M. Cappa

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An observational study comparing continuous subcutaneous insulin infusion (CSII) and insulin glargine in children with type 1 diabetes

R. Schiaffini, P. Ciampalini, S. Spera, 2005, Diabetes/metabolism research and reviews.

Expression of PD-1 Molecule on Regulatory T Lymphocytes in Patients with Insulin-Dependent Diabetes Mellitus

R. Schiaffini, M. Cappa, A. Crinò, 2015, International journal of molecular sciences.

Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy: Report of Seven Additional Sicilian Patients and Overview of the Overall Series from Sicily

S. Barollo, M. Cappa, A. Fierabracci, 2014, Hormone Research in Paediatrics.

Inside out the Ragbag of Glucose Intolerance in Obese Adolescents

G. Bedogni, A. Tura, M. Manco, 2017, Hormone Research in Paediatrics.

Impact of short stature on quality of life: A systematic literature review.

M. Dattani, P. Backeljauw, W. Kiess, 2021, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Is subclinical adrenal failure in adrenoleukodystrophy/adrenomyeloneuropathy reversible?

M. Cappa, C. Aiello, C. Bizzarri, 2011, Journal of endocrinological investigation.

Growth in Children With Noonan Syndrome and Effects of Growth Hormone Treatment on Adult Height

M. Maghnie, M. Digilio, G. Ferrero, 2021, Frontiers in Endocrinology.

Abnormal glucose tolerance in children with cystic fibrosis: the predictive role of continuous glucose monitoring system.

V. Lucidi, R. Schiaffini, M. Cappa, 2010, European journal of endocrinology.

Somatostatin infusion withdrawal: studies in the acute and recovery phase of anorexia nervosa, and in obesity.

F. Cavagnini, M. Scacchi, M. Cappa, 2003, European journal of endocrinology.

Altered B cell homeostasis and Toll-like receptor 9-driven response in patients affected by autoimmune polyglandular syndrome Type 1: Altered B cell phenotype and dysregulation of the B cell function in APECED patients.

S. Barollo, E. Gianchecchi, M. Cappa, 2017, Immunobiology.

An 8-year-old boy with autoimmune hepatitis and Candida onychosis as the first symptoms of autoimmune polyglandular syndrome (APS1): identification of a new homozygous mutation in the autoimmune regulator gene (aire)

C. Lintas, M. Cappa, A. Fierabracci, 2008, European Journal of Pediatrics.

Does Graves’ Disease during Puberty Influence Adult Bone Mineral Density?

M. Cappa, F. Rigon, G. Radetti, 2002, Hormone Research in Paediatrics.

Case Report: Precision COVID-19 Immunization Strategy to Overcome Individual Fragility: A Case of Generalized Lipodystrophy Type 4

B. Dallapiccola, E. Agolini, A. Novelli, 2022, Frontiers in Immunology.

Simpson‐golabi‐behmel syndrome: An X‐linked encephalo‐tropho‐schisis syndrome

J. Opitz, G. Neri, M. Cappa, 1988, American journal of medical genetics. Part A.

Pre-diabetes in Italian obese children and youngsters

G. Valerio, P. Ciampalini, M. Cappa, 2011, Journal of endocrinological investigation.

Th 1 cytokine production by peripheral blood mononuclear cells in X-linked adrenoleukodystrophy

M. Cappa, A. Biase, S. Salvati, 2001, Journal of the Neurological Sciences.

Impact of long-term use of eHealth systems in adolescents with type 1 diabetes treated with sensor-augmented pump therapy

R. Schiaffini, P. Ciampalini, M. Cappa, 2016, Journal of telemedicine and telecare.

REDUCED GROWTH HORMONE RESPONSE TO GROWTH HORMONE‐RELEASING HORMONE IN CHILDREN WITH SIMPLE OBESITY: EVIDENCE FOR SOMATOMEDIN‐C MEDIATED INHIBITION

S. Loche, M. Cappa, A. Crinò, 1987, Clinical endocrinology.

Effect of the enhancement of the cholinergic tone by pyridostigmine on the exercise-induced growth hormone release in man

E. Ghigo, S. Loche, F. Drago, 1993, Journal of endocrinological investigation.

Pyridostigmine counteracts the blunted growth hormone response to growth hormone-releasing hormone of obese children.

E. Ghigo, V. Locatelli, S. Loche, 1989, Acta endocrinologica.

Adult height in patients with permanent growth hormone deficiency with and without multiple pituitary hormone deficiencies.

R. Lorini, M. Maghnie, C. Tinelli, 2006, The Journal of clinical endocrinology and metabolism.

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

A. Salvatoni, A. Franzese, L. Beccaria, 2008, American journal of medical genetics. Part A.

Growth hormone (GH) response to combined pyridostigmine and GH-releasing hormone administration in patients with Prader-Labhard-Willi syndrome.

E. Ghigo, D. Carta, S. Loche, 1993, Hormone research.

Pituitary-ovarian responses to leuprolide acetate testing in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

S. Bernasconi, L. Ibáñez, L. Ghizzoni, 1996 .

New compositional data on ancient mortars from Hagia Sophia (Istanbul, Turkey)

Hasan Bora Yavuz, G. M. Crisci, A. Pecci, 2017, Archaeological and Anthropological Sciences.

1-Hour plasma glucose in obese youth

S. Caprio, M. Manco, L. Perrone, 2012, Acta Diabetologica.

Prevalence of prediabetes in children and adolescents by class of obesity

L. Ravà, A. Deodati, M. Manco, 2022, Pediatric obesity.

The bricks of Hagia Sophia (Istanbul, Turkey): a new hypothesis to explain their compositional difference

G. M. Crisci, F. Chiaravalloti, A. Pecci, 2019, Journal of Cultural Heritage.

No Protective Effect of Calcitriol on β-Cell Function in Recent-Onset Type 1 Diabetes

G. Ghirlanda, N. Napoli, P. Pozzilli, 2010, Diabetes Care.

Computer use, free time activities and metabolic control in patients with type 1 diabetes.

P. Pozzilli, D. Pitocco, S. Spera, 2010, Diabetes research and clinical practice.

A case of primary selective hypoaldosteronism carrying three mutations in the aldosterone synthase (Cyp11b2) gene.

A. Masotti, M. Cappa, C. Bizzarri, 2012, Gene.

ZnT8 antibodies in patients with cystic fibrosis: an expression of secondary beta-cell damage?

V. Lucidi, M. Cappa, C. Bizzarri, 2013, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Basal insulin supplementation in Type 1 diabetic children: A long-term comparative observational study between continuous subcutaneous insulin infusion and glargine insulin

R. Schiaffini, P. Ciampalini, M. Cappa, 2007, Journal of endocrinological investigation.

Consensus statement - Prader-Willi syndrome: Growth hormone (GH)/insulin-like growth factor axis deficiency and GH treatment

D. Wilson, M. Cappa, G. Chiumello, 2000 .

Sexual dimorphism of body composition and insulin sensitivity across pubertal development in obese Caucasian subjects.

O. Porzio, M. Manco, R. Schiaffini, 2009, European journal of endocrinology.

Metabolic Syndrome in Italian Obese Children and Adolescents: Stronger Association with Central Fat Depot than with Insulin Sensitivity and Birth Weight

M. Cappa, C. Brufani, F. Barbetti, 2011, International journal of hypertension.

Susceptibility to oxidation of plasma low-density lipoprotein in X-linked adrenoleukodystrophy: effects of simvastatin treatment.

