Hasil Pencarian - Berenice B Mendonça

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  1. 1
    Adrenal Insufficiency and Glucocorticoid Use During the COVID-19 Pandemic

    Adrenal Insufficiency and Glucocorticoid Use During the COVID-19 Pandemic oleh Madson Q. Almeida, Berenice B. Mendonca

    Diterbitkan 2020-06-01
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  2. 2
    Adrenal crisis and mortality rate in adrenal insufficiency and congenital adrenal hyperplasia

    Adrenal crisis and mortality rate in adrenal insufficiency and congenital adrenal hyperplasia oleh Lia Mesquita Lousada, Berenice B. Mendonca, Tania A. S. S. Bachega

    Diterbitkan 2021-07-01
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  3. 3
    Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency

    Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency oleh Larissa G. Gomes, Guiomar Madureira, Berenice B. Mendonca, Tania A. S. S. Bachega

    Diterbitkan 2013-01-01
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  4. 4
    An update of genetic basis of PCOS pathogenesis

    An update of genetic basis of PCOS pathogenesis oleh Raiane P. Crespo, Tania A. S. S. Bachega, Berenice B. Mendonça, Larissa G. Gomes

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  5. 5
    Impact of glucocorticoid receptor gene polymorphisms on the metabolic profile of adult patients with the classical form of 21-hydroxylase deficiency.

    Impact of glucocorticoid receptor gene polymorphisms on the metabolic profile of adult patients with the classical form of 21-hydroxylase deficiency. oleh Ricardo P P Moreira, Larissa G Gomes, Berenice B Mendonca, Tânia A S S Bachega

    Diterbitkan 2012-01-01
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  6. 6
    Frequency of genetic polymorphisms of PXR gene in the Brazilian population

    Frequency of genetic polymorphisms of PXR gene in the Brazilian population oleh Ricardo P. P. Moreira, Alexander A. L. Jorge, Berenice B. Mendonca, Tânia A. S. S. Bachega

    Diterbitkan 2011-01-01
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  7. 7
    Influence of the A3669G Glucocorticoid Receptor Gene Polymorphism on the Metabolic Profile of Pediatric Patients with Congenital Adrenal Hyperplasia

    Influence of the A3669G Glucocorticoid Receptor Gene Polymorphism on the Metabolic Profile of Pediatric Patients with Congenital Adrenal Hyperplasia oleh Ricardo P. P. Moreira, Larissa G. Gomes, Guiomar Madureira, Berenice B. Mendonca, Tânia A. S. S. Bachega

    Diterbitkan 2014-01-01
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  8. 8
    Applicability of a novel mathematical model for the prediction of adult height and age at menarche in girls with idiopathic central precocious puberty

    Applicability of a novel mathematical model for the prediction of adult height and age at menarche in girls with idiopathic central precocious puberty oleh Mateus Cavarzan Lopes, Carolina Oliveira Ramos, Ana Claudia Latronico, Berenice B. Mendonça, Vinicius N. Brito

    Diterbitkan 2018-07-01
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  9. 9
    Performance of mutation pathogenicity prediction tools on missense variants associated with 46,XY differences of sex development

    Performance of mutation pathogenicity prediction tools on missense variants associated with 46,XY differences of sex development oleh Luciana R. Montenegro, Antônio M. Lerário, Miriam Y. Nishi, Alexander A.L. Jorge, Berenice B. Mendonca

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  10. 10
    Primary malignant tumors of the adrenal glands

    Primary malignant tumors of the adrenal glands oleh Madson Q. Almeida, Joao Evangelista Bezerra-Neto, Berenice B. Mendonça, Ana Claudia Latronico, Maria Candida B.V. Fragoso

    Diterbitkan 2018-12-01
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  11. 11
    Mutation analysis of NANOS3 in Brazilian women with primary ovarian failure

    Mutation analysis of NANOS3 in Brazilian women with primary ovarian failure oleh Braian Lucas A. Sousa, Mirian Yumie Nishi, Mariza Gerdulo Santos, Vinicius Nahime Brito, Sorahia Domenice, Berenice B. Mendonca

