Manjiri Karlekar

Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center Experience and Systematic Review.

N. Shah, V. Sarathi, S. Memon, 2023, Calcified tissue international.

Genetic spectrum of Kallmann syndrome: Single‐center experience and systematic review

N. Shah, V. Sarathi, S. Memon, 2022, Clinical endocrinology.

Giant prolactinoma in children and adolescents: a single-center experience and systematic review

N. Shah, V. Sarathi, S. Memon, 2022, Pituitary.

Pediatric Macrocorticotropinoma: Do They Differ from Microcorticotropinoma?

N. Shah, V. Sarathi, S. Memon, 2023, Neuroendocrinology.

Octreotide-LAR is a Useful Alternative for the Management of Diazoxide-Responsive Congenital Hyperinsulinism

S. Flanagan, N. Shah, V. Sarathi, 2021, Hormone and Metabolic Research.

Genotype–Phenotype Correlations in Asian Indian Children and Adolescents with Primary Hyperparathyroidism

V. Sarathi, P. Hira, Anima Sharma, 2022, Calcified Tissue International.

Vitamin D deficiency or resistance and hypophosphatemia.

V. Sarathi, A. Lila, M. Dhananjaya, 2024, Best practice & research. Clinical endocrinology & metabolism.

Genotypic Spectrum and its Correlation with Alopecia and Clinical Response in Hereditary Vitamin D Resistant Rickets: Our Experience and Systematic Review

A. Kunwar, Robin Garg, V. Sarathi, 2023, Calcified Tissue International.

Sellar Paraganglioma.

N. Shah, A. Lila, T. Bandgar, 2018, Clinical nuclear medicine.