Khushnandan Rai

发表

17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature

A. Kunwar, N. Shah, V. Sarathi, 2022, Journal of the Endocrine Society.

Side‐chain cleavage enzyme deficiency: Systematic review and case series

A. Kunwar, V. Sarathi, S. Memon, 2022, Clinical endocrinology.

Expanding genetic spectrum and discriminatory role of steroid profiling by LC‐MS/MS in 11β‐hydroxylase deficiency

A. Kunwar, N. Shah, V. Sarathi, 2020, Clinical endocrinology.

Homozygous p.Val89Leu plays an important pathogenic role in 5α-reductase type 2 deficiency patients with homozygous p.Arg246Gln in SRD5A2.

A. Kunwar, N. Shah, K. Khadilkar, 2020, European journal of endocrinology.