A. Di Biase, M. Cappa, A. Biase, 2000, Molecular genetics and metabolism.

Low Birthweight Increases the Likelihood of Severe Steatosis in Pediatric Non-Alcoholic Fatty Liver Disease

M. Raponi, A. Alisi, E. Bugianesi, 2017, The American Journal of Gastroenterology.

Obese children with low birth weight demonstrate impaired beta-cell function during oral glucose tolerance test.

O. Porzio, M. Cappa, C. Brufani, 2009, The Journal of clinical endocrinology and metabolism.

Word Count : 5897 ( including all parts ) Number of table and Figures : 4 Tables and 2 Figures

A. Alisi, E. Bugianesi, A. Dotta, 2022 .

Thyroid Nodules and Carcinoma

A. Mussa, M. Cappa, A. Corrias, 2015 .

Next-Generation Sequencing Identifies Different Genetic Defects in 2 Patients with Primary Adrenal Insufficiency and Gonadotropin-Independent Precocious Puberty

A. Novelli, S. Loche, M. Mucciolo, 2018, Hormone Research in Paediatrics.

Use of testosterone gel compared to intramuscular formulation for puberty induction in males with constitutional delay of growth and puberty: a preliminary study

M. Cappa, D. Fintini, L. Chioma, 2018, Journal of Endocrinological Investigation.

Routine screening by brain magnetic resonance imaging is not indicated in every girl with onset of puberty between the ages of 6 and 8 years.

M. Cappa, S. Cianfarani, S. Pedicelli, 2014, The Journal of clinical endocrinology and metabolism.

Growth hormone treatment started in the first year of life in infants with chronic renal failure

F. Emma, M. Cappa, D. Kiepe, 2009, Pediatric Nephrology.

Final Height in Girls With Central Idiopathic Precocious Puberty Treated With Gonadotropin-Releasing Hormone Analog and Oxandrolone

S. Bernasconi, L. Ghizzoni, S. Loche, 2006 .

Final height in girls with central idiopathic precocious puberty treated with gonadotropin-releasing hormone analog and oxandrolone.

S. Bernasconi, L. Ghizzoni, S. Loche, 2006, The Journal of clinical endocrinology and metabolism.

Altered Bone Mineral Density in Patients with Complete Androgen Insensitivity Syndrome

G. Saggese, M. Cappa, R. Lala, 1998, Hormone Research in Paediatrics.

Turner Syndrome and Diabetes

M. Cappa, A. Grossi, 2017 .

Succinic semialdehyde dehydrogenase deficiency: clinical, biochemical and molecular characterization of a new patient with severe phenotype and a novel mutation

R. Carrozzo, A. Novelletto, K. Gibson, 2006, Clinical genetics.

Birth weight influences the clinical phenotype and the metabolic control of patients with type 1 diabetes (T1D)

L. Ravà, R. Schiaffini, P. Ciampalini, 2013, Diabetes/metabolism research and reviews.

P. Pozzilli, D. Pitocco, M. Cappa, 2012, Diabetes Care.

Incidence of Type 1 Diabetes Has Doubled in Rome and the Lazio Region in the 0- to 14-Year Age-Group: A 6-Year Prospective Study (2004–2009)

P. Pozzilli, S. Petrucci, M. Cappa, 2010, Diabetes Care.

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.

Bone mineral density and body composition in male children with hypogonadism

M. Cappa, C. Brufani, D. Fintini, 2009, Journal of endocrinological investigation.

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.

Water Balance and ‘Salt Wasting' in the First Year of Life: The Role of Aldosterone-Signaling Defects

M. Cappa, C. Bizzarri, S. Cianfarani, 2016, Hormone Research in Paediatrics.

The use of prohibited substances for therapeutic reasons in athletes affected by endocrine diseases and disorders: the therapeutic use exemption (TUE) in clinical endocrinology

F. Pigozzi, L. Frati, A. Gianfrancesco, 2019, Journal of Endocrinological Investigation.

A mixture of oleic, erucic and conjugated linoleic acids modulates cerebrospinal fluid inflammatory markers and improve somatosensorial evoked potential in X-linked adrenoleukodystrophy female carriers

Massimiliano Valeriani, C. Vollono, S. Banni, 2011, Journal of Inherited Metabolic Disease.

High dose immunoglobulin IV treatment in adrenoleukodystrophy.

E. Bertini, A. Di Biase, M. Cappa, 1994, Journal of neurology, neurosurgery, and psychiatry.

Blood Pressure and Left Ventricular Characteristics in Young Patients with Classical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

L. Ravà, M. Cappa, C. Bizzarri, 2010, International journal of pediatric endocrinology.

Prevalence of elevated 1-h plasma glucose and its associations in obese youth.

S. Bernardini, M. Cappa, C. Brufani, 2016, Diabetes research and clinical practice.

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..

Profile of mecasermin for the long-term treatment of growth failure in children and adolescents with severe primary IGF-1 deficiency

M. Cappa, C. Brufani, D. Fintini, 2009, Therapeutics and clinical risk management.

Children with Prader-Willi syndrome exhibit more evident meal-induced responses in plasma ghrelin and peptide YY levels than obese and lean children.

A. Salvatoni, A. Sartorio, M. Cappa, 2010, European journal of endocrinology.

Lipoprotein (a) in childhood: Correlations with family history of cardiovascular disease

R. Bernabei, A. Verrotti, M. Cappa, 2003, Journal of endocrinological investigation.

Glutathione imbalance in patients with X-linked adrenoleukodystrophy☆

E. Bertini, S. Petrillo, M. Cappa, 2013, Molecular genetics and metabolism.

Metabolic syndrome in adult patients with Prader-Willi syndrome.

G. Bedogni, A. Salvatoni, P. Brambilla, 2013, Nutrition, metabolism, and cardiovascular diseases : NMCD.

Interaction of free fatty acids and arginine on growth hormone secretion in man.

E. Ghigo, S. Loche, M. Cappa, 1994, Metabolism: clinical and experimental.

Growth Hormone-Releasing Hormone Resistance in Pseudohypoparathyroidism Type Ia: New Evidence for Imprinting of the Gsα Gene

E. Menis, M. Maghnie, P. Beck‐Peccoz, 2003 .

Glucose tolerance status in 510 children and adolescents attending an obesity clinic in Central Italy

P. Ciampalini, M. Cappa, C. Brufani, 2010, Pediatric diabetes.

The growth hormone response to hexarelin in children: reproducibility and effect of sex steroids.

E. Ghigo, S. Loche, A. Colao, 1997, The Journal of clinical endocrinology and metabolism.

Bone mineral density in adolescent girls with early onset of anorexia nervosa.

M. Cappa, M. Castro, C. Bizzarri, 2007, Clinical nutrition.

Residual β-Cell Mass Influences Growth of Prepubertal Children With Type 1 Diabetes

M. Cappa, C. Bizzarri, S. Cianfarani, 2013, Hormone Research in Paediatrics.

Ovarian hyperandrogenism in adolescents and young women with type I diabetes is primarily related to birth weight and body mass index.

