Works by Weber, Giovanna

Results: 53

Surgical management of pediatric Graves' disease: an effective definitive treatment.

Published in:

Pediatric Surgery International, 2012, v. 28, n. 6, p. 609, doi. 10.1007/s00383-012-3095-5

By:

Peroni, Elena;
Angiolini, Maria;
Vigone, Maria;
Mari, Gilberto;
Chiumello, Giuseppe;
Beretta, Edoardo;
Weber, Giovanna

Publication type:

Article

Different Efficacy of Burosumab on Physical Performance and Serum Phosphate in Adult Patients with X-Linked Hyphophosphatemic Rickets during the First Six-Month of Treatment.

Published in:

Journal of Clinical Medicine, 2023, v. 12, n. 8, p. 2906, doi. 10.3390/jcm12082906

By:

Arcidiacono, Teresa;
Foligno, Nadia E.;
Brioni, Elena;
Bologna, Arianna;
Weber, Giovanna;
Mora, Stefano;
Pitea, Marco;
Vitale, Corrado;
Vezzoli, Giuseppe

Publication type:

Article

STUDY OF THE EFFECTS OF BROMOCRIPTINE ON SEXUAL IMPOTENCE.

Published in:

Clinical Endocrinology, 1977, v. 7, n. 5, p. 417, doi. 10.1111/j.1365-2265.1977.tb03351.x

By:

AMBROSI, B.;
BARA, ROSSELLA;
TRAVAGLINI, P.;
WEBER, GIOVANNA;
PECCOZ, P. BECK;
RONDENA, M.;
ELLI, R.;
FAGLIA, G.

Publication type:

Article

Post-Surgical Metabolic Imbalance in Adolescents with Renal Hypophosphatemic Rickets.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2000, v. 13, n. 6, p. 657, doi. 10.1515/jpem.2000.13.6.657

By:

Prinster, Chiara;
Weber, Giovanna;
Beccio, Sabrina;
Meneghel, Marta;
Mora, Stefano;
Chiumello, Giuseppe

Publication type:

Article

Crying Abnormalities in Congenital Hypothyroidism: Preliminary Spectrographic Study.

Published in:

Journal of Child Neurology, 2000, v. 15, n. 9, p. 603

By:

Boero, Daniela Lenti;
Weber, Giovanna;
Vigone, Maria Cristina;
Lenti, Carlo

Publication type:

Article

Bone Density and Bone Metabolism Are Normal After Long-Term Gluten-Free Diet in Young Celiac Patients.

Published in:

American Journal of Gastroenterology (Springer Nature), 1999, v. 94, n. 2, p. 398, doi. 10.1111/j.1572-0241.1999.867_r.x

By:

Mora, Stefano;
Barera, Graziano;
Beccio, Sabrina;
Proverbio, Maria Carla;
Weber, Giovanna;
Bianchi, Cesare;
Chiumello, Giuseppe

Publication type:

Article

Pseudohypoparathyroidism: application of the Italian common healthcare-pathway for a homogeneous clinical approach and a shared follow up.

Published in:

Italian Journal of Pediatrics, 2021, v. 47, n. 1, p. 1, doi. 10.1186/s13052-021-01000-z

By:

Tessaris, Daniele;
Bonino, Elisa;
Weber, Giovanna;
Wasniewska, Malgorzata;
Corica, Domenico;
Pitea, Marco;
Scirè, Giuseppe;
Caruso-Nicoletti, Manuela;
Fintini, Danilo;
de Sanctis, Luisa

Publication type:

Article

Decreased Parietal Cortex Activity during Mental Rotation in Children with Congenital Hypothyroidism.

Published in:

Neuroendocrinology, 2009, v. 89, n. 1, p. 56, doi. 10.1159/000151397

By:

Blasi, Valeria;
Longaretti, Roberta;
Giovanettoni, Chiara;
Baldoli, Cristina;
Pontesilli, Silvia;
Vigone, Cristina;
Saccuman, Cristina;
Nigro, Francesco;
Chiumello, Giuseppe;
Scotti, Giuseppe;
Weber, Giovanna

Publication type:

Article

Implications of deferred diagnosis of paediatric intracranial germ cell tumours.

