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Physical activity modulates effects of some genetic polymorphisms affecting cardiovascular risk in men aged over 40 years

Nutrition, metabolism, and cardiovascular diseases, 2003-08, Vol.13 (4), p.202-210

2003

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Analysis of LDL receptor gene mutations in Italian patients with homozygous familial hypercholesterolemia

Arteriosclerosis, thrombosis, and vascular biology, 1999-02, Vol.19 (2), p.408

1999

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Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia

Atherosclerosis, 2004-05, Vol.174 (1), p.57-65

2004

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Pseudodominance of lipoprotein lipase (LPL) deficiency due to a nonsense mutation (Tyr302>Term) in exon 6 of LPL gene in an Italian family from Sardinia (LPLOlbia)

Clinical genetics, 2000-02, Vol.57 (2), p.140-147

2000

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Lipoprotein(a) levels in hemodialysis patients: relation to glucose intolerance and hemodialysis duration

Nephron (2015), 1995, Vol.70 (4), p.500

1995

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Sepsis bundles: just think about it?

Critical care (London, England), 2009, Vol.13 (Suppl 1), p.P341-P341

2009

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Partial duplication of the EGF precursor homology domain of the LDL-receptor protein causing familial hypercholesterolemia (FH-Salerno)

Journal of lipid research, 1994-08, Vol.35 (8), p.1422-1430

1994

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Sensitivity and specificity of a triage score dedicated to trauma patients in a tertiary-level hospital: preliminary results

Critical care (London, England), 2007, Vol.11 (Suppl 2), p.P354-P354

2007

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Four novel partial deletions of LDL-receptor gene in Italian patients with familial hypercholesterolemia

Arteriosclerosis, thrombosis, and vascular biology, 1995-01, Vol.15 (1), p.81

1995

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Identification of regulatory residues of the yeast adenylyl cyclase

The EMBO journal, 1991-02, Vol.10 (2), p.349-359

1991

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Lipid control with low-dosage simvastatin in patients with moderate hypercholesterolaemia. An Italian multicentre double-blind placebo-controlled study

European heart journal, 1992-07, Vol.13 (suppl-B), p.11-16

1992

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Influence of beta(0)-thalassemia on the phenotypic expression of heterozygous familial hypercholesterolemia : a study of patients with familial hypercholesterolemia from Sardinia

Arteriosclerosis, thrombosis, and vascular biology, 2000-01, Vol.20 (1), p.236

2000

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Intact human lymphocyte membranes respond to muscarinic receptor stimulation by oxotremorine with marked changes in microviscosity and an increase in cyclic GMP

FEBS letters, 1985-11, Vol.192 (2), p.194-198

1985

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Measurement of fetal surfactant production by fluorescence polarization of amniotic fluid in complicated pregnancies

Clinica chimica acta, 1987-09, Vol.168 (2), p.137-142

1987

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RFLPs of the LDL-Receptor Gene: Their Use in the Diagnosis of FH and in Evaluation of Different Levels of Gene Expression on Normal Subjects

European journal of epidemiology, 1992-05, Vol.8 (S1), p.18-25

1992

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Biochemical characterization of the hepatic effects in mice and rats of 1,4-bis[2-(3,5-dichloropyridyloxy)]benzene, a hepatic neoplasm promoter

Toxicology and applied pharmacology, 1986-04, Vol.83 (2), p.379-385

1986

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Circadian rhythmicity of prolactin secretion in elderly subjects: changes during bromocriptine treatment

Journal of endocrinological investigation, 1981-07, Vol.4 (3), p.317-321

1981

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Apolipoprotein E epsilon 4 allele frequency is not increased in progressive supranuclear palsy

Neurology, 1995-09, Vol.45 (9), p.1764

1995

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P55 Effects of equal doses of pravastatin, simvastain and atorvastatin in heterozygous patients with familial hypercholesterolemia

