BARONIO, FEDERICO
BARONIO, FEDERICO
DIPARTIMENTO DI SCIENZE GINECOLOGICHE, OSTETRICHE E PEDIATRICHE
46, XX DSD due to androgen excess in monogenic disorders of steroidogenesis: Genetic, biochemical, and clinical features
2019 Federico Baronio, Rita Ortolano, Soara Menabò, Alessandra Cassio, Lilia Baldazzi, Valeria Di Natale, Giacomo Tonti, Benedetta Vestrucci, Antonio Balsamo
A Case of Acrodermatitis Dysmetabolica in a Child Affected by Citrullinemia Type I: When Early Diagnosis and Timely Treatment Are Not Enough
2023 Bruni L.; Cassio A.; Di Natale V.; Baronio F.; Ortolano R.; Pession A.; Piraccini B.M.; Neri I.
A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism
2005 Balsamo A.; Antelli A.; Baldazzi L.; Baronio F.; Lazareva D.; Cassio A.; Cicognani A.
A NOVEL FRAME-SHIFT MUTATION IN THE SHOX GENE IN A SUBJECT WITH LERI-WEIL DYSCHONDROSTEOSIS.
2005 Nicoletti A.; Baldazzi L.; Antelli A.; Mazzanti L.; Baronio F.; Menabò S.; Pirazzoli P.
A novel frame-shift mutation in the SHOX gene in a subject with Léri-Weill dyschondrosteosis
2005 Nicoletti A.; Baldazzi L.; Antelli A.; Mazzanti L.; Baronio F.; Menabò S.; Pirazzoli P.; Cicognani A.
AutoimmunePolyendocrinopathyCandidiasisEctodermalDystrophy Syndrome(APECED) clinical and molecular features in three patients from southernItaly.
2008 F.Baronio;A Cassio; G.Tonini; E.Faleschini; M.Gallucci; C.Betterle; ; A .Cicognani
Autosomal dominant pseudohypoaldosteronism type 1 (PHA1) in the Italian population: functional characterization of two novel hMR (NR3C2) gene mutations and frequency and function of three NR3C2 gene SNPs
2007 Antonio Balsamo; Alessandro Cicognani; Monia Gennari; Wolfgang G Sippel; Soara Menabò; Federico Baronio; Wolfgang G Riepe
Autosomal dominant pseudohypoaldosteronism type 1 (PHA1) in the Italian population: functional characterization of two novel hMR (NR3C2) gene mutations and frequency and function of three gene SNPs
2007 Balsamo A.; Cicognani A.; Gennari M.; Sippel W.G.; Menabò S.; Baronio F.; Riepe F.
Beta-ketothiolase (T2) deficiency detected with newborn screening (NBS)
2012 I.Bettocchi; F.Baronio; A.Martini; M.Bal; A.Marsigli; A.Cassio
Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes.
2006 Balsamo A.; Wasniewska M.; Di Pasquale G.; Salzano G.; Baronio F.; Bombaci S.; De Luca F.
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype.
2006 A.Balsamo; M.Wasniewska; G.Di Pasquale; G.Salzano; G.Zirilli; F.Baronio; M.Valenzise; F.De Luca.
Body Mass Index (BMI) evaluation in survivors from childhood cancer
2007 Federico Baronio; Andrea Pasini; Giulio Maltoni; Enrico De Cristofaro; Laura Castiglioni; Stefano Gualandi; Alessandro Cicognani
Carnitine longitudinal pattern in preterm infants <1800 g body weight: a case–control study
2019 Baronio F.; Righi B.; Righetti F.; Bettocchi I.; Ortolano R.; Faldella G.; Rondelli R.; Pession A.; Cassio A.
Comment on "complete androgen insensitivity syndrome: optimizing diagnosis and management"
2014 Balsamo, Antonio; Baronio, Federico; Berra, Marta; Bertelloni, Silvano; D'Alberton, Franco; Marrocco, Giacinto; Vallasciani, Santiago
Comparison between Liquid and Tablet Formulations of Levothyroxine in the Initial Treatment of Congenital Hypothyroidism
2013 Cassio A.; Monti S.; Rizzello A.; Bettocchi I.; Baronio F.; D'Addabbo G.; Bal M.O.; Balsamo A. .
Congenital hypothyroidism (CH): the re-evaluation of diagnosis in CH patients with in situ gland identified by newborn screening
2018 Rita Ortolano, Maria Bitelli, Federico Baronio, Alessandra Cassio
CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency.
