Sai B. Sanka

Bengaluru, KA, India

Last Updated: 09/26/2026

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Found 13 publications

Myofibrillar Myopathy: Clinico-Genetic Spectrum From a Neuromuscular Center in South India.

Myofibrillar Myopathy: Clinico-Genetic Spectrum From a Neuromuscular Center in South India.

Journal: Journal of clinical neuromuscular disease

Published: June 13, 2025

MICU1 related myopathy - a rare report from India.

MICU1 related myopathy - a rare report from India.

Journal: Journal of neuromuscular diseases

Published: February 20, 2025

Acute myeloneuropathy due to Glutaric aciduria-1: Expanding the phenotypic spectrum.

Acute myeloneuropathy due to Glutaric aciduria-1: Expanding the phenotypic spectrum.

Journal: Global medical genetics

Published: December 17, 2024

GNE Myopathy: Genotype - Phenotype Correlation and Disease Progression in an Indian Cohort.

GNE Myopathy: Genotype - Phenotype Correlation and Disease Progression in an Indian Cohort.

Journal: Journal of neuromuscular diseases

Published: August 30, 2024

Phenotype-Genotype Correlation of a Cohort of Patients with Congenital Myopathy: A Single Centre Experience from India.

Phenotype-Genotype Correlation of a Cohort of Patients with Congenital Myopathy: A Single Centre Experience from India.

Journal: Journal of neuromuscular diseases

Published: July 05, 2024

Spinal melanoma with optic neuropathy -rare manifestation of Neurocutaneous melanosis and PET-MRI findings.

Spinal melanoma with optic neuropathy -rare manifestation of Neurocutaneous melanosis and PET-MRI findings.

Journal: eNeurologicalSci

Published: January 13, 2024

Novel Variant of the Desert Hedgehog Gene in an Indian Patient of 46, XY Gonadal Dysgenesis with Peripheral Neuropathy.

Novel Variant of the Desert Hedgehog Gene in an Indian Patient of 46, XY Gonadal Dysgenesis with Peripheral Neuropathy.

Journal: Neurology India

Published: December 20, 2023

A Novel Mutation in Frabin (FGD4) Causing a Mild Phenotype of CMT4H in an Indian Patient.

A Novel Mutation in Frabin (FGD4) Causing a Mild Phenotype of CMT4H in an Indian Patient.

Journal: Journal of neuromuscular diseases

Published: December 18, 2023

Monomelic Amyotrophy/Hirayama Disease: Surgical Outcome in a Large Cohort of Indian Patients.

Monomelic Amyotrophy/Hirayama Disease: Surgical Outcome in a Large Cohort of Indian Patients.

Journal: World neurosurgery

Published: September 02, 2023

Atypical Presentation of Tangier Disease-Expanding the Clinical Spectrum.

Atypical Presentation of Tangier Disease-Expanding the Clinical Spectrum.

Journal: Journal of clinical neuromuscular disease

Published: August 23, 2023

Childhood-Onset Myopathy With Preserved Ambulation Caused by a Recurrent ADSSL1 Missense Variant.

Childhood-Onset Myopathy With Preserved Ambulation Caused by a Recurrent ADSSL1 Missense Variant.

Journal: Neurology. Genetics

Published: July 27, 2023

MYH2-related Myopathy: Expanding the Clinical Spectrum of Chronic Progressive External Ophthalmoplegia (CPEO).

MYH2-related Myopathy: Expanding the Clinical Spectrum of Chronic Progressive External Ophthalmoplegia (CPEO).

Journal: Journal of neuromuscular diseases

Published: May 08, 2023

Showing 1-12 of 13

Last Updated: 09/26/2026