Lista de obras - Luciano Cavallo - Dominio Público Uruguay

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

artículo científico publicado en 2009

A large deletion causes apparent homozygosity for the D1152H mutation in the cystic fibrosis transmembrane regulator (CFTR) gene.

artículo científico publicado en 2012

A novel HESX1 splice mutation causes isolated GH deficiency by interfering with mRNA processing.

artículo científico publicado en 2011

A novel heterozygous SOX2 mutation causing congenital bilateral anophthalmia, hypogonadotropic hypogonadism and growth hormone deficiency

artículo científico publicado en 2013

A randomized controlled trial of Lactobacillus GG in children with functional abdominal pain

artículo científico publicado en 2010

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 endothelial protein C receptor gene and metabolic profile in Prader-Willi syndrome and obese subjects

artículo científico publicado en 2011

Best determinants of nonalcoholic fatty liver disease and intra-abdominal fat in prepubertal children born small for gestational age: ultrasound technique versus anthropometric data

artículo científico publicado en 2013

Bone health in children and adolescents with steroid-sensitive nephrotic syndrome assessed by DXA and QUS.

artículo científico publicado en 2014

Bulimia and cough: psychogenic or organic?

artículo científico publicado en 2009

Cardiac function in congenital hypothyroidism: impairment and response to L-T4 therapy

scientific article published on 01 January 1991

Clarithromycin-resistant genotypes and eradication of Helicobacter pylori.

artículo científico publicado en 2010

Clinical, serologic, and histologic features of gluten sensitivity in children.

artículo científico publicado en 2013

Comparison of esophageal pH and multichannel intraluminal impedance testing in pediatric patients with suspected gastroesophageal reflux

artículo científico publicado en 2010

Congenital cataract and evolutive myopia. Relationship with hypophyseal-adrenal cortical axis function.

artículo científico publicado en 1986

Diagnostic value of growth hormone-releasing hormone test in children and adolescents with idiopathic growth hormone deficiency

artículo científico publicado el 1 de abril de 1992

Effect of recombinant insulin-like growth factor-1 treatment on short-term linear growth in a child with Majewski osteodysplastic primordial dwarfism type II and hepatic insufficiency

artículo científico publicado en 2013

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

article

Evaluation of the growth-hormone-releasing hormone test in short normal and growth-hormone-deficient children

scientific article published on 01 January 1990

Evidence that fibrinolytic changes in paediatric obesity translate into a hypofibrinolytic state

article

Factors predicting final height in early treated congenital hypothyroid patients

artículo científico publicado en 2006

Gastroesophageal reflux in preterm infants: how acid should it be?

artículo científico publicado en 2008

Genotype-phenotype correlation in juvenile Paget disease: role of molecular alterations of the TNFRSF11B gene

artículo científico publicado en 2012

Glucocorticoid-induced osteoporosis in children with 21-hydroxylase deficiency

artículo científico publicado en 2013

Helicobacter pylori eradication: can't we do better?

artículo científico publicado en 2011

High dickkopf-1 levels in sera and leukocytes from children with 21-hydroxylase deficiency on chronic glucocorticoid treatment.

artículo científico publicado en 2013

High serum sclerostin levels in children with haemophilia A.

artículo científico publicado en 2015

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

artículo científico publicado en 2010

Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure

artículo científico publicado en 2006

Improved efficacy of 10-Day sequential treatment for Helicobacter pylori eradication in children: a randomized trial

artículo científico publicado en 2005

Increased prevalence of celiac disease among pediatric patients with irritable bowel syndrome: a 6-year prospective cohort study

artículo científico publicado en 2014

Infantile colic, regurgitation, and constipation: an early traumatic insult in the development of functional gastrointestinal disorders in children?

artículo científico publicado en 2014

Lactobacillus reuteri Strain Combination In Helicobacter pylori Infection

artículo científico publicado en 2014

Lactobacillus reuteri accelerates gastric emptying and improves regurgitation in infants.

artículo científico publicado en 2010

Lactobacillus reuteri therapy to reduce side-effects during anti-Helicobacter pylori treatment in children: a randomized placebo controlled trial.

