Carla R. P. Oliveira

Author

Also Known As

C R P Oliveira, C. R. P. Oliveira, Carla Oliveira, Carla R P Oliveira, Carla R. P. Oliveira, Carla R.P Oliveira, Carla R.P. Oliveira, Carla RP Oliveira, Oliveira, Carla R. P.

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Universidade Federal de Sergipe Johns Hopkins University Johns Hopkins Medicine Universidade de São Paulo Sidney Kimmel Comprehensive Cancer Center

About

Carla R. P. Oliveira is an author at Universidade Federal de Sergipe specializing in medicine, endocrinology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	11	195
2	Health Sciences	3	3	56
3	Education	2	2	53
4	Arts	1	1	25
5	Engineering	1	1	20

Carla R. P. Oliveira

Publications

895

Citations

H-Index

Page 1

	Year	Citations
Longevity in Untreated Congenital Growth Hormone Deficiency Due to a Homozygous Mutation in the GHRH Receptor Gene Manuel H. Aguiar‐Oliveira, Francielle T. Oliveira, Rossana M. C. Pereira, The Journal of Clinical Endocrinology & Metabolism	2009	114
Congenital Growth Hormone (GH) Deficiency and Atherosclerosis: Effects of GH Replacement in GH-Naive Adults Joselina Luzia Menezes Oliveira, Manuel H. Aguiar‐Oliveira, Argemiro D’Oliveira, The Journal of Clinical Endocrinology & Metabolism	2007	66
Insulin Sensitivity and β-Cell Function in Adults with Lifetime, Untreated Isolated Growth Hormone Deficiency Carla R. P. Oliveira, Roberto Salvatori, José Augusto Soares Barreto-Filho, The Journal of Clinical Endocrinology & Metabolism	2011	54
Adipokine Profile and Urinary Albumin Excretion in Isolated Growth Hormone Deficiency Carla R. P. Oliveira, Roberto Salvatori, Rafael Alexandre Meneguz‐Moreno, The Journal of Clinical Endocrinology & Metabolism	2009	40
Sizes of abdominal organs in adults with severe short stature due to severe, untreated, congenital GH deficiency caused by a homozygous mutation in the GHRH receptor gene Carla R. P. Oliveira, Roberto Salvatori, Luciana Michele A. Nóbrega, Clinical Endocrinology	2008	40
Phenotypic Variation Among Four Family Members with Congenital Hypothyroidism Caused by Two Distinct Thyroglobulin Gene Mutations Viviane Pardo, Ileana Gabriela Sanchez Rubio, Meyer Knobel, Thyroid	2008	38
Heterozygosity for a Mutation in the Growth Hormone-Releasing Hormone Receptor Gene Does Not Influence Adult Stature, But Affects Body Composition Rossana M. C. Pereira, Manuel H. Aguiar‐Oliveira, Alessia Sagazio, The Journal of Clinical Endocrinology & Metabolism	2007	35
Metabolic effects of growth hormone (GH) replacement in children and adolescents with severe isolated GH deficiency due to a GHRH receptor mutation Helena Gleeson, Elenilde S. de A. Barreto, Roberto Salvatori, Clinical Endocrinology	2007	34
Increased Visceral Adiposity and Cortisol to Cortisone Ratio in Adults With Congenital Lifetime Isolated GH Deficiency Elenilde Gomes-Santos, Roberto Salvatori, Thiago O. Ferrão, The Journal of Clinical Endocrinology & Metabolism	2014	33
Quality of life in congenital, untreated, lifetime isolated growth hormone deficiency Jorge Antônio Rodrigues Barbosa, Roberto Salvatori, Carla R. P. Oliveira, Psychoneuroendocrinology Growth HormoneHuman GrowthNeuroendocrinologyPediatricsEducation	2009	32

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