Hasil Pencarian - Biswaroop Chakrabarty
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Management of wilson disease: The quest continues oleh Gautam Kamila, Biswaroop Chakrabarty
Diterbitkan 2022-01-01
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DIAGNOSTIC AND TREATMENT OPTIONS IN AUTISTIC SPECTRUM DIDORDERS – AN OVERVIEW oleh Sheffali GULATI, Biswaroop CHAKRABARTY
Diterbitkan 2014-03-01
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A genetically proven case of Pelizaeus-Merzbacher disease: Clinicoradiological clues oleh Lokesh Saini, Biswaroop Chakrabarty, Atin Kumar, Sheffali Gulati
Diterbitkan 2016-01-01
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Moyamoya disease; suspecting on conventional MRI brain without angiography oleh Anil Israni, Biswaroop Chakrabarty, Sheffali Gulati, Atin Kumar
Diterbitkan 2015-01-01
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Recurrent headache in a five year old boy oleh Lokesh Saini, Ranjith M Kumar, Biswaroop Chakrabarty, Sheffali Gulati
Diterbitkan 2016-01-01
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A case of congenital myopathy masquerading as paroxysmal dyskinesia oleh Harsh Patel, Biswaroop Chakrabarty, Sheffali Gulati, Mehar C Sharma, Lokesh Saini
Diterbitkan 2014-01-01
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Acquired demyelinating disorders of central nervous system: A pediatric cohort oleh Sheffali Gulati, Biswaroop Chakrabarty, Atin Kumar, Puneet Jain, Harsh Patel, Lokesh Saini
Diterbitkan 2015-01-01
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Bilateral facial palsy in lymphomatous meningitis oleh Priyanka Madaan, Prashant Jauhari, Biswaroop Chakrabarty, Atin Kumar, Sarthak Tripathy, Nishikant Damle, Sheffali Gulati
Diterbitkan 2021-01-01
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Development of All India Institute of Medical Sciences-Modified International Clinical Epidemiology Network Diagnostic Instrument for Neuromotor Impairments in Children Aged 1 Mont... oleh Sheffali Gulati, Harsh Patel, Biswaroop Chakrabarty, Rachana Dubey, N. K. Arora, R. M. Pandey, Vinod K. Paul, Konanki Ramesh, Vyshakh Anand, Ankit Meena
Diterbitkan 2017-11-01
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Genetically confirmed first Indian dentatorubral–pallidoluysian atrophy kindred: A case report oleh Pooja Sharma, Raja G Shaikh, Uzma Shamim, Vaishakh Anand, Biswaroop Chakrabarty, Sheffali Gulati, Akhilesh K Sonakar, Istaq Ahmad, Ajay Garg, Achal K Srivastava, Mohammed Faruq
Diterbitkan 2020-01-01
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