Lista de obras - Maria F. Faienza - Dominio Público Uruguay

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

artículo científico publicado en 2009

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

artículo científico publicado en 2011

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

artículo científico publicado en 2016

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

artículo científico publicado en 2013

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 cyclin-dependent kinase inhibitor genes (CDKN2A, CDKN2B, andCDKN2C) in childhood rhabdomyosarcoma

article

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

artículo científico publicado en 2011

Autoimmune haematological disorders in two Italian children with Kabuki syndrome

artículo científico publicado en 2014

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

Childhood obesity, cardiovascular and liver health: a growing epidemic with age

scientific article published on 04 February 2020

Editorial: Special Issue on "Molecular Mechanisms Regulating Osteoclastogenesis"

artículo científico publicado en 2020

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

Elevated endothelin-1 (ET-1) levels may contribute to hypoadiponectinemia in childhood obesity

artículo científico publicado en 2013

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

article

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

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

Growth plate gene involment and isolated short stature

artículo científico publicado en 2020

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

Insulin resistance and endothelial function in children and adolescents

artículo científico publicado en 2014

Interstitial and large chromosome 1p deletion occurs in localized and disseminated neuroblastomas and predicts an unfavourable outcome

artículo científico publicado en 1998

Issues in pediatric haemophilia care

artículo científico publicado en 2013

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

Monitoring and maintaining bone health in patients with Turner syndrome

artículo científico publicado en 2020

Neonatal hyperbilirubinemia and Gilbert's syndrome

artículo científico publicado en 2002

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

artículo científico publicado en 2013

Osteoblasts display different responsiveness to TRAIL-induced apoptosis during their differentiation process

artículo científico

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

Osteoporosis and obesity: Role of Wnt pathway in human and murine models

artículo científico publicado en 2014

Osteotropic Cancers: From Primary Tumor to Bone

Overview of the Potential Beneficial Effects of Carotenoids on Consumer Health and Well-Being

artículo científico publicado en 2023

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

Peculiarities of presentation and evolution over time of Hashimoto's thyroiditis in children and adolescents with Down's syndrome

artículo científico publicado en 2015

Polyphenols and obesity prevention: critical insights on molecular regulation, bioavailability and dose in preclinical and clinical settings

scientific article published on 21 May 2020

Postmenopausal osteoporosis: the role of immune system cells

artículo científico publicado en 2013

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

Risk factors for subclinical atherosclerosis in diabetic and obese children

artículo científico publicado en 2013

Role of antithyroid autoimmunity as a predictive biomarker of chronic immune thrombocytopenia

artículo científico publicado en 2018

SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations

artículo científico publicado en 2011

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

artículo científico publicado en 2008

Shedding "LIGHT" on the Link between Bone and Fat in Obese Children and Adolescents ⬇️

scientific article published on 03 July 2020

Skeleton and glucose metabolism: a bone-pancreas loop

artículo científico publicado en 2015

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 association with Turner syndrome significantly affects the course of Hashimoto’s thyroiditis in children, irrespective of karyotype

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

artículo científico publicado en 2015

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

Treatment of osteoporosis in children with glucocorticoid-treated diseases

artículo científico publicado en 2014

Venous Thromboembolism in Children: From Diagnosis to Management

scientific article published on 11 July 2020

Lista de obras de Maria F. Faienza

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

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

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

A novel heterozygous SOX2 mutation causing congenital bilateral anophthalmia, hypogonadotropic hypogonadism 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 cyclin-dependent kinase inhibitor genes (CDKN2A, CDKN2B, andCDKN2C) in childhood rhabdomyosarcoma

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

Autoimmune haematological disorders in two Italian children with Kabuki syndrome

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.

Childhood obesity, cardiovascular and liver health: a growing epidemic with age

Editorial: Special Issue on "Molecular Mechanisms Regulating Osteoclastogenesis"

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

Elevated endothelin-1 (ET-1) levels may contribute to hypoadiponectinemia in childhood obesity

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

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

Factors predicting final height in early treated congenital hypothyroid patients

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

Glucocorticoid-induced osteoporosis in children with 21-hydroxylase deficiency

Growth plate gene involment and isolated short stature

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

Insulin resistance and endothelial function in children and adolescents

Interstitial and large chromosome 1p deletion occurs in localized and disseminated neuroblastomas and predicts an unfavourable outcome

Issues in pediatric haemophilia care

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

Monitoring and maintaining bone health in patients with Turner syndrome

Neonatal hyperbilirubinemia and Gilbert's syndrome

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

Osteoblasts display different responsiveness to TRAIL-induced apoptosis during their differentiation process

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

Osteoporosis and obesity: Role of Wnt pathway in human and murine models

Osteotropic Cancers: From Primary Tumor to Bone

Overview of the Potential Beneficial Effects of Carotenoids on Consumer Health and Well-Being

Oxidative Stress in Obesity and Metabolic Syndrome in Children and Adolescents

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

Peculiarities of presentation and evolution over time of Hashimoto's thyroiditis in children and adolescents with Down's syndrome

Polyphenols and obesity prevention: critical insights on molecular regulation, bioavailability and dose in preclinical and clinical settings

Postmenopausal osteoporosis: the role of immune system cells

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

Risk factors for subclinical atherosclerosis in diabetic and obese children

Role of antithyroid autoimmunity as a predictive biomarker of chronic immune thrombocytopenia

SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations

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

Shedding "LIGHT" on the Link between Bone and Fat in Obese Children and Adolescents ⬇️

Skeleton and glucose metabolism: a bone-pancreas loop

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

The association with Turner syndrome significantly affects the course of Hashimoto’s thyroiditis in children, irrespective of karyotype

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

To test or not to test…this is the problem

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

Treatment of osteoporosis in children with glucocorticoid-treated diseases

Venous Thromboembolism in Children: From Diagnosis to Management