artículo científico publicado en 2006

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

Mechanisms of enhanced osteoclastogenesis in girls and young women with Turner's Syndrome

artículo científico publicado en 2015

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

artículo científico publicado en 2014

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

artículo científico publicado en 2011

New insights into childhood Vernal keratoconjunctivitis-associated factors

scientific article published on 11 September 2012

Nonalcoholic fatty liver disease in prepubertal children born small for gestational age: influence of rapid weight catch-up growth

artículo científico publicado en 2013

Osteoclastogenesis in children with 21-hydroxylase deficiency on long-term glucocorticoid therapy: the role of receptor activator of nuclear factor-kappaB ligand/osteoprotegerin imbalance.

artículo científico publicado en 2009

Osteoclastogenic potential of peripheral blood mononuclear cells in cleidocranial dysplasia

artículo científico publicado en 2014

Oxidative Stress in Obesity and Metabolic Syndrome in Children and Adolescents

artículo científico publicado en 2012

PTPN11 gene mutation and severe neonatal hypertrophic cardiomyopathy: what is the link?

artículo científico publicado en 2009

Physiological basis of food intolerance in VLBW ⬇️

artículo científico publicado el 1 de octubre de 2011

Postmenopausal osteoporosis: the role of immune system cells

artículo científico publicado en 2013

Prebiotics improve gastric motility and gastric electrical activity in preterm newborns

artículo científico publicado en 2009

Prevention of functional gastrointestinal disorders in neonates: clinical and socioeconomic impact.

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

Propranolol for infantile haemangiomas and neuroglycopenic seizures.

artículo científico publicado en 2010

Randomised clinical trial: Lactobacillus reuteri DSM 17938 vs. placebo in children with acute diarrhoea--a double-blind study

artículo científico publicado en 2012

Risk factors for subclinical atherosclerosis in diabetic and obese children

artículo científico publicado en 2013

SOX2 plays a critical role in the pituitary, forebrain, and eye during human embryonic development

artículo científico publicado en 2008

Skeleton and glucose metabolism: a bone-pancreas loop

artículo científico publicado en 2015

Subcutaneous growth hormone administration in growth-hormone-deficient children. Continuous plus pulsatile overnight versus single daily injection: effects on growth rate velocity

artículo científico publicado en 1994

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

The acid-labile subunit of human ternary insulin-like growth factor-binding protein complex in girls with central precocious puberty before and during gonadotropin-releasing hormone analog therapy

artículo científico publicado en 2002

The effect of different growth hormone administration frequencies on growth in growth hormone-deficient patients

article published in 1998

The effects of probiotics on feeding tolerance, bowel habits, and gastrointestinal motility in preterm newborns.

artículo científico publicado en 2007

The p53 family member p73 modulates the proproliferative role of IGFBP3 in short children born small for gestational age

artículo científico publicado en 2015

The role of post-transplantation cyclosporine treatment in the course of cystic fibrosis pulmonary disease: a case report.

artículo científico publicado en 2012

Thyroid function after prolonged treatment for congenital hypothyroidism

scientific article published on 01 December 1990

To test or not to test…this is the problem

artículo científico publicado en 2011

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

artículo científico publicado en 2005

Unusual pediatric co-morbility: autoimmune thyroiditis and cortico-resistant nephrotic syndrome in a 6-month-old Italian patient.

artículo científico publicado en 2012

Lista de obras de Luciano Cavallo

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

A large deletion causes apparent homozygosity for the D1152H mutation in the cystic fibrosis transmembrane regulator (CFTR) gene.

A novel HESX1 splice mutation causes isolated GH deficiency by interfering with mRNA processing.

A novel heterozygous SOX2 mutation causing congenital bilateral anophthalmia, hypogonadotropic hypogonadism and growth hormone deficiency

A randomized controlled trial of Lactobacillus GG in children with functional abdominal pain

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

Analysis of endothelial protein C receptor gene and metabolic profile in Prader-Willi syndrome and obese subjects

Best determinants of nonalcoholic fatty liver disease and intra-abdominal fat in prepubertal children born small for gestational age: ultrasound technique versus anthropometric data

Bone health in children and adolescents with steroid-sensitive nephrotic syndrome assessed by DXA and QUS.

Bulimia and cough: psychogenic or organic?

Cardiac function in congenital hypothyroidism: impairment and response to L-T4 therapy

Clarithromycin-resistant genotypes and eradication of Helicobacter pylori.

Clinical, serologic, and histologic features of gluten sensitivity in children.