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  12. 12
    An activating mutation in the CRHR1 gene is rarely associated with pituitary-dependent hyperadrenocorticism in poodles

    An activating mutation in the CRHR1 gene is rarely associated with pituitary-dependent hyperadrenocorticism in poodles oleh Viviani De-Marco, Luciani R. Carvalho, Mariana F. Guzzo, Paulo S.L. Oliveira, Larissa G. Gomes, Berenice B. Mendonca

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  13. 13
    Population and mutation analysis of Y-STR loci in a sample from the city of São Paulo (Brazil)

    Population and mutation analysis of Y-STR loci in a sample from the city of São Paulo (Brazil) oleh José A. Soares-Vieira, Ana E.C. Billerbeck, Edna S.M. Iwamura, Berenice B. Mendonca, Leonor Gusmão, Paulo A. Otto

    Diterbitkan 2008-01-01
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  14. 14
    PROP1 and CTNNB1 expression in adamantinomatous craniopharyngiomas with or without β-catenin mutations

    PROP1 and CTNNB1 expression in adamantinomatous craniopharyngiomas with or without β-catenin mutations oleh Carolina M.G Cani, Hamilton Matushita, Luciani R. S Carvalho, Ibere C Soares, Luciana P Brito, Madson Q Almeida, Berenice B Mendonça

    Diterbitkan 2011-01-01
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  15. 15
    Modulatory effect of BclI GR gene polymorphisms on the obesity phenotype in Brazilian patients with Cushing's disease

    Modulatory effect of BclI GR gene polymorphisms on the obesity phenotype in Brazilian patients with Cushing's disease oleh Ricardo P.P. Moreira, Tânia A.S.S. Bachega, Márcio C. Machado, Berenice B. Mendonca, Marcello D. Bronstein, Maria Candida B. Villares Fragoso

    Diterbitkan 2013-05-01
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  16. 16
    Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

    Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency oleh Ricardo P. P. Moreira, Alexander A. L. Jorge, Larissa G. Gomes, Laura C. Kaupert, João Massud Filho, Berenice B. Mendonca, Tânia A. S. S. Bachega

    Diterbitkan 2011-01-01
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  17. 17
    Long-term follow-up of a female with congenital adrenal hyperplasia due to P450-oxidoreductase deficiency

    Long-term follow-up of a female with congenital adrenal hyperplasia due to P450-oxidoreductase deficiency oleh Beatriz D. S. F. Bonamichi, Stella L. M. Santiago, Débora R. Bertola, Chong A. Kim, Nivaldo Alonso, Berenice B. Mendonca, Tania A. S. S. Bachega, Larissa G. Gomes

    Diterbitkan 2016-10-01
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  18. 18
    PROP1 overexpression in corticotrophinomas: evidence for the role of PROP1 in the maintenance of cells committed to corticotrophic differentiation

    PROP1 overexpression in corticotrophinomas: evidence for the role of PROP1 in the maintenance of cells committed to corticotrophic differentiation oleh Ricardo V. Araujo, Claudia V. Chang, Valter A. S. Cescato, Maria Candida B. V. Fragoso, Marcello D. Bronstein, Berenice B. Mendonca, Ivo J. P. Arnhold, Luciani R. S. Carvalho

    Diterbitkan 2013-06-01
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  19. 19
    ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome

    ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome oleh Renata C Scalco, Ericka B Trarbach, Edoarda V A Albuquerque, Thais K Homma, Thais H Inoue-Lima, Mirian Y Nishi, Berenice B Mendonca, Alexander A L Jorge

    Diterbitkan 2019-12-01
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  20. 20
    Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery

    Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery oleh Fernanda A. Correa, Marilena Nakaguma, João L. O. Madeira, Mirian Y. Nishi, Milena G. Abrão, Alexander A. L. Jorge, Luciani R. Carvalho, Ivo J. P. Arnhold, Berenice B. Mendonça

    Diterbitkan 2019-05-01
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