Hydroxyapatite nanorods loaded with parathyroid hormone (PTH) synergistically enhance the net formative effect of PTH anabolic therapy by Dave, Jay R., Dewle, Ankush M., Mhaske, Suhas T., Phulpagar, Prashant T., Mathe, Vikas L., More, Supriya E., Khan, Ayesha A., Murthy, Appala Venkata Ramana, Datar, Suwarna S., Jog, Ajay J., Page, Megha, Tomar, Geetanjali B.

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Clinicogenetic Characterization of Patients with PD and Heterozygous GBA1 Variants in an Indian Cohort by Kamath, Sneha D, Holla, Vikram V., Phulpagar, Prashant, Kamble, Nitish, Yadav, Ravi, Muthusamy, Babylakshmi, Pal, Pramod Kumar

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Novel CWF19L1 mutations in patients with spinocerebellar ataxia, autosomal recessive 17 by Phulpagar, Prashant, Holla, Vikram V, Tomar, Deepti, Kamble, Nitish, Yadav, Ravi, Pal, Pramod Kumar, Muthusamy, Babylakshmi

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Genetic architecture of a single cohort of 230 Indian Parkinson's Disease patients by Kamath, Sneha D., Phulpagar, Prashant, Holla, Vikram V., Kamble, Nitish, Yadav, Ravi, Muthusamy, Babylakshmi, Kumar Pal, Pramod

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Effective Visualization and Easy Tracking of Extracellular Vesicles in Glioma Cells by Mondal, Abir, Ashiq, K A, Phulpagar, Prashant, Singh, Divya Kumari, Shiras, Anjali

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A splice altering variant in NDRG1 gene causes Charcot-Marie-Tooth disease, type 4D by Pravinbabu, Pooja, Holla, Vikram V., Phulpagar, Prashant, Kamble, Nitish, Netravathi, Manjunath, Yadav, Ravi, Pal, Pramod Kumar, Muthusamy, Babylakshmi

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Whole exome sequencing and transcript analysis discover a novel pathogenic splice site mutation in DCAF17 gene underlying Woodhouse‐Sakati syndrome by Kumari, Riyanka, Holla, Vikram V., Phulpagar, Prashant, Sriram, Neeharika, Hegde, Aditya G., Vengalil, Seena, Kamble, Nitish, Saini, Jitender, Yadav, Ravi, Pal, Pramod Kumar, Muthusamy, Babylakshmi

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Spinocerebellar ataxia recessive type 7 due to novel compound heterozygous variants in TPP1: First report from India by Holla, Vikram V., Jha, Shreyasi, Pal, Pramod Kumar, Yadav, Ravi, Phulpagar, Prashant, Muthusamy, Babylakshmi, Arunachal, Gautham

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Clinico-Genetic Profiles of Seven Patients With PINK1-Related Parkinson’s Disease: A Case Series From a Tertiary Care Centre in India and a Review of the Literature by Gunasekaran, Aravind, Holla, Vikram V, Phulpagar, Prashant, Kamath, Sneha D, Kamble, Nitish, Yadav, Ravi, Muthusamy, Babylakshmi, Pal, Pramod Kumar

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CLCN2‐Related Leukoencephalopathy in Two Unrelated Patients Due to Novel Variants by Holla, Vikram V., Phulpagar, Prashant, Saini, Jitender, Kamble, Nitish, Pal, Pramod Kumar, Yadav, Ravi, Muthusamy, Babylakshmi, Netravathi, Manjunath

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The Clinical, Radiological and Genetic Spectrum of PLA2G6 -Associated Neurodegeneration: An Experience From a Tertiary Center by Holla, Vikram V, Samim, M M, Kumari, Riyanka, Dhar, Debjyoti, Phulpagar, Prashant, Sriram, Neeharika, Prasad, Shweta, Saini, Jitender, Kamble, Nitish, Yadav, Ravi, Muthusamy, Babylakshmi, Pal, Pramod Kumar

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A Rare Case of Ophthalmoplegia with Ataxia in Genetically Proven Abetalipoproteinemia by Gurram, Sandeep, Holla, Vikram V., Sriram, Neeharika, Phulpagar, Prashant, Jha, Shreyashi, Sharma, Praveen, Mallithavana, Siddaya, Kamble, Nitish, Netravathi, Manjunath, Yadav, Ravi, Muthusamy, Babylakshmi, Pal, Pramod Kumar

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