Hasil Pencarian - Mainak Bardhan
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Rise in cholera amid COVID-19: Spotlight on Pakistan and Bangladesh oleh Syed Hassan Ahmed, Taha Gul Shaikh, Summaiyya Waseem, Mohammad Mehedi Hasan, Mainak Bardhan, Nobendu Mukerjee
Diterbitkan 2022-09-01Dapatkan teks lengkap
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Self-medication prevalence and associated factors among adult population in Northern India: A community-based cross-sectional study oleh Khushboo Juneja, Ambren Chauhan, Tuhina Shree, Priyanka Roy, Mainak Bardhan, Absar Ahmad, Amit Singh Pawaiya, Ayush Anand
Diterbitkan 2024-03-01Dapatkan teks lengkap
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Vaccine apartheid: the separation of the world’s poorest and most vulnerable and the birth of Omicron oleh Sakshi Prasad, Abia Shahid, Edzel Lorraine F. Co, Govinda Khatri, Huzaifa Ahmad Cheema, Ian Christopher N. Rocha, Mainak Bardhan, Mohammad Mehedi Hasan
Diterbitkan 2022-06-01Dapatkan teks lengkap
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Exploring Health Care Disparities in Genetic Testing and Research for Hereditary Cardiomyopathy: Current State and Future Perspectives oleh Helen Huang, Jay Verma, Valerie Mok, Hareesha R. Bharadwaj, Maen M. Alrawashdeh, Adarsh Aratikatla, Sourav Sudan, Suprateeka Talukder, Minatoullah Habaka, Gary Tse, Mainak Bardhan
Diterbitkan 2024-01-01Dapatkan teks lengkap
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Expanding the Phenotypic Spectrum of <i>ECEL1</i>-Associated Distal Arthrogryposis oleh Akshata Huddar, Kiran Polavarapu, Veeramani Preethish-Kumar, Mainak Bardhan, Gopikrishnan Unnikrishnan, Saraswati Nashi, Seena Vengalil, Priyanka Priyadarshini, Karthik Kulanthaivelu, Gautham Arunachal, Hanns Lochmüller, Atchayaram Nalini
Diterbitkan 2021-10-01Dapatkan teks lengkap
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Identification of a Novel Intronic Mutation in <i>VMA21</i> Associated with a Classical Form of X-Linked Myopathy with Autophagy oleh Mainak Bardhan, Kiran Polavarapu, Dipti Baskar, Veeramani Preethish-Kumar, Seena Vengalil, Saraswati Nashi, Valakunja H. Ganaraja, Dinesh Sharma, Karthik Kulanthaivelu, B.N. Nandeesh, Atchayaram Nalini
Diterbitkan 2024-06-01Dapatkan teks lengkap
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Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathy oleh Shamita Sanga, Sudipta Chakraborty, Mainak Bardhan, Kiran Polavarapu, Veeramani Preethish Kumar, Chandrika Bhattacharya, Saraswati Nashi, Seena Vengalil, Thenral S. Geetha, Vedam Ramprasad, Atchayaram Nalini, Analabha Basu, Moulinath Acharya
Diterbitkan 2023-09-01Dapatkan teks lengkap
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Mutation spectrum of primary lipid storage myopathies oleh Seena Vengalil, Kiran Polavarapu, Veeramani Preethish-Kumar, Saraswati Nashi, Gautham Arunachal, Tanushree Chawla, Mainak Bardhan, Dhaarini Mohan, Rita Christopher, Nandeesh Bevinahalli, Karthik Kulanthaivelu, Ichizo Nishino, Mohammad Faruq, Atchayaram Nalini
Diterbitkan 2022-01-01Dapatkan teks lengkap
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Phenotypic Heterogeneity in ORAI-1-Associated Congenital Myopathy oleh Dipti Baskar, Seena Vengalil, Kiran Polavarapu, Veeramani Preethish-Kumar, Gautham Arunachal, Ramya Sukrutha, Mainak Bardhan, Akshata Huddar, Gopikrishnan Unnikrishnan, Girish Baburao Kulkarni, Yasha T. Chickabasaviah, Rashmi Santhosh Kumar, Atchayaram Nalini, Saraswati Nashi
Diterbitkan 2024-12-01Dapatkan teks lengkap
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PET-MRI in idiopathic inflammatory myositis: a comparative study of clinical and immunological markers with imaging findings oleh Manu Santhappan Girija, Ravindu Tiwari, Seena Vengalil, Saraswati Nashi, Veeramani Preethish-Kumar, Kiran Polavarapu, Karthik Kulanthaivelu, Arpana Arbind, Mainak Bardhan, Akshata Huddar, Gopikrishnan Unnikrishnan, Valasani Ravi Kiran, Tanushree Chawla, Bevinahalli Nandeesh, Chandana Nagaraj, Atchayaram Nalini
Diterbitkan 2022-10-01Dapatkan teks lengkap
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Disease Progression and Mutation Pattern in a Large Cohort of LGMD R1/LGMD 2A Patients from India oleh Valakunja H. Ganaraja, Kiran Polavarapu, Mainak Bardhan, Veeramani Preethish-Kumar, Shingavi Leena, Ram M. Anjanappa, Seena Vengalil, Saraswati Nashi, Gautham Arunachal, Swetha Gunasekaran, Dhaarini Mohan, Sanita Raju, Gopikrishnan Unnikrishnan, Akshata Huddar, Valasani Ravi-Kiran, Priya T. Thomas, Atchayaram Nalini
Diterbitkan 2022-03-01Dapatkan teks lengkap
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Qualitative and quantitative electrocardiogram parameters in a large cohort of children with duchenne muscle dystrophy in comparison with age-matched healthy subjects: A study from... oleh Manu S Girija, Deepak Menon, Kiran Polavarapu, Veeramani Preethish-Kumar, Seena Vengalil, Saraswati Nashi, Madassu Keertipriya, Mainak Bardhan, Priya T Thomas, Valasani R Kiran, Vikas Nishadham, Arun Sadasivan, Akshata Huddar, Gopi K Unnikrishnan, Ganagarajan Inbaraj, Arjun Krishnamurthy, Boris W Kramer, Talakad N Sathyaprabha, Atchayaram Nalini
Diterbitkan 2024-01-01Dapatkan teks lengkap
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TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease oleh Lindsey Van Haute, Emily O’Connor, Héctor Díaz-Maldonado, Benjamin Munro, Kiran Polavarapu, Daniella H. Hock, Gautham Arunachal, Alkyoni Athanasiou-Fragkouli, Mainak Bardhan, Magalie Barth, Dominique Bonneau, Nicola Brunetti-Pierri, Gerarda Cappuccio, Nikeisha J. Caruana, Natalia Dominik, Himanshu Goel, Guy Helman, Henry Houlden, Guy Lenaers, Karine Mention, David Murphy, Bevinahalli Nandeesh, Catarina Olimpio, Christopher A. Powell, Veeramani Preethish-Kumar, Vincent Procaccio, Rocio Rius, Pedro Rebelo-Guiomar, Cas Simons, Seena Vengalil, Maha S. Zaki, Alban Ziegler, David R. Thorburn, David A. Stroud, Reza Maroofian, John Christodoulou, Claes Gustafsson, Atchayaram Nalini, Hanns Lochmüller, Michal Minczuk, Rita Horvath
Diterbitkan 2023-02-01Dapatkan teks lengkap
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