Ivo J Arnhold, MD, PHD

Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
Disciplina de Endocrinologia e Metabologia - Laboratório de Hormônios e Genética Molecular/ LIM42
Papers:
Molecular and Gene Network Analysis of Thyroid Transcription Factor 1 (TTF1) and Enhanced at Puberty 1 (EAP1) Genes in Patients with GnRH-Dependent Pubertal Disorders
REVISITING THE PHENOTYPE OF ORGANIC AND IDIOPATHIC CENTRAL PRECOCIOUS PUBERTY IN A LARGE BRAZILIAN COHORT
Molecular analysis of SOX3 gene in patients with combined pituitary hormone deficiency (CPHD) by MLPA technique
Gender Auto-perception, Psycho-social and Sexual Aspects in Patients with Disorders of Sex Development 46,XY Exposed to Low or Normal Testosterone Levels in the Prenatal Period
OR20-3 Decreased growth hormone (GH) expression due to double homozygous mutations in the GH1 promoter region is associated to isolated growth hormone deficiency (IGHD) in 3 siblings
OR20-4 Mild growth and immunological phenotypes in individuals heterozygous for STAT5B mutations