Published in:

Pediatric Blood & Cancer, 2023, v. 70, n. 3, p. 1, doi. 10.1002/pbc.30168

By:

Partenope, Cristina;
Pozzobon, Gabriella;
Weber, Giovanna;
Carceller, Fernando;
Albanese, Assunta

Publication type:

Article

Neutralizing Anti-Cytokine Autoantibodies Against Interferon-α in Immunodysregulation Polyendocrinopathy Enteropathy X-Linked.

Published in:

Frontiers in Immunology, 2018, p. 1, doi. 10.3389/fimmu.2018.00544

By:

Rosenberg, Jacob M.;
Maccari, Maria E.;
Barzaghi, Federica;
Allenspach, Eric J.;
Pignata, Claudio;
Weber, Giovanna;
Torgerson, Troy R.;
Utz, Paul J.;
Bacchetta, Rosa

Publication type:

Article

Mild TSH resistance: Clinical and hormonal features in childhood and adulthood.

Published in:

Clinical Endocrinology, 2017, v. 87, n. 5, p. 587, doi. 10.1111/cen.13387

By:

Vigone, Maria Cristina;
Di Frenna, Marianna;
Guizzardi, Fabiana;
Gelmini, Giulia;
Filippis, Tiziana;
Mora, Stefano;
Caiulo, Silvana;
Sonnino, Micol;
Bonomi, Marco;
Persani, Luca;
Weber, Giovanna

Publication type:

Article

A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH).

Published in:

Clinical Endocrinology, 2009, v. 71, n. 5, p. 739, doi. 10.1111/j.1365-2265.2009.03568.x

By:

Corbetta, Carlo;
Weber, Giovanna;
Cortinovis, Francesca;
Calebiro, Davide;
Passoni, Arianna;
Vigone, Maria C.;
Beck-Peccoz, Paolo;
Chiumello, Giuseppe;
Persani, Luca

Publication type:

Article

Absence of sonic hedgehog (Shh) germline mutations in patients with thyroid dysgenesis.

Published in:

2008

By:

Muzza, Marina;
Persani, Luca;
Filippis, Tiziana de;
Gastaldi, Roberto;
Vigone, Maria Cristina;
Sala, Davide;
Weber, Giovanna;
Lorini, Renata;
Beck-Peccoz, Paolo;
Fugazzola, Laura

Publication type:

Letter

Recombinant human TSH testing is a valuable tool for differential diagnosis of congenital hypothyroidism during l-thyroxine replacement.

Published in:

Clinical Endocrinology, 2003, v. 59, n. 2, p. 230, doi. 10.1046/j.1365-2265.2003.01830.x

By:

Fugazzola, Laura;
Persani, Luca;
Mannavola, Deborah;
Reschini, Eugenio;
Vannucchi, Guia;
Weber, Giovanna;
Beck-Peccoz, Paolo

Publication type:

Article

Congenital Hypothyroidism Treatment in Infants: A Comparative Study between Liquid and Tablet Formulations of Levothyroxine.

Published in:

Hormone Research in Paediatrics, 2014, v. 81, n. 1, p. 50, doi. 10.1159/000356047

By:

Peroni, Elena;
Vigone, Maria Cristina;
Mora, Stefano;
Bassi, Lorenzo andrea;
Pozzi, Clara;
Passoni, arianna;
Weber, Giovanna

Publication type:

Article

Levothyroxine Treatment in Pediatric Benign Thyroid Nodules.

Published in:

Hormone Research in Paediatrics, 2011, v. 75, n. 4, p. 246, doi. 10.1159/000321841

By:

Corrias, Andrea;
Mussa, Alessandro;
Wasniewska, Malgorzata;
Segni, Maria;
Cassio, Alessandra;
Salerno, Mariacarolina;
Gastaldi, Roberto;
Vigone, Maria Cristina;
Bal, Milva;
Matarazzo, Patrizia;
Weber, Giovanna;
De Luca, Filippo

Publication type:

Article

Prevalence of Thyroid Autoantibodies and Thyroid Autoimmune Disease in Diabetic Children and Adolescents.

Published in:

Diabetes Care, 1994, v. 17, n. 7, p. 782, doi. 10.2337/diacare.17.7.782

By:

Cerai, Laura M. Prina;
Weber, Giovanna;
Meschi, Franco;
Mora, Stefano;
Bognetti, Emilio;
Siragusa, Virginia;
di Natale, Berardo

Publication type:

Article

Validation of food frequency questionnaire for assessing dietary macronutrients and calcium intake in Italian children and adolescents.

