Copy number variation associated with Kallmann syndrome: new genetics insights from genome-wide studies

著者: Trarbach, Ericka B
出版事項 2011

Evaluation of Downstream Regulatory Element Antagonistic Modulator Gene in Human Multinodular Goiter

著者: Shinzato, Amanda, Lerario, Antonio M., Lin, Chin J., Danilovic, Debora S., Marui, Suemi, Trarbach, Ericka B.
出版年 Med Sci Monit Basic Res (2015)

ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome

著者: Scalco, Renata C, Trarbach, Ericka B, Albuquerque, Edoarda V A, Homma, Thais K, Inoue-Lima, Thais H, Nishi, Mirian Y, Mendonca, Berenice B, Jorge, Alexander A L
出版年 Endocr Connect (2019)

A GPR54-Activating Mutation in a Patient with Central Precocious Puberty

著者: Teles, Milena Gurgel, Bianco, Suzy D.C., Brito, Vinicius Nahime, Trarbach, Ericka B., Kuohung, Wendy, Xu, Shuyun, Seminara, Stephanie B., Mendonca, Berenice B., Kaiser, Ursula B., Latronico, Ana Claudia
出版事項 2008

Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency

著者: Trarbach, Ericka B., Abreu, Ana Paula, Silveira, Leticia Ferreira Gontijo, Garmes, Heraldo Mendes, Baptista, Maria Tereza M., Teles, Milena Gurgel, Costa, Elaine M. F., Mohammadi, Moosa, Pitteloud, Nelly, Mendonca, Berenice B., Latronico, Ana Claudia
出版事項 2010

Mutational Analysis of TAC3 and TACR3 Genes in Patients with Idiopathic Central Pubertal Disorders

著者: Tusset, Cintia, Noel, Sekoni D., Trarbach, Ericka B., Silveira, Letícia F. G., Jorge, Alexander A. L., Brito, Vinicius N., Cukier, Priscila, Seminara, Stephanie B., de Mendonça, Berenice B., Kaiser, Ursula B., Latronico, Ana Claudia
出版事項 2012

Role of GnRH receptor mutations in patients with a wide spectrum of pubertal delay

著者: Beneduzzi, Daiane, Trarbach, Ericka B., Min, Le, Jorge, Alexander A. L., Garmes, Heraldo M., Renk, Alessandra Covallero, Fichna, Marta, Fichna, Piotr, Arantes, Karina A., Costa, Elaine M. F., Zhang, Anna, Adeola, Oluwaseun, Wen, Junping, Carroll, Rona S., Mendonça, Berenice B., Kaiser, Ursula B., Latronico, Ana Claudia, Silveira, Letícia F. G.
出版事項 2014

FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies

著者: Correa, Fernanda A, Trarbach, Ericka B, Tusset, Cintia, Latronico, Ana Claudia, Montenegro, Luciana R, Carvalho, Luciani R, Franca, Marcela M, Otto, Aline P, Costalonga, Everlayny F, Brito, Vinicius N, Abreu, Ana Paula, Nishi, Mirian Y, Jorge, Alexander A L, Arnhold, Ivo J P, Sidis, Yisrael, Pitteloud, Nelly, Mendonca, Berenice B
出版年 Endocr Connect (2015)

New Insights Into Pheochromocytoma Surveillance of Young Patients With VHL Missense Mutations

著者: Fagundes, Gustavo F C, Petenuci, Janaina, Lourenco, Delmar M, Trarbach, Ericka B, Pereira, Maria Adelaide A, Correa D’Eur, Joya Emilie, Hoff, Ana O, Lerario, Antonio M, Zerbini, Maria Claudia N, Siqueira, Sheila, Yamauchi, Fernando, Srougi, Victor, Tanno, Fabio Y, Chambo, Jose Luis, Latronico, Ana Claudia, Mendonca, Berenice B, Fragoso, Maria Candida B V, Almeida, Madson Q
出版年 J Endocr Soc (2019)