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List of works by Maurizio Delvecchio

17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence.

scientific article

A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2.

scientific article

A novel OTX2 gene frameshift mutation in a child with microphthalmia, ectopic pituitary and growth hormone deficiency

scientific article published on 12 March 2016

Acute pancreatitis in a girl with panhypopituitarism due to craniopharyngioma on growth hormone treatment. A combination of risk factors

scientific article

Analysis of Circulating Mediators of Bone Remodeling in Prader-Willi Syndrome.

scientific article published on 20 January 2018

Anti-pituitary antibodies in children with newly diagnosed celiac disease: a novel finding contributing to linear-growth impairment

scientific article published on 10 November 2009

Autoimmune pituitary involvement in Prader-Willi syndrome: new perspective for further research

scientific article published on 02 July 2018

CHARGE syndrome and common variable immunodeficiency: A case report and review of literature

scientific article published on 03 May 2016

Can HbA1c combined with fasting plasma glucose help to assess priority for GCK-MODY vs HNF1A-MODY genetic testing?

scientific article published on 13 June 2018

Clinical heterogeneity of abnormal glucose homeostasis associated with the HNF4A R311H mutation.

scientific article published on 19 June 2014

Clinical, endocrine, and molecular findings in 17beta-hydroxysteroid dehydrogenase type 3 deficiency.

scientific article published on January 2008

Coeliac children treated for growth hormone deficiency reach normal final height.

scientific article published in June 2011

Constitutional delay of growth and puberty

scientific article published in October 2001

Diagnostic performance of the atopy patch test with inhalant allergens

scientific article published in January 2015

Disorders of glucose metabolism in Prader-Willi syndrome: Results of a multicenter Italian cohort study

scientific article published on 3 June 2016

Effects of moderate-severe exercise on blood glucose in Type 1 diabetic adolescents treated with insulin pump or glargine insulin.

scientific article published in June 2009

Endothelial dysfunction and cardiovascular risk factors in childhood acute lymphoblastic leukemia survivors

scientific article published on 9 November 2016

Evaluation of impact of steroid replacement treatment on bone health in children with 21-hydroxylase deficiency

article

Factors associated with different results of allergy tests in children with dust mite-induced atopic dermatitis

scientific article published on 30 July 2014

Factors predicting final height in early treated congenital hypothyroid patients

scientific article published in November 2006

Final height in Italian patients with congenital hypothyroidism detected by neonatal screening: a 20-year observational study.

scientific article

Final height in short polytransfused thalassemia major patients treated with recombinant growth hormone

scientific article published in April 2005

Graves disease in children: thyroid-stimulating hormone receptor antibodies as remission markers.

scientific article published on 8 February 2014

Growth hormone deficiency and antipituitary antibodies in a patient with common variable immunodeficiency

scientific article

Growth hormone treatment improves final height and nutritional status of children with chronic kidney disease and growth deceleration

scientific article published on 17 August 2017

Growth hormone treatment in prepubertal children with celiac disease and growth hormone deficiency.

scientific article

High Sclerostin and Dickkopf-1 (DKK-1) Serum Levels in Children and Adolescents With Type 1 Diabetes Mellitus

scientific article published in April 2017

IGF2 gene variants and risk of hypertension in obese children and adolescents

scientific article published in April 2010

Identification of candidate children for maturity-onset diabetes of the young type 2 (MODY2) gene testing: a seven-item clinical flowchart (7-iF).

scientific article

Impaired bone remodeling in children with osteogenesis imperfecta treated and untreated with bisphosphonates: the role of DKK1, RANKL, and TNF-α.

scientific article published on 8 February 2016

In congenital hypothyroidism bone maturation at birth may be a predictive factor of psychomotor development during the first Year of life irrespective of other variables related to treatment

scientific article

Incidence of Type 1 Diabetes among Children and Adolescents in Italy between 2009 and 2013: The Role of a Regional Childhood Diabetes Registry.

scientific article published on 22 March 2016

Isolated increased serum TSH response to TRH is prevalent in celiac disease and predicts poor response to treatment

scientific article published on 01 October 2005

Levothyroxine requirement in congenital hypothyroidism: a 12-year longitudinal study

scientific article

Longitudinal Assessment of Levo-Thyroxine Therapy for Congenital Hypothyroidism: Relationship with Aetiology, Bone Maturation and Biochemical Features

scientific article published on 28 February 2007

Low prevalence of HNF1A mutations after molecular screening of multiple MODY genes in 58 Italian families recruited in the pediatric or adult diabetes clinic from a single Italian hospital

scientific article

MODY type 2 P59S GCK mutant: founder effect in South of Italy

article

Metabolic Outcomes, Bone Health, and Risk of Polycystic Ovary Syndrome in Girls with Idiopathic Central Precocious Puberty Treated with Gonadotropin-Releasing Hormone Analogues

scientific article

Metabolic syndrome in childhood leukemia survivors: a meta-analysis.

scientific article published on 26 August 2014

Metabolic syndrome in children with Prader–Willi syndrome: the effect of obesity

scientific article published on 20 January 2010

Metabolic, inflammatory, endothelial and haemostatic markers in a group of Italian obese children and adolescents

scientific article published on 6 January 2011

Microdeletion of 12q24.31: Report of a girl with intellectual disability, stereotypies, seizures and facial dysmorphisms

scientific article published on 26 November 2014

Monogenic Diabetes Accounts for 6.3% of Cases Referred to 15 Italian Pediatric Diabetes Centers During 2007 to 2012.

scientific article published on 16 February 2017

Neonatal hearing screening during the first and second day of life

scientific article published in August 2005

Non-alcoholic fatty liver disease is associated with early left ventricular dysfunction in childhood acute lymphoblastic leukaemia survivors.

scientific article

Prevalence of positive atopy patch test in an unselected pediatric population.

scientific article published on 7 May 2015

Prolactin may be increased in newly diagnosed celiac children and adolescents and decreases after 6 months of gluten-free diet

scientific article published on 5 March 2014

Sleep-disordered breathing in obese children: the southern Italy experience.

scientific article published on 5 February 2010

Sodium fraction excretion rate in nocturnal enuresis correlates with nocturnal polyuria and osmolality.

scientific article published in June 2004

Sulfonylurea treatment in a girl with neonatal diabetes (KCNJ11 R201H) and celiac disease: impact of low compliance to the gluten free diet

scientific article

Survey on etiological diagnosis of diabetes in 1244 Italian diabetic children and adolescents: impact of access to genetic testing

scientific article published on 20 January 2015

The Effect of Gaseous Ozone Therapy in Conjunction with Periodontal Treatment on Glycated Hemoglobin Level in Subjects with Type 2 Diabetes Mellitus: An Unmasked Randomized Controlled Trial

scientific article published on 29 July 2020

The Italian National Survey for Prader–Willi syndrome: An epidemiologic study

article

The prevalence of growth hormone deficiency and celiac disease in short children.

scientific article

Thyroid function and thyroid autoimmunity in childhood acute lymphoblastic leukemia off-therapy patients treated only with chemotherapy.

scientific article published on 28 July 2009

Thyroid function in patients with Prader-Willi syndrome: an Italian multicenter study of 339 patients

article

Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation.

scientific article

Vascular Function and Myocardial Performance Indices in Children Born Small for Gestational Age

scientific article published on 10 February 2016

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