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Mutational analysis of the SHH, Gli2 and BMP4 genes in patients with congenital hypopituitarism and/or midline cerebral defects

Grant number: 10/11510-1
Support Opportunities:Scholarships in Brazil - Doctorate (Direct)
Start date: November 01, 2010
End date: October 31, 2012
Field of knowledge:Health Sciences - Medicine
Principal Investigator:Sonir Roberto Rauber Antonini
Grantee:Sabrina Soares Paulo
Host Institution: Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da USP (HCMRP). Secretaria da Saúde (São Paulo - Estado). Ribeirão Preto , SP, Brazil
News published in Agência FAPESP Newsletter about the scholarship:
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Scientific publications
(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)
PAULO, SABRINA SOARES; FERNANDES-ROSA, FABIO L.; TURATTI, WENDY; COELI-LACCHINI, FERNANDA BORCHERS; MARTINELLI, CARLOS E., JR.; NAKIRI, GUILHERME S.; MOREIRA, AYRTON C.; SANTOS, ANTONIO C.; DE CASTRO, MARGARET; ANTONINI, SONIR R.. Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects. CLINICAL ENDOCRINOLOGY, v. 82, n. 4, p. 8-pg., . (10/11510-1)
PAULO, SABRINA SOARES; FERNANDES-ROSA, FABIO L.; TURATTI, WENDY; COELI-LACCHINI, FERNANDA BORCHERS; MARTINELLI, JR., CARLOS E.; NAKIRI, GUILHERME S.; MOREIRA, AYRTON C.; SANTOS, ANTONIO C.; DE CASTRO, MARGARET; ANTONINI, SONIR R.. Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects. Clinical Endocrinology, v. 82, n. 4, p. 562-569, . (10/11510-1)