Romolo Sandrini - Concepedia

Author

Romolo Sandrini

Universidade Federal do Paraná

Also Known As

Romolo Sandrini

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

Universidade Federal do Paraná St. Jude Children's Research Hospital University of Tennessee Health Science Center Georgetown University National Institutes of Health

About

Romolo Sandrini is an author at Universidade Federal do Paraná specializing in medicine, adrenal disease, and pediatrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	325
2	Public Health	1	1	220
3	Diabetes	1	1	10
4	Epidemiology	1	1	220
5	Neurology	1	1	10

Romolo Sandrini

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
An inherited <i>p53</i> mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma Raul C. Ribeiro, Fabiano Sandrini, Bonald C. Figueiredo, Proceedings of the National Academy of Sciences	2001	530
Childhood Adrenocortical Tumors<sup>1</sup> Romolo Sandrini, Raul C. Ribeiro, Luiz DeLacerda The Journal of Clinical Endocrinology & Metabolism Population ChildrenAdrenal GlandEndocrine OncologyPediatric EpidemiologySurgical Pathology	1997	220
Amplification of the Steroidogenic Factor 1 Gene in Childhood Adrenocortical Tumors Bonald C. Figueiredo, Luciane R. Cavalli, Mara Albonei Dudeque Pianovski, The Journal of Clinical Endocrinology & Metabolism	2005	131
Comparative Genomic Hybridization Analysis of Adrenocortical Tumors of Childhood<sup>1</sup> Bonald C. Figueiredo, Constantine A. Stratakis, Romolo Sandrini, The Journal of Clinical Endocrinology & Metabolism	1999	116
Correlation of Pathologic Features with Clinical Outcome in Pediatric Adrenocortical Neoplasia:<i>A Study of a Brazilian Population</i> Michael F. Bugg, Raul C. Ribeiro, Paula K. Roberson, American Journal of Clinical Pathology Surgical OncologyHistologic ClassificationPathologyAdrenal GlandOncology	1994	95
Clinical characteristics of small functioning adrenocortical tumors in children Edson Michalkiewicz, Romolo Sandrini, Michael F. Bugg, Medical and Pediatric Oncology	1997	59
<i>In vitro</i> and <i>in vivo</i> responses to short‐term recombinant human insulin‐like growth factor‐1 (IGF‐I) in a severely growth‐retarded girl with ring chromosome 15 and deletion of a single allele for the type 1 IGF receptor gene Luiz de Lacerda, Julienne Ângela Ramires de Carvalho, Bethel Stannard, Clinical Endocrinology	1999	38
An Intron 9 CYP19 Gene Variant (IVS9+5G>A), Present in an Aromatase-Deficient Girl, Affects Normal Splicing and Is Also Present in Normal Human Steroidogenic Tissues Nora Saraco, Suzana Nesi-França, Romina Sainz, Hormone Research in Paediatrics	2015	12
Evaluation of sensorimotor polyneuropathy in children and adolescents with type I diabetes: associations with microalbuminuria and retinopathy Lúcia Helena Coutinho dos Santos, Isac Bruck, Sérgio Antônio Antoniuk, Pediatric Diabetes Diabetic RetinopathyNormal ControlsOphthalmologyMedicineMicrovascular Dysfunction	2002	10

Page 1