Vasculitic neuropathy in elderly: A study from a tertiary care university hospital in South India

by Anish Lawrence, Madhu Nagappa, Anita Mahadevan, Arun B Taly
Published 2016-01-01

Hypereosinophilia as a cause of recurrent stroke

by Srikant Venkatakrishnan, Anupam Gupta, Meeka Khanna, Madhu Nagappa, Cecil Ross
Published 2020-01-01

Prevalence of fatigue in Guillain-Barre syndrome in neurological rehabilitation setting

by Prajna Ranjani, Meeka Khanna, Anupam Gupta, Madhu Nagappa, Arun B Taly, Partha Haldar
Published 2014-01-01

Differential improvement of the sleep quality among patients with juvenile myoclonic epilepsy with valproic acid: A longitudinal sleep questionnaire-based study

by Chetan Nayak, Sanjib Sinha, Chaitra T Ramachandraiah, Madhu Nagappa, Kandivali Thennarasu, Arun B Taly, Parthasarathy Satishchandra
Published 2015-01-01

Clinical, hematological, and imaging observations in a 25-year-old woman with abetalipoproteinemia

by Madhu Nagappa, Parayil S Bindu, Sikandar Adwani, Sangeeta K Seshagiri, Jitender Saini, Sanjib Sinha, Arun B Taly
Published 2014-01-01

Tangier′s disease: An uncommon cause of facial weakness and non-length dependent demyelinating neuropathy

by Madhu Nagappa, Arun B Taly, Anita Mahadevan, M Pooja, P S Bindu, Y T Chickabasaviah, N Gayathri, Sanjib Sinha
Published 2016-01-01

An uncommon cause of bifacial weakness and non-length-dependent demyelinating neuropathy

by Madhu Nagappa, Arun B Taly, Anita Mahadevan, Mailankody Pooja, Parayil Sankaran Bindu, Yasha T Chickabasaviah, Narayanappa Gayathri, Sanjib Sinha
Published 2015-01-01

Pulmonary Involvement in Patients with Guillain–Barré Syndrome in Subacute Phase

by Meeka Khanna, Nidhi Rawat, Anupam Gupta, Madhu Nagappa, Arun B. Taly, M. R. Rukmani, T. N. Sathyaprabha, Partha Haldar
Published 2017-07-01

Spectrum and evolution of EEG changes in Anti-NMDAR encephalitis

by Lakshminarayanapuram Gopal Viswanathan, Shreedhara A Siddappa, Madhu Nagappa, Anita Mahadevan, Shishir Duble, Parayil S Bindu, Arun B Taly, Sanjib Sinha
Published 2021-01-01

Utility of immunohistochemistry and western blot in profiling clinically suspected cases of congenital muscular dystrophy

by Radhika Mhatre, Deepha Sekar, Jessiena Ponmalar, Madhu Nagappa, Preethish-Kumar Veeramani, Kiran Polavarapu, Seena Vengalil, Nalini Atchayaram, Gayathri Narayanappa
Published 2021-01-01

Clinical profile and treatment response in patients with CASPR2 antibody-associated neurological disease

by Sumanth Shivaram, Madhu Nagappa, Doniparthi V Seshagiri, Anita Mahadevan, Yashwanth Gangadhar, T N Sathyaprabha, Vijay Kumavat, Rose D Bharath, Sanjib Sinha, Arun B Taly
Published 2021-01-01

Genetic analysis of ATP7B in 102 south Indian families with Wilson disease.

by Nivedita Singh, Pradeep Kallollimath, Mohd Hussain Shah, Saketh Kapoor, Vishwanath Kumble Bhat, Lakshminarayanapuram Gopal Viswanathan, Madhu Nagappa, Parayil S Bindu, Arun B Taly, Sanjib Sinha, Arun Kumar
Published 2019-01-01

Ictal Generalized EEG Attenuation (IGEA) and hypopnea in a child with occipital type 1 cortical dysplasia - Is it a biomarker for SUDEP?

by Ganne Chaitanya, Santosh N Subbareddy, Jayabal Velmurugan, Arima Arivazhagan, Bharath D Rose, Anita Mahadevan, Madhu Nagappa, Parayil S Bindu, Malla Bhaskara Rao, Arun B Taly, Parthasarathy Satishchandra, Sanjib Sinha
Published 2015-01-01

Vogt-koyanagi-harada syndrome - A neurologist's perspective

by Sumanth Shivaram, Madhu Nagappa, Doniparthi V Seshagiri, Jayanth Shimoga Shanthakumar, Swayang Sudha Panda, Ravi Anadure, B N Nandeesh, Yasha T Chickabasaviah, Rose D Bharath, Joy Vijayan, Bakula Kashyap, Sanjib Sinha, Arun B Taly
Published 2021-01-01

Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex.

by Saketh Kapoor, Mohd Hussain Shah, Nivedita Singh, Mohammad Iqbal Rather, Vishwanath Bhat, Sindhura Gopinath, Parayil Sankaran Bindu, Arun B Taly, Sanjib Sinha, Madhu Nagappa, Rose Dawn Bharath, Anita Mahadevan, Gayathri Narayanappa, Yasha T Chickabasaviah, Arun Kumar
Published 2016-01-01

Identification and functional characterization of two novel mutations in KCNJ10 and PI4KB in SeSAME syndrome without electrolyte imbalance

by Ravi K. Nadella, Anirudh Chellappa, Anand G. Subramaniam, Ravi Prabhakar More, Srividya Shetty, Suriya Prakash, Nikhil Ratna, V. P. Vandana, Meera Purushottam, Jitender Saini, Biju Viswanath, P. S. Bindu, Madhu Nagappa, Bhupesh Mehta, Sanjeev Jain, Ramakrishnan Kannan
Published 2019-10-01