Lorenzo Iughetti
A5075683382- Growth Hormone and Insulin-like Growth Factors
- Diabetes Management and Research
- Diabetes and associated disorders
- Genetic Syndromes and Imprinting
- Lipoproteins and Cardiovascular Health
- Pancreatic function and diabetes
- Obesity, Physical Activity, Diet
- Neonatal Respiratory Health Research
- Sexual Differentiation and Disorders
- Diet and metabolism studies
- Hypothalamic control of reproductive hormones
- Birth, Development, and Health
- Celiac Disease Research and Management
- Genetics and Neurodevelopmental Disorders
- Childhood Cancer Survivors' Quality of Life
- Educational and Social Studies
- Diabetes, Cardiovascular Risks, and Lipoproteins
- Ovarian function and disorders
- Prenatal Screening and Diagnostics
- Effects and risks of endocrine disrupting chemicals
- Genomic variations and chromosomal abnormalities
- Liver Disease Diagnosis and Treatment
- Congenital heart defects research
- Neonatal and Maternal Infections
- Hyperglycemia and glycemic control in critically ill and hospitalized patients
University of Modena and Reggio Emilia
2016-2025
Azienda Ospedaliero-Universitaria di Modena
2003-2025
Azienda Sanitaria Unità Locale di Reggio Emilia
2024
Azienda Unita' Sanitaria Locale Di Modena
2024
Ospedale Sacro Cuore Don Calabria
2023
Istituti di Ricovero e Cura a Carattere Scientifico
2023
Tokai University
2023
National Institute of Infectious Diseases
2023
Nagoya University
2023
Santa Maria Nuova Hospital
2023
The thyroid gland regulates most of the physiological processes. Environmental factors, including climate change, pollution, nutritional changes, and exposure to chemicals, have been recognized impact function health. Thyroid disorders cancer increased in last decade, latter increasing by 1.1% annually, suggesting that environmental contaminants must play a role. This narrative review explores current knowledge on relationships among factors anatomy function, reporting recent data,...
Until early 2000, permanent and transient neonatal diabetes mellitus (NDM), defined as with onset within 6 weeks from birth that requires insulin therapy for at least 2 weeks, were considered exceedingly rare conditions, a global incidence of 1:500,000–1:400,000 live births. The new definition NDM recently adopted, includes patients months age, has prompted studies have set the form alone between 1:210,000 1:260,000 Aim present work was to ascertain (i.e. + form) in Italy years 2005–2010....
Background/Objective To minimize the wide spread of coronavirus disease (COVID-19) pandemic, Italy was placed in an almost complete lockdown state that forced people to “stay at home”. Aim this study evaluate effects on glycemic control children and adolescents with type 1 diabetes (T1D) followed through telemedicine. Subjects/Methods This observational involved patients T1D using real-time continuous glucose monitoring (CGM) Dexcom G6 ® . Ambulatory profile data from 3-months before schools...
Objective Being overweight or obese is one of the most common reasons that children and adolescents are teased at school. We carried out a study in order to investigate: i) relation between weight status school bullying ii) categories types victimization an outpatient sample Italian with different degrees from minimal up severe obesity. Participants/Methods Nine-hundred-forty-seven (age range 6.0–14.0 years) were recruited 14 hospitals distributed over country Italy. The participants...
An etiologic diagnosis of diabetes can affect the therapeutic strategy and prognosis chronic complications. The aim present study was to establish relative percentage different subtypes in patients attending Italian pediatric centers influence an on therapy. This a retrospective study. clinical records 3781 consecutive (age, 0 18 years) referred 15 clinics with or impaired fasting glucose from January 1, 2007 December 31, 2012 were examined. characteristics at their first referral centers,...
Mowat-Wilson syndrome (MWS) is a rare intellectual disability/multiple congenital anomalies caused by heterozygous mutation of the ZEB2 gene. It generally underestimated because its rarity and phenotypic variability sometimes make it difficult to recognize. Here, we aimed better delineate phenotype, natural history, genotype-phenotype correlations MWS.In collaborative study, analyzed clinical data for 87 patients with molecularly confirmed diagnosis. We described prevalence all aspects,...
Background . Type 1 diabetes mellitus (T1DM) is the most common endocrine disorder in children and adolescents worldwide. While data about prevalence, treatment, complications are recorded many countries, few exist for Sub-Saharan Africa. The aim of this study was to determine degree control patients with T1DM aged 1–19 years over a 6-month period 3 outpatient Kenyan clinics. It also sought how influenced by parameters patient treatment. Methods Eighty-two were included study. Clinical...
Familial hypercholesterolemia (FH) is an autosomal dominant disease characterized by elevated plasma levels of LDL-cholesterol that confers increased risk premature atherosclerotic cardiovascular disease. Early identification and treatment FH patients can improve prognosis reduce the burden mortality. Aim this study was to perform mutational analysis identified through a collaboration 20 Lipid Clinics in Italy (LIPIGEN Study). We recruited 1592 individuals with clinical diagnosis definite or...
Kawasaki disease (KD) is a febrile systemic vasculitis of unknown etiology and the main cause acquired heart among children in developed world. To date, abdominal involvement at presentation not recognized as risk factor for more severe form disease.To evaluate whether presenting manifestations identify group major Intravenous immunoglobulin (IVIG)-resistance coronary lesions.Retrospective study KD patients diagnosed between 2000 2015 13 pediatric units Italy. Patients were divided into 2...
Primary dyslipidemias are a heterogeneous group of disorders characterized by abnormal levels circulating lipoproteins. Among them, familial hypercholesterolemia is the most common lipid disorder that predisposes for premature cardiovascular disease. We set up an Italian nationwide network aimed at facilitating clinical and genetic diagnosis named LIPIGEN (LIpid TransPort Disorders GEnetic Network). Observational, multicenter, retrospective prospective study involving about 40 centers....