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Paradoxes in longevity: sequence analysis of mtDNA haplogroup J in centenarians
EUROPEAN JOURNAL OF HUMAN GENETICS
Low-density lipoprotein apheresis in a patient aged 3.5 years
ACTA PAEDIATRICA
Updated analysis of epsilon '/epsilon in the standard model with hadronic matrix elements from the chiral quark model - art. no. 056009
PHYSICAL REVIEW D
Educazione Ambientale nella scuola dell'infanzia: uno spazio per documentere, raccontare, riflettere e confrontarsi
Infanzia
Rapid sizing of microsatellite alleles by gel electrophoresis on microfabricated channels: Application to the D19S394 tetranucleotide repeat for cosegregation study of familial hypercholesterolemia
ELECTROPHORESIS
Autosomal recessive hypercholesterolemia caused by mutations in a putativeLDL receptor adaptor protein
SCIENCE
Hypocomplementemic type II membranoproliferative glomerulonephritis in a male patient with familial lecithin-cholesterol acyltransferase deficiency due to two different allelic mutations
NEPHRON
Phenotypic expression of familial hypobetalipoproteinemia in three kindreds with mutations of apolipoprotein B gene
JOURNAL OF LIPID RESEARCH
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease
ATHEROSCLEROSIS
Identification of an alternative transcript of ABCA1 gene in different human cell types
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Polymorphisms of drug-metabolizing enzymes in healthy nonagenarians and centenarians: Difference at GSTT1 locus
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Clinical expression of familial hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotype
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
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
A study of fatty liver disease and plasma lipoproteins in a kindred with familial hypobetalipoproteinemia due to a novel truncated form of apolipoprotein B (APO B-54.5)
JOURNAL OF HEPATOLOGY
Theory of the CP-violating parameter epsilon '/epsilon
REVIEWS OF MODERN PHYSICS
Pseudodominance of lipoprotein lipase (LPL) deficiency due to a nonsense mutation (Tyr(302) > Term) in exon 6 of LPL gene in an Italian family from Sardinia (LPLOlbia)
CLINICAL GENETICS
Gabrielle Suchon, a voluntary celibate life, or life without commitment
AUSTRALIAN JOURNAL OF FRENCH STUDIES
Analysis of LDL receptor gene mutations in Italian patients with homozygous familial hypercholesterolemia
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
Lattice matrix elements confronting the experimental value of epsilon '/epsilon
JOURNAL OF HIGH ENERGY PHYSICS
Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans
FASEB JOURNAL
GH, IGFBP-1, and IGFBP-3 response to oral glucose tolerance test in perimenopausal women: no influence of body mass index
MATURITAS
Apolipoprotein E and alpha-1-antichymotrypsin allele polymorphism in sporadic and familial Alzheimer's disease
NEUROSCIENCE LETTERS
