Publications by authors named "K Polavarapu"

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Novel muscle MRI features in Desmin related myasthenic myopathy.
Dipti Baskar, Seetam Kumar Tumulu, Kiran Polavarapu, Akshata Huddar, Gopikrishnan Unnikrishnan

Neuromuscul Disord· December 2025

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A systematic analysis of mitochondrial aminoacyl tRNA synthetase variants in a rare disease cohort.
Thiloka E Ratnaike, M Eren Kule, Ida Paramonov, Leslie Matalonga, Kiran Polavarapu

Eur J Hum Genet· December 2025

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Unveiling MYH2-related myopathy: Histological-genetic insights from a case series and systematic review.
Beatrice Labella, Guy Brochier, Maud Beuvin, Emmanuelle Lacene, Anais Chanut, Kiran Polavarapu

J Neuromuscul Dis· November 2025

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The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease.
Vicente A Yépez, German Demidov, Kornelia Ellwanger, Steven Laurie, Rebeka Luknárová, Kiran Polavarapu

Nat Genet· October 2025

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An interesting report of POPDC3 limb girdle muscular dystrophy R26 from India.
Dipti Baskar, Kiran Polavarapu, Ananthapadmanabha Kotambail, Gautham Arunachal, Seetam Kumar Tumulu

J Neuromuscul Dis· September 2025

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