Published in:

2005

By:

Bertoli, Simona;
Petroni, Maria Letizia;
Pagliato, Emanuela;
Mora, Stefano;
Weber, Giovanna;
Chiumello, Giuseppe;
Testolin, Giulio

Publication type:

journal article

Autosomal Dominant Hypocalcemia in Monozygotic Twins Caused by a De Novo Germline Mutation Near the Amino-Terminus of the Human Calcium Receptor.

Published in:

Journal of Bone & Mineral Research, 2004, v. 19, n. 4, p. 578, doi. 10.1359/JBMR.040106

By:

Hu, Jianxin;
Mora, Stefano;
Weber, Giovanna;
Zamproni, Ilaria;
Proverbio, Maria Carla;
Spiegel, Allen M

Publication type:

Article

Longitudinal Changes of Bone Density and Bone Resorption in Hyperthyroid Girls During Treatment.

Published in:

Journal of Bone & Mineral Research, 1999, v. 14, n. 11, p. 1971, doi. 10.1359/jbmr.1999.14.11.1971

By:

Mora, Stefano;
Weber, Giovanna;
Marenzi, Karen;
Signorini, Elisabetta;
Rovelli, Rosanna;
Proverbio, Maria Carla;
Chiumello, Giuseppe

Publication type:

Article

Analysis of 21-deoxycortisol, a marker of congenital adrenal hyperplasia, in blood by atmospheric pressure chemical ionization and electrospray ionization using multiple reaction monitoring.

Published in:

Rapid Communications in Mass Spectrometry: RCM, 2004, v. 18, n. 1, p. 77, doi. 10.1002/rcm.1284

By:

Simone Cristoni;
Debora Cuccato;
Mariateresa Sciannamblo;
Luigi Rossi Bernardi;
Ida Biunno;
Piermario Gerthoux;
Gianni Russo;
Giovanna Weber;
Stefano Mora

Publication type:

Article

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

Published in:

Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 9, p. 4070, doi. 10.1210/jc.2002-022028

By:

MANTOVANI, GIOVANNA;
MAGHNIE, MOHAMAD;
WEBER, GIOVANNA;
DE MENIS, ERNESTO;
BRUNELLI, VALERIA;
CAPPA, MARCO;
LOLI, PAOLA;
BECK-PECCOZ, PAOLO;
SPADA, ANNA

Publication type:

Article

Germline Mutations of TSH Receptor Gene as Cause of Nonautoimmune Subclinical Hypothyroidism.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 6, p. 2549, doi. 10.1210/jcem.87.6.8536

By:

ALBERTI, LUISELLA;
PROVERBIO, MARIA CARLA;
COSTAGLIOLA, SABINE;
ROMOLI, ROBERTO;
BOLDRIGHINI, BENEDETTA;
VIGONE, MARIA CRISTINA;
WEBER, GIOVANNA;
CHIUMELLO, GIUSEPPE;
BECK-PECCOZ, PAOLO;
PERSANI, LUCA

Publication type:

Article

Hyperplastic Pituitary Gland, High Serum Glycoprotein Hormoneα -Subunit, and Variable Circulating Thyrotropin (TSH) Levels as Hallmark of Central Hypothyroidism due to Mutations of the TSHβ Gene

Published in:

Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 4, p. 1600, doi. 10.1210/jcem.86.4.7411

By:

Bonomi, Marco;
Proverbio, Maria Carla;
Weber, Giovanna;
Chiumello, Giuseppe;
Beck-Peccoz, Paolo;
Persani, Luca

Publication type:

Article

Molecular Analysis of the Pendred’s Syndrome Gene and Magnetic Resonance Imaging Studies of the Inner Ear Are Essential for the Diagnosis of True Pendred’s Syndrome.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 7, p. 2469, doi. 10.1210/jcem.85.7.6694

By:

FUGAZZOLA, LAURA;
MANNAVOLA, DEBORAH;
CERUTTI, NADIA;
MAGHNIE, MOHAMED;
PAGELLA, FABIO;
BIANCHI, PAOLO;
WEBER, GIOVANNA;
LUCA, LUCA;
BECK-PECCOZ, PAOLO

Publication type:

Article

Endocrine manifestations of paediatric intracranial germ cell tumours: from diagnosis to long-term follow-up.

