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Results 1-10 of 117 (Search time: 0.004 seconds).
Issue DateTitleAuthor(s)
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
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
2019Probably Pathogenic Variants in New Candidate Genes in Patients with Pituitary Stalk Interruption Syndrome (PSIS) Revealed by Whole-Exome SequencingCORREA, F. A.; NAKAGUMA, M.; JORGE, A. A. L.; FUNARI, M. F. A.; LERARIO, A. M.; CARVALHO, L. R. S.; ARNHOLD, I. J. P.; MENDONCA, B. B.
2019An Extremely Rare Novel Missense Variant p.M304V in SOX3 Gene is Responsible for an X-Linked GH Deficiency in a Brazilian PatientBENEDETTI, A. F. F.; SILVA, J. M.; BISCOTTO, I. P.; FERREIRA, N. P.; ARNHOLD, I. J. P.; MENDONCA, B. B.; CARVALHO, L. R. S.
2019Low Frequency of Pathogenic Allelic Variants in the 46,XY Differences of Sex Development (DSD)-Related Genes in Small for Gestational Age Children with HypospadiasBRAGA, B. L.; GOMES, L. N.; NISHI, M. Y.; FREIRE, B. L.; BATISTA, R. L.; FUNARI, M. F. A.; COSTA, E. M. F.; LERARIO, A. M.; DOMENICE, S.; JUNIOR, J. A. D. F.; JORGE, A. A. L.; MENDONCA, B. B.
2019Clinical and Genetic Evaluation of Prepubertal Children with Short Stature and Advanced Bone AgeVASQUES, G. A.; ANDRADE, N. L. M.; FUNARI, M. F. A.; HOMMA, T. K.; FREIRE, B. L.; NISHI, M. Y.; MALAQUIAS, A. C.; MENDONCA, B. B.; ARNHOLD, I. J. P.; JORGE, A. A. L.
2019Long-Term Outcome In Leydig Cell HypoplasiaBONCOMPAGNI, Alessandra; BRYCE, Jillian; LUCACCIONI, Laura; IUGHETTI, Lorenzo; ACERINI, Carlo; CUCCARO, Rieko T.; BERTELLONI, Silvano; HANNEMA, Sabine E.; DARENDELILER, F. Feyza; POYRAZOGLU, Sukran; DENZER, Friederike; BATISTA, Rafael L.; DOMENICE, Sorahia; LATRONICO, Ana C.; MENDONCA, Berenice B.; REY, Rodolfo; AHMED, S. Faisal
2019Global Practice of Glucocorticoid and Mineralocorticoid Treatment in Children and Adults with Congenital Adrenal Hyperplasia - Insights from the I-CAH RegistryBACILA, Irina-Alexandra; BLANKENSTEIN, Oliver; NEUMANN, Uta; GRINTEN, Hedi L. Claahsen-van der; KRONE, Ruth; ACERINI, Carlo; BACHEGA, Tania S. S.; MIRANDA, Mirella C.; MENDONCA, Berenice; BIRKEBAEK, Niels H.; COOLS, Martine; MILENKOVIC, Tatjana; BONFIG, Walter; TOMLINSON, Jeremy; ELSEDFY, Heba; BALSAMO, Antonio; HANNEMA, Sabine; HIGHAM, Claire; ATAPATTU, Navoda; LICHIARDOPOL, Corina; GURAN, Tulay; ABALI, Zehra; MOHNIKE, Klaus; FINKEN, Martijn J. J.; VIEITES, Ana; DARENDELILER, Feyza; GUVEN, Ayla; KORBONITS, Marta; VRIE, Liat De; COSTA, Eduardo; EINAUDI, Silvia; KAMP, Hetty van der; IOTOVA, Violeta; ROSS, Richard; AHMED, S. Faisal; KRONE, Nils P.
2019Large spectrum of DSD phenotype caused by pathogenic variants in Wilms tumor suppressor gene 1FERRARI, Maria Tereza Martins; DOMENICE, Sorahia; MENDONCA, Berenice Bilharino; MORAES, Daniela Rodrigues; BATISTA, Rafael Loch; GOMES, Nathalia Lisboa; NISHI, Mirian Yumie; SIRCILI, Maria Helena; PAULA, Tatiana Evelin; COSTA, Eduardo; COSTA, Elaine Maria Frade