M. Salerno

发表

Beta-cell dysfunction in classic transient neonatal diabetes is characterized by impaired insulin response to glucose but normal response to glucagon.

A. Franzese, G. Valerio, J. Shield, 2004, Diabetes care.

JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid Defects.

M. Maghnie, L. Persani, P. Prontera, 2016, The Journal of clinical endocrinology and metabolism.

The R156H variation in IL-12Rβ1 is not a mutation

G. Giardino, C. Pignata, L. Palamaro, 2013, Italian Journal of Pediatrics.

Left ventricular mass and function in children with GH deficiency before and during 12 months GH replacement therapy

A. Colao, G. Lombardi, L. T. de Horatio, 2004, Clinical endocrinology.

New strategies for the treatment of lysosomal storage diseases (review).

C. Pignata, P. Vajro, G. Parenti, 2013, International journal of molecular medicine.

Impaired protein stability and nuclear localization of NOBOX variants associated with premature ovarian insufficiency.

L. Persani, A. Ferlin, I. Ferrari, 2016, Human molecular genetics.

Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome.

L. Notarangelo, V. Lougaris, A. Plebani, 2011, Clinical immunology.

Subtle alterations of cardiac performance in children with growth hormone deficiency: results of a two-year prospective, case-control study.

A. Colao, G. Lombardi, A. Lo Vecchio, 2009, The Journal of clinical endocrinology and metabolism.

0021-972X/06/$15.00/0 The Journal of Clinical Endocrinology & Metabolism 91(4):1288–1295 Printed in U.S.A. Copyright © 2006 by The Endocrine Society doi: 10.1210/jc.2005-0981 Improvement of Cardiac Performance and Cardiovascular Risk Factors in Children w

A. Colao, A. Colao, A. Umbaldo, 2022 .

Alterations of the autoimmune regulator transcription factor and failure of central tolerance: APECED as a model

V. Gallo, G. Giardino, C. Pignata, 2013, Expert review of clinical immunology.

Genetic Basis of Altered Central Tolerance and Autoimmune Diseases: A Lesson from AIRE Mutations

V. Gallo, G. Giardino, E. Cirillo, 2012, International reviews of immunology.

Cardiovascular abnormalities and impaired exercise performance in adolescents with congenital adrenal hyperplasia.

A. Lenzi, A. Isidori, A. Cittadini, 2015, The Journal of clinical endocrinology and metabolism.

Genetics of Autoimmune Regulator (AIRE) and Clinical Implications in Childhood

M. Salerno, D. Capalbo, N. Improda, 2021, Endocrinology.

Effects of long-term L-thyroxine treatment on endothelial function and arterial distensibility in young adults with congenital hypothyroidism.

A. Cittadini, G. Bosso, M. Salerno, 2010, European journal of endocrinology.

Subclinical hypothyroidism in childhood — current knowledge and open issues

M. Salerno, F. Luca, D. Capalbo, 2016, Nature Reviews Endocrinology.

Diagnostic features of thyroid nodules in pediatrics.

M. Segni, L. Beccaria, A. Mussa, 2010, Archives of pediatrics & adolescent medicine.

Linear growth and intellectual outcome in children with long-term idiopathic subclinical hypothyroidism.

D. Bruzzese, C. Bravaccio, M. Salerno, 2011, European journal of endocrinology.

GH secretion in a cohort of children with pseudohypoparathyroidism type Ia

L. Ghizzoni, D. Concolino, M. Salerno, 2007, Journal of endocrinological investigation.

Growth hormone deficiency in a patient with lysinuric protein intolerance

G. Parenti, G. Sebastio, M. Salerno, 2006, European Journal of Pediatrics.

Longitudinal growth, sexual maturation and final height in patients with congenital hypothyroidism detected by neonatal screening.

A. Tenore, M. Micillo, M. Salerno, 2001, European journal of endocrinology.

Near Final Height after GnRH Agonist Treatment in Central Precocious Puberty

M. Micillo, M. Salerno, S. Di Maio, 2000, Journal of pediatric endocrinology & metabolism : JPEM.

Central Precocious Puberty: A Single Blood Sample after Gonadotropin-Releasing Hormone Agonist Administration in Monitoring Treatment

A. Tenore, A. Mariano, M. Salerno, 1998, Hormone Research in Paediatrics.

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy from the pediatric perspective

C. Pignata, M. Salerno, F. Barbieri, 2013, Journal of Endocrinological Investigation.

Influence of Hashimoto Thyroiditis on the Development of Thyroid Nodules and Cancer in Children and Adolescents

S. Loche, M. Cappa, G. Radetti, 2019, Journal of the Endocrine Society.

Therapeutic options in pediatric non alcoholic fatty liver disease: current status and future directions

C. Pignata, P. Vajro, G. Parenti, 2012, Italian Journal of Pediatrics.

The natural history of the normal/mild elevated TSH serum levels in children and adolescents with Hashimoto’s thyroiditis and isolated hyperthyrotropinaemia: a 3‐year follow‐up

S. Loche, A. Mussa, M. Cappa, 2012, Clinical endocrinology.

Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious puberty.