Atherosclerosis, 1999-07, Vol.145, p.S24-S24

1999

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Thyrotropin and prolactin responses to different doses of thyrotropin-releasing hormone in depression

Neuropsychobiology, 1988-01, Vol.20 (3), p.120

1988

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Role of alveolar phospholipids in bleomycin-induced pulmonary fibrosis in the rat

Respiration, 1987, Vol.51 Suppl 1, p.23

1987

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Two homozygous children and several heterozygotes carrying FH Pavia mutation (deletion of exons 2–12 of LDL-R gene) in a large family from north-western Italy

Atherosclerosis, 1999-05, Vol.144, p.19-20

1999

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Neuroendocrinological signs of central neurotransmission disorders

Cephalalgia, 1983-08, Vol.3 (1_suppl), p.122-128

1983

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N-acetyl-β- d-glucosaminidase (NAG) levels in amniotic fluid or urine in prenatal and postnatal life

Early human development, 1986-12, Vol.14 (3), p.229-232

1986

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Effects of a single oral dose of phenobarbital on prolactin, growth hormone and luteinizing hormone in normal women

Acta endocrinologica (Copenhagen), 1983-07, Vol.103 (3), p.309

1983

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Physical activity modulates effects of some genetic polymorphisms affecting cardiovascular risk in men aged over 40 years

Analysis of LDL receptor gene mutations in Italian patients with homozygous familial hypercholesterolemia

Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia

Pseudodominance of lipoprotein lipase (LPL) deficiency due to a nonsense mutation (Tyr302>Term) in exon 6 of LPL gene in an Italian family from Sardinia (LPLOlbia)

Lipoprotein(a) levels in hemodialysis patients: relation to glucose intolerance and hemodialysis duration

Sepsis bundles: just think about it?

Partial duplication of the EGF precursor homology domain of the LDL-receptor protein causing familial hypercholesterolemia (FH-Salerno)

Sensitivity and specificity of a triage score dedicated to trauma patients in a tertiary-level hospital: preliminary results

Four novel partial deletions of LDL-receptor gene in Italian patients with familial hypercholesterolemia

Identification of regulatory residues of the yeast adenylyl cyclase

Lipid control with low-dosage simvastatin in patients with moderate hypercholesterolaemia. An Italian multicentre double-blind placebo-controlled study

Influence of beta(0)-thalassemia on the phenotypic expression of heterozygous familial hypercholesterolemia : a study of patients with familial hypercholesterolemia from Sardinia

Intact human lymphocyte membranes respond to muscarinic receptor stimulation by oxotremorine with marked changes in microviscosity and an increase in cyclic GMP

Measurement of fetal surfactant production by fluorescence polarization of amniotic fluid in complicated pregnancies

RFLPs of the LDL-Receptor Gene: Their Use in the Diagnosis of FH and in Evaluation of Different Levels of Gene Expression on Normal Subjects

Biochemical characterization of the hepatic effects in mice and rats of 1,4-bis[2-(3,5-dichloropyridyloxy)]benzene, a hepatic neoplasm promoter

Circadian rhythmicity of prolactin secretion in elderly subjects: changes during bromocriptine treatment

Apolipoprotein E epsilon 4 allele frequency is not increased in progressive supranuclear palsy

P55 Effects of equal doses of pravastatin, simvastain and atorvastatin in heterozygous patients with familial hypercholesterolemia

Thyrotropin and prolactin responses to different doses of thyrotropin-releasing hormone in depression

Role of alveolar phospholipids in bleomycin-induced pulmonary fibrosis in the rat

Two homozygous children and several heterozygotes carrying FH Pavia mutation (deletion of exons 2–12 of LDL-R gene) in a large family from north-western Italy

Neuroendocrinological signs of central neurotransmission disorders

N-acetyl-β- d-glucosaminidase (NAG) levels in amniotic fluid or urine in prenatal and postnatal life

Effects of a single oral dose of phenobarbital on prolactin, growth hormone and luteinizing hormone in normal women

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