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Pituitary|July 13, 2007
Genetic insights into human isolated gonadotropin deficiencyEricka Barbosa Trarbach, Leticia Gontijo Silveira, Ana Claudia Latronico
Molecular and Cellular Endocrinology|March 2, 2010
Genetics basis for GnRH-dependent pubertal disorders in humansLeticia Ferreira Gontijo Silveira, Ericka Barbosa Trarbach, Ana Claudia Latronico
Endocrine Oncology (Bristol, England)|April 21, 2025
HHLA2: a potential biomarker and therapeutic target in endocrine-related cancerChristiane Gruetzmacher, Bruna Sousa Pessoa, Flora Ladeira Craveiro, et al.
Clinics (Sao Paulo, Brazil)|February 24, 2012
Genotype analysis of the human endostatin variant p.D104N in benign and malignant adrenocortical tumorsBeatriz Marinho de Paula Mariani, Ericka Barbosa Trarbach, Tamaya Castro Ribeiro, et al.
Pituitary|May 29, 2007
Two cases of Kallmann syndrome associated with empty sellaCristina Micheletto Dallago, Denise Dotta Abech, Julia Fernanda Semmelmann Pereira-Lima, et al.
The Journal of Clinical Endocrinology and Metabolism|August 3, 2006
Novel fibroblast growth factor receptor 1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmiaEricka Barbosa Trarbach, Elaine Maria Frade Costa, Beatriz Versiani, et al.
World Neurosurgery|August 24, 2018
Nonfunctioning Pituitary Adenoma Recurrence and Its Relationship with Sex, Size, and Hormonal Immunohistochemical ProfileRafael Loch Batista, Ericka Barbosa Trarbach, Mateus Diniz Marques, et al.
Frontiers in Endocrinology|April 7, 2017
Transcriptome Analysis Showed a Differential Signature between Invasive and Non-invasive CorticotrophinomasLeonardo Jose Tadeu de Araújo, Antonio Marcondes Lerario, Margaret de Castro, et al.
The Journal of Clinical Endocrinology and Metabolism|August 7, 2008
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndromeAna Paula Abreu, Ericka Barbosa Trarbach, Margaret de Castro, et al.
European Journal of Endocrinology|May 6, 2011
Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadismDaiane Beneduzzi, Anita K Iyer, Ericka Barbosa Trarbach, et al.
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