N. de Roux, J. Carel, M. Salerno, 2016, European journal of endocrinology.

Subclinical hypothyroidism and Down’s syndrome; studies on myocardial structure and function

G. Limongelli, G. Andria, E. D. del Giudice, 2003, Archives of disease in childhood.

Long-term cardiovascular effects of levothyroxine therapy in young adults with congenital hypothyroidism.

L. Saccá, A. Cittadini, M. Salerno, 2008, The Journal of clinical endocrinology and metabolism.

Accuracy and Limitations of the Growth Hormone (GH) Releasing Hormone-Arginine Retesting in Young Adults With Childhood-Onset GH Deficiency

M. Maghnie, S. Parodi, S. Loche, 2019, Front. Endocrinol..

Muscle and skeletal health in children and adolescents with GH deficiency.

M. Salerno, A. Esposito, D. Capalbo, 2016, Best practice & research. Clinical endocrinology & metabolism.

Serum homocysteine concentrations in children with growth hormone (GH) deficiency before and after 12 months GH replacement

M. Salerno, S. Di Biase, D. Labella, 2004, Clinical endocrinology.

Cardiovascular risk factors in children with long-standing untreated idiopathic subclinical hypothyroidism.

R. Meli, G. Mattace Raso, M. Salerno, 2014, The Journal of clinical endocrinology and metabolism.

Thyroid function in children and adolescents with Hashimoto's thyroiditis after l-thyroxine discontinuation

M. Rotondi, S. Loche, M. Cappa, 2017, Endocrine connections.

A new case of familial nonautoimmune hyperthyroidism caused by the M463V mutation in the TSH receptor with anticipation of the disease across generations: a possible role of iodine supplementation.

P. Macchia, G. Fenzi, M. Salerno, 2007, Thyroid : official journal of the American Thyroid Association.

Screening for mutations in the ISL1 gene in patients with thyroid dysgenesis

P. Macchia, I. C. Nettore, G. Fenzi, 2011, Journal of endocrinological investigation.

Pubertal Growth, Sexual Maturation, and Final Height in Children With IDDM: Effects of age at onset and metabolic control

A. Tenore, M. Salerno, S. Di Maio, 1997, Diabetes Care.

Sedentary lifestyle and precocious puberty in girls during the COVID-19 pandemic: an Italian experience

M. Maghnie, S. Loche, M. Cappa, 2021, Endocrine connections.

Betamethasone therapy in ataxia telangiectasia: unraveling the rationale of this serendipitous observation on the basis of the pathogenesis

V. Gallo, G. Giardino, C. Pignata, 2013, European journal of neurology.

Androgen insensitivity syndrome: somatic mosaicism of the androgen receptor in seven families and consequences for sex assignment and genetic counseling.

P. Czernichow, G. Pinto, B. Köhler, 2005, The Journal of clinical endocrinology and metabolism.

Imbalanced cortisol concentrations in glycogen storage disease type I: evidence for a possible link between endocrine regulation and metabolic derangement

R. Ferrigno, D. Melis, G. Parenti, 2020, Orphanet Journal of Rare Diseases.

Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)

V. Tillmann, P. Chanson, M. Dattani, 2020, Orphanet Journal of Rare Diseases.

Mild Hypothyroidism in Childhood: Who, When, and How Should Be Treated?

M. Salerno, G. Weber, M. Vigone, 2018, Journal of the Endocrine Society.

Prospective evaluation of the natural course of idiopathic subclinical hypothyroidism in childhood and adolescence.

A. Mussa, M. Salerno, G. Zirilli, 2009, European journal of endocrinology.

HYDROCORTISONE THERAPY AND GROWTH TRAJECTORY IN CHILDREN WITH CLASSICAL CONGENITAL ADRENAL HYPERPLASIA.

