A. Corrias

发表

Ultrasound surveillance for radiation-induced thyroid carcinoma in adult survivors of childhood cancer.

E. Brignardello, F. Fagioli, G. Isolato, 2016, European journal of cancer.

Patients with Hashimoto's Disease Treated with L-Thyroxine and Followed for Three Years

A. Corrias, L. Silvestro, G. Mussa, 1998, Journal of pediatric endocrinology & metabolism : JPEM.

Final height in girls with central precocious puberty: comparison of two different luteinizing hormone‐releasing hormone agonist treatments

S. Bernasconi, M. Cisternino, L. Tatò, 1994, Acta paediatrica.

Use of combined Gn-RH agonist and hGH therapy for better attining the goals in precocious puberty treatment.

A. Pasquino, M. Cisternino, L. Tatò, 1995, Hormone research.

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

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

Newborn of mothers affected by autoimmune thyroiditis: the importance of thyroid function monitoring in the first months of life

F. Mosca, R. Rovelli, G. Chiumello, 2010, Italian journal of pediatrics.

Effect of cholinergic enhancement by pyridostigmine on growth hormone secretion in obese adults and children.

E. Arvat, E. Ghigo, E. Müller, 1989, Metabolism: clinical and experimental.

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.

GH replacement therapy and second neoplasms in adult survivors of childhood cancer: a retrospective study from a single institution

C. Sacerdote, E. Arvat, U. Ricardi, 2015, Journal of Endocrinological Investigation.

Thyroid Nodules and Carcinoma

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

Thyroid Nodules in Pediatrics: Which Ones Can Be Left Alone, Which Ones Must be Investigated, When and How

A. Mussa, A. Corrias, 2012, Journal of clinical research in pediatric endocrinology.

Diagnostic features of thyroid nodules in pediatrics.

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

Etiology of Central Precocious Puberty in Males: The Results of the Italian Study Group for Physiopathology of Puberty

A. Pasquino, M. Cisternino, A. Pilotta, 2000, Journal of pediatric endocrinology & metabolism : JPEM.

Factors Influencing Final/Near-Final Height in 12 Boys with Central Precocious Puberty Treated with Gonadotrophin-Releasing Hormone Agonists

A. Pasquino, M. Cisternino, V. De Sanctis, 2000, Journal of pediatric endocrinology & metabolism : JPEM.

Growth Hormone Treatment in Irradiated Children with Brain Tumors

M. Garrè, P. Picco, A. Corrias, 1997, Journal of pediatric endocrinology & metabolism : JPEM.

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.

Gonadal status in long-term male survivors of childhood cancer

G. Ciccone, E. Brignardello, F. Fagioli, 2016, Journal of Cancer Research and Clinical Oncology.

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 TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis

P. Macchia, M. Zannini, G. Fenzi, 2009, Journal of endocrinological investigation.

Influence of age, gender, and glucose tolerance on fasting and fed acylated ghrelin in Prader Willi syndrome.

A. Franzese, F. Prodam, E. Di Battista, 2009, Clinical nutrition.

Metabolic syndrome in adult patients with Prader-Willi syndrome.

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

The natural history of euthyroid Hashimoto's thyroiditis in children.

S. Loche, G. Radetti, G. Bona, 2006, The Journal of pediatrics.

Subclinical hypothyroidism in children and adolescents: a wide range of clinical, biochemical, and genetic factors involved.

A. Monzani, L. Tatò, V. De Sanctis, 2009, The Journal of clinical endocrinology and metabolism.

Defective function of Fas in T cells from paediatric patients with autoimmune thyroid diseases

A. Chiocchetti, U. Dianzani, I. Dianzani, 2003, Clinical and experimental immunology.

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

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

Thyroid diseases in patients treated during pre-puberty for medulloblastoma with different radiotherapic protocols

U. Ricardi, L. Genitori, A. Corrias, 2001, Journal of endocrinological investigation.

Thyroid dysfunction as a late effect in childhood medulloblastoma: a comparison of hyperfractionated versus conventionally fractionated craniospinal radiotherapy.