L. Ravà, R. Schiaffini, P. Ciampalini, 2011, Fertility and sterility.

Fatty liver and insulin resistance in children with hypobetalipoproteinemia: the importance of aetiology

M. Cappa, C. Brufani, V. Nobili, 2013, Clinical endocrinology.

KBG syndrome: Common and uncommon clinical features based on 31 new patients

M. Digilio, B. Dallapiccola, M. Rinelli, 2020, American journal of medical genetics. Part A.

The growth hormone response to hexarelin in patients with Prader-Willi syndrome

G. Raguso, G. Neri, S. Loche, 1998, Journal of endocrinological investigation.

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

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

Different Sports in Adolescence: Effect on Lipid Profile, Glucose Metabolism, Body Composition, Bone Density, Bone Quality, Bone Markers, Vascular Function and Structure, Pituitary and Hypothalamic Antibodies

A. Bellis, M. Cappa, D. Gatti, 2015 .

Thyroid Function Tests in Obese Prepubertal Children: Correlations with Insulin Sensitivity and Body Fat Distribution

M. Manco, M. Cappa, C. Brufani, 2012, Hormone Research in Paediatrics.

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

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

Exogenous growth hormone administration does not inhibit the growth hormone response to hexarelin in normal men

G. Federici, D. Carta, S. Loche, 1995, Journal of endocrinological investigation.

Pituitary magnetic resonance imaging in idiopathic and genetic growth hormone deficiency.

M. Maghnie, S. Loche, M. Cappa, 2003, The Journal of clinical endocrinology and metabolism.

Pyridostigmine potentiates growth hormone (GH)-releasing hormone-induced GH release in both men and women.

R. Valcavi, F. Casanueva, E. Arvat, 1993, The Journal of clinical endocrinology and metabolism.

Bone and body composition analyzed by Dual-energy X-ray Absorptiometry (DXA) in clinical and nutritional evaluation of young patients with Cystic Fibrosis: a cross-sectional study.

V. Lucidi, S. Bella, M. Cappa, 2009, BMC pediatrics.

Early Glucose Derangement Detected by Continuous Glucose Monitoring and Progression of Liver Fibrosis in Nonalcoholic Fatty Liver Disease: An Independent Predictive Factor?

D. Liccardo, A. Alisi, R. Schiaffini, 2015, Hormone Research in Paediatrics.

Hypogonadism in Male Infants and Adolescents: New Androgen Formulations

M. Cappa, L. Chioma, 2021, Hormone Research in Paediatrics.

The growth hormone response to hexarelin in patients with different hypothalamic-pituitary abnormalities.

M. Maghnie, C. Tinelli, S. Loche, 1998, The Journal of clinical endocrinology and metabolism.

The growth hormone response to pyridostigmine plus growth hormone releasing hormone is not influenced by pubertal maturation

S. Loche, M. Cappa, R. Salvatori, 1991, Journal of endocrinological investigation.

Neurophysiological abnormalities in adrenoleukodystrophy carriers. Evidence of different degrees of central nervous system involvement.

E. Bertini, A. Oliviero, Massimiliano Valeriani, 1997, Brain : a journal of neurology.

Thyroid autoimmunity in children with coeliac disease: a prospective survey

R. Guglielmi, M. Cappa, M. Crisogianni, 2011, Archives of Disease in Childhood.

Cushing's Syndrome in a 6-month-old Boy: A Rare Side-effect due to Inadequate use of Topical Corticosteroids.

M. Cappa, C. Bizzarri, M. El Hachem, 2016, Acta dermato-venereologica.

Glucose tolerance affects pubertal growth and final height of children with cystic fibrosis

V. Lucidi, M. Cappa, C. Bizzarri, 2015, Pediatric pulmonology.

MKRN3 circulating levels in Prader–Willi syndrome: a pilot study

M. Manco, E. D. del Giudice, M. Cappa, 2022, Journal of Endocrinological Investigation.

Wrist circumference is a biomarker of adipose tissue dysfunction and cardiovascular risk in children with obesity

M. Cappa, R. Buzzetti, L. D'Onofrio, 2020, Journal of Endocrinological Investigation.

Non‐Alcoholic Fatty Liver Disease (NAFLD) in children and adolescents with Prader–Willi Syndrome (PWS)

M. Cappa, A. Crinò, C. Brufani, 2016, Pediatric obesity.

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.

Growth hormone-releasing hormone resistance in pseudohypoparathyroidism type ia: new evidence for imprinting of the Gs alpha gene.

M. Maghnie, P. Beck‐Peccoz, M. Cappa, 2003, The Journal of clinical endocrinology and metabolism.

Final height after growth hormone therapy in non-growth-hormone-deficient children with short stature.

D. Carta, S. Loche, M. Cappa, 1994, The Journal of pediatrics.

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.

Exploiting novel tailored immunotherapies of type 1 diabetes: Short interfering RNA delivered by cationic liposomes enables efficient down-regulation of variant PTPN22 gene in T lymphocytes.

S. De Santis, S. Petrini, M. Cappa, 2019, Nanomedicine : nanotechnology, biology, and medicine.

Identification of GAD65 AA 114-122 reactive 'memory-like' NK cells in newly diagnosed Type 1 diabetic patients by HLA-class I pentamers

E. Gianchecchi, M. Andreani, M. Cappa, 2017, PloS one.

Efficacy of short-term induction therapy with low-dose testosterone as a diagnostic tool in the workup of delayed growth and puberty in boys

M. Cappa, T. Todisco, D. Fintini, 2022, Journal of Endocrinological Investigation.

Disorders of Pubertal Development: Precocious Puberty

M. Cappa, L. Chioma, 2021, Pediatric and Adolescent Andrology.

Growth hormone excess in children with neurofibromatosis type‐1 and optic glioma

A. Cacchione, R. Capolino, A. Mastronuzzi, 2017, American journal of medical genetics. Part A.

Clinical features suggestive of non-classical 21-hydroxylase deficiency in children presenting with precocious pubarche

L. Ravà, O. Porzio, M. Cappa, 2012, Journal of pediatric endocrinology & metabolism : JPEM.

Ontogeny of Hypothalamus-Pituitary Gonadal Axis and Minipuberty: An Ongoing Debate?

M. Cappa, C. Bizzarri, 2020, Frontiers in Endocrinology.

Metabolic factors affecting residual beta cell function assessed by C-peptide secretion in patients with newly diagnosed type 1 diabetes.

P. Pozzilli, D. Pitocco, M. Cappa, 2006, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

Rachitismo ipofosforemico X-linked

F. Emma, M. Cappa, D. Fintini, 2020, Medico e Bambino.

X-linked hypophosphatemic rickets: an Italian experts’ opinion survey

M. Maghnie, M. Brandi, F. Emma, 2019, Italian Journal of Pediatrics.

Frequent TSH receptor genetic alterations with variable signaling impairment in a large series of children with nonautoimmune isolated hyperthyrotropinemia.

H. Biebermann, D. Libri, C. Mian, 2012, The Journal of clinical endocrinology and metabolism.

The growth hormone-releasing activity of hexarelin, a new synthetic hexapeptide, in short normal and obese children and in hypopituitary subjects.

D. Carta, S. Loche, B. Imbimbo, 1995, The Journal of clinical endocrinology and metabolism.

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

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

Acute administration of hexarelin stimulates GH secretion during day and night in normal men

S. Loche, A. Colao, B. Imbimbo, 1997, Clinical endocrinology.

Somatotropic function in short stature: evaluation by integrated auxological and hormonal indices in 214 children. The Italian Collaborative Group of Neuroendocrinology.

F. Dammacco, E. Ghigo, S. Loche, 1993, The Journal of clinical endocrinology and metabolism.

Central adrenal insufficiency in young adults with Prader‐Willi Syndrome

A. Salvatoni, S. Andrulli, L. Beccaria, 2013, Clinical endocrinology.

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.

