Výsledky vyhledávání - "Vânia F, Tonetto-Fernandes"

Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency

Autor: Odete H. Nakamura, Claudio E. Kater, José Gilberto H. Vieira, Tânia A.S.S. Bachega, Flávia A. Costa-Barbosa, Vânia F. Tonetto-Fernandes, Vivian Moura, Valdemir Melechco Carvalho

Publikováno v: Clinical Endocrinology. 73:700-706

Summary Background Congenital adrenal hyperplasia caused by classic 21-hydroxylase deficiency (21OHD) is an autosomal recessive disorder with a high prevalence of asymptomatic heterozygote carriers (HTZ) in the general population, making case detecti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a6a3d20f0a49cecc0594b1fb2aa06907
https://doi.org/10.1111/j.1365-2265.2010.03871.x

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Hiperplasia adrenal congênita: estudo qualitativo sobre doença e tratamento, dúvidas, angústias e relacionamentos (parte I)

Autor: Claudio E. Kater, Paulo Schiller, Vânia F. Tonetto-Fernandes, Mariana Telles-Silveira

OBJETIVO: Compreender significados e pensamentos de um grupo de pais, pacientes e médicos sobre a hiperplasia adrenal congênita (HAC) e analisar angústias, dúvidas e ansiedades. MÉTODOS: Foram selecionados 21 sujeitos: 7 especialistas de cinco i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02426d4066d91db9067a6d94603a06de
https://doi.org/10.1590/s0004-27302009000900008

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Development of a radioimmunoassay for serum 21-deoxycortisol and its potential application in the diagnosis of congenital adrenal hyperplasia

Autor: Claudio E. Kater, José Gilberto H. Vieira, Jean Fiet, Vânia F. Tonetto-Fernandes, Luciane M. Ribeiro-Neto, Ieda Therezinha do Nascimento Verreschi

Publikováno v: Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 47, Issue: 2, Pages: 171-176, Published: APR 2003
Arquivos Brasileiros de Endocrinologia & Metabologia v.47 n.2 2003
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM

O 21-deoxicortisol (21DF) sérico tem sido considerado um excelente marcador para o diagnóstico da hiperplasia adrenal congênita (HAC) por deficiência de 21-hidroxilase (D21OH). Embora vários métodos de radioimunoensaio (RIE) tenham sido descrit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fde5576c7eb154b79698d23bcc344f3e
https://doi.org/10.1590/s0004-27302003000200010

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Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency

Autor: Flávia A, Costa-Barbosa, Vânia F, Tonetto-Fernandes, Valdemir M, Carvalho, Odete H, Nakamura, Vivian, Moura, Tânia A S S, Bachega, José G H, Vieira, Claudio E, Kater

Publikováno v: Clinical endocrinology. 73(6)

Congenital adrenal hyperplasia caused by classic 21-hydroxylase deficiency (21OHD) is an autosomal recessive disorder with a high prevalence of asymptomatic heterozygote carriers (HTZ) in the general population, making case detection desirable by rou

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1b8d9544099e707da5ea6973c38947fb
https://pubmed.ncbi.nlm.nih.gov/20846292

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Hiperplasia adrenal congênita: estudo qualitativo sobre definição e redefinição sexual, cirurgia de dilatação e apoio psicológico (parte II)

Autor: Claudio E. Kater, Mariana Telles-Silveira, Paulo Schiller, Vânia F. Tonetto-Fernandes

Publikováno v: Arquivos Brasileiros de Endocrinologia & Metabologia v.53 n.9 2009
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 53, Issue: 9, Pages: 1125-1136, Published: DEC 2009

OBJETIVO: Identificar questões relacionadas à definição e redesignação sexual e à cirurgia corretiva em pacientes com hiperplasia adrenal congênita (HAC) e compreender a inserção do psicólogo no seu atendimento. MÉTODOS: Selecionaram-se 2

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75c3a11b4b52f3c03c20436292f582e0
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302009000900009

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[Congenital adrenal hyperplasia: a qualitative study on disease and treatment, doubts, anguishes and relationships (part I)]

Autor: Mariana, Telles-Silveira, Vânia F, Tonetto-Fernandes, Paulo, Schiller, Claudio E, Kater

Publikováno v: Arquivos brasileiros de endocrinologia e metabologia. 53(9)

To understand the meanings/thoughts of a group of parents, patients and physicians regarding congenital adrenal hyperplasia (CAH), and to evaluate their anguishes, doubts and anxieties.We selected 21 subjects: 7 pediatric endocrinologists from five B

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::023b4dffa131ed22105ad7ede9ce2db7
https://pubmed.ncbi.nlm.nih.gov/20126869

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[Congenital adrenal hyperplasia: a qualitative study on sex definition and redesignation dilation surgery and psychological support (part II)]

Autor: Mariana, Telles-Silveira, Vânia F, Tonetto-Fernandes, Paulo, Schiller, Claudio E, Kater

Publikováno v: Arquivos brasileiros de endocrinologia e metabologia. 53(9)

To identify relevant questions related to sex definition and re-designation and reconstructive surgery in patients with congenital adrenal hyperplasia (CAH), and to understand the role of the psychologist in providing care for these patients.We selec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4b913f2e0f3abaac32f58d37e81b0d94
https://pubmed.ncbi.nlm.nih.gov/20126870

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21-Hydroxylase Deficiency Transiently Mimicking Combined 21- and 11β-Hydroxylase Deficiency

Autor: Claudio E. Kater, Sofia Helena Valente de Lemos-Marini, Luciane M. Ribeiro-Neto, Maricilda Palandi de Mello, Vânia F. Tonetto-Fernandes

Publikováno v: Journal of Pediatric Endocrinology and Metabolism. 21

21-Hydroxylase deficiency (21OHD) is the commonest form of congenital adrenal hyperplasia, while 11betaOHD represents 5% of cases. Although both result from mutations in distinct genes, cases of 'apparent' combined 21OHD and 11betaOHD (AC21,11OHD) ha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a517c4dfe69425081cd329590fff024
https://doi.org/10.1515/jpem.2008.21.5.487

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