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Indian Pediatrics
|
March 28, 2008
Chikungunya infection in neonates
Gouri Rao, Yasmin Zakarya Khan, D S Chitnis
Journal of Indian Association of Pediatric Surgeons
|
July 12, 2017
Early Thoracoscopic Plication of Diaphragm in a Newborn with Brachial Plexus Palsy and Concurrent Phrenic Nerve Palsy
Saurabh Shyam Garge, Gouri Rao Passi, Devendra Ghanekar
Journal of Pediatric Neurosciences
|
December 19, 2022
Case Report of Congenital Kyphoscoliosis with Myotonic Dystrophy Type 1: Perioperative and Anesthetic Considerations
Arpit Agrawal, Tanvi Dhawale, Varinder Kaur, et al.
Indian Pediatrics
|
August 2, 2021
Management of Neurocysticercosis in Children: Association of Child Neurology Consensus Guidelines
Naveen Sankhyan, Razia Adam Kadwa, Mahesh Kamate, et al.
Brain & Development
|
January 3, 2022
Cerebral creatine deficiency disorders - A clinical, genetic and follow up study from India
Gouri Rao Passi, Swati Pandey, Akella Radha Rama Devi, et al.
American Journal of Medical Genetics. Part A
|
July 7, 2020
An Indian child with Coats plus syndrome due to mutations in STN1
Gouri Rao Passi, Uzma Shamim, Surabhi Rathore, et al.
Indian Journal of Community Medicine : Official Publication of Indian Association of Preventive & Social Medicine
|
November 29, 2016
Neonatal Cholestasis - Single Centre Experience in Central India
Mayank Jain, Sagar Adkar, Chandrashekhar Waghmare, et al.
Pediatric Neurology
|
September 18, 2025
Validation and Modified Application of the 2023 International Expert Consensus Criteria for Diagnosing Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Among Children With Acquired Demyelination in Resource-Limited Regions
Vishal Sondhi, Neelu Desai, Lokesh Lingappa, et al.
Acta Neuropathologica
|
December 11, 2019
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases
Elena Perenthaler, Anita Nikoncuk, Soheil Yousefi, et al.
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of 2
Search research articles
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Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Indian Pediatrics
|
March 28, 2008
Chikungunya infection in neonates
Gouri Rao, Yasmin Zakarya Khan, D S Chitnis
Journal of Indian Association of Pediatric Surgeons
|
July 12, 2017
Early Thoracoscopic Plication of Diaphragm in a Newborn with Brachial Plexus Palsy and Concurrent Phrenic Nerve Palsy
Saurabh Shyam Garge, Gouri Rao Passi, Devendra Ghanekar
Journal of Pediatric Neurosciences
|
December 19, 2022
Case Report of Congenital Kyphoscoliosis with Myotonic Dystrophy Type 1: Perioperative and Anesthetic Considerations
Arpit Agrawal, Tanvi Dhawale, Varinder Kaur, et al.
Indian Pediatrics
|
August 2, 2021
Management of Neurocysticercosis in Children: Association of Child Neurology Consensus Guidelines
Naveen Sankhyan, Razia Adam Kadwa, Mahesh Kamate, et al.
Brain & Development
|
January 3, 2022
Cerebral creatine deficiency disorders - A clinical, genetic and follow up study from India
Gouri Rao Passi, Swati Pandey, Akella Radha Rama Devi, et al.
American Journal of Medical Genetics. Part A
|
July 7, 2020
An Indian child with Coats plus syndrome due to mutations in STN1
Gouri Rao Passi, Uzma Shamim, Surabhi Rathore, et al.
Indian Journal of Community Medicine : Official Publication of Indian Association of Preventive & Social Medicine
|
November 29, 2016
Neonatal Cholestasis - Single Centre Experience in Central India
Mayank Jain, Sagar Adkar, Chandrashekhar Waghmare, et al.
Pediatric Neurology
|
September 18, 2025
Validation and Modified Application of the 2023 International Expert Consensus Criteria for Diagnosing Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Among Children With Acquired Demyelination in Resource-Limited Regions
Vishal Sondhi, Neelu Desai, Lokesh Lingappa, et al.
Acta Neuropathologica
|
December 11, 2019
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases
Elena Perenthaler, Anita Nikoncuk, Soheil Yousefi, et al.
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of 2