| Nome |
# |
|
Multiple food hypersensitivity as a cause of refractory chronic constipation in adults, file e3ad891b-0587-da0e-e053-3705fe0a2b96
|
621
|
|
TERAPIA CON STATINE IN PAZIENTI SICILIANI AFFETTI DA IPERLIPIDEMIA FAMILIARE COMBINATA, file e3ad8915-e39f-da0e-e053-3705fe0a2b96
|
606
|
|
Myristic acid is associated to low plasma HDL cholesterol levels in a Mediterranean population and increases HDL catabolism by enhancing HDL particles trapping to cell surface proteoglycans in a liver hepatoma cell model, file e3ad8919-33ed-da0e-e053-3705fe0a2b96
|
393
|
|
Lomitapide: a novel drug for homozygous familial hypercholesterolemia, file e3ad8916-d927-da0e-e053-3705fe0a2b96
|
392
|
|
IgA anti-actin antibodies ELISA in coeliac disease: A multicentre study., file e3ad891a-9d8e-da0e-e053-3705fe0a2b96
|
376
|
|
Food hypersensitivity as a cause of rectal bleeding in adults, file e3ad891a-ee32-da0e-e053-3705fe0a2b96
|
373
|
|
Plasma calprotectin levels in patients suffering from acute pancreatitis., file e3ad891b-0355-da0e-e053-3705fe0a2b96
|
263
|
|
Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an “FCS score”, file e3ad891d-3a66-da0e-e053-3705fe0a2b96
|
253
|
|
Enhanced Lipid Peroxidation and Platelet Activation as Potential Contributors to Increased Cardiovascular Risk in the Low-HDL Phenotype, file e3ad8919-893a-da0e-e053-3705fe0a2b96
|
251
|
|
LIPASE MATURATION FACTOR 1 IS REQUIRED FOR ENDOTHELIAL LIPASE ACTIVITY, file e3ad8916-b4bf-da0e-e053-3705fe0a2b96
|
239
|
|
Rapid degradation of ABCA1 protein following cAMP withdrawal and treatment with PKA inhibitor suggests ABCA1 is a short-lived protein primarily regulated at the transcriptional level, file e3ad8923-d81d-da0e-e053-3705fe0a2b96
|
235
|
|
The ANP Genetic Variant RS5068 is Associated With a Favorable Cardiometabolic Phenotype in a Mediterranean Population, file e3ad8917-0ce9-da0e-e053-3705fe0a2b96
|
226
|
|
Determinants of enhanced thromboxane biosynthesis in renal transplantation, file e3ad8919-35ab-da0e-e053-3705fe0a2b96
|
218
|
|
Lack of Correlation of Plasma HDL With Fecal Cholesterol and Plasma Cholesterol Efflux Capacity Suggests Importance of HDL Functionality in Attenuation of Atherosclerosis, file e3ad891d-acd4-da0e-e053-3705fe0a2b96
|
191
|
|
Individual analysis of patients with HoFH participating in a phase 3 trial with lomitapide: The Italian cohort, file e3ad8919-344b-da0e-e053-3705fe0a2b96
|
190
|
|
CLINICAL CHARACTERISTICS AND PLASMA
LIPIDS IN SUBJECTS WITH FAMILIAL
COMBINED HYPOLIPIDEMIA:
A POOLED ANALYSIS, file e3ad8917-1507-da0e-e053-3705fe0a2b96
|
188
|
|
Role of Nutraceuticals in Hypolipidemic Therapy, file e3ad8917-d2c9-da0e-e053-3705fe0a2b96
|
162
|
|
Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score, file e3ad891e-5cea-da0e-e053-3705fe0a2b96
|
162
|
|
Exome sequencing in suspected monogenic dyslipidemias, file e3ad8917-b1a2-da0e-e053-3705fe0a2b96
|
156
|
|
Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN), file e3ad891b-da22-da0e-e053-3705fe0a2b96
|
149
|
|
Prothrombotic gene variants as risk factors of acute myocardial infarction in young women., file e3ad8916-5a09-da0e-e053-3705fe0a2b96
