Tectal glioma with hydrocephalus presenting with spastic and ataxic quadriparesis

Por Shukla, Dhaval, Bindu, Parayil Sankaran, Devi, Bhagvatula Indira
Publicado em 2014

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

Por Nagappa, Madhu, Bindu, Parayil S., Adwani, Sikandar, Seshagiri, Sangeeta K., Saini, Jitender, Sinha, Sanjib, Taly, Arun B.
Publicado em 2014

Speech-Language and swallowing manifestations and rehabilitation in an 11-year-old girl with MELAS syndrome

Por Vandana, V. P., Bindu, Parayil Sankaran, Sonam, Kothari, Taly, Arun B., Gayathri, N., Madhu, N., Sinha, S.
Publicado no J Pediatr Neurosci (2015)

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

Por Nagappa, Madhu, Taly, Arun B., Mahadevan, Anita, Pooja, Mailankody, Bindu, Parayil Sankaran, Chickabasaviah, Yasha T., Gayathri, Narayanappa, Sinha, Sanjib
Publicado no Ann Indian Acad Neurol (2015)

Genetic analysis of an Indian family with members affected with Waardenburg syndrome and Duchenne muscular dystrophy

Por Kapoor, Saketh, Bindu, Parayil Sankaran, Taly, Arun B., Sinha, Sanjib, Gayathri, Narayanappa, Rani, S. Vasantha, Chandak, Giriraj Ratan, Kumar, Arun
Publicado em 2012

Self-limiting symptomatic peri-ictal bradyarryhthmia due to junctional AV rhythm

Por Babarao, Hanmantrao Darku, Madhu, Nagappa, Sinha, Sanjib, Prasad, Chandrajit, Somasekhar, Nagaraju, Ahmad, Naveed, Bindu, Parayil Sankaran, Taly, Arun B
Publicado em 2013

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

Por Chaitanya, Ganne, Santosh, N. Subbareddy, Velmurugan, Jayabal, Arivazhagan, Arima, Bharath, Rose D., Mahadevan, Anita, Nagappa, Madhu, Bindu, Parayil S, Rao, Malla Bhaskara, Taly, Arun B., Satishchandra, Parthasarathy, Sinha, Sanjib
Publicado no Ann Indian Acad Neurol (2015)

Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish

Por Southgate, Laura, Dafou, Dimitra, Hoyle, Jacqueline, Li, Nan, Kinning, Esther, Critchley, Peter, Németh, Andrea H., Talbot, Kevin, Bindu, Parayil S., Sinha, Sanjib, Taly, Arun B., Raghavendra, Seetharam, Müller, Ferenc, Maher, Eamonn R., Trembath, Richard C.
Publicado em 2010

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

Por Kapoor, Saketh, Shah, Mohd Hussain, Singh, Nivedita, Rather, Mohammad Iqbal, Bhat, Vishwanath, Gopinath, Sindhura, Bindu, Parayil Sankaran, Taly, Arun B., Sinha, Sanjib, Nagappa, Madhu, Bharath, Rose Dawn, Mahadevan, Anita, Narayanappa, Gayathri, Chickabasaviah, Yasha T., Kumar, Arun
Publicado no PLoS One (2016)