A third major locus for autosomal dominant hypercholesterolemia maps to 1p34.1-p32
AMERICAN JOURNAL OF HUMAN GENETICS
p53 variants predisposing to cancer are present in healthy centenarians
AMERICAN JOURNAL OF HUMAN GENETICS
Gene/longevity association studies at four autosomal loci (REN, THO, PARP,SOD2)
EUROPEAN JOURNAL OF HUMAN GENETICS
B-]S-GAMMA-GAMMA TRANSITION IN SOFTLY BROKEN SUPERSYMMETRY
Physical review. D. Particles and fields
THE DELTA-I=1 2 RULE AND (B)OVER-CAP-B-K AT O(P(4)) IN THE CHIRAL EXPANSION/
Nuclear physics. B
EPSILON' EPSILON AT O(P(4)) IN THE CHIRAL EXPANSION/
Nuclear physics. B
SOMATOTROPIC AXIS AND BODY-WEIGHT IN PREMENOPAUSAL AND POSTMENOPAUSALWOMEN - EVIDENCE FOR A NEUROENDOCRINE DERANGEMENT, IN ABSENCE OF CHANGES OF INSULIN-LIKE-GROWTH-FACTOR BINDING-PROTEIN CONCENTRATIONS
Human reproduction
LABORATORY PARAMETERS OF ITALIAN CENTENARIANS
Archives of gerontology and geriatrics
ASSESSMENT OF SENSE OF TASTE IN ITALIAN CENTENARIANS
Archives of gerontology and geriatrics
ANALYSIS OF 2 DUPLICATIONS OF THE LDL RECEPTOR GENE AFFECTING INTRACELLULAR-TRANSPORT, CATABOLISM, AND SURFACE BINDING OF THE LDL RECEPTOR
Journal of lipid research
SIMPLE DETECTION OF A POINT MUTATION IN LDL RECEPTOR GENE CAUSING FAMILIAL HYPERCHOLESTEROLEMIA IN SOUTHERN ITALY BY ALLELE-SPECIFIC POLYMERASE-CHAIN-REACTION
Journal of lipid research
A DE-NOVO POINT MUTATION OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENEIN AN ITALIAN SUBJECT WITH PRIMARY HYPERCHOLESTEROLEMIA
Clinical genetics
LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE MUTATION IN A NONAGENARIAN
Clinical chemistry
GENE POLYMORPHISMS PREDICTING HIGH PLASMA-LEVELS OF COAGULATION AND FIBRINOLYSIS PROTEINS - A STUDY IN CENTENARIANS
Arteriosclerosis, thrombosis, and vascular biology
EFFICACY AND SAFETY OF ATORVASTATIN COMPA RED TO PRAVASTATIN IN PATIENTS WITH HYPERCHOLESTEROLEMIA
Perfusion
HORMONAL REPLACEMENT THERAPY AFFECTS CALCITONIN-GENE-RELATED PEPTIDE AND ATRIAL-NATRIURETIC-PEPTIDE SECRETION IN POSTMENOPAUSAL WOMEN
European journal of endocrinology
THE PHYSICS OF K-0-(K)OVER-BAR(0) MIXING - (B)OVER-CAP(K) AND DELTA-M-LS IN THE CHIRAL QUARK-MODEL
Nuclear physics. B
THROMBOTIC EVENTS IN RHEUMATOID-ARTHRITIS - RELATIONSHIP BETWEEN LIPOPROTEIN (A) AND ANTICARDIOLIPIN ANTIBODIES
Thrombosis and haemostasis
LIPID PROFILE AND ANTICARDIOLIPIN ANTIBODIES IN RHEUMATOID-ARTHRITIS PATIENTS WITH THROMBOTIC COMPLICATIONS
Thrombosis and haemostasis
EPIDEMIOLOGIC AND SOCIOECONOMIC ASPECTS OF ITALIAN CENTENARIANS
Archives of gerontology and geriatrics
LDL APHERESIS WITH DEXTRAN SULFATE AND ANGIOTENSIN RECEPTOR ANTAGONIST (LOSARTAN)
Artificial organs
LDL APHERESIS IN A HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIC CHILD AGED 4.5
Artificial organs
4 NOVEL MUTATIONS OF STEROL 27-HYDROXYLASE GENE IN ITALIAN PATIENTS WITH CEREBROTENDINOUS XANTHOMATOSIS
Journal of lipid research
DEVELOPMENT OF RAPID TESTS FOR POINT MUTATIONS IN LDL-RECEPTOR GENE CAUSING FAMILIAL HYPERCHOLESTEROLEMIA IN SOUTHERN ITALY
