Spectrum and Pattern of Movement Disorders in Patients with Sporadic Creutzfeldt-Jakob Disease

por Gurram, Sandeep, Holla, Vikram V., Sharma, Praveen, Kamble, Nitish, Saini, Jitender, Netravathi, Manjunath, Yadav, Ravi, Pal, Pramod Kumar
Publicado 2023

Clinical Spectrum, Radiological Correlation and Outcome of Movement Disorders in Wilson’s Disease

por Mahale, Rohan R., Stezin, Albert, Prasad, Shweta, Kamble, Nitish, Holla, Vikram V., Netravathi, Manjunath, Yadav, Ravi, Pal, Pramod Kumar
Publicado 2023

Utility of Clinical Exome Sequencing in Dystonia: A Single-Center Study From India

por Holla, Vikram Venkappayya, Neeraja, Koti, Stezin, Albert, Prasad, Shweta, Surisetti, Bharat Kumar, Netravathi, Manjunath, Kamble, Nitish, Yadav, Ravi, Pal, Pramod Kumar
Publicado 2022

Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation

por Netravathi, Manjunath, Kumari, Renu, Kapoor, Saketh, Dakle, Pushkar, Dwivedi, Manish Kumar, Roy, Sumitabho Deb, Pandey, Paritosh, Saini, Jitender, Ramakrishna, Anil, Navalli, Devaraddi, Satishchandra, Parthasarathy, Pal, Pramod Kumar, Kumar, Arun, Faruq, Mohammed
Publicado 2015