2 results for author:"Pereira M.A.A." in Literature citations
Results Customize
› Repeat search in UniProtKB (5)
| Cushing's syndrome secondary to adrenocorticotropin-independent macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene. Fragoso M.C.B.V., Domenice S., Latronico A.C., Martin R.M., Pereira M.A.A., Zerbini M.C.N., Lucon A.M., Mendonca B.B. J. Clin. Endocrinol. Metab. 88:2147-2151(2003) · UniProtKB (4) |
| Gonadotropin-independent precocious puberty due to luteinizing hormone receptor mutations in Brazilian boys: a novel constitutively activating mutation in the first transmembrane helix. Latronico A.C., Shinozaki H., Guerra G. Jr., Pereira M.A.A., Lemos Marini S.H.V., Baptista M.T.M., Arnhold I.J.P., Fanelli F., Mendonca B.B., Segaloff D.L. J. Clin. Endocrinol. Metab. 85:4799-4805(2000) · UniProtKB (1) |