2004 Balsamo A; Cicognani A; Baldazzi L; Barbaro M; Baronio F; Gennari M; Bal M; Cassio A; Kontaxaki K; Cacciari E.
Cystathionine Beta-Synthase Deficiency: Three Consecutive Cases Detected in 40 Days by Newborn Screening in Emilia Romagna (Italy) and a Comprehensive Review of the Literature
2023 Candela, Egidio; Zagariello, Michele; Di Natale, Valeria; Ortolano, Rita; Righetti, Francesca; Assirelli, Valentina; Biasucci, Giacomo; Cassio, Alessandra; Pession, Andrea; Baronio, Federico
Diagnosis, treatment, and follow-up of a case of Wolman disease with hemophagocytic lymphohistiocytosis
2022 Baronio F.; Conti F.; Miniaci A.; Carfagnini F.; Di Natale V.; Di Donato G.; Testi M.; Totaro C.; De Fanti A.; Boenzi S.; Dionisi-Vici C.; Esposito S.; Pession A.
Diagnostic features of thyroid nodules in pediatrics
2010 Andrea Corrias; Alessandro Mussa; Federico Baronio; Teresa Arrigo; Mariacarolina Salerno; Maria Segni; Maria Cristina Vigone; Roberto Gastaldi; Giuseppa Zirilli; Gerdi Tuli; Luciano Beccaria; Lorenzo Iughetti; Silvia Einaudi; Giovanna Weber; Filippo De Luca; Alessandra Cassio; Study Group for Thyroid Diseases of Italian Society for Pediatric Endocrinology and Diabetology (SIEDP/ISPED)
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| 46, XX DSD due to androgen excess in monogenic disorders of steroidogenesis: Genetic, biochemical, and clinical features | Federico Baronio, Rita Ortolano, Soara Menabò, Alessandra Cassio, Lilia Baldazzi, Valeria Di Nata...le, Giacomo Tonti, Benedetta Vestrucci, Antonio Balsamo | 2019-01-01 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | - | 1.01 Articolo in rivista | 46,XX DSD.pdf; ijms-20-04605-s001.pdf |
| A Case of Acrodermatitis Dysmetabolica in a Child Affected by Citrullinemia Type I: When Early Diagnosis and Timely Treatment Are Not Enough | Bruni L.; Cassio A.; Di Natale V.; Baronio F.; Ortolano R.; Pession A.; Piraccini B.M.; Neri I. | 2023-01-01 | CHILDREN | - | 1.01 Articolo in rivista | - |
| A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism | Balsamo A.; Antelli A.; Baldazzi L.; Baronio F.; Lazareva D.; Cassio A.; Cicognani A. | 2005-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART A | - | 1.01 Articolo in rivista | - |
| A NOVEL FRAME-SHIFT MUTATION IN THE SHOX GENE IN A SUBJECT WITH LERI-WEIL DYSCHONDROSTEOSIS. | Nicoletti A.; Baldazzi L.; Antelli A.; Mazzanti L.; Baronio F.; Menabò S.; Pirazzoli P. | 2005-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| A novel frame-shift mutation in the SHOX gene in a subject with Léri-Weill dyschondrosteosis | Nicoletti A.; Baldazzi L.; Antelli A.; Mazzanti L.; Baronio F.; Menabò S.; Pirazzoli P.; Cicognan...i A. | 2005-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| AutoimmunePolyendocrinopathyCandidiasisEctodermalDystrophy Syndrome(APECED) clinical and molecular features in three patients from southernItaly. | F.Baronio;A Cassio; G.Tonini; E.Faleschini; M.Gallucci; C.Betterle; ; A .Cicognani | 2008-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| Autosomal dominant pseudohypoaldosteronism type 1 (PHA1) in the Italian population: functional characterization of two novel hMR (NR3C2) gene mutations and frequency and function of three NR3C2 gene SNPs |
Antonio Balsamo; Alessandro Cicognani; Monia Gennari; Wolfgang G Sippel; Soara Menabò; Federico ...Baronio; Wolfgang G Riepe |
2007-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| Autosomal dominant pseudohypoaldosteronism type 1 (PHA1) in the Italian population: functional characterization of two novel hMR (NR3C2) gene mutations and frequency and function of three gene SNPs | Balsamo A.; Cicognani A.; Gennari M.; Sippel W.G.; Menabò S.; Baronio F.; Riepe F. | 2007-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| Beta-ketothiolase (T2) deficiency detected with newborn screening (NBS) | I.Bettocchi; F.Baronio; A.Martini; M.Bal; A.Marsigli; A.Cassio | 2012-01-01 | JOURNAL OF INHERITED METABOLIC DISEASE | - | 4.02 Riassunto (Abstract) | - |
| Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes. | Balsamo A.; Wasniewska M.; Di Pasquale G.; Salzano G.; Baronio F.; Bombaci S.; De Luca F. | 2006-01-01 | EUROPEAN JOURNAL OF PEDIATRICS | - | 1.01 Articolo in rivista | - |
| Birth length and weight in congenital adrenal hyperplasia according to the different phenotype. | A.Balsamo; M.Wasniewska; G.Di Pasquale; G.Salzano; G.Zirilli; F.Baronio; M.Valenzise; F.De Luca. | 2006-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| Body Mass Index (BMI) evaluation in survivors from childhood cancer |
Federico Baronio; Andrea Pasini; Giulio Maltoni; Enrico De Cristofaro; Laura Castiglioni; Stefan...o Gualandi; Alessandro Cicognani |
2007-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| Carnitine longitudinal pattern in preterm infants <1800 g body weight: a case–control study | Baronio F.; Righi B.; Righetti F.; Bettocchi I.; Ortolano R.; Faldella G.; Rondelli R.; Pession A....; Cassio A. | 2019-01-01 | PEDIATRIC RESEARCH | - | 1.01 Articolo in rivista | - |
| Comment on "complete androgen insensitivity syndrome: optimizing diagnosis and management" | Balsamo, Antonio; Baronio, Federico; Berra, Marta; Bertelloni, Silvano; D'Alberton, Franco; Marro...cco, Giacinto; Vallasciani, Santiago | 2014-01-01 | CASE REPORTS IN OBSTETRICS AND GYNECOLOGY | - | 1.04 Replica / breve intervento (e simili) | - |
| Comparison between Liquid and Tablet Formulations of Levothyroxine in the Initial Treatment of Congenital Hypothyroidism | Cassio A.; Monti S.; Rizzello A.; Bettocchi I.; Baronio F.; D'Addabbo G.; Bal M.O.; Balsamo A. . | 2013-01-01 | THE JOURNAL OF PEDIATRICS | - | 1.01 Articolo in rivista | - |
| Congenital hypothyroidism (CH): the re-evaluation of diagnosis in CH patients with in situ gland identified by newborn screening | Rita Ortolano, Maria Bitelli, Federico Baronio, Alessandra Cassio | 2018-01-01 | - | Lowell T. Duncan, Nova Science Publishers | 2.01 Capitolo / saggio in libro | - |
| CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency. | Balsamo A; Cicognani A; Baldazzi L; Barbaro M; Baronio F; Gennari M; Bal M; Cassio A; Kontaxaki K...; Cacciari E. | 2004-01-01 | THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM | - | 1.01 Articolo in rivista | - |
| Cystathionine Beta-Synthase Deficiency: Three Consecutive Cases Detected in 40 Days by Newborn Screening in Emilia Romagna (Italy) and a Comprehensive Review of the Literature | Candela, Egidio; Zagariello, Michele; Di Natale, Valeria; Ortolano, Rita; Righetti, Francesca; As...sirelli, Valentina; Biasucci, Giacomo; Cassio, Alessandra; Pession, Andrea; Baronio, Federico | 2023-01-01 | CHILDREN | - | 1.01 Articolo in rivista | children-10-00396.pdf |
| Diagnosis, treatment, and follow-up of a case of Wolman disease with hemophagocytic lymphohistiocytosis | Baronio F.; Conti F.; Miniaci A.; Carfagnini F.; Di Natale V.; Di Donato G.; Testi M.; Totaro C.;... De Fanti A.; Boenzi S.; Dionisi-Vici C.; Esposito S.; Pession A. | 2022-01-01 | MOLECULAR GENETICS AND METABOLISM REPORTS | - | 1.01 Articolo in rivista | main.pdf |
| Diagnostic features of thyroid nodules in pediatrics | Andrea Corrias; Alessandro Mussa; Federico Baronio; Teresa Arrigo; Mariacarolina Salerno; Maria S...egni; Maria Cristina Vigone; Roberto Gastaldi; Giuseppa Zirilli; Gerdi Tuli; Luciano Beccaria; Lorenzo Iughetti; Silvia Einaudi; Giovanna Weber; Filippo De Luca; Alessandra Cassio; Study Group for Thyroid Diseases of Italian Society for Pediatric Endocrinology and Diabetology (SIEDP/ISPED) | 2010-01-01 | ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE | - | 1.01 Articolo in rivista | - |