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Fingerprint Dive into the research topics where Andrea Bartuli is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

Medicine & Life Sciences

Exome
Mutation
Hyperlipoproteinemia Type II
Genes
Beckwith-Wiedemann Syndrome
Methylation
Lipids
Hyperammonemia
Newborn Infant
Genetic Association Studies
Hypertriglyceridemia
Liver
Fetal Development
Down Syndrome
Maple Syrup Urine Disease
Triglycerides
Inborn Errors Metabolism
Lipoprotein Lipase
LDL Cholesterol
Incidental Findings
Obesity
Inborn Genetic Diseases
Plasminogen
Neonatal Intensive Care Units
Uniparental Disomy
Pediatrics
Phenotype
Hyperlipoproteinemia Type I
Dialysis
Atherosclerosis
Dyslipidemias
Hypobetalipoproteinemia, Familial, Apolipoprotein B
Critical Illness
Italy
Lipoproteins
Retinitis Pigmentosa
Coma
Renal Dialysis
Hypoglycemia
Therapeutics
Adenylosuccinate Lyase
Netherton Syndrome
Missense Mutation
Blood Component Removal
Essential Osteolysis
Ornithine Carbamoyltransferase Deficiency Disease
Basal Ganglia
Early Diagnosis
Hypercholesterolemia
Thalamus