|
143
|
|
A NOVEL APOB MUTATION IDENTIFIED
BY EXOME SEQUENCING COSEGREGATES
WITH STEATOSIS, LIVER CANCER
AND HYPOCHOLESTEROLEMIA, file e3ad8917-150a-da0e-e053-3705fe0a2b96
|
143
|
|
Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study, file e3ad891b-c805-da0e-e053-3705fe0a2b96
|
143
|
|
RT-PCR and in situ hybridization analysis of apolipoprotein H expression in rat normal tissues, file e3ad8915-f813-da0e-e053-3705fe0a2b96
|
141
|
|
eNOS activation by HDL is impaired in genetic CETP deficiency, file e3ad8916-b4bd-da0e-e053-3705fe0a2b96
|
140
|
|
PREVALENCE OF ANGPTL3 AND APOB
GENE MUTATIONS IN SUBJECTS WITH
COMBINED HYPOLIPIDEMIA, file e3ad8917-1383-da0e-e053-3705fe0a2b96
|
136
|
|
The pathophysiology of intestinal lipoprotein production, file e3ad8917-b653-da0e-e053-3705fe0a2b96
|
121
|
|
Plasma levels of lipoproteins and apolipoproteins in congenital hypothyroidism: effects of L-thyroxine substitution therapy, file e3ad8916-f667-da0e-e053-3705fe0a2b96
|
107
|
|
Hyperalphalipoproteinemia and Beyond: The Role of HDL in Cardiovascular Diseases, file e3ad8927-2dd8-da0e-e053-3705fe0a2b96
|
77
|
|
Lipoprotein(a) Genotype Influences the Clinical Diagnosis of Familial Hypercholesterolemia, file a949c7ff-c4f5-4be1-91e4-a40a0aba7829
|
74
|
|
rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography, file 1b4920a3-5d2f-43b3-8096-705f21f2486e
|
54
|
|
PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study, file e3ad8920-7873-da0e-e053-3705fe0a2b96
|
50
|
|
RUOLO DEL POLIMORFISMO ILE148MET DEL GENE PNPLA3 NELLA STEATOSI ASSOCIATA ALLA IPOBETALIPOPROTEINEMIA FAMILIARE, file e3ad8917-6c13-da0e-e053-3705fe0a2b96
|
48
|
|
An unusual case of chronic diarrhea: a case report, file f7b6bc8d-9844-4344-9ec9-b456090a7914
|
46
|
|
Lipoprotein abnormalities in chronic kidney disease and renal transplantation, file e3ad8927-2858-da0e-e053-3705fe0a2b96
|
45
|
|
Association between plasma lipid levels and migraine in subjects aged > or =50 years: preliminary data from the Zabùt Aging Project, file e3ad8915-fa14-da0e-e053-3705fe0a2b96
|
43
|
|
Long-term efficacy of lipoprotein apheresis and lomitapide in the treatment of homozygous familial hypercholesterolemia (HoFH): a cross-national retrospective survey, file e3ad8927-72bb-da0e-e053-3705fe0a2b96
|
43
|
|
Twelve Variants Polygenic Score for Low-Density Lipoprotein Cholesterol Distribution in a Large Cohort of Patients With Clinically Diagnosed Familial Hypercholesterolemia With or Without Causative Mutations, file e3ad8928-1e00-da0e-e053-3705fe0a2b96
|
38
|
|
Efficacy and safety of lomitapide in familial chylomicronaemia syndrome, file 9e6ef88d-38b6-43a2-97ca-4ddb44dd95af
|
36
|
|
A subgroup analysis of the ODYSSEY APPRISE study: Safety and efficacy of alirocumab in the Italian cohort, file 70a0d8d3-eb6a-419b-8752-5cf40a58c390
|
25
|
|
Effects of PCSK9 inhibitors on HDL cholesterol efflux and serum cholesterol loading capacity in familial hypercholesterolemia subjects: a multi-lipid-center real-world evaluation, file 33366139-af4a-4bac-aa4c-7ddbaf8ca576
|
23
|
|