Comparison of esophageal pH and multichannel intraluminal impedance testing in pediatric patients with suspected gastroesophageal reflux

Congenital cataract and evolutive myopia. Relationship with hypophyseal-adrenal cortical axis function.

Diagnostic value of growth hormone-releasing hormone test in children and adolescents with idiopathic growth hormone deficiency

Effect of recombinant insulin-like growth factor-1 treatment on short-term linear growth in a child with Majewski osteodysplastic primordial dwarfism type II and hepatic insufficiency

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

Evaluation of the growth-hormone-releasing hormone test in short normal and growth-hormone-deficient children

Evidence that fibrinolytic changes in paediatric obesity translate into a hypofibrinolytic state

Factors predicting final height in early treated congenital hypothyroid patients

Gastroesophageal reflux in preterm infants: how acid should it be?

Genotype-phenotype correlation in juvenile Paget disease: role of molecular alterations of the TNFRSF11B gene

Glucocorticoid-induced osteoporosis in children with 21-hydroxylase deficiency

Helicobacter pylori eradication: can't we do better?

High dickkopf-1 levels in sera and leukocytes from children with 21-hydroxylase deficiency on chronic glucocorticoid treatment.

High serum sclerostin levels in children with haemophilia A.

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

Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure

Improved efficacy of 10-Day sequential treatment for Helicobacter pylori eradication in children: a randomized trial

Increased prevalence of celiac disease among pediatric patients with irritable bowel syndrome: a 6-year prospective cohort study

Infantile colic, regurgitation, and constipation: an early traumatic insult in the development of functional gastrointestinal disorders in children?

Lactobacillus reuteri Strain Combination In Helicobacter pylori Infection

Lactobacillus reuteri accelerates gastric emptying and improves regurgitation in infants.

Lactobacillus reuteri therapy to reduce side-effects during anti-Helicobacter pylori treatment in children: a randomized placebo controlled trial.

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

Mechanisms of enhanced osteoclastogenesis in girls and young women with Turner's Syndrome

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

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

New insights into childhood Vernal keratoconjunctivitis-associated factors

Nonalcoholic fatty liver disease in prepubertal children born small for gestational age: influence of rapid weight catch-up growth

Osteoclastogenesis in children with 21-hydroxylase deficiency on long-term glucocorticoid therapy: the role of receptor activator of nuclear factor-kappaB ligand/osteoprotegerin imbalance.

Osteoclastogenic potential of peripheral blood mononuclear cells in cleidocranial dysplasia

Oxidative Stress in Obesity and Metabolic Syndrome in Children and Adolescents

PTPN11 gene mutation and severe neonatal hypertrophic cardiomyopathy: what is the link?

Physiological basis of food intolerance in VLBW ⬇️

Postmenopausal osteoporosis: the role of immune system cells

Prebiotics improve gastric motility and gastric electrical activity in preterm newborns

Prevention of functional gastrointestinal disorders in neonates: clinical and socioeconomic impact.

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

Propranolol for infantile haemangiomas and neuroglycopenic seizures.

Randomised clinical trial: Lactobacillus reuteri DSM 17938 vs. placebo in children with acute diarrhoea--a double-blind study

Risk factors for subclinical atherosclerosis in diabetic and obese children

SOX2 plays a critical role in the pituitary, forebrain, and eye during human embryonic development

Skeleton and glucose metabolism: a bone-pancreas loop

Subcutaneous growth hormone administration in growth-hormone-deficient children. Continuous plus pulsatile overnight versus single daily injection: effects on growth rate velocity

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

The acid-labile subunit of human ternary insulin-like growth factor-binding protein complex in girls with central precocious puberty before and during gonadotropin-releasing hormone analog therapy

The effect of different growth hormone administration frequencies on growth in growth hormone-deficient patients

The effects of probiotics on feeding tolerance, bowel habits, and gastrointestinal motility in preterm newborns.

The p53 family member p73 modulates the proproliferative role of IGFBP3 in short children born small for gestational age

The role of post-transplantation cyclosporine treatment in the course of cystic fibrosis pulmonary disease: a case report.

Thyroid function after prolonged treatment for congenital hypothyroidism

To test or not to test…this is the problem

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

Unusual pediatric co-morbility: autoimmune thyroiditis and cortico-resistant nephrotic syndrome in a 6-month-old Italian patient.