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

A. Salvatoni, A. Franzese, L. Mazzanti, 2016, Nutrition, metabolism, and cardiovascular diseases : NMCD.

Pianeta Nutrizione kids: international pediatric conference on food, physical activity, growth and well-being

A. Veicsteinas, M. Clerici, S. Nicklaus, 2016, Italian Journal of Pediatrics.

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

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

Growth Hormone Response to Standard Provocative Stimuli and Combined Tests in Very Young Children with Prader-Willi Syndrome

S. Spera, M. Cappa, A. Crinò, 2014, Hormone Research in Paediatrics.

Multiple forms of hypogonadism of central, peripheral or combined origin in males with Prader–Willi syndrome

A. Lenzi, S. Spera, M. Cappa, 2012, Clinical endocrinology.

BioEnterics Intragastric Balloon for Treatment of Morbid Obesity in Prader–Willi Syndrome: Specific Risks and Benefits

E. Ceriati, P. Marchetti, S. Spera, 2008, Obesity Surgery.

Polycystic ovary syndrome in perimenarchal obese adolescents: experience with magnetic resonance imaging

A. Pasquino, M. Cappa, P. Cambiaso, 2008 .

Pituitary-ovarian responses to leuprolide acetate testing in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

S. Bernasconi, L. Ibáñez, L. Ghizzoni, 1996, The Journal of clinical endocrinology and metabolism.

PYRIDOSTIGMINE DOES NOT REVERSE DEXAMETHASONE‐INDUCED GROWTH HORMONE INHIBITION

M. Cappa, J. Gertner, P. Balzo, 1990, Clinical endocrinology.

Parathyroid hormone levels in pubertal uremic adolescents treated with growth hormone

G. Ardissino, G. Rizzoni, G. Montini, 2003, Pediatric Nephrology.

Mechanisms of acute hypercalcemia in pediatric patients following the interruption of Denosumab

E. Levtchenko, A. Deodati, M. Cappa, 2021, Journal of Endocrinological Investigation.

Relationship between non‐alcoholic steatohepatitis, PNPLA3 I148M genotype and bone mineral density in adolescents

C. Byrne, M. Cappa, A. Zicari, 2018, Liver international : official journal of the International Association for the Study of the Liver.

Streptococcus pneumoniae oropharyngeal colonization in school-age children and adolescents with type 1 diabetes mellitus: Impact of the heptavalent pneumococcal conjugate vaccine

C. Maffeis, S. Esposito, N. Principi, 2016, Human vaccines & immunotherapeutics.

Exercise-induced GH secretion is related to puberty

M. Cappa, C. Bizzarri, L. Di Luigi, 2020, Journal of Endocrinological Investigation.

Growth Trajectory in Children with Type 1 Diabetes Mellitus: The Impact of Insulin Treatment and Metabolic Control

M. Cappa, C. Bizzarri, S. Cianfarani, 2018, Hormone Research in Paediatrics.

Early retesting by GHRH + arginine test shows normal GH response in most children with idiopathic GH deficiency

G. Bedogni, M. Cappa, C. Bizzarri, 2015, Journal of Endocrinological Investigation.

Sexual dimorphism in growth and insulin-like growth factor-I in children with type 1 diabetes mellitus.

M. Cappa, C. Bizzarri, Marco Anziano, 2014, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Sexual dimorphismingrowth and insulin-like growth factor-I inchildren with type 1 diabetes mellitus

M. Cappa, C. Bizzarri, Marco Anziano, 2014 .

Growth hormone response to physical exercise in growing patients with classic congenital adrenal hyperplasia

L. Ravà, S. Loche, M. Cappa, 2009 .

GENETIC DISORDERS: CLINICAL AND THERAPEUTICAL ASPECTS

E. Bertini, G. Uziel, M. Cappa, 1994 .

Natural history of a cohort of ABCD1 variant female carriers

E. Bertini, G. Vasco, M. Petrarca, 2018, European journal of neurology.

Effects of Exogenous Hexacosanoic Acid on Biochemical Myelin Composition in Weaning and Post-Weaning Rats

A. Di Biase, M. Cappa, S. Salvati, 1997, Neurochemical Research.

Possible role of vitamin D in Covid-19 infection in pediatric population

P. D’argenio, M. Cappa, P. Rossi, 2020, Journal of Endocrinological Investigation.

Plasma Levels of Adrenomedullin in Patients with Adrenoleukodystrophy/Adrenomyeloneuropathy

A. Di Biase, M. Cappa, C. Letizia, 2005, Hormone Research in Paediatrics.

Gender differences in bone mineral density in obese children during pubertal development

M. Cappa, C. Brufani, D. Fintini, 2011, Journal of endocrinological investigation.

Efficacy of short-term induction therapy with low-dose testosterone as a diagnostic tool in the workup of delayed growth and puberty in boys

M. Cappa, T. Todisco, D. Fintini, 2022, Journal of Endocrinological Investigation.

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

M. Cappa, C. Bizzarri, M. Giordano, 2018, Journal of Endocrinological Investigation.

Responses to GHRH plus arginine test are more concordant with IGF-I circulating levels than responses to arginine and clonidine provocative tests

A. Deodati, M. Cappa, P. Cambiaso, 2011, Journal of Endocrinological Investigation.

Somatostatinergic tone in children on chronic haemodialysis and after renal transplantation

G. Rizzoni, M. Cappa, P. Borrelli, 1991, Pediatric Nephrology.

ABCD1 gene mutation in an Italian family with X-linkedadrenoleukodystrophy: case series

A. Mohn, C. Giannini, M. Cappa, 2021, Endocrinology, diabetes & metabolism case reports.

X-linked adrenoleukodystrophy: first report of the Italian Study Group

E. Bertini, G. Uziel, M. Rimoldi, 1998, The Italian Journal of Neurological Sciences.

Long-term results of the surgical treatment of craniopharyngioma: the experience at the Policlinico Gemelli, Catholic University, Rome

L. Massimi, M. Cappa, G. Tamburrini, 2005, Child's Nervous System.

Growth hormone treatment in non-growth hormone-deficient short children

S. Loche, M. Cappa, G. Ubertini, 2005, Journal of endocrinological investigation.

Non‐conventional use of growth hormone therapy

M. Cappa, P. Cambiaso, R. Fiori, 2006 .

Effect of p53 activation through targeting MDM2/MDM4 heterodimer on T regulatory and effector cells in the peripheral blood of Type 1 diabetes patients

F. Moretti, A. Arena, M. Andreani, 2020, PloS one.

Family history and ethnicity influencing clinical presentation of type 1 diabetes in childhood

M. Cappa, A. Fierabracci, C. Bizzarri, 2015, Journal of Endocrinological Investigation.

Parental origin of Gsalpha mutations in the McCune-Albright syndrome and in isolated endocrine tumors.

P. Chanson, P. Beck‐Peccoz, E. Di Battista, 2004, Journal of Clinical Endocrinology and Metabolism.

McCune-Albright Syndrome: A Clinical Longitudinal Study of 32 Patients

M. Segni, M. Cisternino, L. Ghizzoni, 1999, Journal of pediatric endocrinology & metabolism : JPEM.

Functional and Structural Analysis of Four Novel Mutations of CYP21A2 Gene in Italian Patients with 21-Hydroxylase Deficiency

L. Federici, L. Ghizzoni, O. Porzio, 2014, Hormone and Metabolic Research.

Divergent phenotype of two siblings human leukocyte antigen identical, affected by nonclassical and classical congenital adrenal hyperplasia caused by 21-hydroxylase deficiency.

