Search Results - "del Giudice, E. Miraglia"

Association between non-alcoholic fatty liver disease and subclinical hypothyroidism in children with obesity by Di Sessa, A., Cembalo Sambiase Sanseverino, N., De Simone, R. F., Marrapodi, M. M., Cirillo, G., Umano, G. R., Guarino, S., Papparella, A., Miraglia del Giudice, E., Marzuillo, P.

“…Purpose We aimed (i) evaluating the relationship between non-alcoholic fatty liver disease (NAFLD) and thyroid function tests, (ii) testing if the relationship…”
Get full text

High uric acid, reduced glomerular filtration rate and non-alcoholic fatty liver in young people with obesity by Di Bonito, P., Valerio, G., Licenziati, M. R., Miraglia del Giudice, E., Baroni, M. G., Morandi, A., Maffeis, C., Campana, G., Spreghini, M. R., Di Sessa, A., Morino, G., Crinò, A., Chiesa, C., Pacifico, L., Manco, M.

“…Objective To evaluate the association between high uric acid (UA), reduced estimated glomerular filtration rate (eGFR), and non-alcoholic fatty liver disease…”
Get full text

A new DLK1 defect in a family with idiopathic central precocious puberty: elucidation of the male phenotype by Palumbo, S., Cirillo, G., Sanchez, G., Aiello, F., Fachin, A., Baldo, F., Pellegrin, M. C., Cassio, A., Salerno, M., Maghnie, M., Faienza, M. F., Wasniewska, M., Fintini, D., Giacomozzi, C., Ciccone, S., Miraglia del Giudice, E., Tornese, G., Grandone, A.

“…Purpose We aimed to investigate a cohort of female and male patients with idiopathic central precocious puberty (CPP), negative for Makorin Ring Finger Protein…”
Get full text

Impaired fasting glucose and impaired glucose tolerance in children and adolescents with overweight/obesity by Di Bonito, P., Pacifico, L., Chiesa, C., Valerio, G., Miraglia del Giudice, E., Maffeis, C., Morandi, A., Invitti, C., Licenziati, M. R., Loche, S., Tornese, G., Franco, F., Manco, M., Baroni, M. G.

“…Objective To investigate in a large sample of overweight/obese (OW/OB) children and adolescents the prevalence of prediabetic phenotypes such as impaired…”
Get full text

Effect of body mass index reduction on serum hepcidin levels and iron status in obese children by Amato, A, Santoro, N, Calabrò, P, Grandone, A, Swinkels, D.W, Perrone, L, Miraglia del Giudice, E

“…Iron deficiency has been linked to obesity. Hepcidin is the main regulator of iron homeostasis and is higher in obese children compared to controls. To gain…”
Get full text

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 by Di Bonito, P, Valerio, G, Grugni, G, Licenziati, M.R, Maffeis, C, Manco, M, Miraglia del Giudice, E, Pacifico, L, Pellegrin, M.C, Tomat, M, Baroni, M.G

“…Abstract Background and aims Lipid ratios to estimate atherosclerotic disease risk in overweight/obese children are receiving great attention. We aimed to…”
Get full text

Association between cannabinoid receptor type 2 Q63R variant and oligo/polyarticular juvenile idiopathic arthritis by Bellini, G, Olivieri, AN, Grandone, A, Alessio, M, Gicchino, MF, Nobili, B, Perrone, L, Maione, S, Miraglia del Giudice, E, Rossi, F

“…Objectives: To investigate whether the functional variant Q63R of the cannabinoid 2 (CB2) receptor is associated with susceptibility to oligo/poly-articular…”
Get full text

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 by Cirillo, G., Marini, R., Ito, S., Wakamatsu, K., Scianguetta, S., Bizzarri, C., Romano, A., Grandone, A., Perrone, L., Cappa, M., Miraglia del Giudice, E.

Get full text

Molecular screening of the ghrelin gene in Italian obese children: the Leu72Met variant is associated with an earlier onset of obesity by DEL GIUDICE, E. Miraglia, SANTORO, N, CIRILLO, G, RAIMONDO, P, GRANDONE, A, D'ANIELLO, A, DI NARDO, A, PERRONE, L

“…To test whether ghrelin variants could play a role in modulating some aspects of the obese phenotype during childhood. We screened the ghrelin gene in 300…”
Get full text

Subclinical hypothyroidism and myocardial function in obese children by Brienza, C, Grandone, A, Di Salvo, G, Corona, A.M, Di Sessa, A, Pascotto, C, Calabrò, R, Toraldo, R, Perrone, L, Miraglia del Giudice, E

“…Abstract Background and aims Pediatric obesity is an important health problem representing a major public health concern worldwide in the last decades. An…”
Get full text

New treatment modalities for obesity by Grandone, A., Di Sessa, A., Umano, G.R., Toraldo, R., Miraglia del Giudice, E.