Metabolomic analysis of plasma from Alzheimer disease patients, file e3ad8917-11c2-da0e-e053-3705fe0a2b96
|
22
|
|
LA LIPIDOMICA DELLA NON ALCOHOLIC FATTY LIVER DISEASE: ANALISI DELLA CINETICA DELL’ACIDO PALMITICO MEDIANTE L’USO DI UN ISOTOPO STABILE IN UN MODELLO IN VITRO, file e3ad8917-6478-da0e-e053-3705fe0a2b96
|
21
|
|
DeepSRE: Identification of sterol responsive elements and nuclear transcription factors Y proximity in human DNA by Convolutional Neural Network analysis, file e3ad8927-f09c-da0e-e053-3705fe0a2b96
|
17
|
|
NEXT GENERATION SEQUENCIN: A NEW METHODOLOGICAL APPROACH FOR THE MOLECULAR DIAGNOSIS OF GENETIC DYSLIPIDEMIAS, file e3ad8917-70ec-da0e-e053-3705fe0a2b96
|
16
|
|
FragClust and TestClust, two informatics tools for chemical structure hierarchical clustering analysis applied to lipidomics. The example of Alzheimer's disease, file e3ad8919-4046-da0e-e053-3705fe0a2b96
|
16
|
|
Efficacy of Long-Term Treatment of Autosomal Recessive Hypercholesterolemia With Lomitapide: A Subanalysis of the Pan-European Lomitapide Study, file 66dce40a-9b7c-4330-9db3-2bb0bc75281c
|
15
|
|
Long-term hepatic safety of lomitapide in homozygous familial hypercholesterolaemia, file cf03ee1d-8d94-486b-9442-96ac8a88e25d
|
13
|
|
Circulating Molecular Chaperones in Subjects with Amnestic Mild Cognitive Impairment and Alzheimer's Disease: Data from the Zabùt Aging Project, file e3ad891e-8b33-da0e-e053-3705fe0a2b96
|
12
|
|
Identification of a novel ANGPTL3 mutation splicing associeted to severe hypobetalipoproteinemia, file e3ad8917-1389-da0e-e053-3705fe0a2b96
|
11
|
|
FUNCTIONAL EFFECT OF NOVEL AMINO ACID VARIANTS OF APOLIPOPROTEIN B IN FAMILIAL HYPOBETALIPOPROTEINEMIA, file e3ad8917-0e74-da0e-e053-3705fe0a2b96
|
10
|
|
Six novel mutations of the LDL receptor gene in FH kindred of Sicilian and Paraguayan descent, file 0c1f6393-ac16-4da2-a156-6099b58dfde5
|
7
|
|
Automated untargeted stable isotope assisted lipidomics of liver cells on high glucose shows alteration of sphingolipid kinetics, file e3ad8923-f441-da0e-e053-3705fe0a2b96
|
7
|
|
FUNCTIONAL CHARACTERIZATION OF NOVEL AMINO ACID VARIANTS IN APOB IN FAMILIAL HYPOBETALIPOPROTEINEMIA, file e3ad8917-1518-da0e-e053-3705fe0a2b96
|
6
|
|
Therapeutic options for homozygous familial hypercholesterolemia: the role of Lomitapide, file e3ad8920-b1d9-da0e-e053-3705fe0a2b96
|
6
|
|
Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study, file e3ad8921-c809-da0e-e053-3705fe0a2b96
|
6
|
|
APOC-III: a Gatekeeper in Controlling Triglyceride Metabolism, file 58badf58-bd87-4c2c-bc1e-3b7884b20c50
|
5
|
|
Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study, file 8ae92fcd-37b3-4ca4-8148-f6ab90e576f1
|
5
|
|
Clinical, molecular and functional characterization of two novel mutations associated to compound heterozygous FHBL, file e3ad8917-11ce-da0e-e053-3705fe0a2b96
|
5
|
|
PCSK9-D374Y mediated LDL-R degradation can be functionally inhibited by EGF-A and truncated EGF-A peptides: An in vitro study, file e3ad8921-1937-da0e-e053-3705fe0a2b96
|
5
|
|
Heparin induces an accumulation of atherogenic lipoproteins during hemodialysis in normolipidemic end-stage renal disease patients., file e3ad8921-a24e-da0e-e053-3705fe0a2b96
