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Resultado 1-10 de 683.
DataTítuloAutor(es)
2017Functional Impact of Novel Androgen Receptor Mutations on the Clinical Manifestation of Androgen Insensitivity SyndromePETROLI, Reginaldo J.; HIORT, Olaf; STRUVE, Dagmar; GESING, Julia K.; SOARDI, Fernanda C.; SPINOLA-CASTRO, Angela M.; MELO, Karla; ARNHOLD, Ivo J. Prado; MACIEL-GUERRA, Andrea T.; GUERRA-JUNIOR, Gil; WERNER, Ralf; MELLO, Maricilda P. de
2017Tumores corticais da suprarrenalALMEIDA, Madson Queiroz; ANTONINI, Sonir Roberto Rauber; FRAGOSO, Maria Candida Barrison Villares
2017Hirsutismo e síndrome dos ovários policísticosMARCONDES, José Antonio Miguel; HAYASHIDA, Sylvia Asaka Yamashita; GOMES, Larissa Garcia
2018A Lower Ki 67 Labelling Index (LI) Cut-Point Improves the Prognostic Assessment and Might Aid in the Diagnosis of Adult Adrenocortical TumorsMARTINS FILHO, Sebastiao N.; ALMEIDA, Madson Q.; SOARES, Ibere C.; WAKAMATSU, Alda; ALVES, Venancio; FRAGOSO, Maria C.; ZERBINI, Maria
2018A Simple Yet Powerful Algorithm Including Ki67 Labeling Index (LI) Helps Predict Outcome Pediatric Adrenocortical Tumors (ACT)MARTINS FILHO, Sebastiao N.; ALMEIDA, Madson Q.; WAKAMATSU, Alda; ALVES, Venancio; FRAGOSO, Maria C.; ZERBINI, Maria
2016The Frequency of Pathogenic Copy Number Variants in Children with Short Stature of Unknown EtiologyCANTON, A.; HOMMA, T.; FURUYA, T.; ROELA, R.; ARNHOLD, I; JORGE, A.
2017DEFINING THE DOSE, TYPE AND TIMING OF GLUCOCORTICOID AND MINERALOCORTICOID REPLACEMENT IN 256 CHILDREN AND ADULTS WITH CONGENITAL ADRENAL HYPERPLASIA (CAH) IN THE I-CAH REGISTRYDANIEL, Eleni; SANDRK, Marija; BLANKENSTEIN, Oliver; NEUMANN, Uta; GRINTEN, Hedi Claahsen-Van der; LINDE, Annelieke Van der; DARENDELILER, Feyza; PYRAZOGLU, Sukran; MENDONCA, Berenice B.; BACHEGA, Tania S. S.; MIRANDA, Mirela C.; ACERINI, Carlo; GURAN, Tulay; BIRKEBAEK, Niels H.; COOLS, Martine; MILENKOVIC, Tatjana; BONFIG, Walter; TOMLINSON, Jeremy W.; AHMED, Syed Faisal; ELSEDFY, Heba; BALSAMO, Antonio; HANNEMA, Sabine E.; HIGHAM, Claire; ATAPATTU, Navoda; LICHIARDOPOL, Corina; KRONE, Ruth E.; MOHNIKE, Klaus; KRONE, Nils
2017A common CHRNE mutation (c.130dupG) in Brazilian patients with congenital myasthenic syndromeESTEPHAN, E.; SILVA, A.; MENDONCA, R.; CALDAS, V.; ZAMBON, A.; MARCHIORI, P.; HEISE, C.; REED, U.; ZANOTELI, E.
2017PATERNALLY INHERITED DLK1 DELETION AS A NOVEL CAUSE OF FAMILIAL CENTRAL PRECOCIOUS PUBERTYDAUBER, Andrew; CUNHA-SILVA, Marina; MACEDO, Delanie; BRITO, Vinicius; ABREU, Ana Paula; ROBERTS, Stephanie; MONTENEGRO, Luciana; ANDREW, Melissa; KRIBY, Andrew; WEIRAUCH, Matthew; LABILLOY, Guillaume; BESSA, Danielle; CARROLL, Rona; JACOBS, Dakota; CHAPPELL, Patrick; MENDONCA, Berenice B.; HAIG, David; KAISER, Ursula; LATRONICO, Ana Claudia
2013Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiencyGOMES, Larissa G.; MADUREIRA, Guiomar; MENDONCA, Berenice B.; BACHEGA, Tania A. S. S.