Milena Beranova

The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics.

W. Crowley, S. Seminara, E. Schipani, 2001, The Journal of clinical endocrinology and metabolism.

Genetics of hypogonadotropic hypogonadism

W. Crowley, S. Seminara, F. Hayes, 2000, Journal of endocrinological investigation.

Successful use of pulsatile gonadotropin-releasing hormone (GnRH) for ovulation induction and pregnancy in a patient with GnRH receptor mutations.

W. Crowley, J. Hall, S. Seminara, 2000, The Journal of clinical endocrinology and metabolism.

Prevalence, phenotypic spectrum, and modes of inheritance of gonadotropin-releasing hormone receptor mutations in idiopathic hypogonadotropic hypogonadism.

W. Crowley, J. Hall, G. Bédécarrats, 2001, The Journal of clinical endocrinology and metabolism.

Four naturally occurring mutations in the human GnRH receptor affect ligand binding and receptor function

K. Linher, P. Conn, J. Janovick, 2003, Molecular and Cellular Endocrinology.

Conventional renal cell carcinoma with granulomatous reaction: a report of three cases

O. Hes, M. Sulc, T. Vaněček, 2003, Virchows Archiv.