O. Porzio, M. Cappa, M. Salerno, 2017, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

Expert Opinion on the Management of Growth Hormone Deficiency in Brain Tumor Survivors: Results From an Italian Survey

M. Maghnie, L. D'Incerti, I. Sardi, 2022, Frontiers in Endocrinology.

Clinical benefits of sex steroids given as a priming prior to GH provocative test or as a growth‐promoting therapy in peripubertal growth delays: Results of a retrospective study among ENDO‐ERN centres

M. Dattani, L. Persani, M. Bonomi, 2020, Clinical endocrinology.

Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients

S. Masiero, A. Stigliano, F. Bogazzi, 2021, Journal of Endocrinological Investigation.

PROKR2 in Girls with Idiopathic Central Precocious Puberty

G. Cirillo, A. Grandone, M. Salerno, 2019 .

Allogeneic bone marrow transplantation restores IGF-I production and linear growth in a γ-SCID patient with abnormal growth hormone receptor signaling

C. Pignata, M. Salerno, B. Rotoli, 2004, Bone Marrow Transplantation.

Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations.

M. Maghnie, S. Perrotta, F. Ragione, 2015, European journal of endocrinology.

Reliability of clonidine testing for the diagnosis of growth hormone deficiency in children and adolescents

M. Maghnie, S. Loche, M. Cappa, 2018, Clinical endocrinology.

Atypical X‐linked SCID phenotype associated with growth hormone hyporesponsiveness

C. Pignata, A. Apicella, M. Ursini, 2002, Clinical and experimental immunology.

A novel recessive splicing mutation in the POU1F1 gene causing combined pituitary hormone deficiency

Y. Carlomagno, M. Godi, M. Salerno, 2009, Journal of endocrinological investigation.

Clinical Heterogeneity in two patients with Noonan-like Syndrome associated with the same SHOC2 mutation

C. Pignata, L. Palamaro, D. Melis, 2012, Italian Journal of Pediatrics.

Noonan‐like syndrome with loose anagen hair associated with growth hormone insensitivity and atypical neurological manifestations

C. Pignata, L. Palamaro, D. Melis, 2012, American journal of medical genetics. Part A.

Hypertransaminasemia and fatal lung disease: a case report

C. Pignata, G. Parenti, M. Salerno, 2013, Italian Journal of Pediatrics.

In children with autoimmune thyroid diseases the association with Down syndrome can modify the clustering of extra-thyroidal autoimmune disorders

L. Iughetti, M. Salerno, F. De Luca, 2016, Journal of pediatric endocrinology & metabolism : JPEM.

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

A. Mussa, L. Iughetti, G. Radetti, 2015, Hormones.

The cardiovascular risk of GH-deficient adolescents.

F. Orio, A. Colao, G. Lombardi, 2002, The Journal of clinical endocrinology and metabolism.

Delayed gastric emptying: a novel gastrointestinal finding in Turner's syndrome.

A. Staiano, P. Strisciuglio, G. Marsullo, 1996, Archives of disease in childhood.

Effect of long-term L-thyroxine treatment on bone mineral density in young adults with congenital hypothyroidism.

A. Carpinelli, M. Salerno, A. del Puente, 2004, European journal of endocrinology.

Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH).

M. Maghnie, A. Isidori, P. Duminuco, 2018, European journal of endocrinology.

Bone health in children with long–term idiopathic subclinical hypothyroidism

C. Pignata, C. Mainolfi, M. Salerno, 2012, Italian Journal of Pediatrics.

Effect of initial levothyroxine dose on neurodevelopmental and growth outcomes in children with congenital hypothyroidism

D. Bruzzese, A. Mussa, C. Bravaccio, 2022, Frontiers in Endocrinology.

The growth hormone-insulin-like growth factor axis in glycogen storage disease type 1: evidence of different growth patterns and insulin-like growth factor levels in patients with glycogen storage disease type 1a and 1b.

A. Colao, G. Andria, D. Melis, 2010, The Journal of pediatrics.

Subclinical hyperthyroidism when presenting as initial manifestation of juvenile Hashimoto’s thyroiditis: first report on its natural history

G. Salzano, A. Mussa, M. Salerno, 2014, Journal of Endocrinological Investigation.

Treatment of children with chronic viral hepatitis: what is available and what is in store

C. Pignata, P. Vajro, G. Parenti, 2013, World Journal of Pediatrics.

Long-term effects of growth hormone (GH) replacement therapy on hematopoiesis in a large cohort of children with GH deficiency

C. Pignata, M. Salerno, A. Esposito, 2016, Endocrine.

Thyroid Function Patterns at Hashimoto’s Thyroiditis Presentation in Childhood and Adolescence Are Mainly Conditioned by Patients’ Age

