Lista de obras - Maurizio Delvecchio - Dominio Público Uruguay

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

artículo científico publicado en 2009

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

artículo científico publicado en 2014

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

artículo científico publicado en 2016

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

artículo científico publicado en 2009

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

artículo científico publicado en 2018

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

artículo científico publicado en 2009

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

artículo científico publicado en 2018

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

artículo científico publicado en 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.

artículo científico publicado en 2014

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

artículo científico publicado en 2008

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

artículo científico publicado en 2011

Constitutional delay of growth and puberty

artículo científico publicado en 2001

Diagnostic performance of the atopy patch test with inhalant allergens

artículo científico publicado en 2015

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

artículo científico publicado en 2016

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

artículo científico publicado en 2009

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

artículo científico publicado en 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

artículo científico publicado en 2014

Factors predicting final height in early treated congenital hypothyroid patients

artículo científico publicado en 2006

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

artículo científico publicado en 2015

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

artículo científico publicado en 2005

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

artículo científico publicado en 2014

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

artículo científico publicado en 2009

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

artículo científico publicado en 2017

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

artículo científico publicado en 2007

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

artículo científico publicado en 2017

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

artículo científico publicado en 2010

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

artículo científico publicado en 2013

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

artículo científico publicado en 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

artículo científico publicado en 2003

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

artículo científico publicado en 2016

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

artículo científico publicado en 2005

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

artículo científico publicado en 2015

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

artículo científico publicado en 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

artículo científico publicado en 2014

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.

artículo científico publicado en 2017

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

artículo científico publicado en 2014

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

artículo científico publicado en 2010

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

artículo científico publicado en 2011

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

artículo científico publicado en 2014

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

artículo científico publicado en 2017

Neonatal hearing screening during the first and second day of life

artículo científico publicado en 2005

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

artículo científico publicado en 2017

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

artículo científico publicado en 2015

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

artículo científico publicado en 2014

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

artículo científico publicado en 2010

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

artículo científico publicado en 2004

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

artículo científico publicado en 2009

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

artículo científico publicado en 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

artículo científico publicado en 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.

artículo científico publicado en 2006

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

artículo científico publicado en 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.

artículo científico publicado en 2005

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

artículo científico publicado en 2016

Lista de obras de Maurizio Delvecchio

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

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

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

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

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

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

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

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

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

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

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

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

Constitutional delay of growth and puberty

Diagnostic performance of the atopy patch test with inhalant allergens

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

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

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

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

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

Factors predicting final height in early treated congenital hypothyroid patients

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Neonatal hearing screening during the first and second day of life

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

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

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

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

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

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

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

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

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

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

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

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

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

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