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Nonalcoholic Fatty liver disease/non-alcoholic steatohepatitis in childhood: endocrine-metabolic "mal-programming".Partially hydrolyzed guar gum in pediatric functional abdominal painInflammatory Bowel Disease: Genetics, Epigenetics, and Pathogenesis.Autoimmune liver disease in Noonan Syndrome.A de novo 0.63 Mb 6q25.1 deletion associated with growth failure, congenital heart defect, underdeveloped cerebellar vermis, abnormal cutaneous elasticity and joint laxity.New patients with Temple syndrome caused by 14q32 deletion: Genotype-phenotype correlations and risk of thyroid cancerLMNA gene mutation as a model of cardiometabolic dysfunction: from genetic analysis to treatment response
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P50
description
onderzoeker
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researcher
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հետազոտող
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Italia Loddo
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Italia Loddo
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Italia Loddo
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Italia Loddo
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Italia Loddo
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Italia Loddo
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Italia Loddo
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Italia Loddo
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Italia Loddo
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Italia Loddo
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Italia Loddo
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Italia Loddo
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P106
P1153
37081050600
P31
P496
0000-0002-4400-1596