Published in:

Endocrine (1355008X), 2022, v. 77, n. 3, p. 546, doi. 10.1007/s12020-022-03121-9

By:

Partenope, Cristina;
Pozzobon, Gabriella;
Weber, Giovanna;
Arya, Ved Bhushan;
Carceller, Fernando;
Albanese, Assunta

Publication type:

Article

Growth hormone therapy in children: predictive factors and short-term and long-term response criteria.

Published in:

Endocrine (1355008X), 2019, v. 66, n. 3, p. 614, doi. 10.1007/s12020-019-02057-x

By:

Pozzobon, Gabriella;
Partenope, Cristina;
Mora, Stefano;
Garbetta, Gisella;
Weber, Giovanna;
Barera, Graziano

Publication type:

Article

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

Published in:

Endocrine (1355008X), 2015, v. 50, n. 3, p. 674, doi. 10.1007/s12020-015-0574-1

By:

Delvecchio, Maurizio;
Salerno, Mariacarolina;
Vigone, Maria;
Wasniewska, Malgorzata;
Popolo, Pietro;
Lapolla, Rosa;
Mussa, Alessandro;
Tronconi, Giulia;
D'Acunzo, Ida;
Mase, Raffaella;
Falcone, Rosa;
Corrias, Andrea;
Luca, Filippo;
Weber, Giovanna;
Cavallo, Luciano;
Faienza, Maria

Publication type:

Article

Thyroid scintigraphy and perchlorate test after recombinant human TSH: a new tool for the differential diagnosis of congenital hypothyroidism during infancy.

Published in:

European Journal of Nuclear Medicine & Molecular Imaging, 2007, v. 34, n. 9, p. 1498, doi. 10.1007/s00259-007-0377-6

By:

Fugazzola, Laura;
Persani, Luca;
Vannucchi, Guia;
Carletto, Marco;
Mannavola, Deborah;
Vigone, Maria;
Cortinovis, Francesca;
Beccaria, Luciano;
Longari, Virgilio;
Weber, Giovanna;
Beck-Peccoz, Paolo

Publication type:

Article

Vitamin D in childhood and adolescence: an expert position statement.

Published in:

European Journal of Pediatrics, 2015, v. 174, n. 5, p. 565, doi. 10.1007/s00431-015-2524-6

By:

Saggese, Giuseppe;
Vierucci, Francesco;
Boot, Annemieke;
Czech-Kowalska, Justyna;
Weber, Giovanna;
Camargo, Carlos;
Mallet, Eric;
Fanos, Margherita;
Shaw, Nick;
Holick, Michael

Publication type:

Article

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

Published in:

2016

By:

de Filippis, Tiziana;
Marelli, Federica;
Nebbia, Gabriella;
Porazzi, Patrizia;
Corbetta, Sabrina;
Fugazzola, Laura;
Gastaldi, Roberto;
Vigone, Maria Cristina;
Biffanti, Roberta;
Frizziero, Daniela;
Mandarà, Luana;
Prontera, Paolo;
Salerno, Mariacarolina;
Maghnie, Mohamad;
Tiso, Natascia;
Radetti, Giorgio;
Weber, Giovanna;
Persani, Luca

Publication type:

journal article

Congenital hypothyroidism due to defects of thyroid development and mild increase of TSH at screening: data from the Italian National Registry of infants with congenital hypothyroidism.

Published in:

2013

By:

Olivieri, Antonella;
Corbetta, Carlo;
Weber, Giovanna;
Vigone, Maria Cristina;
Fazzini, Cristina;
Medda, Emanuela;
Italian Study Group for Congenital Hypothyroidism

Publication type:

journal article

Congenital hypothyroidism with eutopic thyroid gland: analysis of clinical and biochemical features at diagnosis and after re-evaluation.

Published in:

2013

By:

Rabbiosi, Sarah;
Vigone, Maria Cristina;
Cortinovis, Francesca;
Zamproni, Ilaria;
Fugazzola, Laura;
Persani, Luca;
Corbetta, Carlo;
Chiumello, Giuseppe;
Weber, Giovanna

Publication type:

journal article

Frequent TSH Receptor Genetic Alterations with Variable Signaling Impairment in a Large Series of Children with Nonautoimmune Isolated Hyperthyrotropinemia.

