Duchenne Muscular Dystrophy and Becker Muscular Dystrophy Confirmed by Multiplex Ligation-Dependent Probe Amplification: Genotype-Phenotype Correlation in a Large Cohort
Vengalil, Seena, Preethish-Kumar, Veeramani, Polavarapu, Kiran, Mahadevappa, Manjunath, Sekar, Deepha, Purushottam, Meera, Thomas, Priya Treesa, Nashi, Saraswathi, Nalini, Atchayaram
Published in Journal of clinical neurology (Seoul, Korea) (01.01.2017)
Published in Journal of clinical neurology (Seoul, Korea) (01.01.2017)
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Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) masquerading primary progressive aphasia
Goyal, Sheetal, Darshini, K, Sharma, Dinesh, Nashi, Saraswathi, Arshad, Faheem, Vandana, V, Alladi, Suvarna
Published in Annals of the Indian Academy of Neurology (01.07.2022)
Published in Annals of the Indian Academy of Neurology (01.07.2022)
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Journal Article
Palliative care needs and care giver burden in neurodegenerative diseases: A cross sectional study
Lithin, Zacharias, Thomas, Priya, Warrier, G, Bhaskar, Adhin, Nashi, Saraswathi, Vengalil, Seena, Polavarapu, Kiran, Kumar, Preethish, Yadav, Ravi, Alladi, Suvarna, Atchayaram, Nalini, Pal, Pramod
Published in Annals of the Indian Academy of Neurology (01.05.2020)
Published in Annals of the Indian Academy of Neurology (01.05.2020)
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P-NU003. Estimation of cross-sectional area reference values of nerves in the upper and lower extremities using ultrasonography in the Indian population
Sindhu, D.M., Vengalil, Seena, Nashi, Saraswathi, Saini, Jitender, Bhatala, Lokesh, Raju, Sanita, Nalini, A.
Published in Clinical neurophysiology (01.08.2021)
Published in Clinical neurophysiology (01.08.2021)
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P-PN036. Loss of function mutation in HINT1 gene presenting with neuromyotonia and hereditary neuropathy
Shingavi, Leena, Vengalil, Seena, Polavarapu, Kiran, Preethish-Kumar, Veeramani, Nashi, Saraswathi, Nalini, Atchayaram
Published in Clinical neurophysiology (01.08.2021)
Published in Clinical neurophysiology (01.08.2021)
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