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Association between non-alcoholic fatty liver disease and subclinical hypothyroidism in children with obesity

Journal of endocrinological investigation, 2023-09, Vol.46 (9), p.1835-1842

2023

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High uric acid, reduced glomerular filtration rate and non-alcoholic fatty liver in young people with obesity

Journal of endocrinological investigation, 2020-04, Vol.43 (4), p.461-468

2020

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A new DLK1 defect in a family with idiopathic central precocious puberty: elucidation of the male phenotype

Journal of endocrinological investigation, 2023-06, Vol.46 (6), p.1233-1240

2023

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Impaired fasting glucose and impaired glucose tolerance in children and adolescents with overweight/obesity

Journal of endocrinological investigation, 2017-04, Vol.40 (4), p.409-416

2017

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Effect of body mass index reduction on serum hepcidin levels and iron status in obese children

International Journal of Obesity, 2010-12, Vol.34 (12), p.1772-1774

2010

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Comparison of non-HDL-cholesterol versus triglycerides-to-HDL-cholesterol ratio in relation to cardiometabolic risk factors and preclinical organ damage in overweight/obese children: The CARITALY study

Nutrition, metabolism, and cardiovascular diseases, 2015-05, Vol.25 (5), p.489-494

2015

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Association between cannabinoid receptor type 2 Q63R variant and oligo/polyarticular juvenile idiopathic arthritis

Scandinavian journal of rheumatology, 2015-07, Vol.44 (4), p.284-287

2015

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Lack of red hair phenotype in a North-African obese child homozygous for a novel POMC null mutation: nonsense-mediated decay RNA evaluation and hair pigment chemical analysis

British journal of dermatology (1951), 2012-12, Vol.167 (6), p.1393-1395

2012

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New treatment modalities for obesity

Baillière's best practice & research. Clinical endocrinology & metabolism, 2018-08, Vol.32 (4), p.535-549

2018

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Molecular screening of the ghrelin gene in Italian obese children: the Leu72Met variant is associated with an earlier onset of obesity

International Journal of Obesity, 2004-03, Vol.28 (3), p.447-450

2004

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Phenotypes of prediabetes and metabolic risk in Caucasian youths with overweight or obesity

Journal of endocrinological investigation, 2022-09, Vol.45 (9), p.1719-1727

2022

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MKRN3 circulating levels in girls with central precocious puberty caused by MKRN3 gene mutations

Journal of endocrinological investigation, 2024-06, Vol.47 (6), p.1477-1485

2024

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TM6SF2 Glu167Lys polymorphism is associated with low levels of LDL-cholesterol and increased liver injury in obese children

Pediatric obesity, 2016-04, Vol.11 (2), p.115-119

2016

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Subclinical hypothyroidism and myocardial function in obese children

Nutrition, metabolism, and cardiovascular diseases, 2013-09, Vol.23 (9), p.898-902

2013

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Association between MBOAT7 rs641738 polymorphism and non-alcoholic fatty liver in overweight or obese children

Nutrition, metabolism, and cardiovascular diseases, 2021-05, Vol.31 (5), p.1548-1555

2021

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Screening for hypertension in young people with obesity: Feasibility in the real life

Nutrition, metabolism, and cardiovascular diseases, 2022-05, Vol.32 (5), p.1301-1307

2022

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Preclinical signs of liver and cardiac damage in youth with metabolically healthy obese phenotype

Nutrition, metabolism, and cardiovascular diseases, 2018-12, Vol.28 (12), p.1230-1236

2018

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Patients affected by dent disease 2 could be predisposed to hidradenitis suppurativa

Journal of the European Academy of Dermatology and Venereology, 2018-08, Vol.32 (8), p.e309-e311

2018

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Abdominal fat interacts with PNPLA3 I148M, but not with the APOC3 variant in the pathogenesis of liver steatosis in chronic hepatitis C

Journal of viral hepatitis, 2013-08, Vol.20 (8), p.517-523

2013

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Adolescents carrying a missense mutation in the CART gene exhibit increased anxiety and depression

Depression and anxiety, 2006, Vol.23 (2), p.90-92

2006

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Expanding the phenotype of RTTN variations: a new family with primary microcephaly, severe growth failure, brain malformations and dermatitis

Clinical genetics, 2016-11, Vol.90 (5), p.445-450

2016

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‘Frequently recurring’ nocturnal polyuria is predictive of response to desmopressin in monosymptomatic nocturnal enuresis in childhood

Journal of pediatric urology, 2019-04, Vol.15 (2), p.166.e1-166.e7

2019

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White blood cell count may identify abnormal cardiometabolic phenotype and preclinical organ damage in overweight/obese children

Nutrition, metabolism, and cardiovascular diseases, 2016-06, Vol.26 (6), p.502-509

2016

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Screening for impaired glucose tolerance in obese children and adolescents: a validation and implementation study

Pediatric obesity, 2014-02, Vol.9 (1), p.17-25

2014

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A new index to simplify the screening of hypertension in overweight or obese youth

Nutrition, metabolism, and cardiovascular diseases, 2017-09, Vol.27 (9), p.830-835

2017

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Association between non-alcoholic fatty liver disease and subclinical hypothyroidism in children with obesity

High uric acid, reduced glomerular filtration rate and non-alcoholic fatty liver in young people with obesity

A new DLK1 defect in a family with idiopathic central precocious puberty: elucidation of the male phenotype

Impaired fasting glucose and impaired glucose tolerance in children and adolescents with overweight/obesity

Effect of body mass index reduction on serum hepcidin levels and iron status in obese children

Comparison of non-HDL-cholesterol versus triglycerides-to-HDL-cholesterol ratio in relation to cardiometabolic risk factors and preclinical organ damage in overweight/obese children: The CARITALY study

Association between cannabinoid receptor type 2 Q63R variant and oligo/polyarticular juvenile idiopathic arthritis

Lack of red hair phenotype in a North-African obese child homozygous for a novel POMC null mutation: nonsense-mediated decay RNA evaluation and hair pigment chemical analysis

New treatment modalities for obesity

Molecular screening of the ghrelin gene in Italian obese children: the Leu72Met variant is associated with an earlier onset of obesity

Phenotypes of prediabetes and metabolic risk in Caucasian youths with overweight or obesity

MKRN3 circulating levels in girls with central precocious puberty caused by MKRN3 gene mutations

TM6SF2 Glu167Lys polymorphism is associated with low levels of LDL-cholesterol and increased liver injury in obese children

Subclinical hypothyroidism and myocardial function in obese children

Association between MBOAT7 rs641738 polymorphism and non-alcoholic fatty liver in overweight or obese children

Screening for hypertension in young people with obesity: Feasibility in the real life

Preclinical signs of liver and cardiac damage in youth with metabolically healthy obese phenotype

Patients affected by dent disease 2 could be predisposed to hidradenitis suppurativa

Abdominal fat interacts with PNPLA3 I148M, but not with the APOC3 variant in the pathogenesis of liver steatosis in chronic hepatitis C

Adolescents carrying a missense mutation in the CART gene exhibit increased anxiety and depression

Expanding the phenotype of RTTN variations: a new family with primary microcephaly, severe growth failure, brain malformations and dermatitis

‘Frequently recurring’ nocturnal polyuria is predictive of response to desmopressin in monosymptomatic nocturnal enuresis in childhood

White blood cell count may identify abnormal cardiometabolic phenotype and preclinical organ damage in overweight/obese children

Screening for impaired glucose tolerance in obese children and adolescents: a validation and implementation study

A new index to simplify the screening of hypertension in overweight or obese youth

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