G. Federici, O. Porzio, M. Testi, 2006, The Journal of clinical endocrinology and metabolism.

Evaluation of growth disorders in the paediatric clinic.

S. Loche, M. Cappa, 2003, Journal of endocrinological investigation.

A Novel Mutation in RPL10 (Ribosomal Protein L10) Causes X‐Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo‐Epiphyseal Dysplasia

S. Klauck, E. Bertini, S. Haas, 2015, Human mutation.

Noonan syndrome: improving recognition and diagnosis

M. Zenker, M. Cappa, J. Blair, 2022, Archives of Disease in Childhood.

25OH vitamin D levels in pediatric patients affected by Prader–Willi syndrome

M. Cappa, G. Grugni, C. Bizzarri, 2018, Journal of Endocrinological Investigation.

Secondary hyperparathyroidism is not always an obstacle to improved growth during recombinant human growth hormone treatment.

G. Rizzoni, M. Cappa, S. Picca, 1997, Nephron.

In Search for the Missing Link in APECED-like Conditions: Analysis of the AIRE Gene in a Series of 48 Patients

C. Cancrini, M. Cappa, A. Fierabracci, 2022, Journal of clinical medicine.

Multiorgan autoimmunity in a Turner syndrome patient with partial monosomy 2q and trisomy 10p.

A. Novelli, G. Zanni, M. Cappa, 2013, Gene.

Biallelic Inactivating TUB Variants Cause Retinal Ciliopathy Impairing Biogenesis and the Structure of the Primary Cilium

A. Bruselles, M. Tartaglia, M. Varano, 2022, International journal of molecular sciences.

Indirect methods for TSH reference interval: at last fit for purpose?

M. Cappa, M. Muraca, P. Cambiaso, 2011, American journal of clinical pathology.

Serum melatonin in children with early and delayed puberty

M. Cappa, P. Cambiaso, A. Attanasio, 1983 .

Current Concepts in Tall Stature and Overgrowth Syndromes

M. Cappa, N. Greggio, S. Drop, 2001, Journal of pediatric endocrinology & metabolism : JPEM.

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.

Microsurgical treatment of varicocele in children

G. Fabbrini, M. Cappa, F. Bergami, 1989, Pediatric Surgery International.

Lack of red hair phenotype in a North‐African obese child homozygous for a novel POMC null mutation: nonsense‐mediated decay RNA evaluation and hair pigment chemical analysis

K. Wakamatsu, L. Perrone, M. Cappa, 2012, The British journal of dermatology.

Deficiency of immunoregulatory indoleamine 2,3-dioxygenase 1in juvenile diabetes.

S. Bicciato, D. Fuchs, U. Grohmann, 2018, JCI insight.

Endocrine autoimmunity in Turner syndrome

M. Cappa, A. Crinò, A. Fierabracci, 2013, Italian Journal of Pediatrics.

How does long-term parenteral nutrition impact the bone mineral status of children with intestinal failure?

M. Cappa, M. Castro, A. Daniele, 2010, Journal of Bone and Mineral Metabolism.

Early alterations of cortical thickness and gyrification in migraine without aura: a retrospective MRI study in pediatric patients

Massimiliano Valeriani, M. Cappa, D. Longo, 2021, The Journal of Headache and Pain.

Hyperparathyroidism during growth hormone treatment: a role for puberty?

G. Rizzoni, M. Cappa, S. Picca, 2000, Pediatric Nephrology.

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

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

Lipoid congenital adrenal hyperplasia by steroidogenic acute regulatory protein (STAR) gene mutation in an Italian infant: an uncommon cause of adrenal insufficiency

A. Novelli, M. Mucciolo, M. Cappa, 2017, Italian Journal of Pediatrics.

Unilateral cryptorchidism corrected in prepubertal age: evaluation of sperm parameters, hormones, and antisperm antibodies in adult age.

A. Lenzi, M. Cappa, F. Culasso, 1997, Fertility and sterility.

Antisperm antibodies in young boys

A. Lenzi, M. Cappa, P. Nardini, 2009, Andrologia.

Autoimmune Thyroid Diseases in Children

M. Cappa, C. Bizzarri, F. Crea, 2010, Journal of thyroid research.

Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

T. Yuen, M. Gribaa, S. Haider, 2017, Proceedings of the National Academy of Sciences.

A New Homozygous Frameshift Mutation in the HSD3B2 Gene in an Apparently Nonconsanguineous Italian Family

L. Federici, S. Loche, O. Porzio, 2016, Hormone Research in Paediatrics.

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.

Congenital primary adrenal insufficiency and selective aldosterone defects presenting as salt-wasting in infancy: a single center 10-year experience

M. Cappa, P. Cambiaso, C. Bizzarri, 2016, Italian Journal of Pediatrics.

Prolactinomas in children and adolescents. Clinical presentation and long-term follow-up.

S. Loche, A. Colao, G. Lombardi, 1998, The Journal of clinical endocrinology and metabolism.

Retracted: Identification of seven novel mutations in ABCD1 by a DHPLC‐based assay in Italian patients with X‐linked adrenoleukodystrophy

C. Piantadosi, F. Santorelli, A. Di Biase, 2005, Human mutation.

Cutis verticis gyrata and chromosomal abnormalities.

G. Neri, M. Cappa, R. Marini, 1989, American journal of diseases of children.

The Opitz syndrome: a new designation for the clinically indistinguishable BBB and G syndromes.

G. Neri, M. Cappa, R. Marini, 1987, American journal of medical genetics.

Effects of total urogenital mobilization on lower urinary tract function in children with congenital adrenal hyperplasia

M. Cappa, C. Bizzarri, G. Mosiello, 2008 .

Altered B Cell Homeostasis and Toll-Like Receptor 9-Driven Response in Type 1 Diabetes Carriers of the C1858T PTPN22 Allelic Variant: Implications in the Disease Pathogenesis

E. Gianchecchi, M. Cappa, A. Crinò, 2014, PloS one.

The Gly972-->Arg IRS-1 variant is associated with type 1 diabetes in continental Italy.

L. Nisticò, G. Sesti, M. Federici, 2003, Diabetes.

“Impact of COVID-19 pandemic lockdown on early onset of puberty: experience of an Italian tertiary center”

M. Cappa, C. Bizzarri, S. Pedicelli, 2021, Italian Journal of Pediatrics.

Thyroid morphology and subclinical hypothyroidism in children and adolescents with Williams syndrome.

M. Digilio, R. Capolino, S. Loche, 2007, The Journal of pediatrics.

The response to gonadotropin releasing hormone (GnRH) stimulation test does not predict the progression to true precocious puberty in girls with onset of premature thelarche in the first three years of life.

M. Cappa, C. Bizzarri, S. Cianfarani, 2014, The Journal of clinical endocrinology and metabolism.

The adolescent «Female Athlete Triad»

M. Cappa, C. Bizzarri, G. Ubertini, 2002 .

Prevalence of copy number variants (CNVs) and rhGH treatment efficacy in an Italian cohort of children born small for gestational age (SGA) with persistent short stature associated with a complex clinical phenotype

A. Novelli, M. Mucciolo, A. Deodati, 2021, Journal of Endocrinological Investigation.

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.

Renal Tubular Dysfunction Fully Accounts for Plasma Biochemical Abnormalities in Type 1A Pseudohypoparathyroidism.