A. Mussa, M. Salerno, S. Bombaci, 2012, Hormone Research in Paediatrics.

Outcomes of Children with Hashitoxicosis

A. Mussa, F. Lombardo, M. Salerno, 2012, Hormone Research in Paediatrics.

Acute adrenal failure as the presenting feature of primary antiphospholipid syndrome in a child

C. Pignata, L. Palamaro, M. Salerno, 2012, Italian Journal of Pediatrics.

A case of galactosemia misdiagnosed as cow’s milk intolerance

C. Pignata, P. Vajro, G. Parenti, 2012, Italian Journal of Pediatrics.

Interleukin 12 receptor deficiency in a child with recurrent bronchopneumonia and very high IgE levels

G. Giardino, C. Pignata, L. Palamaro, 2012, Italian Journal of Pediatrics.

Cognitive function in children with idiopathic subclinical hypothyroidism: effects of two years of levothyroxine therapy.

C. Bravaccio, M. Salerno, A. Esposito, 2020, The Journal of clinical endocrinology and metabolism.

High-resolution melting analysis (HRM) for mutational screening of Dnajc17 gene in patients affected by thyroid dysgenesis

P. Macchia, I. C. Nettore, A. Colao, 2018, Journal of Endocrinological Investigation.

Growth hormone treatment of adolescents with growth hormone deficiency (GHD) during the transition period: results of a survey among adult and paediatric endocrinologists from Italy. Endorsed by SIEDP/ISPED, AME, SIE, SIMA

S. Cannavò, M. Maghnie, V. Toscano, 2015, Journal of Endocrinological Investigation.

Glycogen storage disease type Ia (GSDIa) but not Glycogen storage disease type Ib (GSDIb) is associated to an increased risk of metabolic syndrome: possible role of microsomal glucose 6-phosphate accumulation

G. Muscogiuri, P. Formisano, G. Andria, 2015, Orphanet Journal of Rare Diseases.

Tryptophan hydroxylase autoantibodies as markers of a distinct autoimmune gastrointestinal component of autoimmune polyendocrine syndrome type 1.

S. Masiero, L. Ghizzoni, R. Giordano, 2013, The Journal of clinical endocrinology and metabolism.

The Evolution of Thyroid Function after Presenting with Hashimoto Thyroiditis Is Different between Initially Euthyroid Girls with and Those without Turner Syndrome

L. Mazzanti, M. Salerno, F. De Luca, 2016, Hormone Research in Paediatrics.

Five-year prospective evaluation of thyroid function in girls with subclinical mild hypothyroidism of different etiology.

A. Mussa, M. Salerno, F. De Luca, 2015, European journal of endocrinology.

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

L. Mazzanti, A. Mussa, M. Salerno, 2015, Endocrine.

Antipituitary antibodies recognizing growth hormone (GH)-producing cells in children with idiopathic GH deficiency and in children with idiopathic short stature.

G. Bellastella, A. Bellastella, A. De Bellis, 2006, The Journal of clinical endocrinology and metabolism.

EXTENSIVE CLINICAL EXPERIENCE Antipituitary Antibodies Recognizing Growth Hormone (GH)-Producing Cells in Children with Idiopathic GH Deficiency and in Children with Idiopathic Short Stature

G. Bellastella, A. Bellastella, A. Bellis, 2006 .

Rare forms of genetic paediatric adrenal insufficiency: Excluding congenital adrenal hyperplasia

A. Lenzi, R. Ferrigno, V. Hasenmajer, 2023, Reviews in Endocrine and Metabolic Disorders.

Precocious puberty in Turner Syndrome: report of a case and review of the literature

C. Pignata, P. Vajro, G. Parenti, 2012, Italian Journal of Pediatrics.

Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort

F. Prodam, M. Salerno, F. De Luca, 2015, Clinical endocrinology.

Primary Adrenal Insufficiency in childhood: data from a large nationwide cohort.