Atherosclerosis
APOE4 ALLELE FREQUENCY DECREASES WITH AGE AND IS LOWEST IN CENTENARIANS - RESULTS FROM A STUDY IN NORTHERN ITALY
Atherosclerosis
FH CLUSTERS IN SOUTHERN ITALY
Atherosclerosis
A TETRANUCLEOTIDE INSERTION IN EXON-8 OF LDL-RECEPTOR GENE IN AN ITALIAN FH PATIENT
Atherosclerosis
A FOUNDER-RELATED LDL RECEPTOR GENE MUTATION IN THE LIGURIA REGION OFITALY
Atherosclerosis
FAMILIAL HYPOBETALIPOPROTEINEMIA CAUSED BY A TRUNCATED APOLIPOPROTEIN-B (B-33.4) IS NOT PROTECTIVE AGAINST CAROTID-ARTERY DISEASE
Atherosclerosis
A DE-NOVO POINT MUTATION OF LDL RECEPTOR GENE
Atherosclerosis
MUTATIONS IN APOLIPOPROTEIN-B GENE IN FAMILIAL HYPOBETALIPOPROTEINEMIA
Atherosclerosis
MOLECULAR-GENETICS OF FAMILIAL HYPERCHOLESTEROLEMIA IN ITALY - OUTCOMES AND FUTURE-PROSPECTS
Atherosclerosis
ABNORMAL LDL METABOLISM IN A CASE OF RECESSIVE FORM OF FAMILIAL HYPERCHOLESTEROLEMIA
Atherosclerosis
APOLIPOPROTEIN-E (APO-E) PHENOTYPE AND GENOTYPE IN ISCHEMIC CEREBROVASCULAR-DISEASE (S), ALZHEIMER-DISEASE (AD) AND IN MULTI-INFARCTUAL DEMENTIA (MID)
Atherosclerosis
IN-VIVO LDL KINETIC AND IN-VITRO LDL METABOLISM IN A CASE OF RECESSIVE FAMILIAL HYPERCHOLESTEROLEMIA (RFH)
Atherosclerosis
VARIABLE PHENOTYPIC-EXPRESSION OF THE MUTATION PADUA-1 OF LDL-R GENE IN HOMOZYGOUS PATIENTS
Atherosclerosis
NEW MINUTE OR POINT MUTATIONS OF LDL-R GENE IN PATIENTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA
Atherosclerosis
A NEW MUTATION OF THE LECITHIN-CHOLESTEROL ACYLTRANSFERASE (LCAT) GENE CAUSING FISH-EYE DISEASE
Atherosclerosis
EFFICACY AND SAFETY OF ATORVASTATIN COMPARED TO PRAVASTATIN IN PATIENTS WITH HYPERCHOLESTEROLEMIA
Atherosclerosis
THE DD GENOTYPE OF THE ACE GENE, BUT NOT THE VAL VAL GENOTYPE OF THE MTHFR GENE, IS STRONGLY ASSOCIATED WITH CHD IN SUBJECTS WITH HETEROZYGOUS FH/
Atherosclerosis
3 MUTATIONS IN THE GLUCOKINASE GENE IN ITALIAN SUBJECTS WITH MATURITY-ONSET-DIABETES OF THE YOUNG (MODY)
Diabetes
PRESENCE OF SOLUBLE AMYLOID BETA-PEPTIDE PRECEDES AMYLOID PLAQUE-FORMATION IN DOWNS-SYNDROME
Nature medicine
A NEW ESTIMATE OF EPSILON' EPSILON
Nuclear physics. B
THE DELTA-S=1 WEAK CHIRAL LAGRANGIAN AS THE EFFECTIVE THEORY OF THE CHIRAL QUARK-MODEL
Nuclear physics. B
THE DELTA-I=1 2 SELECTION RULE
Nuclear physics. B
LIPOPROTEINS, ANTICARDIOLIPIN ANTIBODIES AND THROMBOTIC EVENTS IN RHEUMATOID-ARTHRITIS
Clinical and experimental rheumatology
MUTANT FACTOR-V (ARG506GLN) IN HEALTHY CENTENARIANS
Lancet
CEREBROTENDINOUS XANTHOMATOSIS CAUSED BY 2 NEW MUTATIONS OF THE STEROL-27-HYDROXYLASE GENE THAT DISRUPT MESSENGER-RNA SPLICING
Journal of lipid research
PARTIAL DELETION OF THE GENE ENCODING STEROL 27-HYDROXYLASE IN A SUBJECT WITH CEREBROTENDINOUS XANTHOMATOSIS
Journal of lipid research
2 NOVEL PARTIAL DELETIONS OF LDL-RECEPTOR GENE IN ITALIAN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA (FHSIRACUSA AND FHREGGIO EMILIA)
Atherosclerosis
SERUM-LIPID LEVELS DURING INTERFERON THERAPY IN PATIENTS WITH CHRONICHEPATITIS-C
