Publications by authors named "Shingavi Leena"

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Disease Progression and Mutation Pattern in a Large Cohort of LGMD R1/LGMD 2A Patients from India.
Valakunja H Ganaraja, Kiran Polavarapu, Mainak Bardhan, Veeramani Preethish-Kumar, Shingavi Leena

Glob Med Genet· March 2022

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Distinct and Recognisable Muscle MRI Pattern in a Series of Adults Harbouring an Identical GMPPB Gene Mutation.
Shahyan Siddiqui, Kiran Polavarapu, Mainak Bardhan, Veeramani Preethish-Kumar, Aditi Joshi, Shingavi Leena

J Neuromuscul Dis· February 2022

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Hyperglycemic Hyperosmolar Syndrome Presenting With Unique Craniofacial Involuntary Movements.
Manu Santhappan Girija, Ravi Yadav, Atchayaram Nalini, Jagadish Annapureddy, Manisha Gupta, Leena Shingavi

Neurol Clin Pract· December 2021

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Lead Encephalopathy with Distinctive Brain Magnetic Resonance Imaging Findings.
Ameya Patwardhan, Nalini Atchayaram, Jitender Saini, Manu S Girija, Jagadish Annapureddy, Leena Shingavi

Neurol India· November 2021

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A founder mutation in the GMPPB gene [c.1000G > A (p.Asp334Asn)] causes a mild form of limb-girdle muscular dystrophy/congenital myasthenic syndrome (LGMD/CMS) in South Indian patients.
Kiran Polavarapu, Aradhna Mathur, Aditi Joshi, Saraswati Nashi, Veeramani Preethish-Kumar, Leena Shingavi

Neurogenetics· October 2021

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Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome.
Mainak Bardhan, Kiran Polavarapu, Nandeesh N Bevinahalli, Preethish-Kumar Veeramani, Ram Murthy Anjanappa, Leena Shingavi

J Hum Genet· August 2021

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Correction: Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome.
Mainak Bardhan, Kiran Polavarapu, Nandeesh N Bevinahalli, Veeramani Preethish-Kumar, Ram Murthy Anjanappa, Leena Shingavi

J Hum Genet· August 2021

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Nemaline Rod/Cap Myopathy Due to Novel Homozygous Mutations: The First Report from South Asia and Comprehensive Literature Review.
Kiran Polavarapu, Mainak Bardhan, Ram Murthy Anjanappa, Seena Vengalil, Veeramani Preethish-Kumar, Leena Shingavi

J Clin Neurol· July 2021

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Novel variants broaden the phenotypic spectrum of PLEKHG5-associated neuropathies.
Zhongbo Chen, Reza Maroofian, A Nazlı Başak, Leena Shingavi, Mert Karakaya

Eur J Neurol· April 2021

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Altered REM sleep architecture in patients with Myotonic dystrophy type 1: is related to sleep apnea?
Doniparthi Venkata Seshagiri, Akshata Huddar, Saraswati Nashi, Somdattaa Ray, Palanyswamy Ramaswamy, Leena Shingavi

Sleep Med· March 2021

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Social Cognition Deficits Are Pervasive across Both Classical and Overlap Frontotemporal Dementia Syndromes.
Faheem Arshad, Avanthi Paplikar, Shailaja Mekala, Feba Varghese, Vandana Valiyaparambath Purushothaman, Leena Shingavi

Dement Geriatr Cogn Dis Extra· November 2020

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