M. Maghnie, M. Cappa, F. Baronio, 2020, The Journal of clinical endocrinology and metabolism.

Novel Findings into AIRE Genetics and Functioning: Clinical Implications

E. Cirillo, C. Pignata, M. Salerno, 2016, Front. Pediatr..

Congenital Hypothyroidism: A 2020–2021 Consensus Guidelines Update—An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology

D. Luton, M. Polak, H. Krude, 2020, Thyroid : official journal of the American Thyroid Association.

Adult height in children with short stature and idiopathic delayed puberty after different management

M. Maghnie, M. Cisternino, S. Zucchini, 2008, European Journal of Pediatrics.

What microRNAs could tell us about the human X chromosome

C. Gravholt, M. Salerno, N. Potenza, 2020, Cellular and Molecular Life Sciences.

Menstrual cycle pattern during the first gynaecological years in girls with precocious puberty following gonadotropin-releasing hormone analogue treatment

A. Pasquino, L. Iughetti, M. Salerno, 2006, European Journal of Pediatrics.

Adolescent Girls with Idiopathic Central Precocious Puberty: Typical Character Traits

M. Micillo, M. Salerno, S. Di Maio, 2000, Journal of pediatric endocrinology & metabolism : JPEM.

APECED: A Paradigm of Complex Interactions between Genetic Background and Susceptibility Factors

C. Pignata, M. Salerno, D. Capalbo, 2013, Front. Immunol..

Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy: Insights into Genotype-Phenotype Correlation

G. Giardino, C. Pignata, P. Vajro, 2012, International journal of endocrinology.

Molecular background and genotype-phenotype correlation in autoimmune-polyendocrinopathy-candidiasis-ectodermal-distrophy patients from Campania and in their relatives

C. Pignata, E. Arvat, R. Giordano, 2011, Journal of Endocrinological Investigation.

Neurodevelopmental Outcomes in Children with Congenital Hypothyroidism

M. Salerno, M. Cerbone, L. D. Martino, 2015 .

Molecular Analysis of the GNAS1 Gene for the Correct Diagnosis of Albright Hereditary Osteodystrophy and Pseudohypoparathyroidism

M. Maghnie, I. Dianzani, S. Maio, 2003, Pediatric Research.

Expression of growth hormone receptor by peripheral blood lymphocytes in children: evaluation in clinical conditions of impaired growth

R. Badolato, M. Waters, S. Venuta, 1997, Clinical endocrinology.

Use of office hysteroscopy to empty a very large hematometra in a young virgin patient with mosaic Turner's syndrome.

M. Guida, A. Di Spiezio Sardo, G. Bifulco, 2007, Fertility and sterility.

Metamorphic thyroid autoimmunity in Down Syndrome: from Hashimoto’s thyroiditis to Graves’ disease and beyond

L. Iughetti, G. Radetti, M. Salerno, 2015, Italian Journal of Pediatrics.

Peculiarities of Graves' disease in children and adolescents with Down's syndrome.

A. Mussa, G. Radetti, M. Salerno, 2010, European journal of endocrinology.

Hormonal and neuropsychological evaluation of two 47,XYY patients with pituitary abnormalities

E. Giudice, M. Salerno, D. Capalbo, 2008, American journal of medical genetics. Part A.

Prospective evaluation of autoimmune and non-autoimmune subclinical hypothyroidism in Down syndrome children.

A. Alibrandi, G. Pajno, I. Scala, 2020, European journal of endocrinology.

In young patients with Turner or Down syndrome, Graves' disease presentation is often preceded by Hashimoto's thyroiditis.

F. Lombardo, M. Salerno, F. De Luca, 2014, Thyroid : official journal of the American Thyroid Association.

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

A. Pistorio, A. Mussa, M. Salerno, 2014, The Journal of pediatrics.

MANAGEMENT OF ENDOCRINE DISEASE Subclinical hypothyroidism in children.

M. Salerno, D. Capalbo, N. Improda, 2020, European journal of endocrinology.

Frequency of Hashimoto’s Thyroiditis Antecedents in the History of Children and Adolescents with Graves’ Disease

A. Mussa, F. Lombardo, M. Salerno, 2010, Hormone Research in Paediatrics.

Five-Year Prospective Evaluation of Thyroid Function Test Evolution in Children with Hashimoto's Thyroiditis Presenting with Either Euthyroidism or Subclinical Hypothyroidism.

M. Salerno, F. De Luca, M. Valenzise, 2016, Thyroid : official journal of the American Thyroid Association.

Underlying Hashimoto's thyroiditis negatively affects the evolution of subclinical hypothyroidism in children irrespective of other concomitant risk factors.

A. Mussa, F. Lombardo, M. Salerno, 2015, Thyroid : official journal of the American Thyroid Association.

Intellectual outcome at 12 years of age in congenital hypothyroidism.

A. Tenore, C. Bravaccio, M. Salerno, 1999, European journal of endocrinology.

The structure of human STAT5A and B genes reveals two regions of nearly identical sequence and an alternative tissue specific STAT5B promoter.

