Guiomar Madureira - Concepedia

Author

Guiomar Madureira

Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo

Also Known As

Guiomar Madureira, Madureira Guiomar

Publications

964

Citations

H-Index

Concepts

All Affiliations

Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo Universidade de São Paulo

About

Guiomar Madureira is an author at Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo specializing in adrenal health, obstetrics, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	164
2	Obstetrics	3	3	164
3	Endocrinology	2	2	139
4	Public Health	1	1	92
5	Metabolism	1	1	92

Guiomar Madureira

Publications

906

Citations

H-Index

Page 1

	Year	Citations
Clinical, Hormonal and Pathological Findings in a Comparative Study of Adrenocortical Neoplasms in Childhood and Adulthood Berenice B. Mendonça, Antonio Marmo Lucón, C A V Menezes, The Journal of Urology	1995	112
Molecular Genotyping in Brazilian Patients with the Classical and Nonclassical Forms of 21-Hydroxylase Deficiency<sup>1</sup> Tânia A.S.S. Bachega, Ana Elisa C. Billerbeck, Guiomar Madureira, The Journal of Clinical Endocrinology & Metabolism	1998	107
Influence of different genotypes on 17‐hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21‐hydroxylase deficiency Tânia A.S.S. Bachega, Ana Elisa C. Billerbeck, José Antônio Miguel Marcondes, Clinical Endocrinology Human GrowthGeneticsGenetic EpidemiologyGynecologyPathology	2000	92
Molecular CYP21A2 diagnosis in 480 Brazilian patients with congenital adrenal hyperplasia before newborn screening introduction Daniel Fonseca de Carvalho, Mirela Costa de Miranda, Larissa Garcia Gomes, European Journal of Endocrinology	2016	84
Three Novel Mutations in CYP21 Gene in Brazilian Patients with the Classical Form of 21-Hydroxylase Deficiency Due to a Founder Effect Ana Elisa C. Billerbeck, Berenice B. Mendonça, Emília M. Pinto, The Journal of Clinical Endocrinology & Metabolism	2002	64
ANATOMICAL AND FUNCTIONAL OUTCOMES OF FEMINIZING GENITOPLASTY FOR AMBIGUOUS GENITALIA IN PATIENTS WITH VIRILIZING CONGENITAL ADRENAL HYPERPLASIA Maria Helena Palma Sircili, Berenice B. Mendonça, Francisco Tibor Dénes, Clinics	2006	57
Neonatal 17‐hydroxyprogesterone levels adjusted according to age at sample collection and birthweight improve the efficacy of congenital adrenal hyperplasia newborn screening Giselle Yuri Hayashi, Daniel Fonseca de Carvalho, Mirela Costa de Miranda, Clinical Endocrinology	2016	50
Variable ACTH-Stimulated 17-Hydroxyprogesterone Values in 21-Hydroxylase Deficiency Carriers Are Not Related to the Different CYP21 Gene Mutations Tânia A.S.S. Bachega, Enecy M.L. Brenlha, Ana Elisa C. Billerbeck, The Journal of Clinical Endocrinology & Metabolism Cutoff LevelMendelian DisorderHuman GrowthGenetic DisorderGenetics	2002	47
Substitutions in the <i>CYP21A2</i> promoter explain the simple‐virilizing form of 21‐hydroxylase deficiency in patients harbouring a P30L mutation Rogério Santiago Araújo, Ana Elisa C. Billerbeck, Guiomar Madureira, Clinical Endocrinology	2005	40
A Novel Missense Mutation, GLY424SER, in Brazilian Patients with 21-Hydroxylase Deficiency<sup>1</sup> Ana Elisa C. Billerbeck, Tânia A.S.S. Bachega, Eliana T. Frazzatto, The Journal of Clinical Endocrinology & Metabolism	1999	40

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