The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non‐Morrocan ancestry von Ali, Taccyanna M., Linnenkamp, Bianca D. W., Yamamoto, Guilherme L., Honjo, Rachel S., Cabral de Menezes Filho, Hamilton, Kim, Chong Ae, Bertola, Débora R.

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Tamoxifen Improves Final Height Prediction in Girls with McCune-Albright Syndrome: A Long Follow-Up von de G. Buff Passone, Caroline, Kuperman, Hilton, Cabral de Menezes-Filho, Hamilton, Spassapan Oliveira Esteves, Lygia, Lana Obata Giroto, Rachel, Damiani, Durval

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Identification and functional analysis of a novel inactivating mutation (A804D) of the calcium-sensing receptor gene von Miyashiro, Kozue, Kasamatsu, Teresa Sayoko, Steinmetz, Leandra, De Menezes Filho, Hamilton Cabral, Damiani, Durval, Setian, Nuvarte, Hauache, Omar Magid

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Síndrome metabólica em crianças e adolescentes: dúvidas na terminologia, mas não nos riscos cardiometabólicos von Damiani, Durval, Kuba, Valesca Mansur, Cominato, Louise, Damiani, Daniel, Dichtchekenian, Vaê, Menezes Filho, Hamilton Cabral de

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Novel mutation in MCT8 gene in a Brazilian boy with thyroid hormone resistance and severe neurologic abnormalities von Filho, Hamilton Cabral de Menezes, Marui, Suemi, Manna, Thais Della, Brust, Ester Saraiva, Radonsky, Vanessa, Kuperman, Hilton, Dichtchekenian, Vaê, Setian, Nuvarte, Damiani, Durval

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Pesquisa de tecido prostático em pacientes 46,XX portadoras da forma clássica de hiperplasia congênita das suprarrenais von Paulino, Mariana da Costa Rose, Steinmetz, Leandra, Menezes Filho, Hamilton Cabral de, Kuperman, Hilton, Della Manna, Thaís, Vieira, José Gilberto Henriques, Blasbalg, Roberto, Baroni, Ronaldo, Setian, Nuvarte, Damiani, Durval

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Metabolic syndrome in children and adolescents: doubts about terminology but not about cardiometabolic risks von Damiani, Durval, Kuba, Valesca Mansur, Cominato, Louise, Damiani, Daniel, Dichtchekenian, Vaê, Menezes Filho, Hamilton Cabral de

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A novel DAX1/NR0B1 mutation in a patient with adrenal hypoplasia congenita and hypogonadotropic hypogonadism von Battistin, Claudilene, Menezes Filho, Hamilton Cabral de, Domenice, Sorahia, Nishi, Mirian Yumie, Della Manna, Thais, Kuperman, Hilton, Steinmetz, Leandra, Dichtchekenian, Vaê, Setian, Nuvarte, Damiani, Durval

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Search of prostatic tissue in 46,XX congenital adrenal hyperplasia von Paulino, Mariana da Costa Rose, Steinmetz, Leandra, Menezes Filho, Hamilton Cabral de, Kuperman, Hilton, Della Manna, Thaís, Vieira, José Gilberto Henriques, Blasbalg, Roberto, Baroni, Ronaldo, Setian, Nuvarte, Damiani, Durval

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The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry von Ali, Taccyanna M, Linnenkamp, Bianca D W, Yamamoto, Guilherme L, Honjo, Rachel S, Cabral de Menezes Filho, Hamilton, Kim, Chong Ae, Bertola, Débora R

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Síndrome metabólica em crianças e adolescentes: dúvidas na terminologia, mas não nos riscos cardiometabólicos von Damiani, Durval, Kuba, Valesca Mansur, Cominato, Louise, Damiani, Daniel, Dichtchekenian, Vaê, Menezes Filho, Hamilton Cabral de

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Pesquisa de tecido prostático em pacientes 46,XX portadoras da forma clássica de hiperplasia congênita das suprarrenais von Paulino, Mariana da Costa Rose, Steinmetz, Leandra, Menezes Filho, Hamilton Cabral de, Kuperman, Hilton, Della Manna, Thaís, Vieira, José Gilberto Henriques, Blasbalg, Roberto, Baroni, Ronaldo, Setian, Nuvarte, Damiani, Durval

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Identification and functional analysis of a novel inactivating mutation (A804D) of the calcium-sensing receptor gene von Miyashiro, Kozue, Kasamatsu, Teresa Sayoko, Steinmetz, Leandra, de Menezes Filho, Hamilton Cabral, Damiani, Durval, Setian, Nuvarte, Hauache, Omar Magid

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