Published in:

2012

By:

Calebiro, Davide;
Gelmini, Giulia;
Cordella, Daniela;
Bonomi, Marco;
Winkler, Franziska;
Biebermann, Heike;
de Marco, Alessandro;
Marelli, Federica;
Libri, Domenico V.;
Antonica, Francesco;
Vigone, Maria Cristina;
Cappa, Marco;
Mian, Caterina;
Sartorio, Alessandro;
Beck-Peccoz, Paolo;
Radetti, Giorgio;
Weber, Giovanna;
Persani, Luca

Publication type:

Journal Article

Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism.

Published in:

2008

By:

Zamproni, Ilaria;
Grasberger, Helmut;
Cortinovis, Francesca;
Vigone, Maria Cristina;
Chiumello, Giuseppe;
Mora, Stefano;
Onigata, Kazumichi;
Fugazzola, Laura;
Refetoff, Samuel;
Persani, Luca;
Weber, Giovanna

Publication type:

journal article

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

Published in:

Italian Journal of Pediatrics, 2015, v. 14, p. 1, doi. 10.1186/s13052-015-0190-y

By:

Delvecchio, Maurizio;
Vigone, Maria Cristina;
Wasniewska, Malgorzata;
Weber, Giovanna;
Lapolla, Rosa;
Popolo, Pietro Pio;
Tronconi, Giulia Maria;
Di Mase, Raffaella;
De Luca, Filippo;
Cavallo, Luciano;
Salerno, Mariacarolina;
Faienza, Maria Felicia

Publication type:

Article

Persistent mild hypothyroidism associated with novel sequence variants of the DUOX2 gene in two siblings.

Published in:

Human Mutation, 2005, v. 26, n. 4, p. 395, doi. 10.1002/humu.9372

By:

Vigone, Maria Cristina;
Fugazzola, Laura;
Zamproni, Ilaria;
Passoni, Arianna;
Di Candia, Stefania;
Chiumello, Giuseppe;
Persani, Luca;
Weber, Giovanna

Publication type:

Article

Treatment of congenital hypothyroidism: comparison between L-thyroxine oral solution and tablet formulations up to 3 years of age.

Published in:

European Journal of Endocrinology, 2022, v. 186, n. 1, p. 45, doi. 10.1530/EJE-20-1444

By:

Vigone, Maria Cristina;
Ortolano, Rita;
Vincenzi, Gaia;
Pozzi, Clara;
Ratti, Micol;
Assirelli, Valentina;
Vissani, Sofia;
Cavarzere, Paolo;
Mussa, Alessandro;
Gastaldi, Roberto;
Di Mase, Raffaella;
Salerno, Mariacarolina;
Street, Maria Elisabeth;
Trombatore, Jessica;
Weber, Giovanna;
Cassio, Alessandra

Publication type:

Article

A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidism.

Published in:

European Journal of Endocrinology, 2001, v. 145, n. 3, p. 249, doi. 10.1530/eje.0.1450249

By:

Alberti, Luisella;
Proverbio, Maria Carla;
Costagliola, Sabine;
Weber, Giovanna;
Beck-Peccoz, Paolo;
Chiumello, Giuseppe;
Persani, Luca

Publication type:

Article

Snyder-Robinson syndrome: A novel nonsense mutation in spermine synthase and expansion of the phenotype.

Published in:

American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 9, p. 2316, doi. 10.1002/ajmg.a.36116

By:

Peron, Angela;
Spaccini, Luigina;
Norris, Joy;
Bova, Stefania M.;
Selicorni, Angelo;
Weber, Giovanna;
Wood, Tim;
Schwartz, Charles E.;
Mastrangelo, Massimo

Publication type:

Article

Suprasellar granular cell tumor of the neurohypophysis in a child: unusual presentation in pediatric age of a rare tumor.

