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Mostrando ítems 1-10 de 38

[11beta-hydroxylase Deficiency].

Mello, Maricilda Palandi; Penachioni, Junia Yara; Amaral, Fernando C do; Castro, Margaret de (2004)

Mutation distribution and CYP21/C4 locus variability in Brazilian families with the classical form of the 21-hydroxylase deficiency

Paulino, LC; Araujo, M; Guerra, G; Marini, SHVL; De Mello, MP (Scandinavian University PressOsloNoruega, 1999)

Molecular Analysis Of Cyp21 And C4 Genes In Brazilian Families With The Classical Form Of Steroid 21-hydroxylase Deficiency.

de-Araujo, M; Sanches, M R; Suzuki, L A; Guerra, G; Farah, S B; de-Mello, M P (1996)

Female Pseudohermaphroditism Due To Classical 21-hydroxylase Deficiency In A Girl With Turner Syndrome.

Maciel-Guerra, A T; Guerra, G; Marini, S H; Matias Baptista, M T; Marques-de-Faria, A P (1997)

Classical Congenital Adrenal Hyperplasia Due To 21-hydroxylase Deficiency: A Cross-sectional Study Of Factors Involved In Bone Mineral Density.

de Almeida Freire, Patrícia Oliveira; de Lemos-Marini, Sofia Helena Valente; Maciel-Guerra, Andréa Trevas; Morcillo, André Moreno; Matias Baptista, Maria Tereza; de Mello, Maricilda Palandi; Guerra, Gil (2003)

H28+C insertion in the CYP21 gene: A novel frameshift mutation in a Brazilian patient with the classical form of 21-hydroxylase deficiency

Lau, IF; Soardi, FC; Lemos-Marini, SHV; Guerra, G; Baptista, MTM; De Mello, MP (Endocrine SocChevy ChaseEUA, 2001)

H28+c Insertion In The Cyp21 Gene: A Novel Frameshift Mutation In A Brazilian Patient With The Classical Form Of 21-hydroxylase Deficiency.

Lau, I F; Soardi, F C; Lemos-Marini, S H; Guerra Jr, G; Baptista, M T; De Mello, M P (2001)

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)

Complement 4 Phenotypes And Genotypes In Brazilian Patients With Classical 21-hydroxylase Deficiency.

Guerra-Junior, G; Grumach, A Sevciovic; de Lemos-Marini, S H Valente; Kirschfink, M; Condino Neto, A; de Araujo, M; De Mello, M Palandi (2009)

[congenital Adrenal Hyperplasia Due To 21-hydroxylase Deficiency: Final Height In 27 Patients With The Classical Form].

Lemos-Marini, Sofia H V; Guerra-Júnior, Gil; Morcillo, André M; Baptista, Maria Tereza M; Silva, Luciana O; Maciel-Guerra, Andréa T (2005)