Longui, Carlos A.
Irmandade da Santa Casa de Misericórdia de São Paulo · Faculdade de Ciências Médicas da Santa Casa de São Paulo
4 papers on CoChatORCID 0000-0002-6361-5235
Most cited papers
- Verified
Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3
Abreu, A. P., Dauber, A., Macedo, D. B., Noel, S. D., Brito, V. N., Gill, J. C., Cukier, P., Thompson, I. R., Navarro, V. M., Gagliardi, P. C., et al. (2013) · New England Journal of Medicine
Hypothalamic control of reproductive hormonesGenetic Syndromes and Imprinting
Cited by 534
- Verified
Molecular Genotyping in Brazilian Patients with the Classical and Nonclassical Forms of 21-Hydroxylase Deficiency1
Bachega, T. A. S. S., Billerbeck, A. E. C., Madureira, G., Marcondes, J. A. M., Longui, C. A., Leite, M. V., Arnhold, I. J. P., & Mendonca, B. B. (1998) · The Journal of Clinical Endocrinology & Metabolism
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 108
- Verified
The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene
Rocha, R. O., Billerbeck, A. E. C., Pinto, E. M., Melo, K. F. S., Lin, C. J., Longui, C. A., Mendonca, B. B., & Bachega, T. A. S. S. (2008) · Clinical Endocrinology
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 43
- Verified
Neonatal detection of Turner syndrome by real-time PCR gene quantification of the ARSE and MAGEH1 genes
Corrêa, S. C., Rocha, M. N., Richeti, F., Kochi, C., Silva e Lima, L. A., Magalhães, M., & Longui, C. A. (2014) · Genetics and Molecular Research
Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesSexual Differentiation and Disorders
Cited by 11
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