Employment
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Education
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Nimhans DM
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Publications (181)
- Clinical profile and treatment outcomes of patients with chronic presentations of autoimmune encephalitis: expanding the spectrum Save
- Magnetic resonance imaging in idiopathic inflammatory myopathies: deciphering the pattern of muscle involvement Save
- Genetic spectrum of neuronal ceroid lipofuscinosis & its genotype-phenotype correlation –A single centre experience of 56 cases Save
- Autoantibody-Based Clinicoradiopathologic Phenotyping of Idiopathic Inflammatory Myopathies: An Indian Cohort Save
- Phenotypic Heterogeneity in ORAI-1-Associated Congenital Myopathy Save
- Phenotype-genotype spectrum of a cohort of congenital muscular dystrophies: a single-centre experience from India Save
- Childhood-Onset Myopathy With Preserved Ambulation Caused by a Recurrent ADSSL1 Missense Variant Save
- A Novel Mutation in Frabin (FGD4) Causing a Mild Phenotype of CMT4H in an Indian Patient Save
- A novel DHTKD1 gene mutation with ALS like presentation: a case report Save
- A synonymous codon change in the DYSF gene alters mRNA splicing and causes autosomal recessive limb girdle muscular dystrophy type 2B Save