Journal of interferon & cytokine research
4 NOVEL PARTIAL DELETIONS OF LDL-RECEPTOR GENE IN ITALIAN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA
Arteriosclerosis, thrombosis, and vascular biology
STUDYING EPSILON' EPSILON IN THE CHIRAL QUARK-MODEL - GAMMA(5)-SCHEMEINDEPENDENCE AND NLO HADRONIC MATRIX-ELEMENTS/
Nuclear physics. B
LIPID PROFILE AND ANTICARDIOLIPIN ANTIBODIES IN RHEUMATOID-ARTHRITIS
Clinical and experimental rheumatology
LIPOPROTEIN (A) AND ANTICARDIOLIPIN ANTIBODIES AS RISK-FACTORS FOR VASCULAR-DISEASE IN RHEUMATOID-ARTHRITIS
Thrombosis and haemostasis
SUPERSYMMETRIC PREDICTIONS FOR THE INCLUSIVE B-]S-GAMMA DECAY
Zeitschrift fur Physik. C, Particles and fields
LIPOPROTEIN (A) IS INCREASED IN ACUTE CORONARY SYNDROMES (UNSTABLE ANGINA-PECTORIS AND MYOCARDIAL-INFARCTION), BUT IT IS NOT PREDICTIVE OF THE SEVERITY OF CORONARY LESIONS
Clinical cardiology
APOLIPOPROTEIN-E EPSILON-4 ALLELE FREQUENCY IS NOT INCREASED IN PROGRESSIVE SUPRANUCLEAR PALSY
Neurology
PARTIAL DETECTION OF STEROL 27-HYDROXYLASE GENE IN AN ITALIAN PATIENTWITH CEREBROTENDINOUS XANTHOMATOSIS
Neurology
APOLIPOPROTEIN-E4 ALLELE FREQUENCY IS NOT INCREASED IN PROGRESSIVE SUPRANUCLEAR PALSY
Neurology
LIPOPROTEIN(A) LEVELS IN HEMODIALYSIS-PATIENTS - RELATION TO GLUCOSE-INTOLERANCE AND HEMODIALYSIS DURATION
Nephron
OCCURRENCE OF MULTIPLE ABERRANTLY SPLICED MESSENGER-RNAS OF THE LDL-RECEPTOR GENE UPON A DONOR SPLICE-SITE MUTATION THAT CAUSES FAMILIAL HYPERCHOLESTEROLEMIA (FHBENEVENTO)
Journal of lipid research
GEMFIBROZIL VERSUS SIMVASTATIN IN PRIMARY MODERATE HYPERCHOLESTEROLEMIA WITH LOW HIGH-DENSITY-LIPOPROTEIN CHOLESTEROL - A MULTICENTER COMPARISON - THE MULTICENTER ITALIAN GEMFIBROZIL SIMVASTATIN (MIGS) STUDY
NMCD. Nutrition Metabolism and Cardiovascular Diseases
THE RELEVANCE OF THE DIPOLE PENGUIN OPERATORS IN EPSILON'EPSILON
Physics letters. Section B
ON SOFT BREAKING AND CP PHASES IN THE SUPERSYMMETRIC STANDARD MODEL
Physics letters. Section B
A NEW MISSENSE MUTATION (CYS(297)-]PHE) OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR IN ITALIAN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA (FH(TRIESTE))
Human genetics
LINKAGE ANALYSIS DOES NOT SUPPORT A ROLE FOR GLUCOKINASE GENE IN THE ETIOLOGY OF TYPE-2 DIABETES-MELLITUS AMONG NORTH-WESTERN ITALIANS
Molecular and cellular endocrinology
REGIONAL CEREBRAL BLOOD-FLOW IN FAMILIAL HYPERCHOLESTEROLEMIA
Stroke
PARTIAL DUPLICATION OF THE EGF PRECURSOR HOMOLOGY DOMAIN OF THE LDL-RECEPTOR PROTEIN CAUSING FAMILIAL HYPERCHOLESTEROLEMIA (FH-SALERNO)
Journal of lipid research
CHORIONIC DNA ANALYSIS FOR THE PRENATAL-DIAGNOSIS OF FAMILIAL HYPERCHOLESTEROLEMIA
Human genetics
ALTERNATIVE SPLICING OF MUTANT LDL-RECEPTOR MESSENGER-RNA IN AN ITALIAN PATIENT WITH FAMILIAL HYPERCHOLESTEROLEMIA DUE TO A PARTIAL DELETION OF LDL-RECEPTOR GENE (FH(POTENZA))
Journal of lipid research
LINKAGE ANALYSIS OF GLUCOKINASE GENE WITH NIDDM IN ITALIAN PEDIGREES
Diabetes