“…The treatment of childhood obesity represents a greater challenge for pediatricians. To date, it is multidisciplinary, including behavioral, dietary,…”
Get full text

Phenotypes of prediabetes and metabolic risk in Caucasian youths with overweight or obesity by Di Bonito, P., Licenziati, M. R., Corica, D., Wasniewska, M. G., Di Sessa, A., del Giudice, E. Miraglia, Morandi, A., Maffeis, C., Faienza, M. F., Mozzillo, E., Calcaterra, V., Franco, F., Maltoni, G., Valerio, G.

“…Purpose To assess the prevalence of pre-diabetes phenotypes, i.e., impaired fasting glucose (IFG), impaired glucose tolerance (IGT), increased HbA1c (IA1c),…”
Get full text

MKRN3 circulating levels in girls with central precocious puberty caused by MKRN3 gene mutations by Aiello, F., Palumbo, S., Cirillo, G., Tornese, G., Fava, D., Wasniewska, M., Faienza, M. F., Bozzola, M., Luongo, C., Festa, A., Miraglia del Giudice, E., Grandone, A.

“…Purpose MKNR3 is a paternally expressed gene whose mutations are the main cause of central precocious puberty (CPP). Protein circulating levels can be easily…”
Get full text

TM6SF2 Glu167Lys polymorphism is associated with low levels of LDL-cholesterol and increased liver injury in obese children by Grandone, A., Cozzolino, D., Marzuillo, P., Cirillo, G., Di Sessa, A., Ruggiero, L., Di Palma, M. R., Perrone, L., Miraglia del Giudice, E.

“…Summary Background The Glu167Lys (E167K) transmembrane 6 superfamily member 2 (TM6SF2) variant has been associated with liver steatosis, high alanine…”
Get full text

Screening for hypertension in young people with obesity: Feasibility in the real life by Di Bonito, P., Licenziati, M.R., Morandi, A., Maffeis, C., Miraglia del Giudice, E., Di Sessa, A., Campana, G., Wasniewska, M., Corica, D., Valerio, G.

“…Screening for pediatric hypertension (HTN) is based on several measurements of blood pressure (BP) in different visits. We aimed to assess its feasibility in…”
Get full text

Association between MBOAT7 rs641738 polymorphism and non-alcoholic fatty liver in overweight or obese children by Zusi, C., Morandi, A., Maguolo, A., Corradi, M., Costantini, S., Mosca, A., Crudele, A., Mantovani, A., Alisi, A., Miraglia del Giudice, E., Targher, G., Maffeis, C.

“…The association between non-alcoholic fatty liver (NAFL) and the variant rs641738 within the membrane bound O-acyltransferase domain-containing 7 (MBOAT7) gene…”
Get full text

Adolescents carrying a missense mutation in the CART gene exhibit increased anxiety and depression by Miraglia del Giudice, E., Santoro, N., Fiumani, P., Dominguez, G., Kuhar, M. J., Perrone, L.

“…A Leu34Phe mutation in the cocaine‐ and amphetamine‐regulated transcript (CART) gene has been associated with severe early‐onset obesity in an affected family…”
Get full text

Preclinical signs of liver and cardiac damage in youth with metabolically healthy obese phenotype by Di Bonito, P., Miraglia del Giudice, E., Chiesa, C., Licenziati, M.R., Manco, M., Franco, F., Tornese, G., Baroni, M.G., Morandi, A., Maffeis, C., Pacifico, L., Valerio, G.

“…We aimed to evaluate whether the metabolically healthy obese (MHO) phenotype was associated with hepatic steatosis (HS) or left ventricular hypertrophy (LVH)…”
Get full text

Patients affected by dent disease 2 could be predisposed to hidradenitis suppurativa by Marzuillo, P., Piccolo, V., Mascolo, M., Apicella, A., Argenziano, G., Della Vecchia, N., Guarino, S., Miraglia del Giudice, E., La Manna, A.

Get full text

Abdominal fat interacts with PNPLA3 I148M, but not with the APOC3 variant in the pathogenesis of liver steatosis in chronic hepatitis C by Zampino, R., Coppola, N., Cirillo, G., Boemio, A., Pisaturo, M., Marrone, A., Macera, M., Sagnelli, E., Perrone, L., Adinolfi, L. E., Miraglia del Giudice, E.

“…Summary The patatin‐like phospholipase domain‐containing 3 gene (PNPLA3) and the apolipoprotein C3 gene (APOC3) have been studied in relation to liver…”
Get full text