about
SOX2 plays a critical role in the pituitary, forebrain, and eye during human embryonic developmentGlucocorticoid-induced osteoporosis in children with 21-hydroxylase deficiencyThe 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 therapyA randomized controlled trial of Lactobacillus GG in children with functional abdominal painBest determinants of nonalcoholic fatty liver disease and intra-abdominal fat in prepubertal children born small for gestational age: ultrasound technique versus anthropometric data.Lactobacillus reuteri therapy to reduce side-effects during anti-Helicobacter pylori treatment in children: a randomized placebo controlled trial.Skeleton and glucose metabolism: a bone-pancreas loop.The p53 family member p73 modulates the proproliferative role of IGFBP3 in short children born small for gestational ageRisk factors for subclinical atherosclerosis in diabetic and obese children.Postmenopausal osteoporosis: the role of immune system cellsGenotype-phenotype correlation in juvenile Paget disease: role of molecular alterations of the TNFRSF11B gene.Prevention of functional gastrointestinal disorders in neonates: clinical and socioeconomic impact.Levothyroxine requirement in congenital hypothyroidism: a 12-year longitudinal study.Unusual pediatric co-morbility: autoimmune thyroiditis and cortico-resistant nephrotic syndrome in a 6-month-old Italian patient.Infantile colic, regurgitation, and constipation: an early traumatic insult in the development of functional gastrointestinal disorders in children?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.Osteoclastogenic potential of peripheral blood mononuclear cells in cleidocranial dysplasia.Propranolol for infantile haemangiomas and neuroglycopenic seizures.Clarithromycin-resistant genotypes and eradication of Helicobacter pylori.IGF2 gene variants and risk of hypertension in obese children and adolescents.The effects of probiotics on feeding tolerance, bowel habits, and gastrointestinal motility in preterm newborns.17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence.Nonalcoholic fatty liver disease in prepubertal children born small for gestational age: influence of rapid weight catch-up growth.Lactobacillus reuteri accelerates gastric emptying and improves regurgitation in infants.Prolactin may be increased in newly diagnosed celiac children and adolescents and decreases after 6 months of gluten-free diet.Clinical, serologic, and histologic features of gluten sensitivity in children.High serum sclerostin levels in children with haemophilia A.Metabolic syndrome in childhood leukemia survivors: a meta-analysis.PTPN11 gene mutation and severe neonatal hypertrophic cardiomyopathy: what is the link?Osteoclastogenesis in children with 21-hydroxylase deficiency on long-term glucocorticoid therapy: the role of receptor activator of nuclear factor-kappaB ligand/osteoprotegerin imbalance.Sulfonylurea treatment in a girl with neonatal diabetes (KCNJ11 R201H) and celiac disease: impact of low compliance to the gluten free diet.Mechanisms of enhanced osteoclastogenesis in girls and young women with Turner's Syndrome.Bone health in children and adolescents with steroid-sensitive nephrotic syndrome assessed by DXA and QUS.Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation.Improved efficacy of 10-Day sequential treatment for Helicobacter pylori eradication in children: a randomized trial.Factors predicting final height in early treated congenital hypothyroid patients.Congenital cataract and evolutive myopia. Relationship with hypophyseal-adrenal cortical axis function.Acute pancreatitis in a girl with panhypopituitarism due to craniopharyngioma on growth hormone treatment. A combination of risk factors.A novel heterozygous SOX2 mutation causing congenital bilateral anophthalmia, hypogonadotropic hypogonadism and growth hormone deficiency.A large deletion causes apparent homozygosity for the D1152H mutation in the cystic fibrosis transmembrane regulator (CFTR) gene.
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Luciano Cavallo
@ast
Luciano Cavallo
@en
Luciano Cavallo
@es
Luciano Cavallo
@nl
type
label
Luciano Cavallo
@ast
Luciano Cavallo
@en
Luciano Cavallo
@es
Luciano Cavallo
@nl
prefLabel
Luciano Cavallo
@ast
Luciano Cavallo
@en
Luciano Cavallo
@es
Luciano Cavallo
@nl
P106
P1153
35562814400
P21
P31
P496
0000-0003-4787-8681