Does Neonatal Sepsis Independently Increase Neurodevelopmental Impairment?

por Bhat, Vishwanath, Bhandari, Vineet
Publicado 2022

Gastroschisis: A State-of-the-Art Review

por Bhat, Vishwanath, Moront, Matthew, Bhandari, Vineet
Publicado 2020

Whole exome sequencing identifies a novel splice-site mutation in ADAMTS17 in an Indian family with Weill-Marchesani syndrome

por Shah, Mohd Hussain, Bhat, Vishwanath, Shetty, Jyoti S., Kumar, Arun
Publicado 2014

Evidence that TSC2 acts as a transcription factor and binds to and represses the promoter of Epiregulin

por Pradhan, Shalmali Avinash, Rather, Mohammad Iqbal, Tiwari, Ankana, Bhat, Vishwanath Kumble, Kumar, Arun
Publicado 2014

A short‐term in vivo model for Merkel Cell Carcinoma

por Bhat, Vishwanath Kumble, Krump, Corinna, Bernhart, Eva, Becker, Jürgen C., Sattler, Wolfgang, Ghaffari‐Tabrizi‐Wizsy, Nassim
Publicado 2018

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

por 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
Publicado 2019

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 2016