A. Urgesi, U. Ricardi, E. Madon, 2001, International journal of radiation oncology, biology, physics.

Features of children perinatally infected with HIV-1 surviving longer than 5 years Italian Register for HIV Infection in Children

C. Giaquinto, R. Consolini, F. Veglia, 1994, The Lancet.

Epidemiology of HIV infection in children in Italy

C. Giaquinto, R. Consolini, F. Mannelli, 1994 .

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.

Auxological and biochemical parameters in assessing treatment of infants and toddlers with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

R. Lala, S. Pagliardini, A. Corrias, 1993, The Journal of pediatric endocrinology.

Assessment of central adrenal insufficiency in children and adolescents with Prader–Willi syndrome

A. Salvatoni, S. Andrulli, L. Beccaria, 2012, Clinical endocrinology.

Thyroid nodules and cancer in children and adolescents affected by autoimmune thyroiditis.

A. Mussa, F. Baronio, G. Weber, 2008, Archives of pediatrics & adolescent medicine.

GH/IGF-I axis in Prader-Willi syndrome: Evaluation of IGF-I levels and of the somatotroph responsiveness to various provocative stimuli

A. Salvatoni, L. Beccaria, P. Ciampalini, 2000, Journal of endocrinological investigation.

Central adrenal insufficiency in young adults with Prader‐Willi Syndrome

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

Thyroid function in patients with Prader-Willi syndrome: an Italian multicenter study of 339 patients

A. Salvatoni, A. Pilotta, A. Crinò, 2019, Journal of pediatric endocrinology & metabolism : JPEM.

Hypogonadism and pubertal development in Prader-Willi syndrome

A. Salvatoni, L. Beccaria, R. Schiaffini, 2003, European Journal of Pediatrics.

Pituitary height and neuroradiological alterations in patients with Prader-Labhart-Willi syndrome

G. Grugni, L. Iughetti, B. Predieri, 2008, European Journal of Pediatrics.

Neonatal hypotonia: don't forget the Prader‐Willi syndrome

A. Crinò, G. Trifiró, A. Corrias, 2003, Acta paediatrica.

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.

Adrenal axis function after high‐dose steroid therapy for childhood acute lymphoblastic leukemia

G. Pastore, E. Barisone, A. Corrias, 2008, Pediatric blood & cancer.

Phalangeal quantitative ultrasound in 1,719 children and adolescents with bone disorders

F. Terlizzi, A. Mussa, R. Lala, 2012, Osteoporosis International.

Growth impairment after TBI of leukemia survivors children: a model- based investigation

A. Gliozzi, D. Nucera, F. Fagioli, 2014, Theoretical Biology and Medical Modelling.

Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes

L. Tatò, A. Gandini, G. Radetti, 2005, Clinical endocrinology.

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.

Fractures and skeletal complications should be the gold standard for validation of methods for bone appraisal in pediatrics

A. Mussa, F. Fagioli, F. Porta, 2010 .

Prospective bone ultrasound patterns during childhood acute lymphoblastic leukemia treatment.

A. Mussa, F. Fagioli, F. Porta, 2010, Bone.

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.

Familial PAX8 small deletion (c.989_992delACCC) associated with extreme phenotype variability.

M. Zannini, I. Dianzani, P. Gianino, 2004, The Journal of clinical endocrinology and metabolism.

Recommendations for Premature Ovarian Insufficiency Surveillance for Female Survivors of Childhood, Adolescent, and Young Adult Cancer: A Report From the International Late Effects of Childhood Cancer Guideline Harmonization Group in Collaboration With the PanCareSurFup Consortium.

U. Dirksen, M. H. van den Berg, M. Hudson, 2016, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Thyroid Abnormalities in Children and Adolescents with McCune-Albright Syndrome

R. Lala, M. Vigone, M. Wasniewska, 2012, Hormone Research in Paediatrics.

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.

