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

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PMP22 Gene–Associated Neuropathies: Phenotypic Spectrum in a Cohort from India von Nagappa, Madhu, Sharma, Shivani, Govindaraj, Periyasamy, Chickabasaviah, Yasha T., Siram, Ramesh, Shroti, Akhilesh, Debnath, Monojit, Sinha, Sanjib, Bindu, Parayil S., Taly, Arun B.

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Management of Anti–N-Methyl-d-Aspartate (NMDA) Receptor Encephalitis in Children von Nagappa, Madhu, Parayil, S. Bindu, Mahadevan, Anita, Sinha, Sanjib, Mathuranath, Pavagada S., Taly, Arun B.

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Spectrum of Sensory Conduction Abnormalities in Guillain Barre Syndrome von Nagappa, Madhu, Wahatule, Rahul, Bindu, Parayil, Sinha, Sanjib, Taly, Arun

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Cranial MRI in Acute Hyperammonemic Encephalopathy von Bindu, Parayil S., DM, Sinha, Sanjib, DM, Taly, Arun B., DM, Christopher, Rita, MD, Kovoor, Jerry M.E., MD

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Characterisation of Patients with SH3TC2 Associated Neuropathy in an Indian Cohort von Nagappa, Madhu, Sharma, Shivani, Govindaraj, Periyasamy, Chickabasaviah, Yasha, Siram, Ramesh, Shroti, Akhilesh, Seshagiri, Doniparthi, Debnath, Monojit, Sinha, Sanjib, Bindu, Parayil, Taly, Arun

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

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Child Neurology: Molybdenum cofactor deficiency von Nagappa, Madhu, Bindu, Parayil S, Taly, Arun B, Sinha, Sanjib, Bharath, Rose D

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Clinical, hematological, and imaging observations in a 25-year-old woman with abetalipoproteinemia von Nagappa, Madhu, Bindu, Parayil S, Adwani, Sikandar, Seshagiri, Sangeeta K, Saini, Jitender, Sinha, Sanjib, Taly, Arun B

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Child Neurology: Sjögren-Larsson syndrome von Nagappa, Madhu, Bindu, Parayil S, Chiplunkar, Shwetha, Gupta, Neelesh, Sinha, Sanjib, Mathuranath, Pavagada S, Bharath, Rose D, Taly, Arun B

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

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Mega-Corpus Callosum, Polymicrogyria, and Psychomotor Retardation Syndrome von Bindu, Parayil S., DM, Taly, Arun B., DM, Sinha, Sanjib, DM, Bharath, Rose D., DM

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Pediatric opsoclonus-myoclonus-ataxia syndrome: Experience from a tertiary care university hospital von Huddar, Akshata, Bindu, Parayil, Nagappa, Madhu, Bharath, Rose, Sinha, Sanjib, Mathuranath, Pavagada, Taly, Arun

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Genetic Spectrum of Inherited Neuropathies in India von Sharma, Shivani, Govindaraj, Periyasamy, Chickabasaviah, Yasha, Siram, Ramesh, Shroti, Akhilesh, Seshagiri, Doniparthi, Debnath, Monojit, Bindu, Parayil, Taly, Arun, Nagappa, Madhu

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Spectrum and evolution of EEG changes in Anti-NMDAR encephalitis von Viswanathan, Lakshminarayanapuram, Siddappa, Shreedhara, Nagappa, Madhu, Mahadevan, Anita, Duble, Shishir, Bindu, Parayil, Taly, Arun, Sinha, Sanjib

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Palatal Tremor Revisited: Disorder with Nosological Diversity and Etiological Heterogeneity von Nagappa, Madhu, Bindu, Parayil S., Sinha, Sanjib, Bharath, Rose D., Sandhya, Mangalore, Saini, Jitender, Mathuranath, Pavagada S., Taly, Arun B.

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Fatal Morvan Syndrome Associated With Myasthenia Gravis von Nagappa, Madhu, Mahadevan, Anita, Sinha, Sanjib, Bindu, Parayil S, Mathuranath, Pavagada S, Bineesh, Cheminikara, Bharath, Rose D, Taly, Arun B

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Non-Wilsonian hepatolenticular degeneration: Clinical and MRI observations in four families from south India von Nagappa, Madhu, Sinha, Sanjib, Saini, Jitender S, Kallolimath, Pradeep, Singh, Nivedita, Kumar, Arun, Bindu, Parayil S, Taly, Arun B

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Panda with "Bright eyes" in Wilson's disease von Kallollimath, Pradeep, Nagappa, Madhu, Sinha, Sanjib, Saini, Jitender, Bindu, Parayil S, Taly, Arun B

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Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery von Scott, Eric M, Halees, Anason, Itan, Yuval, Spencer, Emily G, He, Yupeng, Azab, Mostafa Abdellateef, Gabriel, Stacey B, Belkadi, Aziz, Boisson, Bertrand, Abel, Laurent, Clark, Andrew G, Alkuraya, Fowzan S, Casanova, Jean-Laurent, Gleeson, Joseph G

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