M. D'urso, C. Pignata, M. Ursini, 2002, Gene.

The Italian screening program for primary congenital hypothyroidism: Actions to improve screening, diagnosis, follow-up, and surveillance

V. Stoppioni, F. Mosca, M. Tonacchera, 2013, Journal of Endocrinological Investigation.

Prognostic factors in the intellectual development at 7 years of age in children with congenital hypothyroidism

A. Tenore, S. Maio, G. Valerio, 1995, Journal of endocrinological investigation.

Factors predicting final height in early treated congenital hypothyroid patients

M. Salerno, M. Delvecchio, C. Zecchino, 2006, Clinical endocrinology.

Effect of different starting doses of levothyroxine on growth and intellectual outcome at four years of age in congenital hypothyroidism.

A. Tenore, C. Bravaccio, M. Micillo, 2002, Thyroid : official journal of the American Thyroid Association.

γ Chain transducing element: a shared pathway between endocrine and immune system.

E. Cirillo, C. Pignata, L. Palamaro, 2011, Cellular immunology.

Growth retardation, developmental delay, distinctive face, multiple endocrine abnormalities, and adenylyl cyclase dysfunction: A new syndrome?

G. Andria, M. Lecora, M. Salerno, 2003, American Journal of Medical Genetics. Part A.

Growth Hormone Receptor (GHR) 6Ω Pseudoexon Activation: A Novel Cause of Severe Growth Hormone Insensitivity

C. Pignata, V. Hwa, L. Metherell, 2021, The Journal of clinical endocrinology and metabolism.

Cutaneous vasculitis in patients with autoimmune polyendocrine syndrome type 1: report of a case and brief review of the literature

E. Cirillo, C. Pignata, M. Salerno, 2014, BMC Pediatrics.

High intrafamilial variability in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy: A case study

U. Dianzani, C. Pignata, A. Fusco, 2011, Journal of Endocrinological Investigation.

[Turner syndrome and insulin-dependent diabetes mellitus].

A. Franzese, M. Salerno, A. Argenziano, 1994, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Serum thyrotropin concentration in children with isolated thyroid nodules.

M. Segni, A. Mussa, L. Iughetti, 2013, The Journal of pediatrics.

A frequent oligogenic involvement in congenital hypothyroidism.

D. Larizza, D. Ardissino, S. Duga, 2017, Human molecular genetics.

Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry

M. C. Savanelli, M. T. Pellecchia, G. Argenziano, 2021, Journal of public health.

Case Report: Neonatal Cholestasis as Early Manifestation of Primary Adrenal Insufficiency

M. Salerno, R. Iorio, D. Capalbo, 2021, Frontiers in Pediatrics.

Cut-off limits of the GH response to GHRH plus arginine test and IGF-I levels for the diagnosis of GH deficiency in late adolescents and young adults.

M. Maghnie, L. Ghizzoni, E. Ghigo, 2007, European journal of endocrinology.

Reperti RM in pazienti con deficit di GH

A. D’Amico, M. Salerno, R. Elefante, 1997 .

Growth Hormone Improves Cardiopulmonary Capacity and Body Composition in Children With Growth Hormone Deficiency

F. Giallauria, C. Vigorito, A. Rapacciuolo, 2017, The Journal of clinical endocrinology and metabolism.

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

M. Salerno, G. Weber, F. De Luca, 2015, Italian Journal of Pediatrics.

Evaluation of Adult Height in Patients with Non-Permanent Idiopathic GH Deficiency

S. Loche, M. Cappa, M. Salerno, 2023, Endocrines.

IGF1 for the diagnosis of growth hormone deficiency in children and adolescents: a reappraisal

M. Maghnie, S. Loche, M. Cappa, 2020, Endocrine connections.

Functional SNPs within the intron 1 of the PROP1 gene contribute to combined growth hormone deficiency (CPHD).

F. Prodam, M. Godi, M. Salerno, 2012, The Journal of clinical endocrinology and metabolism.

Efficacy and safety of growth hormone treatment in children with short stature: the Italian cohort of the GeNeSIS clinical study

A. Pasquino, D. Larizza, S. Bernasconi, 2015, Journal of Endocrinological Investigation.

Growth pattern during the first 36 months of life in congenital adrenal hyperplasia (21-hydroxylase deficiency).

A. Tenore, A. Franzese, M. Salerno, 1997, Hormone research.

Abnormal GH receptor signaling in children with idiopathic short stature.