F. Emma, M. Mucciolo, M. Cappa, 2019, The Journal of clinical endocrinology and metabolism.

Nocturnal hypoglycaemia in ACTH and GH deficient children: role of continuous glucose monitoring

G. Pontrelli, R. Schiaffini, M. Cappa, 2013, Clinical endocrinology.

Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria.

G. Scarano, G. Neri, M. Cappa, 1994, American journal of medical genetics.

Influence of gender and pubertal stage at diagnosis on growth outcome in childhood thyrotoxicosis: results of a collaborative study

M. Cappa, G. Weber, G. Bona, 2006, Clinical endocrinology.

Epidemiology, Presentation and Long-Term Evolution of Graves' Disease in Children, Adolescents and Young Adults with Turner Syndrome

L. Mazzanti, A. Mussa, M. Cappa, 2014, Hormone Research in Paediatrics.

Acute suppurative thyroiditis in childhood: relative frequency among thyroid inflammatory diseases

M. Cappa, M. Vigone, M. Wasniewska, 2007, Journal of endocrinological investigation.

Antioxidant Response in Human X-Linked Adrenoleukodystrophy Fibroblasts

G. Vasco, S. Petrillo, M. Cappa, 2022, Antioxidants.

Bilateral testicular masses and adrenal insufficiency: is congenital adrenal hyperplasia the only possible diagnosis? First two cases of TARTS described in Addison-only X-linked adrenoleukodystrophy and a brief review of literature

A. Lenzi, V. Hasenmajer, A. Isidori, 2020, Journal of Endocrinological Investigation.

Serum insulin-like growth factor-I (IGF-I) reference ranges for chemiluminescence assay in childhood and adolescence. Data from a population of in- and out-patients.

G. Bedogni, M. Cappa, M. Muraca, 2012, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Inter-society consensus document on treatment and prevention of bronchiolitis in newborns and infants

C. Minetti, P. Biban, E. Baraldi, 2014, Italian Journal of Pediatrics.

Mutations in the NHEJ component XRCC4 cause primordial dwarfism.

Edward S. Miller, T. Blundell, M. van der Burg, 2015, American journal of human genetics.

Sulfonylurea treatment outweighs insulin therapy in short-term metabolic control of patients with permanent neonatal diabetes mellitus due to activating mutations of the KCNJ11 (KIR6.2) gene

F. Cerutti, M. Vanelli, M. Cappa, 2006, Diabetologia.

Two novel mutations confirm FGD1 is responsible for the Aarskog syndrome

G. Neri, M. May, G. Gillessen‐kaesbach, 2000, European Journal of Human Genetics.

Identification of novel and hotspot mutations in the channel domain of ITPR1 in two patients with Gillespie syndrome

E. Bertini, A. Bruselles, M. Tartaglia, 2017, Gene.

Co-occurrence of mutations in KIF7 and KIAA0556 in Joubert syndrome with ocular coloboma, pituitary malformation and growth hormone deficiency: a case report and literature review

E. Bertini, M. Digilio, B. Dallapiccola, 2020, BMC Pediatrics.

Keppen-Lubinsky syndrome is caused by mutations in the inwardly rectifying K+ channel encoded by KCNJ6.

A. Masotti, B. Dallapiccola, P. Uva, 2015, American journal of human genetics.

Novel point mutation in the splice donor site of exon-intron junction 6 of the androgen receptor gene in a patient with partial androgen insensitivity syndrome.

P. Rossi, R. Geremia, M. Cappa, 2000, The Journal of clinical endocrinology and metabolism.

A novel heterozygous mutation of the AIRE gene in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED).

A. Milillo, E. Bellacchio, M. Cappa, 2012, Gene.

Adrenal crisis in infants and young children with adrenal insufficiency: Management and prevention

M. Cappa, A. Grandone, F. Baronio, 2023, Frontiers in Endocrinology.

IGF2 Methylation Is Associated with Lipid Profile in Obese Children

A. Deodati, M. Cappa, C. Brufani, 2013, Hormone Research in Paediatrics.

Triple A (Allgrove) syndrome: an unusual association with syringomyelia

A. Huebner, M. Cappa, C. Bizzarri, 2013, Italian Journal of Pediatrics.

Longitudinal Neuropsychological Profile in a Patient with Triple A Syndrome

S. Vicari, M. Cappa, L. Mazzone, 2013, Case reports in pediatrics.

COVID-19 pandemic phases and female precocious puberty: The experience of the past 4 years (2019 through 2022) in an Italian tertiary center

M. Cappa, T. Todisco, C. Bizzarri, 2023, Frontiers in Endocrinology.

Early and progressive insulin resistance in young, non‐obese cancer survivors treated with hematopoietic stem cell transplantation

F. Locatelli, M. Cappa, C. Bizzarri, 2015, Pediatric blood & cancer.

Cardiopulmonary response to exercise and cardiac assessment in patients with turner syndrome.

A. Pasquino, B. Marino, M. Cappa, 2011, The American journal of cardiology.

Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.

G. Neri, F. Gurrieri, M. Cappa, 1992, American journal of medical genetics.

Auxological evaluation in patients with DiGeorge/velocardiofacial syndrome (deletion 22q11.2 syndrome)

M. Digilio, A. Giannotti, B. Dallapiccola, 2001, Genetics in Medicine.

The Bones of Children With Obesity

M. Manco, M. Cappa, D. Fintini, 2020, Frontiers in Endocrinology.

Raised C‐reactive protein levels in patients with recent onset type 1 diabetes

P. Pozzilli, M. Cappa, S. Manfrini, 2007, Diabetes/metabolism research and reviews.

Identification of a Novel PROP1 Mutation in a Patient with Combined Pituitary Hormone Deficiency and Enlarged Pituitary

A. Novelli, S. Esposito, M. Cappa, 2019, International journal of molecular sciences.

The Clinical, Genetic and Structural Basis of Congenital Adrenal Hyperplasia Due to 11β- Hydroxylase Deficiency: Results from the International Consortium on Rare Steroid Disorders

T. Yuen, S. Haider, Li Sun, 2017 .

Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe

P. Chanson, J. Bertherat, T. Battelino, 2022, European journal of endocrinology.

Sequential administration of arginine and arginine plus GHRH to test somatotroph function in short children

E. Ghigo, M. Cappa, G. Aimaretti, 2000, Journal of endocrinological investigation.

Reliability of provocative tests to assess growth hormone secretory status. Study in 472 normally growing children.

F. Dammacco, E. Ghigo, S. Loche, 1996, The Journal of clinical endocrinology and metabolism.

Kallmann’s syndrome and normosmic isolated hypogonadotropic hypogonadism: two largely overlapping manifestations of one rare disorder

G. Merlo, M. Maghnie, L. Ghizzoni, 2014, Journal of Endocrinological Investigation.

Summary of Expert Opinion on the Management of Children With Chronic Kidney Disease and Growth Failure With Human Growth Hormone

M. Maghnie, E. Verrina, G. Montini, 2020, Frontiers in Endocrinology.

Brain Magnetic Resonance Imaging as First-Line Investigation for Growth Hormone Deficiency Diagnosis in Early Childhood

M. Cappa, S. Cianfarani, S. Pedicelli, 2015, Hormone Research in Paediatrics.

The growth hormone response to hexarelin in patients with different hypothalamic-pituitary abnormalities.

