Methylome profiling of healthy and central precocious puberty girls
Bessa, Danielle S, Maschietto, Mariana, Aylwin, Carlos Francisco, Canton, Ana P M, Brito, Vinicius N, Macedo, Delanie B, Cunha-Silva, Marina, Palhares, Heloísa M C, de Resende, Elisabete A M R, Borges, Maria de Fátima, Mendonca, Berenice B, Netchine, Irene, Krepischi, Ana C V, Lomniczi, Alejandro, Ojeda, Sergio R, Latronico, Ana Claudia
Published in Clinical epigenetics (22.11.2018)
Published in Clinical epigenetics (22.11.2018)
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Identification of a novel missense mutation in Brazilian patient with a severe form of mucopolysaccharidosis type IVA
Kubaski, Francyne, Brusius-Facchin, Ana Carolina, Palhares, Heloísa M.C., Balarin, Marly Aparecida Spadotto, Viapiana-Camelier, Marli, Guidobono, Regis, Burin, Maira Graeff, Giugliani, Roberto, Leistner-Segal, Sandra
Published in Gene (15.03.2013)
Published in Gene (15.03.2013)
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A single somatic activating Asp578His mutation of the luteinizing hormone receptor causes Leydig cell tumour in boys with gonadotropin-independent precocious puberty
D'Alva, Catarina B., Brito, Vinicius N., Palhares, Heloisa M. C., Carvalho, Filomena M., Arnhold, Ivo J. P., Mendonca, Berenice B., Latronico, Ana Claudia
Published in Clinical endocrinology (Oxford) (01.09.2006)
Published in Clinical endocrinology (Oxford) (01.09.2006)
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Journal Article
A single somatic activating Asp578His mutation of the luteinizing hormone receptor causes Leydig cell tumour in boys with gonadotropin-independent precocious puberty
d'Alva, Catarina B, Brito, Vinicius N, Palhares, Heloisa M C, Carvalho, Filomena M, Arnhold, Ivo J P, Mendonca, Berenice B, Latronico, Ana Claudia
Published in Clinical endocrinology (01.09.2006)
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Published in Clinical endocrinology (01.09.2006)
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