Accuracy of fine needle aspiration biopsy of thyroid nodules in detecting malignancy in childhood: comparison with conventional clinical, laboratory, and imaging approaches.

G Cesaretti, M. Segni, A. Pasquino, 2001, The Journal of clinical endocrinology and metabolism.

Autoimmune Thyroid Disease and Celiac Disease in Children

G. Corrao, R. Lazzari, M. Bonamico, 2003, Journal of pediatric gastroenterology and nutrition.

α-Fetoprotein assay on dried blood spot for hepatoblastoma screening in children with overgrowth-cancer predisposition syndromes

G. Ferrero, M. Silengo, A. Mussa, 2014, Pediatric Research.

Growth impairment after TBI of leukemia survivors children: a model- based investigation

A. Gliozzi, D. Nucera, F. Fagioli, 2014, Theoretical Biology and Medical Modelling.

A significant sex--but not elective cesarean section--effect on mother-to-child transmission of hepatitis C virus infection

J. R. Contreras, S. Polywka, S. Hannam, 2005 .

Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndrome.

D. Ledbetter, S. Christian, P. Simi, 1997, American journal of human genetics.

Final height and body mass index in adult survivors of childhood acute lymphoblastic leukemia treated without cranial radiotherapy: a retrospective longitudinal multicenter Italian study

L. Iughetti, P. Paolucci, M. Street, 2014, BMC Pediatrics.

Endocrine health conditions in adult survivors of childhood cancer: the need for specialized adult-focused follow-up clinics.

G. Ciccone, E. Brignardello, F. Fagioli, 2013, European journal of endocrinology.

Lower lip pits and complete idiopathic precocious puberty in a patient with Kabuki make-up (Niikawa-Kuroki) syndrome.

A. Guala, A. Corrias, P. Franceschini, 1993, American journal of medical genetics.

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.

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.

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.

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.

TSH receptor and Gsα genetic analysis in children with Down’s syndrome and subclinical hypothyroidism

Elena S. Di Martino, A. Pinchera, L. Chiovato, 2003, Journal of endocrinological investigation.

Graves' disease prevalence in a young population with Turner syndrome.

G. Salzano, A. Mussa, M. Valenzise, 2010, Journal of endocrinological investigation.

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.

Graves’ disease prevalence in a young population with Turner syndrome

G. Salzano, F. Luca, A. Corrias, 2010 .

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.

A Multicenter Italian Study on Prader-Willi Syndrome

R. Lorini, A. Salvatoni, P. Brambilla, 1992 .

Death during GH therapy in children with Prader-Willi syndrome: Description of two new cases

A. Sartorio, A. Crinò, G. Grugni, 2005, Journal of endocrinological investigation.

Hyperplastic polyp of the stomach simulating hypertrophic pyloric stenosis.

A. Corrias, C. Sanna, G. Congiu, 1991, Journal of Pediatric Gastroenterology and Nutrition - JPGN.

Factors at Onset Predictive of Lasting Remission in Paediatric Patients with Graves' Disease Followed for at Least Three Years

A. Corrias, L. Silvestro, G. Mussa, 1999, Journal of pediatric endocrinology & metabolism : JPEM.

Four new cases of PHACES syndrome: variable phenotypic expression and endocrine features

M. Silengo, A. Mussa, G. Baldassarre, 2008, Acta paediatrica.

Prevalence of activating thyrotropin receptor and Gsα gene mutations in paediatric thyroid toxic adenomas: a multicentric Italian study

M. Pelizzo, M. Segni, D. Larizza, 2013, Clinical endocrinology.

Serum thyrotropin concentration in children with isolated thyroid nodules.

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

Importance and significance of liver echotomography in Wilson's disease during childhood.

M. Giagheddu, A. Nurchi, A. Corrias, 1987, The Journal of nuclear medicine and allied sciences.

Meningiomas after cranial radiotherapy for childhood cancer: a single institution experience

D. Garbossa, E. Arvat, N. Fortunati, 2015, Journal of Cancer Research and Clinical Oncology.

Carrier detection and early diagnosis of Wilson's disease by restriction fragment length polymorphism analysis.