M. Maghnie, C. Tinelli, S. Loche, 1998, The Journal of clinical endocrinology and metabolism.

The effect of hexarelin on growth hormone (GH) secretion in patients with GH deficiency.

S. Loche, A. Colao, B. Imbimbo, 1995, The Journal of clinical endocrinology and metabolism.

Unresolved Problems Concerning Optimal Therapy of Puberty in Children with Chronic Renal Diseases

A. Hokken-Koelega, P. Saenger, M. Cappa, 2001, Journal of pediatric endocrinology & metabolism : JPEM.

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

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

Results of early reevaluation of growth hormone secretion in short children with apparent growth hormone deficiency.

M. Maghnie, S. Loche, M. Autelli, 2002, The Journal of pediatrics.

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

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

Cut-off limits of the peak GH response to stimulation tests for the diagnosis of GH deficiency in children and adolescents: study in patients with organic GHD.

M. Maghnie, S. Pilia, S. Loche, 2016, European journal of endocrinology.

Growth hormone response to oral clonidine test in normal and short children

E. Ghigo, D. Carta, S. Loche, 1993, Journal of endocrinological investigation.

Long-term first line medical treatment in a 4-year-old girl with Xq26.3 microduplication-negative somatotropinoma. Case report and literature review

G. Colafati, M. Cappa, P. Cambiaso, 2016, Journal of pediatric endocrinology & metabolism : JPEM.

Pituicytoma and Cushing’s Disease in a 7-Year-Old Girl: A Mere Coincidence?

F. Camassei, M. Cappa, D. Longo, 2015, Pediatrics.

Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarche.

M. Maghnie, L. Ghizzoni, D. Carta, 2011, European journal of endocrinology.

Is IGF binding protein‐3 assessment helpful for the diagnosis of GH deficiency?

M. Cappa, G. Argirò, A. Spagnoli, 1995, Clinical endocrinology.

Somatotropic function in short stature: Evaluation by integrated auxological and hormonal indices in 214 children

F. Dammacco, E. Ghigo, S. Loche, 1993 .

Partially Reversible Hypopituitarism in an Adolescent with a Rathke Cleft Cyst

M. Cappa, C. Bizzarri, R. Marini, 2012, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Pain Study in X-Linked Adrenoleukodystrophy in Males and Females

A. Aloisi, G. Cevenini, V. Bachiocco, 2021, Pain and Therapy.

Young elite athletes of different sport disciplines present with an increase in pulsatile secretion of growth hormone compared with non-elite athletes and sedentary subjects

A. Sartorio, M. Cappa, C. Brufani, 2008, Journal of endocrinological investigation.

Somatostatin infusion withdrawal: studies in normal children and in children with growth hormone deficiency.

S. Loche, O. Porzio, M. Cappa, 1999, 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.

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

S. Loche, M. Cappa, L. Iughetti, 2016, Journal of Endocrinological Investigation.

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.

Rhizomelic bone dysplasia with club-like femora. A distinctive, easily recognisable disease. Case report.

M. Cappa, K. Kozłowski, P. Borrelli, 1991, La Radiologia medica.

Dihydrotestosterone (DHT) rapidly increase after maximal aerobic exercise in healthy males: the lowering effect of phosphodiesterase’s type 5 inhibitors on DHT response to exercise-related stress

F. Pigozzi, C. Minganti, C. Antinozzi, 2020, Journal of Endocrinological Investigation.

Growth hormone isoforms release in response to physiological and pharmacological stimuli

M. Cappa, C. Meazza, S. Pagani, 2008, Journal of endocrinological investigation.

Effects of replacement therapy on sleep architecture in children with growth hormone deficiency.

O. Bruni, R. Ferri, M. Cappa, 2012, Sleep medicine.

BioEnterics Intragastric Balloon for Treatment of Morbid Obesity in Prader–Willi Syndrome: Specific Risks and Benefits

E. Ceriati, P. Marchetti, S. Spera, 2008, Obesity surgery.

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

G. Bedogni, A. Salvatoni, P. Brambilla, 2010, Nutrition, metabolism, and cardiovascular diseases : NMCD.

Albuminuria and insulin resistance in children with biopsy proven non-alcoholic fatty liver disease

M. Manco, P. Ciampalini, M. Cappa, 2009, Pediatric Nephrology.

Cardiovascular Fitness, Insulin Resistance and Metabolic Syndrome in Severely Obese Prepubertal Italian Children

P. Ciampalini, M. Cappa, C. Brufani, 2008, Hormone Research in Paediatrics.

The impact of IGF-I, puberty and obesity on early retinopathy in children: a cross-sectional study

M. Cappa, C. Bizzarri, S. Bocchini, 2019, Italian Journal of Pediatrics.

Systematic Review of Metformin Use in Obese Nondiabetic Children and Adolescents

M. Manco, M. Cappa, A. Crinò, 2013, Hormone Research in Paediatrics.

The cientific WorldJOURNAL Clinical Study Central Precocious Puberty : Treatment with Triptorelin 11 . 25 mg

E. Chiocca, M. Cappa, G. Baroncelli, 2014 .

Prenatal hydrocolpos in a male

M. Silveri, M. Cappa, C. Bizzarri, 2015 .

Neurophysiologic follow-up of long-term dietary treatment in adult-onset adrenoleukodystrophy

E. Bertini, A. Oliviero, Massimiliano Valeriani, 1999, Neurology.

Absolute alcohol in esophageal vein sclerosis.

A. Pietroiusti, M. Cappa, P. Paoluzi, 1988, Gastrointestinal endoscopy.

The effect of short-term growth hormone or low-dose oxandrolone treatment in boys with constitutional growth delay

D. Carta, S. Loche, M. Cappa, 1991, Journal of endocrinological investigation.

A rare occurrence of non-classic congenital adrenal hyperplasia and type 1 diabetes mellitus in a girl with Prader-Willi Syndrome: Case report and review of the literature

M. Cappa, A. Crinò, D. Fintini, 2023, Frontiers in Endocrinology.

Use of metformin in pediatric age

M. Cappa, C. Brufani, V. Nobili, 2011, Pediatric diabetes.

Impaired Energy Expenditure Despite Normal Cardiovascular Capacity in Children with Type 1 Diabetes

A. Turchetta, A. Pelliccia, M. Cappa, 2012, Hormone Research in Paediatrics.

Multicentric Italian case–control study on 25OH vitamin D levels in children and adolescents with Prader-Willi syndrome

M. Cappa, A. Crinò, G. Grugni, 2023, Journal of Endocrinological Investigation.

The effect of flutamide on basal and ACTH-stimulated plasma levels of adrenal androgens in patients with advanced prostate cancer

E. Martino, V. Sica, M. Cappa, 1988, Journal of endocrinological investigation.

Metreleptin for the treatment of progressive encephalopathy with/without lipodystrophy (PELD) in a child with progressive myoclonic epilepsy: a case report

M. Cappa, L. de Palma, S. Pedicelli, 2020, Italian Journal of Pediatrics.

Growth hormone receptor gene mutations in two Italian patients with Laron Syndrome

L. Fassone, M. Cappa, G. Aimaretti, 2007, Journal of endocrinological investigation.

The GHRH + arginine stimulated pituitary GH secretion in children and adults with Prader-Willi syndrome shows age- and BMI-dependent and genotype-related differences.

