Genetic analysis of ATP7B in 102 south Indian families with Wilson disease von Singh, Nivedita, Kallollimath, Pradeep, Shah, Mohd Hussain, Kapoor, Saketh, Bhat, Vishwanath Kumble, Viswanathan, Lakshminarayanapuram Gopal, Nagappa, Madhu, Bindu, Parayil S, Taly, Arun B, Sinha, Sanjib, Kumar, Arun

Volltext

Clinical profile and treatment response in patients with CASPR2 antibody-associated neurological disease von Shivaram, Sumanth, Nagappa, Madhu, Seshagiri, Doniparthi, Mahadevan, Anita, Gangadhar, Yashwanth, Sathyaprabha, T, Kumavat, Vijay, Bharath, Rose, Sinha, Sanjib, Taly, Arun

Volltext

Urinary symptoms in patients with Parkinson's disease and progressive supranuclear palsy: Urodynamic findings and management of bladder dysfunction von Gupta, Anupam, Rashmi Krishnan, U, Nageshkumar, Sushruth, Pal, Pramod, Khanna, Meeka, Taly, Arun

Volltext

Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutations von Sonam, Kothari, Khan, Nahid Akthar, Bindu, Parayil Sankaran, Taly, Arun B, Gayathri, N, Bharath, M.M. Srinivas, Govindaraju, C, Arvinda, H.R, Nagappa, Madhu, Sinha, Sanjib, Thangaraj, K

Volltext

Ambulation following spinal cord injury and its correlates von Menon, Nitin, Gupta, Anupam, Khanna, Meeka, Taly, Arun B

Volltext

Vasculitic neuropathy in elderly: A study from a tertiary care university hospital in South India von Lawrence, Anish, Nagappa, Madhu, Mahadevan, Anita, Taly, Arun

Volltext

Post-stroke balance training: Role of force platform with visual feedback technique von Srivastava, Abhishek, Taly, Arun B, Gupta, Anupam, Kumar, Senthil, Murali, Thyloth

Volltext

IL-23/IL-17 immune axis in Guillain Barré Syndrome: Exploring newer vistas for understanding pathobiology and therapeutic implications von Debnath, Monojit, Nagappa, Madhu, Murari, Geetanjali, Taly, Arun B.

Volltext

Oculomotor Apraxia in Gaucher Disease von Nagappa, Madhu, MD, DM, Bindu, Parayil Sankaran, MD, DM, Taly, Arun B., MD, DM, Sinha, Sanjib, MD, DM

Volltext

Child Neurology: Hereditary Folate Malabsorption von Huddar, Akshata, Chiplunkar, Shwetha, Nagappa, Madhu, Govindaraj, Periyasamy, Sinha, Sanjib, Taly, Arun B., Sankaran, Bindu Parayil

Volltext

Mortality in mechanically ventilated patients of Guillain Barré Syndrome von Netto, Archana B, Taly, Arun B, Kulkarni, Girish Baburao, Rao, Umamaheswara G S, Rao, Shivaji

Volltext

Electro-clinical features and magnetic resonance imaging correlates in Menkes disease von Bindu, Parayil Sankaran, Taly, Arun B, Kothari, Sonam, Christopher, Rita, Gayathri, Narayanappa, Sinha, Sanjib, Nagappa, Madhu, Bhatt, Maya, Bharath, Rose Dawn

Volltext

Leukodystrophies and Genetic Leukoencephalopathies in Children Specified by Exome Sequencing in an Expanded Gene Panel von Parayil Sankaran, Bindu, Nagappa, Madhu, Chiplunkar, Shwetha, Kothari, Sonam, Govindaraj, Periyasamy, Sinha, Sanjib, Taly, Arun B.

Volltext

Antecedent infections in Guillain‐Barré syndrome patients from south India von Dutta, Debprasad, Debnath, Monojit, Nagappa, Madhu, Das, Sumit Kumar, Wahatule, Rahul, Sinha, Sanjib, Taly, Arun B., Ravi, Vasanthapuram

Volltext

Prevalence of fatigue in Guillain-Barre syndrome in neurological rehabilitation setting von Ranjani, Prajna, Khanna, Meeka, Gupta, Anupam, Nagappa, Madhu, Taly, Arun B, Haldar, Partha

Volltext

Urodynamic profile of patients with neurogenic bladder following non-traumatic myelopathies von Gupta, Anupam, Taly, Arun

Volltext

Sleep in Myasthenia Gravis: A Questionnaire-Based Study von Kumar, Rakesh, Nayak, Chetan, Nagappa, Madhu, Rao, Shivaji, Sinha, Sanjib, Taly, Arun B

Volltext

Variations within Toll‐like receptor (TLR) and TLR signaling pathway‐related genes and their synergistic effects on the risk of Guillain‐Barré syndrome von Dutta, Debprasad, Nagappa, Madhu, Sreekumaran Nair, Binu V., Das, Sumit Kumar, Wahatule, Rahul, Sinha, Sanjib, Vasanthapuram, Ravi, Taly, Arun B., Debnath, Monojit

Volltext

Ganglioside complex antibodies in an Indian cohort of Guillain‐Barré syndrome von Wahatule, Rahul, Dutta, Debprasad, Debnath, Monojit, Nagappa, Madhu, Mahadevan, Anita, Sinha, Sanjib, Sundaravadivel, Pandarisamy, Rao, Umamaheswara, Periyavan, Sundar, Binu, VS, Rao, Shivaji, Taly, Arun B

Volltext

Leukodystrophy Due to eIF2B Mutations in Adults von Shivaram, Sumanth, Nagappa, Madhu, Seshagiri, Doniparthi Venkata, Saini, Jitender, Govindaraj, Periyasamy, Sinha, Sanjib, Bindu, Parayil Sankaran, Taly, Arun B.

Volltext