Levodopa Non-Responsive Parkinsonism in Tuberculous Cerebral Arteritis: A Rare Occurrence

por Mahale, Rohan, Pon, Arun Gokul, Sandeep, M., Padmanabha, Hansashree, Mailankody, Pooja, Pavagada, Mathuranath
Publicado 2022

ADCY5-Related Dyskinesia: A Genetic Cause of Early-Onset Chorea-Report of Two Cases and a Novel Mutation

por Padmanabha, Hansashree, Ray, Somdattaa, Mahale, Rohan, Arunachal, Gautham, Singhi, Pratibha, Mailankody, Pooja, Pavagada, Mathuranath
Publicado 2021

Autosomal Dominant Cerebral Small Vessel Disease in HTRA1 Gene Mutation

por Mahale, Rohan R., Agarwal, Aakash, Gautam, Jyothi, Varghese, Nibu, Kovoor, Jennifer, Mailankody, Pooja, Padmanabha, Hansashree, Pavagada, Mathuranath
Publicado 2021

Rapidly Progressive Spastic Paraplegia Due to Hyperhomocysteinemia in Child with MTHFR Gene Mutation and Mitochondrial Complex I Deficiency: A Rare Association

por Mahale, Rohan R., Gautam, Jyothi, Arunachal, Gautam, Alappati, Sandhya, Varghese, Nibu, Kovoor, Jennifer, Mailankody, Pooja, Padmanabha, Hansashree, Pavagada, Mathuranath
Publicado 2021

Granulomatous Panuveitis in Multiple Sclerosis: A Rare Occurrence

por Shah, Rutul, Mahale, Rohan R., Babu, Kalpana, Shah, Dhwani, Vincent, Manu, Nanda, Satabdi, Sangeeth, TA, Sriram, Neeharika, Tiwari, Ravindu, Padmanabha, Hansashree, Mailankody, Pooja, Pavagada, Mathuranath S.
Publicado 2022