydrogenase deficiency

Medium‐chain triglyceride loading test in carnitine–acylcarnitine translocase deficiency: Insights on treatment

Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families

Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families

Utility of multimodal evoked potential study and electroencephalography in mitochondrial encephalomyopathy

Muscle cytochrome c oxidase deficiency in two Italian patients with ethylmalonic aciduria and peculiar clinical phenotype

4‐Hydroxybutyric aciduria: Clinical findings and vigabatrin therapy

X-linked adrenoleukodystrophy: first report of the Italian Study Group

A new stable‐isotope dilution method for measurement of orotic acid utilizing solvent‐extracted urine

Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency

4-Hydroxybutyric aciduria: clinical findings and vigabatrin therapy

Antiemetic activity of the new 5-HT3 antagonist DAU 6215 in animal models of cancer chemotherapy and radiation

Debrancher deficiency neuromuscular disorder with pseudohypertrophy in two brothers

Transcorneal Permeation of L-and D-Aspartate Ester Prodrugs of Acyclovir : Delineation of Passive Diffusion Versus Transporter Involvement : Role of transporters in ocular drug delivery system

Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA

Recessive carnitine palmityl transferase deficiency: biochemical studies in tissue cultures and platelets

Cytochrome-C-oxidase deficiency in muscles of a floppy infant without mitochondrial myopathy

A new therapeutic approach for X-linked adrenoleukodystrophy

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