Authors:
Oliveira, LMB
Seminara, SB
Beranova, M
Hayes, FJ
Valkenburgh, SB
Schipani, E
Costa, EMF
Latronico, AC
Crowley, WF
Vallejo, M
Citation: Lmb. Oliveira et al., The importance of autosomal genes in Kallmann syndrome: Genotype-phenotypecorrelations and neuroendocrine characteristics, J CLIN END, 86(4), 2001, pp. 1532-1538
Authors:
Beranova, M
Oliveira, LMB
Bedecarrats, GY
Schipani, E
Vallejo, M
Ammini, AC
Quintos, JB
Hall, JE
Martin, KA
Hayes, FJ
Pitteloud, N
Kaiser, UB
Crowley, WF
Seminara, SB
Citation: M. Beranova et al., Prevalence, phenotypic spectrum, and modes of inheritance of gonadotropin-releasing hormone receptor mutations in idiopathic hypogonadotropic hypogonadism, J CLIN END, 86(4), 2001, pp. 1580-1588
Authors:
Hayes, FJ
Decruz, S
Seminara, SB
Boepple, PA
Crowley, WF
Citation: Fj. Hayes et al., Differential regulation of gonadotropin secretion by testosterone in the human male: Absence of a negative feedback effect of testosterone on follicle-stimulating hormone secretion, J CLIN END, 86(1), 2001, pp. 53-58
Citation: Sb. Seminara et Wf. Crowley, Perspective: The importance of genetic defects in humans in elucidating the complexities of the hypothalamic-pituitary-gonadal axis, ENDOCRINOL, 142(6), 2001, pp. 2173-2177
Authors:
Hayes, FJ
Seminara, SB
Decruz, S
Boepple, PA
Crowley, WF
Citation: Fj. Hayes et al., Aromatase inhibition in the human male reveals a hypothalamic site of estrogen feedback, J CLIN END, 85(9), 2000, pp. 3027-3035
Authors:
Seminara, SB
Beranova, M
Oliveira, LMB
Martin, KA
Crowley, WF
Hall, JE
Citation: Sb. Seminara et al., Successful use of pulsatile gonadotropin-releasing hormone (GnRH) for ovulation induction and pregnancy in a patient with GnRH receptor mutations, J CLIN END, 85(2), 2000, pp. 556-562
Authors:
Seminara, SB
Hall, JE
Taylor, AE
Crowley, WF
Martin, KA
Citation: Sb. Seminara et al., The Reproductive Endocrine Associates of the Massachusetts General Hospital: Fifteen years of integrated clinical practice and investigation, J CLIN END, 84(6), 1999, pp. 1912-1918
Citation: Jc. Achermann et al., Mutational analysis of DAX1 in patients with hypogonadotropic hypogonadismor pubertal delay, J CLIN END, 84(12), 1999, pp. 4497-4500