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Dual burden of Zika and COVID-19 in India: challenges, opportunities and recommendations

Tropical medicine and health, 2021-10, Vol.49 (1), p.83-83, Article 83

2021

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Genetics and Genomics of Chronic Pancreatitis with a Focus on Disease Biology and Molecular Pathogenesis

Global medical genetics, 2023-12, Vol.10 (4), p.324-334

2023

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Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome

Journal of human genetics, 2021-08, Vol.66 (8), p.813-823

2021

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Tuberculosis amidst COVID-19 pandemic in India: unspoken challenges and the way forward

Tropical medicine and health, 2021-10, Vol.49 (1), p.84-84, Article 84

2021

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Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathy

Scientific reports, 2023-09, Vol.13 (1), p.15095-10, Article 15095

2023

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Qualitative and Quantitative Electrocardiogram Parameters in a Large Cohort of Children with Duchenne Muscle Dystrophy in Comparison with Age-Matched Healthy Subjects: A Study from South India

Annals of the Indian Academy of Neurology, 2024-01, Vol.27 (1), p.53-57

2024

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SARS-CoV-2 Vaccination in India: Considerations of Hesitancy and Bioethics in Global Health

Annals of global health, 2021, Vol.87 (1), p.124-124

2021

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Myotonic Dystrophy Type 1 (DM1): Clinical Characteristics and Disease Progression in a Large Cohort

Neurology India, 2024-01, Vol.72 (1), p.83-89

2024

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Muscle ultrasonography in detecting fasciculations: A noninvasive diagnostic tool for amyotrophic lateral sclerosis

Journal of clinical ultrasound, 2022-02, Vol.50 (2), p.286-291

2022

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Correction: Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome

Journal of human genetics, 2021-08, Vol.66 (8), p.841-841

2021

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Vaccine apartheid: the separation of the world’s poorest and most vulnerable and the birth of Omicron

Therapeutic advances in vaccines and immunotherapy, 2022, Vol.10

2022

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Phenotypic Heterogeneity in ORAI-1-Associated Congenital Myopathy

Global medical genetics, 2024-12, Vol.11 (4), p.297-303

2024

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Classical Hirayama disease presenting as progressive spastic quadriparesis

Annals of the Indian Academy of Neurology, 2023-05, Vol.26 (3), p.308-310

2023

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Mutation spectrum of primary lipid storage myopathies

Annals of the Indian Academy of Neurology, 2022-01, Vol.25 (1), p.106-113

2022

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Identification of a Novel Intronic Mutation in VMA21 Associated with a Classical Form of X-Linked Myopathy with Autophagy

Global medical genetics, 2024-06, Vol.11 (2), p.167-174

2024

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Rise in cholera amid COVID-19: Spotlight on Pakistan and Bangladesh

The Lancet regional health. Southeast Asia, 2022-09, Vol.4, p.100041-100041, Article 100041

2022

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Exploring Health Care Disparities in Genetic Testing and Research for Hereditary Cardiomyopathy: Current State and Future Perspectives

Global medical genetics, 2024-01, Vol.11 (1), p.36-47

2024

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Lichtenstein-Knorr syndrome: A rare case of ataxia with sensorineural hearing loss

Annals of the Indian Academy of Neurology, 2022-09, Vol.25 (5), p.970-973

2022

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Animacy effects in fluency task performance in early Alzheimer's Disease-A case-control study

Annals of the Indian Academy of Neurology, 2022-09, Vol.25 (5), p.968-970

2022

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PET-MRI in idiopathic inflammatory myositis: a comparative study of clinical and immunological markers with imaging findings

Neurological research and practice, 2022-10, Vol.4 (1), p.49-49, Article 49

2022

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Expanding the Phenotypic Spectrum of ECEL1-Associated Distal Arthrogryposis

Children (Basel), 2021-10, Vol.8 (10), p.909

2021

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Nemaline Rod/Cap Myopathy Due to Novel Homozygous MYPN Mutations: The First Report from South Asia and Comprehensive Literature Review

Journal of Clinical Neurology, 2021, 17(3), , pp.409-418

2021

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Disease Progression and Mutation Pattern in a Large Cohort of LGMD R1/LGMD 2A Patients from India

Global medical genetics, 2022-03, Vol.9 (1), p.034-041

2022

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Genetic, Epigenetic, and Molecular Biology of Obesity: From Pathology to Therapeutics the Way Forward

Journal of the Association of Physicians of India, 2022-09, Vol.70 (9), p.76-82

2022

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Dual burden of Zika and COVID-19 in India: challenges, opportunities and recommendations

Genetics and Genomics of Chronic Pancreatitis with a Focus on Disease Biology and Molecular Pathogenesis

Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome

Tuberculosis amidst COVID-19 pandemic in India: unspoken challenges and the way forward

Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathy

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

Qualitative and Quantitative Electrocardiogram Parameters in a Large Cohort of Children with Duchenne Muscle Dystrophy in Comparison with Age-Matched Healthy Subjects: A Study from South India

SARS-CoV-2 Vaccination in India: Considerations of Hesitancy and Bioethics in Global Health

Myotonic Dystrophy Type 1 (DM1): Clinical Characteristics and Disease Progression in a Large Cohort

Muscle ultrasonography in detecting fasciculations: A noninvasive diagnostic tool for amyotrophic lateral sclerosis

Correction: Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome

Vaccine apartheid: the separation of the world’s poorest and most vulnerable and the birth of Omicron

Phenotypic Heterogeneity in ORAI-1-Associated Congenital Myopathy

Classical Hirayama disease presenting as progressive spastic quadriparesis

Mutation spectrum of primary lipid storage myopathies

Identification of a Novel Intronic Mutation in VMA21 Associated with a Classical Form of X-Linked Myopathy with Autophagy

Rise in cholera amid COVID-19: Spotlight on Pakistan and Bangladesh

Exploring Health Care Disparities in Genetic Testing and Research for Hereditary Cardiomyopathy: Current State and Future Perspectives

Lichtenstein-Knorr syndrome: A rare case of ataxia with sensorineural hearing loss

Animacy effects in fluency task performance in early Alzheimer's Disease-A case-control study

PET-MRI in idiopathic inflammatory myositis: a comparative study of clinical and immunological markers with imaging findings

Expanding the Phenotypic Spectrum of ECEL1-Associated Distal Arthrogryposis

Nemaline Rod/Cap Myopathy Due to Novel Homozygous MYPN Mutations: The First Report from South Asia and Comprehensive Literature Review

Disease Progression and Mutation Pattern in a Large Cohort of LGMD R1/LGMD 2A Patients from India

Genetic, Epigenetic, and Molecular Biology of Obesity: From Pathology to Therapeutics the Way Forward

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