M. Baptista

发表

Growth in patients with the salt-wasting form of congenital adrenal hyperplasia during the first two years of life

G. Guerra‐Júnior, S. Lemos-Marini, A. Morcillo, 2009 .

Spontaneous puberty in girls with early diagnosis of Turner syndrome.

G. Guerra‐Júnior, A. Maciel-Guerra, A. B. Carvalho, 2012, Arquivos brasileiros de endocrinologia e metabologia.

Turner syndrome: a pediatric diagnosis frequently made by non-pediatricians.

G. Guerra‐Júnior, A. Maciel-Guerra, A. B. Carvalho, 2010, Jornal de pediatria.

Cardiovascular and renal anomalies in Turner syndrome.

A. B. Carvalho, G. Guerra Júnior, M. Baptista, 2010, Revista da Associacao Medica Brasileira.

[Evidences for subclinic chronic autoimmune thyroid disease in girls with Turner Syndrome].

A. Maciel-Guerra, S. Lemos-Marini, G. Guerra Júnior, 2007, Arquivos brasileiros de endocrinologia e metabologia.

Beckwith-Wiedemann syndrome and virilizing cortical adrenal tumor in a child.

G. Guerra‐Júnior, M. Baptista, P. Sabino de Matos, 2000, Journal of pediatric surgery.

Turner's Syndrome and Subclinical Autoimmune Thyroid Disease: A Two-Year Follow-up Study

G. Guerra‐Júnior, A. Maciel-Guerra, E. Camargo, 2009, Journal of pediatric endocrinology & metabolism : JPEM.

Spontaneous Final Height in Turner's Syndrome in Brazil

A. Maciel-Guerra, S. Lemos-Marini, S. H. V. de Lemos-Marini, 2007, Journal of pediatric endocrinology & metabolism : JPEM.

Six new cases confirm the clinical molecular profile of complete combined 17α-hydroxylase/ 17,20-lyase deficiency in Brazil.

G. Guerra‐Júnior, A. Maciel-Guerra, Fernanda Canova Denardi, 2010, Arquivos brasileiros de endocrinologia e metabologia.

Long-term follow-up of an 8-year-old boy with insulinoma as the first manifestation of a familial form of multiple endocrine neoplasia type 1.

G. Guerra‐Júnior, F. C. Soardi, S. Lemos-Marini, 2010, Arquivos brasileiros de endocrinologia e metabologia.

Cytogenetic analysis and detection of KAL-1 gene deletion with fluorescence in situ hybridization (FISH) in patients with Kallmann syndrome

A. Maciel-Guerra, C. Hackel, M. Baptista, 2001 .

Effects of growth hormone on body proportions in Turner syndrome compared with non-treated patients and normal women

G. Guerra‐Júnior, T. Fabbri, A. Maciel-Guerra, 2010 .

Turner's Syndrome and Thyroid Disease: A Transverse Study of Pediatric Patients in Brazil

A. Maciel-Guerra, M. Baptista, C. Medeiros, 2000, Journal of pediatric endocrinology & metabolism : JPEM.

Bone mineralization in Turner syndrome: a transverse study of the determinant factors in 58 patients

A. Maciel-Guerra, S. Lemos-Marini, A. Morcillo, 2002, Journal of Bone and Mineral Metabolism.

A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism.

G. Guerra‐Júnior, M. de Castro, U. Kaiser, 2010, European journal of endocrinology.

Novel fibroblast growth factor receptor 1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia.

M. de Castro, A. Latronico, B. B. de Mendonça, 2006, The Journal of clinical endocrinology and metabolism.

Nonsense mutations in FGF8 gene causing different degrees of human gonadotropin-releasing deficiency.

M. Mohammadi, M. Teles, A. Latronico, 2010, The Journal of clinical endocrinology and metabolism.

Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation‐dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1

M. de Castro, M. Teles, A. Latronico, 2010, Clinical endocrinology.

Molecular analysis of KAL-1, GnRH-R, NELF and EBF2 genes in a series of Kallmann syndrome and normosmic hypogonadotropic hypogonadism patients.

C. Hackel, H. Garmes, M. Baptista, 2005, The Journal of endocrinology.

[Turner syndrome: the patients' view].

L. Magna, M. Baptista, L. Z. Suzigan, 2004, Jornal de Pediatria.

Severe rhabdomyolysis due to adipsic hypernatremia after craniopharyngioma surgery.

D. Zantut-Wittmann, H. Garmes, M. Baptista, 2007, Arquivos brasileiros de endocrinologia e metabologia.

Normalization of height and excess body fat in children with salt-wasting 21-hydroxylase deficiency.

G. Guerra‐Júnior, S. Lemos-Marini, A. Morcillo, 2011, Jornal de pediatria.

Frequency of 677C -> T and 1298A -> C polymorphisms in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene in Turner syndrome individuals

L. Bonadia, S. Lemos-Marini, C. Bertuzzo, 2006 .

Metabolic evaluation of young women with congenital adrenal hyperplasia.

G. Guerra‐Júnior, S. Lemos-Marini, A. Morcillo, 2011, Arquivos brasileiros de endocrinologia e metabologia.

Growth hormone effect on body composition in Turner syndrome

G. Guerra‐Júnior, T. Fabbri, A. Maciel-Guerra, 2011, Endocrine.

Prevalence of Testicular Adrenal Rest Tumor and Factors Associated with Its Development in Congenital Adrenal Hyperplasia

G. Guerra‐Júnior, A. Morcillo, L. C. de Oliveira, 2018, Hormone Research in Paediatrics.

[Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: final height in 27 patients with the classical form].

G. Guerra‐Júnior, A. Maciel-Guerra, S. Lemos-Marini, 2005, Arquivos brasileiros de endocrinologia e metabologia.

Inhibin α-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriers

C. Stratakis, G. Guerra‐Júnior, A. Moreira, 2004, Journal of Medical Genetics.

Turner syndrome and metabolic derangements: another example of fetal programming.

G. Guerra‐Júnior, T. Fabbri, A. Maciel-Guerra, 2012, Early human development.

Normalization of height and excess body fat in children with salt-wasting 21-hydroxylase deficiency.

G. Guerra‐Júnior, S. Lemos-Marini, A. Morcillo, 2011, Jornal de pediatria.