Silvia Einaudi - Concepedia

Author

Silvia Einaudi

Ospedale Regina Margherita

Also Known As

Einaudi, Silvia, Silvia Einaudi

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

Ospedale Regina Margherita University of Turin University of Messina Bambino Gesù Children's Hospital University of Milan

About

Silvia Einaudi is an author at Ospedale Regina Margherita specializing in medicine, adrenal disease, and pediatrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	333
2	Endocrinology	2	2	46
3	Health Sciences	1	1	72
4	Public Health	1	1	144
5	Molecular Genetics	1	1	16

Silvia Einaudi

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
Heterozygous Missense Mutations in Steroidogenic Factor 1 (SF1/Ad4BP, NR5A1) Are Associated with 46,XY Disorders of Sex Development with Normal Adrenal Function Lin Lin, Pascal Philibert, Bruno Ferraz‐de‐Souza, The Journal of Clinical Endocrinology & Metabolism	2007	209
Identification of New Variants of Human<i>BMP15</i>Gene in a Large Cohort of Women with Premature Ovarian Failure Elisa Di Pasquale, Raffaella Rossetti, Anna Marozzi, The Journal of Clinical Endocrinology & Metabolism	2006	199
Prevalence and Characteristics of Familial Hyperaldosteronism Paolo Mulatero, Davide Tizzani, Andrea Viola, Hypertension Metabolic SyndromeHypertensionUrologyFamilial HyperaldosteronismPa Patients	2011	144
Adrenal axis function after high‐dose steroid therapy for childhood acute lymphoblastic leukemia Silvia Einaudi, Nicoletta Bertorello, Nicoletta Masera, Pediatric Blood & Cancer	2007	89
Thyroid dysfunction as a late effect in childhood medulloblastoma: a comparison of hyperfractionated versus conventionally fractionated craniospinal radiotherapy Umberto Ricardi, Andrea Corrias, Silvia Einaudi, International Journal of Radiation OncologyBiologyPhysics Neuro-oncologyLate EffectThyroid DysfunctionThyroid DiseaseThyroid Disorders	2001	72
Elucidating the Underlying Molecular Pathogenesis of<i>NR3C2</i>Mutants Causing Autosomal Dominant Pseudohypoaldosteronism Type 1 Felix G. Riepe, Johannes Finkeldei, Luisa De Sanctis, The Journal of Clinical Endocrinology & Metabolism	2006	65
17α-Hydroxylase/17,20-Lyase Deficiency as a Model to Study Enzymatic Activity Regulation: Role of Phosphorylation* Anna Biason‐Lauber, B. Kempken, E A Werder, The Journal of Clinical Endocrinology & Metabolism	2000	55
Copeptin role in polyuria‐polydipsia syndrome differential diagnosis and reference range in paediatric age Gerdi Tuli, Daniele Tessaris, Silvia Einaudi, Clinical Endocrinology	2018	49
Incidence of primary congenital hypothyroidism and relationship between diagnostic categories and associated malformations Gerdi Tuli, Jessica Munarin, Daniele Tessaris, Endocrine Developmental AnomalyDiagnostic CategoriesThyroid DiseaseThyroid DisordersPrimary Congenital Hypothyroidism	2020	42
Real-World Estimates of Adrenal Insufficiency–Related Adverse Events in Children With Congenital Adrenal Hyperplasia Salma Ali, Jillian Bryce, Houra Haghpanahan, The Journal of Clinical Endocrinology & Metabolism	2020	36

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