C. Pignata, M. Ursini, R. Rosenfeld, 2001, The Journal of clinical endocrinology and metabolism.

Growth Trajectory and Adult Height in Children with Nonclassical Congenital Adrenal Hyperplasia

A. Alibrandi, A. Grandone, F. Baronio, 2020, Hormone Research in Paediatrics.

Adherence to growth hormone (GH) therapy in naïve to treatment GH-deficient children: data of the Italian Cohort from the Easypod Connect Observational Study (ECOS)

S. Bernasconi, S. Loche, L. Persani, 2019, Journal of endocrinological investigation.

Isolated childhood growth hormone deficiency: a 30-year experience on final height and a new prediction model

P. Trerotoli, V. Calcaterra, C. Mameli, 2022, Journal of Endocrinological Investigation.

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

A. Mussa, M. Salerno, G. Weber, 2015, Endocrine.

Assessment of red blood cell indices in growth-hormone-treated children.

R. Badolato, A. Tenore, G. Valerio, 1997, Hormone Research.

Adherence in children with growth hormone deficiency treated with r-hGH and the easypod™ device

S. Loche, M. Cappa, M. Salerno, 2016, Journal of Endocrinological Investigation.

Multisystemic Disease With Involvement of Immune, Endocrine, and Neurologic Systems

C. Pignata, L. Chessa, M. Salerno, 1997, Journal of child neurology.

Effects of L-thyroxine treatment on early markers of atherosclerotic disease in children with subclinical hypothyroidism.

A. Cittadini, G. Mattace Raso, M. Salerno, 2016, European journal of endocrinology.

Evaluation of function and structure of arterial wall in girls and young women with Turner syndrome

A. Colao, L. Mazzanti, G. Radetti, 2015, Journal of Endocrinological Investigation.

Novel GLI2 mutations identified in patients with Combined Pituitary Hormone Deficiency (CPHD): Evidence for a pathogenic effect by functional characterization

F. Prodam, M. Salerno, M. Wasniewska, 2018, Clinical endocrinology.

Liver abnormalities in Turner syndrome

P. Vajro, M. Salerno, S. Di Maio, 1999, European Journal of Pediatrics.

Skeptical Look at the Clinical Implication of Metabolic Syndrome in Childhood Obesity

V. Calcaterra, G. Valerio, C. Maffeis, 2023, Children.

Comparative Evaluation of Therapy with L-Thyroxine versus No Treatment in Children with Idiopathic and Mild Subclinical Hypothyroidism

A. Mussa, F. Lombardo, M. Salerno, 2012, Hormone Research in Paediatrics.

Anemia in infants with congenital hypothyroidism diagnosed by neonatal screening

A. Tenore, A. Franzese, M. Salerno, 1996, Journal of Endocrinological Investigation.

Multiplex Ligation-Dependent Probe Amplification Accurately Detects Turner Syndrome in Girls with Short Stature

L. Perrone, A. Grandone, A. Torella, 2016, Hormone Research in Paediatrics.

The R156H variation in IL-12R beta 1 is not a mutation

G. Giardino, C. Pignata, A. Fusco, 2013 .

Treatment of hypopituitarism in infancy. Effect on head circumference growth.

G. Valerio, M. Salerno, S. Di Maio, 1999, Minerva pediatrica.

Common carotid intima-media thickness in growth hormone (GH)-deficient adolescents: a prospective study after GH withdrawal and restarting GH replacement.

A. Colao, G. Lombardi, M. Salerno, 2005, The Journal of clinical endocrinology and metabolism.

Increased prevalence of thyroid autoimmunity and hypothyroidism in patients with glycogen storage disease type I.

G. Andria, D. Melis, G. Parenti, 2007, The Journal of pediatrics.

Cardiovascular Health in Children and Adolescents With Congenital Adrenal Hyperplasia Due to 21-Hydroxilase Deficiency

M. Salerno, D. Capalbo, F. Barbieri, 2019, Front. Endocrinol..

Premature thelarche in Coffin‐Siris syndrome

N. Brunetti‐Pierri, M. Salerno, V. Esposito, 2003, American journal of medical genetics. Part A.

Hyper IgM syndrome presenting as chronic suppurative lung disease

G. Giardino, C. Pignata, L. Palamaro, 2012, Italian Journal of Pediatrics.

The treatment of obesity in children and adolescents: consensus position statement of the Italian society of pediatric endocrinology and diabetology, Italian Society of Pediatrics and Italian Society of Pediatric Surgery