|
5
|
|
Lomitapide does not alter PCSK9 and Lp(a) levels in homozygous familial hypercholesterolemia patients: Analysis on cytokines and lipid profile, file e3ad8927-2402-da0e-e053-3705fe0a2b96
|
5
|
|
Diagnosis of familial hypercholesterolemia in a large cohort of Italian genotyped hypercholesterolemic patients, file e3ad8928-36f5-da0e-e053-3705fe0a2b96
|
5
|
|
EFFICACY AND SAFETY OF LOMITAPIDE IN HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA: THE PAN-EUROPEAN RETROSPECTIVE OBSERVATIONAL STUDY, file e3ad8928-93b7-da0e-e053-3705fe0a2b96
|
5
|
|
Novel LDL-cholesterol lowering therapies: A step forward a personalized medicine, file 29a16c92-02cb-4c4a-b539-023828fce24a
|
4
|
|
Refinement of the diagnostic approach for the identification of children and adolescents affected by familial hypercholesterolemia: Evidence from the LIPIGEN study, file 3ae68349-f0b3-45b7-a1c9-e8fe1049a4a3
|
4
|
|
Circulating Molecular Chaperones in Subjects with Amnestic Mild Cognitive Impairment and Alzheimer's Disease: Data from the Zabùt Aging Project, file a3ea673a-0a55-4964-bb30-03b570d06b02
|
4
|
|
Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing, file e3ad891b-041d-da0e-e053-3705fe0a2b96
|
4
|
|
Efficacy of Lomitapide in the Treatment of Familial Homozygous Hypercholesterolemia: Results of a Real-World Clinical Experience in Italy, file e3ad891b-b8bb-da0e-e053-3705fe0a2b96
|
4
|
|
Erratum: FragClust and TestClust, two informatics tools for chemical structure hierarchical clustering analysis applied to lipidomics. The example of Alzheimer's disease (Analytical and Bioanalytical Chemistry DOI: 10.1007/s00216-015-9229-6), file e3ad8922-09f4-da0e-e053-3705fe0a2b96
|
4
|
|
EFFECTIVENESS AND SAFETY OF LOMITAPIDE IN A PATIENT WITH FAMILIAL CHYLOMICRONEMIA SYNDROME, file e3ad8928-657c-da0e-e053-3705fe0a2b96
|
4
|
|
Changes in plasma lipids and low-density lipoprotein peak particle size during and after acute myocardial infarction, file e3ad8916-681c-da0e-e053-3705fe0a2b96
|
3
|
|
VASCULOPROTECTIVE FUNCTION OF HDL
FROM CETP-DEFICIENT SUBJECTS, file e3ad8917-1381-da0e-e053-3705fe0a2b96
|
3
|
|
Mutations in MTP gene in abeta- and hypobeta-lipoproteinemia., file e3ad8919-9070-da0e-e053-3705fe0a2b96
|
3
|
|
An unexplained congenital disorder of glycosylation-II in a child with neurohepatic involvement, hypercholesterolemia and hypoceruloplasminemia, file e3ad891d-19e1-da0e-e053-3705fe0a2b96
|
3
|
|
Effectiveness and safety of lomitapide in a patient with familial chylomicronemia syndrome, file e3ad8923-f81b-da0e-e053-3705fe0a2b96
|
3
|
|
rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography, file e3ad8927-72bd-da0e-e053-3705fe0a2b96
|
3
|
|
Genetically determined hypercholesterolaemia results into premature leucocyte telomere length shortening and reduced haematopoietic precursors, file e3ad8927-c99b-da0e-e053-3705fe0a2b96
|
3
|
|
Lifestyle versus ezetimibe plus lifestyle in patients with biopsy-proven non-alcoholic steatohepatitis (LISTEN): A double-blind randomised placebo-controlled trial, file e3ad8927-ee42-da0e-e053-3705fe0a2b96
