Get started
Author

Marianna Di Frenna

Observed names: Di Frenna M, Di Frenna1 M, M. Di Frenna
ORCID: 0000-0001-8853-7694
Observed ORCID: 0000-0001-8853-7694
OpenAlex ID: A5007905366
A frequent oligogenic involvement in congenital hypothyroidism
2017 · Tiziana de Filippis, Giulia Gelmini, et al. · Human Molecular Genetics · 149
PDF
Evolution of Thyroid Function in Preterm Infants Detected by Screening for Congenital Hypothyroidism
2014 · Maria Cristina Vigone, Silvana Caiulo, et al. · The Journal of Pediatrics · 101
Neonatal Screening for Congenital Hypothyroidism: What Can We Learn From Discordant Twins?
2019 · Emanuela Medda, Maria Cristina Vigone, et al. · The Journal of Clinical Endocrinology & Metabolism · 31
PDF
Mild TSH resistance: Clinical and hormonal features in childhood and adulthood
2017 · Maria Cristina Vigone, Marianna Di Frenna, et al. · Clinical Endocrinology · 31
Newborn Screening for Congenital Hypothyroidism: the Benefit of Using Differential TSH Cutoffs in a 2-Screen Program
2020 · Silvana Caiulo, Carlo Corbetta, et al. · The Journal of Clinical Endocrinology & Metabolism · 30
PDF
“Block-and-replace” treatment in Graves’ disease: experience in a cohort of pediatric patients
2019 · M. C. Vigone, E. Peroni, et al. · Journal of Endocrinological Investigation · 20
Difficult treatment of consumptive hypothyroidism in a child with massive parotid hemangioma
2012 · Maria Cristina Vigone, Francesca Cortinovis, et al. · Journal of Pediatric Endocrinology and Metabolism · 20
Novel NKX2-1 Frameshift Mutations in Patients with Atypical Phenotypes of the Brain-Lung-Thyroid Syndrome
2014 · Tiziana de Filippis, Federica Marelli, et al. · European Thyroid Journal · 16
PDF
Heterogeneous phenotype in children affected by non-autoimmune hypothyroidism: an update
2015 · M. C. Vigone, M. Di Frenna, et al. · Journal of Endocrinological Investigation · 14
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism
2022 · D. Gentilini, M. Muzza, et al. · Journal of Endocrinological Investigation · 11
Vitamin D dependent rickets, diagnostic and therapeutic difficulties: two case reports
2011 · Valentina Donghi, Marianna Di Frenna, et al. · Journal of Pediatric Endocrinology and Metabolism · 7
Rare cases of autoimmune hypothyroidism in young children
2013 · Giulia Maria Tronconi, Silvana Caiulo, et al. · Journal of Pediatric Endocrinology and Metabolism · 5
Prolonged asymptomatic SARS‐CoV‐2 infection in a child receiving immunosuppressive therapy
2020 · Daniele Canarutto, Paolo Del Barba, et al. · Pediatric Pulmonology · 3
PDF
Thyroid function and ultrasound surveillance in childhood cancer survivors (CCS): a position paper of the Italian Society of Pediatric Endocrinology and Diabetology (ISPED)
2026 · Gerdi Tuli, Valeria Calcaterra, et al. · Journal of Endocrinological Investigation · 1
PDF
Neonatal screening for congenital hypothyroidism: what can we learn from discordant twins?
2020 · Medda E, Vigone MC, et al. · Yearbook of pediatric endocrinology · 1
L’occhio (non) fa sempre la differenza: quando il sospetto clinico guida per mano la diagnosi
2024 · Andrea Biuso, Stefano Baresi, et al. · Medico e Bambino
Congenital Hypothyroidism (CH) with Delayed TSH Elevation: The Importance of The Second-Screening Strategy and the Evolution of CH in Preterm Infants
2018 · Silvana Caiulo, Maria Cristina Vigone, et al. · 57th Annual ESPE
Mutation of the TSH Receptor Gene: a Longitudinal Study in Children with Non-Autoimmune Subclinical Hypothyroidism
2014 · Maria Cristina Vigone, Micol Sonnino, et al. · ESPE 2014
Ipotiroidismo subclinico nella prima infanzia
2013 · WEBER , GIOVANNA, Di Frenna M, et al. · Archivio Istituzionale della Ricerca - Università Vita-Salute San Raffaele
Clinical re-evaluation of congenital hypothyroidism (CH) in preterm infants with eutopic thyroid
2013 · Vigone MC, Caiulo S, et al. · Archivio Istituzionale della Ricerca - Università Vita-Salute San Raffaele
Comparison between liquid L-thyroxine (L-T4) solution and tablet in congenital hypothyroidism (CH)
2013 · Vigone MC, Peroni E, et al. · Archivio Istituzionale della Ricerca - Università Vita-Salute San Raffaele
Iperparatiroidismo primitivo in paziente con rachitismo ipofosforemico
2011 · F. Rainone, T. Arcidiacono, et al. · Giornale di Clinica Nefrologica e Dialisi
Iperparatiroidismo primitivo in paziente con rachitismo ipofosforemico
2011 · Rainone F, Arcidiacono T, et al. · Archivio Istituzionale della Ricerca - Università Vita-Salute San Raffaele
Neonatal screening of congenital hypothyroidism and Turner's syndrome: diagnostic and therapeutic doubts
2010 · Vigone MC, Maina L, et al. · Archivio Istituzionale della Ricerca - Università Vita-Salute San Raffaele
Clinical outcome of thyroid disfunction in preterm infants
2010 · Vigone MC, Di Frenna M, et al. · Archivio Istituzionale della Ricerca - Università Vita-Salute San Raffaele
Works count: 25
Citation count: 440
H-index: 10
I10-index: 10
Year
Topic
Type