G. Nicolao, G. De Nicolao, A. Sartorio, 2013, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

No thyroid abnormalities in patients submitted to cardiac catheterization in the first eighteen months of life

R. Guglielmi, M. Cappa, P. Cambiaso, 2011, Journal of Endocrinological Investigation.

Dumping syndrome: an unusual cause of severe hyperinsulinemic hypoglycemia in neurologically impaired children with gastrostomy.

R. Schiaffini, M. Cappa, C. Bizzarri, 2011, Minerva pediatrica.

XK‐aprosencephaly and related entities

J. Opitz, L. Chessa, A. Kennedy, 2005, American journal of medical genetics. Part A.

Research Review XK-Aprosencephaly and Related Entities

J. Opitz, L. Chessa, A. Kennedy, 2005 .

Analysis of the autoimmune regulator gene in patients with autoimmune non-APECED polyendocrinopathies.

E. Gianchecchi, M. Cappa, A. Crinò, 2013, Genomics.

Case-control analysis of the ERAP1 polymorphism rs30187 in Italian type 1 diabetes mellitus patients

E. Gianchecchi, M. Cappa, A. Crinò, 2013 .

The ALBA Project: an evaluation of needs, management, fears of Italian young patients with type 1 diabetes in a school setting and an evaluation of parents' and teachers' perceptions

R. Lorini, F. Cerutti, L. Pinelli, 2011, Pediatric diabetes.

Abnormalities of somatosensory and motor evoked potentials in adrenomyeloneuropathy: Comparison with magnetic resonance imaging and clinical findings

E. Bertini, A. Oliviero, Massimiliano Valeriani, 1997, Muscle & nerve.

Use of GLP-1 Receptor Agonists in Prader-Willi Syndrome: Report of Six Cases

M. Cappa, A. Crinò, C. Brufani, 2014, Diabetes Care.

A new multiplex method for the diagnosis of peroxisomal disorders allowing simultaneous determination of plasma very-long-chain fatty acids, phytanic, pristanic, docosahexaenoic and bile acids by high-performance liquid chromatography-atmospheric pressure chemical ionization-tandem mass spectrometry

E. Bertini, C. Dionisi-Vici, S. Boenzi, 2016, Clinica chimica acta; international journal of clinical chemistry.

Effects of Hexarelin on Growth Hormone Secretion in Short Normal Children, in Obese Children, and in Subjects with Growth Hormone Deficiency

D. Carta, S. Loche, B. Imbimbo, 1996 .

The enhancing effect of pyridostigmine on the GH response to GHRH undergoes an accelerated age-related reduction in Down syndrome.

S. Grottoli, E. Arvat, E. Ghigo, 1996, Dementia.

Pyridostigmine potentiates L-dopa- but not arginine- and galanin-induced growth hormone secretion in children.

E. Arvat, E. Ghigo, S. Loche, 1990, Neuroendocrinology.

Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial.

E. Bertini, F. Aarsen, L. de Meirleir, 2019, The lancet. Diabetes & endocrinology.

Congenital hyperinsulinism, neonatal diabetes and the risk of malignancies: an international collaborative study. Preliminary communication

H. Huopio, C. Stanley, M. Polak, 2015, Diabetic medicine : a journal of the British Diabetic Association.

Simpson-Golabi-Behmel syndrome: an X-linked encephalo-tropho-schisis syndrome.

J. Opitz, G. Neri, M. Cappa, 1988, American journal of medical genetics.

European Obesity Summit (EOS) – Joint Congress of EASO and IFSO-EC, Gothenburg, Sweden, June 1 – 4, 2016: Abstracts

Parashu Ram Pal, S. A. Todd, Jimmy D Bell, 2016, Obesity Facts.

Growth hormone (GH) response to GH-releasing hormone in short children: Lack of correlation with endogenous nocturnal GH secretion

S. Loche, M. Cappa, S. Seminara, 1997, Journal of endocrinological investigation.

A novel homozygous variant in COX5A causes an attenuated phenotype with failure to thrive, lactic acidosis, hypoglycemia, and short stature

R. Carrozzo, A. Torraco, M. Castori, 2022, Clinical genetics.

Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study.

E. Bertini, N. Brunetti‐Pierri, M. Polak, 2020, The lancet. Diabetes & endocrinology.

Clinical effects of early treatment with insulin glargine in patients with cystic fibrosis and impaired glucose tolerance

V. Lucidi, S. Bella, P. Ciampalini, 2006, Journal of endocrinological investigation.

Recombinant human GH replacement therapy in children with pseudohypoparathyroidism type Ia: first study on the effect on growth.

M. Maghnie, M. Cisternino, L. Ghizzoni, 2010, The Journal of clinical endocrinology and metabolism.

ESPE Position Statement for Paediatric Endocrinology Subspecialty

L. Federici, J. Charrow, T. Battelino, 2016, Hormone Research in Paediatrics.

Gender-, age-, body composition- and training workloaddependent differences of GH response to a disciplinespecific training session in elite athletes: A study on the field

C. Lafortuna, F. Agosti, A. Sartorio, 2004, Journal of endocrinological investigation.

Growth and pubertal spurt in Williams syndrome

A. Pasquino, A. Giannotti, M. Cappa, 1993 .

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

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

Neuroregulation of Growth Hormone During Exercise in Children

A. Calzolari, A. Turchetta, O. Porzio, 2000, International journal of sports medicine.

Sleep Characteristics in Children with Growth Hormone Deficiency

O. Bruni, R. Ferri, M. Cappa, 2011, Neuroendocrinology.

Non-conventional use of growth hormone therapy.

M. Cappa, P. Cambiaso, R. Fiori, 2006, Acta paediatrica (Oslo, Norway : 1992). Supplement.

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.

Severe Toxoplasma gondii infection in a member of a NFKB2-deficient family with T and B cell dysfunction.

C. Cancrini, G. Colafati, M. Chiriacò, 2017, Clinical immunology.

Detection of mutations in the ALD gene (ABCD1) in seven Italian families: Description of four novel mutations

E. Bertini, G. Uziel, A. Salviati, 2000, Human Mutation.

Safety and Efficacy of Lonapegsomatropin in Children With Growth Hormone Deficiency: enliGHten Trial 2-Year Results

P. Saenger, M. Cappa, P. Hofman, 2022, The Journal of clinical endocrinology and metabolism.

RecoStones: a New Tool to Identify Calabrian Stone Materials Through Image Processing

D. Barca, M. Cappa, G. Fedele, 2021, Geoheritage.

Central Precocious Puberty: Treatment with Triptorelin 11.25 mg

E. Chiocca, M. Cappa, G. Baroncelli, 2012, TheScientificWorldJournal.

Clinical and roentgenographic findings in a patient with primordial microcephalic dwarfism type Caroline Crachami.

A. Pasquino, M. Cappa, G. Marietti, 1996, American journal of medical genetics.

The impact of real practice inappropriateness and devices’ inefficiency to variability in growth hormone consumption

E. Ghigo, F. Chiarelli, R. Castello, 2014, Journal of Endocrinological Investigation.

Insulin Sensitivity from Preschool to School Age in Patients with Severe Obesity

M. Manco, M. Cappa, R. Luciano, 2013, PloS one.

Down Syndrome (Trisomy 21) and Diabetes

M. Cappa, C. Bizzarri, 2017 .

An Incidental Finding of Bilateral Adrenal Lymphoma.

P. Tomà, M. Cappa, P. Cambiaso, 2016, The American journal of the medical sciences.

Cardiovascular fitness is impaired in children born small for gestational age

A. Turchetta, A. Deodati, M. Cappa, 2014, Acta paediatrica.