V. Calcaterra, S. Bernasconi, A. Franzese, 2023, Italian Journal of Pediatrics.

Levothyroxine Treatment in Pediatric Benign Thyroid Nodules

M. Segni, A. Mussa, M. Salerno, 2010, Hormone Research in Paediatrics.

Cluster of cardiometabolic risk factors in children with GH deficiency: a prospective, case–control study

D. Bruzzese, R. Meli, G. Mattace Raso, 2014, Clinical endocrinology.

Analysis of a series of Italian APECED patients with autoimmune hepatitis and gastro-enteropathies

M. Cappa, A. Fierabracci, G. Maggiore, 2023, Frontiers in Immunology.

Spondylocarpotarsal synostosis: Long‐term follow‐up of a case due to FLNB mutations

N. Brunetti‐Pierri, Brendan H. Lee, D. Krakow, 2008, American journal of medical genetics. Part A.

Fetal goiter in a iodine-deficient area

A. Mariano, S. Maio, M. Salerno, 1998, Journal of endocrinological investigation.

Laparoscopy or retroperitoneoscopy for pediatric patients with adrenal masses?

M. Salerno, G. De Filippo, C. Esposito, 2015, Minerva pediatrica.

Real-life long-term efficacy and safety of recombinant human growth hormone therapy in children with short stature homeobox-containing deficiency

L. Iughetti, M. Salerno, M. Wasniewska, 2023, Endocrine Connections.

Non-autoimmune subclinical hypothyroidism due to a mutation in TSH receptor: report on two brothers

C. Pignata, P. Agretti, M. Tonacchera, 2013, Italian Journal of Pediatrics.

Update on early cardiovascular and metabolic risk factors in children and adolescents affected with growth hormone deficiency.

C. Pignata, P. Vajro, G. Parenti, 2012, Minerva endocrinologica.

Quality of life in children and adolescents with growth hormone deficiency and their caregivers: an Italian survey.

M. Cappa, M. Salerno, F. Spandonaro, 2023, Journal of endocrinological investigation.

Identification of three novel SEDL mutations, including mutation in the rare, non‐canonical splice site of exon 4

M. Shaw, J. Gécz, N. Brunetti‐Pierri, 2003, Clinical genetics.

Contents Vol. 77, 2012

F. Kronenberg, V. Tillmann, T. Stijnen, 2012, Hormone Research in Paediatrics.

Management of childhood-onset craniopharyngioma in Italy: A multicenter seven year follow-up study of 145 patients.

C. Marras, M. Maghnie, S. Loche, 2021, The Journal of clinical endocrinology and metabolism.

Cognitive function in children with idiopathic subclinical hypothyroidism: Effects of 2 years of levothyroxine therapy

C. Bravaccio, M. Salerno, D. Capalbo, 2020 .

Treatment of Congenital Hypothyroidism: Comparison Between L-Thyroxine Oral Solution and Tablet Formulations up to 3 years of age.

A. Mussa, M. Salerno, M. Street, 2021, European journal of endocrinology.

Posterior reversible encephalopathy syndrome in a child during an accelerated phase of a severe APECED phenotype due to an uncommon mutation of AIRE

C. Pignata, C. Mazza, M. Salerno, 2008, Clinical endocrinology.

Glucose homeostasis in GHD children during long-term replacement therapy: a case−control study

D. Bruzzese, M. Salerno, F. De Luca, 2018, Endocrine.

New strategies for the treatment of lysosomal storage diseases (review).

C. Pignata, P. Vajro, G. Parenti, 2013, International journal of molecular medicine.

Five-year prospective evaluation of thyroid function in girls with subclinical mild hypothyroidism of different etiology.

A. Mussa, M. Salerno, F. De Luca, 2015, European journal of endocrinology.

A frequent oligogenic involvement in congenital hypothyroidism.

D. Larizza, D. Ardissino, S. Duga, 2017, Human molecular genetics.

Effect of long-term GH treatment in a patient with CHARGE association

D. Melis, M. Salerno, M. Tufano, 2014, Italian Journal of Pediatrics.

Hormonal and neuropsychological evaluation of two 47,XYY patients with pituitary abnormalities

E. Giudice, M. Salerno, D. Capalbo, 2008, American journal of medical genetics. Part A.

Effects of L-thyroxine treatment on early markers of atherosclerotic disease in children with subclinical hypothyroidism.

A. Cittadini, G. Mattace Raso, M. Salerno, 2016, European journal of endocrinology.

Adopted Girls with Idiopathic Central Precocious Puberty: Observations About Character

M. Salerno, V. Esposito, D. Capalbo, 2004, Journal of pediatric endocrinology & metabolism : JPEM.