M. Devoto, A. Nurchi, M. Lai, 1989, Journal of medical genetics.

Predictors of Malignancy in Children with Thyroid Nodules.

A. Mussa, N. Palestini, M. Motta, 2015, The Journal of pediatrics.

Two new PROP1 gene mutations responsible for compound pituitary hormone deficiency

G. Bona, A. Corrias, J. Bellone, 2003, Clinical genetics.

Late Toxicity in Children Undergoing Hematopoietic Stem Cell Transplantation with TBI-containing Conditioning Regimens for Hematological Malignancies

P. Franco, U. Ricardi, F. Fagioli, 2009, Strahlentherapie und Onkologie.

Endocrine late effects after total body irradiation in patients who received hematopoietic cell transplantation during childhood: a retrospective study from a single institution

E. Brignardello, G. Boccuzzi, C. Manieri, 2011, Journal of Cancer Research and Clinical Oncology.

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

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

Iatrogenic acute pancreatitis due to hypercalcemia in a child with pseudohypoparathyroidism

A. Mussa, A. Corrias, L. De Sanctis, 2014, Journal of pediatric endocrinology & metabolism : JPEM.

Two sibs with Malpuech syndrome.

A. Marras, A. Corrias, G. Crisponi, 1999, American journal of medical genetics.

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.

Prevalence of cardiovascular risk factors in long-term survivors of childhood cancer: 16 years follow up from a prospective registry

F. Gaita, E. Arvat, F. D’Ascenzo, 2015, European journal of preventive cardiology.

Two patients with varying combinations of sternal cleft, haemangiomas, midline abdominal raphe, coarctation of the aorta with a right aortic arch.

A. Marras, A. Corrias, L. Memo, 2000, Clinical dysmorphology.

Congenital hypothyroidism, cerebellar atrophy, and the incomplete phenotypic expression of PHACES syndrome.

M. Silengo, E. Biamino, A. Mussa, 2008, Endocrine journal.

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.

Hurthle cell carcinoma in childhood: A retrospective analysis of five cases and review of pediatric literature

G. Pajno, G. Dionigi, G. Zirilli, 2020, Pediatric blood & cancer.

Thyroid Involvement in Two Patients with Bannayan-Riley-Ruvalcaba Syndrome

G. Ferrero, A. Mussa, A. Corrias, 2013, Journal of clinical research in pediatric endocrinology.

Clinical features of thyroid cancer in paediatric age. Experience of a tertiary centre in the 2000–2020 period

N. Palestini, A. Corrias, L. De Sanctis, 2023, Endocrine.

A Survey on Prader-Willi Syndrome in the Italian Population: Prevalence of Historical and Clinical Signs

A. Salvatoni, A. Franzese, G. Valerio, 2009, Journal of pediatric endocrinology & metabolism : JPEM.

Defective function of Fas in patients with type 1 diabetes associated with other autoimmune diseases.

F. Cadario, F. Cerutti, U. Dianzani, 2001, Diabetes.

Bisphosphonate Treatment of Bone Fibrous Dysplasia in McCuneAlbright Syndrome

R. Lala, A. Corrias, J. Bellone, 2006, Journal of pediatric endocrinology & metabolism : JPEM.

Levothyroxine Treatment in Pediatric Benign Thyroid Nodules

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

Complicanze endocrine a lungo temine nei cancer survivors

N. Fortunati, E. Biasin, F. Felicetti, 2014, L'Endocrinologo.

Ultrasound screening for thyroid carcinoma in childhood cancer survivors: a case series.

E. Brignardello, G. Boccuzzi, F. Fagioli, 2008, The Journal of clinical endocrinology and metabolism.

Determinants of thyrotropin rise in congenital hypothyroidism.

A. Mussa, F. Porta, G. Baldassarre, 2011, The Journal of pediatrics.

Contents Vol. 77, 2012

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