Maryam Razzaghy‐Azar

Genotype–phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

Maria I. New, Moolamannil Abraham, Brian D. Gonzalez et al. · Proceedings of the National Academy of Sciences · 2013 · 361 citations · Full text

Life Sciences, Endocrinology, Genetics +17

A mutation in the HSD11B2 gene in a family with apparent mineralocorticoid excess.

Robert C. Wilson, Zygmunt S. Krozowski, K. Li et al. · The Journal of Clinical Endocrinology & Metabolism · 1995 · 198 citations

Life Sciences, Genetics, Molecular Genetics +12

Visfatin in obese children and adolescents and its association with insulin resistance and metabolic syndrome

Mitra Nourbakhsh, Mitra Nourbakhsh, Zafar Gholinejad et al. · Scandinavian Journal of Clinical and Laboratory Investigation · 2015 · 66 citations

Medicine, Endocrinology, Pediatrics +17

Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency

Mabel Yau, Shozeb Haider, Ahmed Khattab et al. · Proceedings of the National Academy of Sciences · 2017 · 63 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A Double-Blind, Placebo-Controlled Comparison of Letrozole to Oxandrolone Effects upon Growth and Puberty of Children with Constitutional Delay of Puberty and Idiopathic Short Stature

Shadab Salehpour, Parvin Alipour, Maryam Razzaghy‐Azar et al. · Hormone Research in Paediatrics · 2010 · 60 citations

Medicine, Endocrinology, Pediatrics +17