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Carmela Ferrari
Carmela Ferrari
University of São Paulo
Endocrinology
Internal medicine
Biology
Receptor
Medicine
4
Papers
157
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Familial growth hormone deficiency with mutated GHRH receptor gene: clinical and hormonal findings in homozygous and heterozygous individuals from Itabaianinha
2000
European Journal of Endocrinology
Cesar Y. Hayashida
Rogério G. Gondo
Carmela Ferrari
Sergio P. A. Toledo
Roberto Salvatori
Michael A. Levine
Marilza C. L Ezabella
N M A Abelin
Daniel Gianella Neto
Bernardo Leo Wajchenberg
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Citations (23)
Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene.
2000
The Journal of Clinical Endocrinology and Metabolism
Flavia Pernasetti
Sergio P. A. Toledo
Vyacheslav V. Vasilyev
Cesar Y. Hayashida
Joy D. Cogan
Carmela Ferrari
Delmar M. Lourenço
Pamela L. Mellon
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Citations (134)
CPHD patients with severe sexual infantilism caused by the PROP1 301-302 2-BASE pair deletion present adrenal insufficiency
1999
Flavia Pernasetti
Sergio P. A. Toledo
Vasilyev
Joy D. Cogan
Carmela Ferrari
Dayse Maria Lourenço
C. Y. Hayashida
Pamela L. Mellon
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IGF-I e IGFBP3 em heterozigotos para mutação no receptor de GHRH
1998
Arquivos Brasileiros De Endocrinologia E Metabologia
Cesar Y. Hayashida
Rogério G. Gondo
Marilza C. L Ezabella
Carmela Ferrari
N M A Abelin
Daniel Gianella Neto
Bernardo Léo Wajchenberg
Sergio P. A. Toledo
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