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Issue Date | Title | Author(s) |
---|---|---|
2016 | The Frequency of Pathogenic Copy Number Variants in Children with Short Stature of Unknown Etiology | CANTON, A.; HOMMA, T.; FURUYA, T.; ROELA, R.; ARNHOLD, I; JORGE, A. |
2017 | DEFINING THE DOSE, TYPE AND TIMING OF GLUCOCORTICOID AND MINERALOCORTICOID REPLACEMENT IN 256 CHILDREN AND ADULTS WITH CONGENITAL ADRENAL HYPERPLASIA (CAH) IN THE I-CAH REGISTRY | DANIEL, 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 |
2017 | PATERNALLY INHERITED DLK1 DELETION AS A NOVEL CAUSE OF FAMILIAL CENTRAL PRECOCIOUS PUBERTY | DAUBER, 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 |
2013 | Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency | GOMES, Larissa G.; MADUREIRA, Guiomar; MENDONCA, Berenice B.; BACHEGA, Tania A. S. S. |
2013 | The benign spectrum of hypothalamic hamartomas: Infrequent epilepsy and normal cognition in patients presenting with central precocious puberty | CUKIER, Priscilla; CASTRO, Luiz Henrique Martins; BANASKIWITZ, Natalie; TELES, Leandro Roberto; FERREIRA, Luiz Roberto Kobuti; ADDA, Carla Cristina; LEITE, Claudia da Costa; ARNHOLD, Ivo J. P.; MENDONCA, Berenice Bilharinho; LATRONICO, Ana Claudia; BRITO, Vinicius Nahime |
2013 | Modulatory effect of BclI GR gene polymorphisms on the obesity phenotype in Brazilian patients with Cushing's disease | MOREIRA, Ricardo P. P.; BACHEGA, Tania A. S. S.; MACHADO, Marcio C.; MENDONCA, Berenice B.; BRONSTEIN, Marcello D.; FRAGOSO, Maria Candida B. Villares |
2013 | PROP1 overexpression in corticotrophinomas: evidence for the role of PROP1 in the maintenance of cells committed to corticotrophic differentiation | ARAUJO, Ricardo V.; CHANG, Claudia V.; CESCATO, Valter A. S.; FRAGOSO, Maria Candida B. V.; BRONSTEIN, Marcello D.; MENDONCA, Berenice B.; ARNHOLD, Ivo J. P.; CARVALHO, Luciani R. S. |
2013 | Heterozygous Mutations in Natriuretic Peptide Receptor-B (NPR2) Gene as a Cause of Short Stature in Patients Initially Classified as Idiopathic Short Stature | VASQUES, Gabriela A.; AMANO, Naoko; DOCKO, Ana J.; FUNARI, Mariana F. A.; QUEDAS, Elisangela P. S.; NISHI, Mirian Y.; ARNHOLD, Ivo J. P.; HASEGAWA, Tomonobu; JORGE, Alexander A. L. |
2013 | Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome | MONTENEGRO, Luciana Ribeiro; SILVEIRA, Leticia F. G.; TUSSET, Cintia; CASTRO, Margaret de; VERSIANI, Beatriz R.; LATRONICO, Ana Claudia; MENDONCA, Berenice Bilharinho; TRARBACH, Ericka B. |
2013 | Molecular and Gene Network Analysis of Thyroid Transcription Factor 1 (TTF1) and Enhanced at Puberty (EAP1) Genes in Patients with GnRH-Dependent Pubertal Disorders | CUKIER, Priscilla; WRIGHT, Hollis; RULFS, Tomke; SILVEIRA, Leticia Ferreira Gontijo; TELES, Milena Gurgel; MENDONCA, Berenice Bilharinho; ARNHOLD, Ivo J. P.; HEGER, Sabine; LATRONICO, Ana Claudia; OJEDA, Sergio R.; BRITO, Vinicius Nahime |
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