Published in:

Child's Nervous System, 2013, v. 29, n. 6, p. 1031, doi. 10.1007/s00381-013-2062-3

By:

Gagliardi, Filippo;
Losa, Marco;
Boari, Nicola;
Franzin, Alberto;
Pozzobon, Gabriella;
Weber, Giovanna;
Mortini, Pietro

Publication type:

Article

Linear growth and puberty in childhood obesity: what is new?

Published in:

Minerva Pediatrics, 2021, v. 73, n. 6, p. 563, doi. 10.23736/S2724-5276.21.06543-5

By:

GIGLIONE, Enza;
LAPOLLA, Rosa;
CIANFARANI, Stefano;
FAIENZA, Maria F.;
FINTINI, Danilo;
WEBER, Giovanna;
DELVECCHIO, Maurizio;
VALERIO, Giuliana

Publication type:

Article

Asymptomatic Thyrotropin-Secreting Pituitary Macroadenoma in a 13-Year-Old Girl: Successful First-Line Treatment with Somatostatin Analogs.

Published in:

Thyroid, 2012, v. 22, n. 10, p. 1076, doi. 10.1089/thy.2012.0077

By:

Rabbiosi, Sarah;
Peroni, Elena;
Tronconi, Giulia Maria;
Chiumello, Giuseppe;
Losa, Marco;
Weber, Giovanna

Publication type:

Article

Total Iodide Organification Defect: Clinical and MolecularCharacterization of an Italian Family.

Published in:

Thyroid, 2005, v. 15, n. 9, p. 1085

By:

Laura Fugazzola;
Deborah Mannavola;
Maria Cristina Vigone;
Valentina Cirello;
Giovanna Weber;
Paolo Beck-Peccoz;
Luca Persani

Publication type:

Article

Diagnosis of hypochondroplasia: the role of radiological interpretation.

Published in:

Pediatric Radiology, 2001, v. 31, n. 3, p. 203, doi. 10.1007/s002470000398

By:

Prinster, Chiara;
Maschio, Maurizia Del;
Beluffi, Giampiero;
Maghnie, Mohamad;
Weber, Giovanna;
Maschio, Alessandro Del;
Chiumello, Giuseppe;
Mora, S.

Publication type:

Article

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

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 2, p. 159, doi. 10.1515/jpem-2018-0388

By:

Iughetti, Lorenzo;
Vivi, Giulia;
Balsamo, Antonio;
Corrias, Andrea;
Crinò, Antonino;
Delvecchio, Maurizio;
Gargantini, Luigi;
Greggio, Nella Augusta;
Grugni, Graziano;
Hladnik, Uros;
Pilotta, Alba;
Ragusa, Letizia;
Salvatoni, Alessandro;
Wasniewska, Malgorzata;
Weber, Giovanna;
Predieri, Barbara

Publication type:

Article

Rare cases of autoimmune hypothyroidism in young children.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 9/10, p. 963, doi. 10.1515/jpem-2012-0423

By:

Tronconi, Giulia Maria;
Caiulo, Silvana;
Di Frenna, Marianna;
Vigone, Maria Cristina;
Chiumello, Giuseppe;
Weber, Giovanna

Publication type:

Article

Difficult treatment of consumptive hypothyroidism in a child with massive parotid hemangioma.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2012, v. 25, n. 1/2, p. 153, doi. 10.1515/jpem.2011.438

By:

Vigone, Maria Cristina;
Cortinovis, Francesca;
Rabbiosi, Sarah;
Di Frenna, Marianna;
Passoni, Arianna;
Persani, Luca;
Chiumello, Giuseppe;
Gelmetti, Carlo;
Weber, Giovanna

Publication type:

Article

Vitamin D dependent rickets, diagnostic and therapeutic difficulties: two case reports.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 9/10, p. 801, doi. 10.1515/JPEM.2011.214

By:

Donghi, Valentina;
Frenna, Marianna Di;
Lascio, Alessandra di;
Chiumello, Giuseppe;
Weber, Giovanna

Publication type:

Article

Clinical Presentation of McCune-Albright Syndrome in Males.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2006, v. 19, p. 619, doi. 10.1515/jpem.2006.19.s2.619

By:

Wasniewska, Malgorzata;
Matarazzo, Patrizia;
Weber, Giovanna;
Russo, Gianni;
Zampolli, Maria;
Salzano, Giuseppina;
Zirilli, Giuseppina;
Bertelloni, Silvano

Publication type:

Article