Rashna S. Dastur

Mumbai, MH, India

Last Updated: 09/26/2026

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Found 9 publications

Enhancing the Performance of a Blood-Based Diagnostic Screening Tool for Dysferlinopathy: Optimising an Immunoassay Across Continents.

Enhancing the Performance of a Blood-Based Diagnostic Screening Tool for Dysferlinopathy: Optimising an Immunoassay Across Continents.

Journal: Neuropathology and applied neurobiology

Published: July 16, 2025

Genetic Appraisal of Hereditary Muscle Disorders In A Cohort From Mumbai, India.

Genetic Appraisal of Hereditary Muscle Disorders In A Cohort From Mumbai, India.

Journal: Journal of neuromuscular diseases

Published: June 20, 2022

Clinical and Genomic Evaluation of 207 Genetic Myopathies in the Indian Subcontinent.

Clinical and Genomic Evaluation of 207 Genetic Myopathies in the Indian Subcontinent.

Journal: Frontiers in neurology

Published: May 05, 2020

Early and consistent pattern of proximal weakness in GNE myopathy.

Early and consistent pattern of proximal weakness in GNE myopathy.

Journal: Muscle & nerve

Published: April 10, 2020

Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients.

Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients.

Journal: Annals of clinical and translational neurology

Published: August 27, 2018

Detection of Dysferlin Gene Pathogenic Variants in the Indian Population in Patients Predicted to have a Dysferlinopathy Using a Blood-based Monocyte Assay and Clinical Algorithm: A Model for Accurate and Cost-effective Diagnosis.

Detection of Dysferlin Gene Pathogenic Variants in the Indian Population in Patients Predicted to have a Dysferlinopathy Using a Blood-based Monocyte Assay and Clinical Algorithm: A Model for Accurate and Cost-effective Diagnosis.

Journal: Annals of Indian Academy of Neurology

Published: September 15, 2017

Limb-girdle muscular dystrophy in the Agarwals: Utility of founder mutations in CAPN3 gene.

Limb-girdle muscular dystrophy in the Agarwals: Utility of founder mutations in CAPN3 gene.

Journal: Annals of Indian Academy of Neurology

Published: March 25, 2016

Ancestral founder mutations in calpain-3 in the Indian Agarwal community: historical, clinical, and molecular perspective.

Ancestral founder mutations in calpain-3 in the Indian Agarwal community: historical, clinical, and molecular perspective.

Journal: Muscle & nerve

Published: December 14, 2012

Identification of deletions and duplications in the Duchenne muscular dystrophy gene and female carrier status in western India using combined methods of multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification.

Identification of deletions and duplications in the Duchenne muscular dystrophy gene and female carrier status in western India using combined methods of multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification.

Journal: Neurology India

Published: January 12, 2012

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Last Updated: 09/26/2026