An insight into the biochemistry of inborn errors of metabolism for a clinical neurologist

por Christopher, Rita, Sankaran, Bindu P.
Publicado 2008

Myasthenia gravis and acetylcholine receptor antibodies: A clinico immunological correlative study on South Indian patients

por Bindu, P. S., Nirmala, M., Patil, S. A., Taly, A. B.
Publicado 2008

Postmastectomy-Postirradiation Atypical Vascular Lesion of the Skin: Report of 2 Cases

por Jayalakshmy, P. S., Sivaram, Aswathy P., Augustine, Joy, Bindu, P.
Publicado 2012

Transition-metal/Lewis acid free synthesis of acyl benzothiophenes via C-C bond forming reaction

por Pal, Sarbani, Khan, Mohammad Ashrafuddin, Bindu, P, Dubey, P K
Publicado 2007

Accidental spinal cord injury during spinal anesthesia: A report

por Netravathi, M., Taly, A. B., Sinha, S., Bindu, P. S., Goel, G.
Publicado 2010

Steroid-responsive encephalopathy in autoimmune thyroiditis: Clinical spectrum and MRI observations in three cases

por Dinkar, K., Sinha, Sanjib, Taly, A. B., Bindu, P. S., Bharath, R. D.
Publicado 2011

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

por Nagappa, Madhu, Taly, Arun B., Mahadevan, Anita, Pooja, M., Bindu, P. S., Chickabasaviah, Y. T., Gayathri, N., Sinha, Sanjib
Publicado 2016

The within-host fitness of HIV-1 increases with age in ART-naïve HIV-1 subtype C infected children

por Nagaraja, Pradeep, Gopalan, Bindu P., D’Souza, Reena R., Sarkar, Debolina, Rajnala, Niharika, Dixit, Narendra M., Shet, Anita
Publicado 2021

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

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

PPA2-associated sudden cardiac death: extending the clinical and allelic spectrum in 20 new families

por Guimier, Anne, Achleitner, Melanie T., Moreau de Bellaing, Anne, Edwards, Matthew, de Pontual, Loïc, Mittal, Kirti, Dunn, Kyla E., Grove, Megan E., Tysoe, Carolyn J., Dimartino, Clémantine, Cameron, Jessie, Kanthi, Anil, Shukla, Anju, van den Broek, Florence, Chatterjee, Diptendu, Alston, Charlotte L., Knowles, Charlotte V., Brett, Laura, Till, Jan A., Homfray, Tessa, French, Paul, Spentzou, Georgia, Elserafy, Noha A., Lichkus, Kate S., Sankaran, Bindu P., Kennedy, Hannah L., George, Peter M., Kidd, Alexa, Wortmann, Saskia B., Fisk, Dianna G., Koopmann, Tamara T., Rafiq, Muhammad A., Merker, Jason D., Parikh, Sumith, Ahimaz, Priyanka, Weintraub, Robert G., Ma, Alan S., Turner, Christian, Ellaway, Carolyn J., Phillips, Liza K., Thorburn, David R., Chung, Wendy K., Kana, Sajel L., Faye-Petersen, Ona M., Thompson, Michelle L., Janin, Alexandre, McLeod, Karen, McGowan, Ruth, McFarland, Robert, Girisha, Katta M., Morris-Rosendahl, Deborah J., Hurst, Anna C. E., Turner, Claire L. S., Hamilton, Robert M., Taylor, Robert W., Bajolle, Fanny, Gordon, Christopher T., Amiel, Jeanne, Mayr, Johannes A., Doudney, Kit
Publicado 2021