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Annals of Indian Academy of Neurology|July 2, 2020
Palliative Care Needs and Care Giver Burden in Neurodegenerative Diseases: A Cross Sectional StudyZacharias Lithin, Priya T Thomas, G Manjusha Warrier, et al.Journal of Neuromuscular Diseases|December 5, 2021
Late Onset Pompe Disease with Novel Mutations and Atypical PhenotypesTanushree Chawla, Veeramani Preethish-Kumar, Kiran Polavarapu, et al.Journal of Neuromuscular Diseases|December 18, 2023
A Novel Mutation in Frabin (FGD4) Causing a Mild Phenotype of CMT4H in an Indian PatientVikas Nishadham, Rashmi Santhoshkumar, Saraswati Nashi, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 25, 2021
Recessive VAMP1 mutations associated with severe congenital myasthenic syndromes - A recognizable clinical phenotypeKiran Polavarapu, Seena Vengalil, Veeramani Preethish-Kumar, et al.Indian Journal of Palliative Care|May 26, 2021
Palliative Care in Duchenne Muscular Dystrophy: A Study on Parents' UnderstandingArun Sadasivan, Manjusha G Warrier, Kiran Polavarapu, et al.Journal of Social Work in End-Of-Life & Palliative Care|August 3, 2019
Family Caregivers' Experiences with Dying and Bereavement of Individuals with Motor Neuron Disease in IndiaManjusha G Warrier, Priya Treesa Thomas, Arun Sadasivan, et al.Journal of Neurology|November 4, 2023
Mutations in PTPN11 could lead to a congenital myasthenic syndrome phenotype: a Noonan syndrome case seriesAlessia Pugliese, Adela Della Marina, Eduardo de Paula Estephan, et al.Scientific Reports|September 12, 2023
Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathyShamita Sanga, Sudipta Chakraborty, Mainak Bardhan, et al.Annals of Indian Academy of Neurology|April 22, 2025
In-Depth Understanding of Hirayama Disease: Dural Detachment Beyond Cervical SpineSeena Vengalil, Vijaykumar Boddu, Karthik Kulanthaivelu, et al.Journal of Neurology|September 10, 2021
Disrupted structural connectome and neurocognitive functions in Duchenne muscular dystrophy: classifying and subtyping based on Dp140 dystrophin isoformVeeramani Preethish-Kumar, Apurva Shah, Kiran Polavarapu, et al.Pageof 12