Apoplexy macroprolactinoma during therapy with cabergoline (2002)
- Authors:
- USP affiliated authors: MENDONCA, BERENICE BILHARINHO DE - FM ; KNOEPFELMACHER, MIRTA - FM
- Unidade: FM
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: San Francisco
- Date published: 2002
- Source:
- Título do periódico: Resumos
- Conference titles: Annual Metting the Endrocrine Society's
-
ABNT
GOMES, Miriam C. e MENDONÇA, Berenice B. e KNOEPFELMACHER, Mirta. Apoplexy macroprolactinoma during therapy with cabergoline. 2002, Anais.. San Francisco: Faculdade de Medicina, Universidade de São Paulo, 2002. . Acesso em: 25 abr. 2024. -
APA
Gomes, M. C., Mendonça, B. B., & Knoepfelmacher, M. (2002). Apoplexy macroprolactinoma during therapy with cabergoline. In Resumos. San Francisco: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Gomes MC, Mendonça BB, Knoepfelmacher M. Apoplexy macroprolactinoma during therapy with cabergoline. Resumos. 2002 ;[citado 2024 abr. 25 ] -
Vancouver
Gomes MC, Mendonça BB, Knoepfelmacher M. Apoplexy macroprolactinoma during therapy with cabergoline. Resumos. 2002 ;[citado 2024 abr. 25 ] - Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
- Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
- Absense of duplication on DAX1 gene in patients with 46,XY sex reversal
- Crescimento linear e estatura final em crianças com tumores adrenais predominantemente virilizantes
- Absense of inactivating mutations and deletions of DAX1 gene in SRY negative 46,XX sex-reversed patients
- Heterogeneidade clínica e molecular do hipogonadismo hipogonadotrófico (HH): importância da avaliação do sistema olfatório no diagnóstico diferencial
- Number of CAG repeats in Exon 1 of androgen receptor gene is not related to gender identity in adult patients with male psudohermaphroditism and male transexualism
- Clinical, hormonal, behavioral, and genetic characteristics of androgen insensitibity syndrome in a brazilian cohort: five novel mutations in the androgen receptor gene
- Microconversão no promotor do gene CYP21A2 envolvendo os sítios de ligação dos fatores de transcrição Sp1 e ASP: nova etiologia molecular da deficiência de 21-hidroxilase (21OHD)
- Clinical and molecular analysis of human reproductive disorders in brazilian patients
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