Two novel exonic and intronic mutations that predict abnormal splicing of the GHRH receptor (GHRHR) gene in patients with sporadic isolated GH deficiency (IGHD)
Suemi Marui Berenice Bilharinho de Mendonca; Vivian Estefan; Ivo Jorge Prado Arnhold; Annual Meeting of the Pediatric Academic Societies (2001 Baltimore)
Pediatric Research Philadelphia v. 49, n. 4 pt. 2, p. 34 res. P2-198, 2001
Philadelphia 2001
Item não circula. Consulte sua biblioteca.(Acessar)
Diagnotic value of ultrasensitive immunofluorometric gonadotropin assays in hypogonadotropic hypogonadism
Elaine M. F. Costa Berenice Bilharinho Mendonca; Ana Claudia Latronico; Ivo J. P Arnhold; Annual Meeting of the Pediatric Academic Societies (2001 Baltimore)
Pediatric Research Philadelphia v. 49, n. 4 pt. 2, p. 138A. res. PI-823, 2001
Philadelphia 2001
Item não circula. Consulte sua biblioteca.(Acessar)
Poor reproducibility of IGF-I and IGFBP-3 generation test in children with short stature
Alexander A. L Jorge Silvia C. A. L Souza; Ivo J. P Arnhold; Berenice Bilharinho Mendonca; Annual Meeting of the Pediatric Academic Societies (2001 Baltimore)
Pediatric Research Philadelphia v. 49, n. 4 pt. 2, p.78A. res. PI-461, 2001
Philadelphia 2001
Item não circula. Consulte sua biblioteca.(Acessar)
21-hydroxylase deficiency (classic form) in black descendents from Bahia molecular, clinical and familial study
Maria Betania M. B. Toralles Ana E. C Billerbeck; Berenice Bilharinho Mendonca; Eliana Azevedo; Annual Meeting of the Pediatric Academic Societies (2001 Baltimore)
Pediatric Research Philadelphia v. 49, n. 4 pt. 2, p. 113A. res. PI-673, 2001
Philadelphia 2001
Item não circula. Consulte sua biblioteca.(Acessar)
Absence of HEXS1 gene mutations in patients with growth hormone deficiency (GHD) associated to cerebral and/or facial midline defects (MLD)
Luciani R. S. Carvalho Berenice Bilharinho de Mendonca; Veronica Mericq; Jose A. M Marcondes; Teresa C. A Vieira; Mirta Knoepfelmacher; Fernando Kok; Ivo J. P Arnhold; Annual Meeting of the Pediatric Academic Societies (2001 Baltimore)
Pediatric Research Philadelphia v. 49, n. 4 pt. 2, p. 33A res. P2-194, 2001
Philadelphia 2001
Item não circula. Consulte sua biblioteca.(Acessar)
A novel mutation (G267S) on the CYP11B1 gene in a patient with 11ß-hydroxylase deficiency causing complete virilization
Maricilda P. de Mello Junia Y Penachioni; Margaret de Castro; Tania A. S. S Bachega; Berenice Bilharinho Mendonca; Annual Meeting of the Pediatric Academic Societies (2001 Baltimore)
Pediatric Research Philadelphia v. 49, n. 4 pt. 2, p. 119A. res. PI-711, 2001
Philadelphia 2001
Item não circula. Consulte sua biblioteca.(Acessar)
Male pseudohermaphroditism associated with low birthweight
Elaine M. F. Costa Rafaela V Correa; Karla F. A. S Melo; Ivo Jorge Prado Arnhold; Berenice Bilharinho Mendonca; Annual Meeting of the Pediatric Academic Societies (2001 Baltimore)
Pediatric Research Philadelphia v. 49, n. 4 pt. 2, p. 57A. res. P3-334, 2001
Philadelphia 2001
Item não circula. Consulte sua biblioteca.(Acessar)
Absence of inactivating mutations in the GH receptor gene (GHR) in children with idiopathic short stature (ISS) and low levels of IGFBP-3
Alexander A. L. Jorge Chin J Lin; Silvia C. A. L Souza; Ivo Jorge Prado arnhold; Berenice Bilharinho Mendonca; Annual Meeting of the Pediatric Academic Societies (2001 Baltimore)
Pediatric Research Philadelphia v. 49, n. 4 pt. 2, p. 69A. res. P1-407, 2001
Philadelphia 2001
Item não circula. Consulte sua biblioteca.(Acessar)
An inherited mutation in homozygous of the p53 tumor suppressor gene in a girl with functioning adrenocortical tumor
Emilia M. Pinto Berenice Bilharinho Mendonca; Adriano Masson; Maria Candida B. V Fragoso; Sorahia Domenice; Regina M Martin; Ana Claudia Latronico; Annual Meeting of the Pediatric Academic Societies (2001 Baltimore)
Pediatric Research Philadelphia v. 49, n. 4 pt. 2, p. 126A. res. PI-750, 2001
Philadelphia 2001
Item não circula. Consulte sua biblioteca.(Acessar)