|
3
|
|
Statin-induced autoimmune myositis: a proposal of an "experience-based" diagnostic algorithm from the analysis of 69 patients, file bbcc7f4f-14a5-4deb-b803-3f6cd9e297a1
|
2
|
|
Variable phenotypic expression of chylomicron retention disease in a kindred carrying a mutation of the Sara2 gene, file e3ad8915-8311-da0e-e053-3705fe0a2b96
|
2
|
|
Nutritional characteristics of a rural Southern Italy population: the Ventimiglia di Sicilia Project, file e3ad8916-6a2f-da0e-e053-3705fe0a2b96
|
2
|
|
ApoE polymorphism in a small Mediterranean island: Relationships with plasma lipids, lipoproteins and LDL particle size, file e3ad8916-6b2e-da0e-e053-3705fe0a2b96
|
2
|
|
Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH gene., file e3ad8916-6b30-da0e-e053-3705fe0a2b96
|
2
|
|
CD14 C(-260)>T gene polymorphism is not a risk factor for myocardial infarction, file e3ad8916-79e4-da0e-e053-3705fe0a2b96
|
2
|
|
CD14 C(-260)>T gene polymorphism is not a risk factor for myocardial infarction, file e3ad8916-79f9-da0e-e053-3705fe0a2b96
|
2
|
|
Transient chylomicronemia preceding the onset of insulin-dependent diabetes in a young girl with no humoral markers of islet autoimmunity., file e3ad8916-8327-da0e-e053-3705fe0a2b96
|
2
|
|
Effects of Steatosis on Hepatic Hemodynamics in Patients with Metabolic Syndrome, file e3ad8917-b656-da0e-e053-3705fe0a2b96
|
2
|
|
Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia, file e3ad8917-bd19-da0e-e053-3705fe0a2b96
|
2
|
|
A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol., file e3ad8919-3c44-da0e-e053-3705fe0a2b96
|
2
|
|
Accumulation of apoE-enriched triglyceride-rich lipoproteins in patients with coronary artery disease, file e3ad891a-26b8-da0e-e053-3705fe0a2b96
|
2
|
|
HDL subfractions distribution in renal transplant recipients: Lack of evidence of a reduction of HDL2 particles, file e3ad891d-daf7-da0e-e053-3705fe0a2b96
|
2
|
|
Homozygous familial hypercholesterolemia in Italy: Clinical and molecular features, file e3ad8923-de4c-da0e-e053-3705fe0a2b96
|
2
|
|
NPC1L1 and ABCG5/8 induction explain synergistic fecal cholesterol excretion in ob/ob mice co-treated with PPAR-α and LXR agonists, file e3ad8923-ffa1-da0e-e053-3705fe0a2b96
|
2
|
|
Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred, file e3ad8926-1e5f-da0e-e053-3705fe0a2b96
|
2
|
|
Lack of phenotypic additive effect of familial defective apolipoprotein B3531 in familial hypercholesterolaemia, file e3ad8927-8ccd-da0e-e053-3705fe0a2b96
|
2
|
|
PCSK9-D374Y MEDIATED LDL-R DEGRADATION CAN BE FUNCTIONALLY INHIBITED BY EGF-A AND TRUNCATED EGF-A PEPTIDES. AN IN VITRO STUDY, file e3ad8928-694f-da0e-e053-3705fe0a2b96
|
2
|
|
PREVALENCE OF STATIN INTOLERANCE IN A COHORT OF OUTPATIENTS IN A LIPID CLINIC, file e3ad8928-b150-da0e-e053-3705fe0a2b96
|
2
|
|
Comparison of two polygenic risk score to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjects: Polygenic hypocholesterolemias, file e3ad8928-d06e-da0e-e053-3705fe0a2b96
|
2
|
|
Lp(a): a genetic cause of clinical FH in children, file 0772acc3-377c-491f-a0d0-96a087d5b874
|
1
|
| Totale |
7.638 |