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17-hydroxyprogesterone deficiency as a cause of sexual infantilism and arterial hypertension: Laboratory and molecular diagnosis - a case report

Benetti-Pinto, CL; Vale, D; Garmes, H; Bedone, A (Parthenon Publishing GroupLancasterInglaterra, 2007)

DISTINCTIVE PLASMA-ALDOSTERONE, 18-HYDROXYCORTICOSTERONE, and 18-HYDROXYDEOXYCORTICOSTERONE PROFILE in the 21-HYDROXYLASE, 17-ALPHA-HYDROXYLASE, and 11-BETA-HYDROXYLASE DEFICIENCY TYPES of CONGENITAL ADRENAL-HYPERPLASIA

Kater, C. E.; Biglieri, E. G.; Kater, C. E.; Biglieri, E. G. (Excerpta Medica Inc, 1983-01-01)

Bases Moleculares da Hiperplasia Adrenal CongênitaMolecular Bases of Congenital Adrenal Hyperplasia

Mello, Maricilda Pallandi de; Bachega, Tânia A.S.S.; Costa-Santos, Marivânia da; Mermejo, Lívia Mara; Castro, Margaret de (Sociedade Brasileira de Endocrinologia e Metabologia, 2002)

Enfermedad de addison en cachorro, hiperplasia adrenal congénita (déficit de 21 alfa hidroxilasa adrenal) e hipoparatiroidismo en perrosAddison disease’s in puppy, congenital adrenal hyperplasia (adrenal 21 alpha hydroxilase deficiency) and Hypoparathyroidism in Dogs

Castillo, Víctor; Ortemberg, L. (2009)

Heterozygosis For Cyp21a2 Mutation Considered As 21-hydroxylase Deficiency In Neonatal Screening.

Soardi, Fernanda Caroline; Lemos-Marini, Sofia Helena V; Coeli, Fernanda Borchers; Maturana, Víctor Gonçalves; Silva, Márcia Duarte Barbosa da; Bernardi, Renan Darin; Justo, Giselle Zenker; de-Mello, Maricilda Palandi (2008)

Deficiencia de la enzima 17Alfa-Hidroxilasa con hiperaldosteronismo17Alpha-Hydroxylase deficiency with hyperaldosteronism

Valencia-West, Angela; Gericke-Brumm, Peter; Reyna-Villasmil, Eduardo (Venezuela, 2022)

Hiperplasia adrenal congénita por déficit de 21 hidroxilasa: un reto diagnóstico y terapéutico

Latorre, Sergio; Garzón, Carolina; Manosalva, Gina; Merchán, Sebastián; Jacomussi, Lorena; Maldonado, Sebastián (Sociedad de Cirugía de Bogotá, Hospital de San José y Fundación Universitaria de Ciencias de la Salud, 2016-06-01)

Phenotype And Genotype Correlation Of The Microconversion From The Cyp21a1p To The Cyp21a2 Gene In Congenital Adrenal Hyperplasia.

Torres, N; Mello, M P; Germano, C M R; Elias, L L K; Moreira, A C; Castro, M (2003)

Phenotype and genotype correlation of the microconversion from the CYP21A1P to the CYP21A2 gene in congenital adrenal hyperplasia

Torres, N.; Mello, M.P.; Germano, C.M.R.; Elias, L.L.K.; Moreira, A.C.; Castro, M. (Associação Brasileira de Divulgação Científica, 2003)

HYPERANDROGENISM DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY WITH ACCESSORY ADRENOCORTICAL TISSUE - A HORMONAL AND METABOLIC EVALUATION

Universidade Estadual Paulista (Unesp) (Associação Brasileira de Divulgação Científica (ABRADIC), 1994-05-01)

1. Adrenal ectopic tissue has been detected in the paragonadal region of normal women. In patients with congenital adrenal hyperplasia due to 21-hydroxylase (21-OH) deficiency, the manifestation of hyperplasia of paragonadal ...