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 · 352 citations · Full text

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

R337c Mutation, Mendelian Disorder, T Transition +13

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 · 62 citations · Full text

Clinical and Endocrine Characteristics in Atypical and Classical Growth Hormone Insensitivity Syndrome

Christine Burren, Katie A. Woods, Steven J. Rose et al. · Hormone Research in Paediatrics · 2001 · 59 citations

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 · 59 citations