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Annals of Indian Academy of Neurology
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March 18, 2024
Adult-onset Leukodystrophy due to <i>TMEM63A</i> Variant Presenting with Rapidly Progressive Dementia with Parkinsonism
Divyani Garg, Ayush Agarwal, Ajay Garg, et al.
Stem Cell Research
|
August 10, 2024
Generation and characterization of human-derived induced pluripotent stem cell line (IGIBi010-A) from a patient with neurodegenerative disease phenotype carrying mutation in SQSTM1/p62 gene
Istaq Ahmad, Himanshi Kapoor, Achal Kumar Srivastava, et al.
Stem Cell Research
|
February 17, 2024
Generation of two human induced pluripotent stem cell lines, IGIBi012-A and IGIBi013-A from Friedreich's ataxia (FRDA) patients with homozygous GAA repeat expansion in FXN gene
Istaq Ahmad, Himanshi Kapoor, Achal Kumar Srivastava, et al.
Nepalese Journal of Ophthalmology : a Biannual Peer-Reviewed Academic Journal of the Nepal Ophthalmic Society : NEPJOPH
|
September 17, 2019
An Unusual case of neurocysticercosis leading to blindness in a young Indian male
Meenakshi Wadhwani, Ananya Panda, Rajpal Vohra, et al.
Stem Cell Research
|
December 23, 2023
Generation and characterization of two human iPSC lines, IGIBi014-A and IGIBi015-A, from Friedreich's ataxia (FRDA) patients with pathogenic (GAA/TTC)n repeat expansion in first intron of the Frataxin (FXN) gene
Istaq Ahmad, Himanshi Kapoor, Achal Kumar Srivastava, et al.
Journal of Movement Disorders
|
February 29, 2024
The First Indian Patient With Benign Hereditary Chorea due to a De Novo Mutation in the NKX2-1 Gene
Divyani Garg, Ayush Agarwal, Mohammed Faruq, et al.
Acta Neurologica Belgica
|
July 24, 2025
Neck muscle hypertrophy in paramyotonia congenita caused by a missense variant in the SCN4A gene (p.Val445Met)
Farsana Mustafa, Divyani Garg, Ayush Agarwal, et al.
Acta Neurologica Belgica
|
December 5, 2024
Examination of the autonomic nervous system at the bedside
Baikuntha Panigrahi, Achal Kumar Srivastava, Divyani Garg, et al.
Neurology
|
April 5, 2022
Teaching NeuroImage: Drug Refractory Epilepsy With Developmental Dysarthria Due to Bilateral Perisylvian Polymicrogyria
Manda Goveen, Ayush Agarwal, Ajay Garg, et al.
Annals of Indian Academy of Neurology
|
August 8, 2022
Genetic Testing in Neurology: What Every Neurologist Must Know
Manish Salunkhe, Ayush Agarwal, Mohd Faruq, et al.
Page
of 19
Search research articles
Search
Showing results (11-20 of 189) with videos related to
Sort By:
Page
of 19
Annals of Indian Academy of Neurology
|
March 18, 2024
Adult-onset Leukodystrophy due to <i>TMEM63A</i> Variant Presenting with Rapidly Progressive Dementia with Parkinsonism
Divyani Garg, Ayush Agarwal, Ajay Garg, et al.
Stem Cell Research
|
August 10, 2024
Generation and characterization of human-derived induced pluripotent stem cell line (IGIBi010-A) from a patient with neurodegenerative disease phenotype carrying mutation in SQSTM1/p62 gene
Istaq Ahmad, Himanshi Kapoor, Achal Kumar Srivastava, et al.
Stem Cell Research
|
February 17, 2024
Generation of two human induced pluripotent stem cell lines, IGIBi012-A and IGIBi013-A from Friedreich's ataxia (FRDA) patients with homozygous GAA repeat expansion in FXN gene
Istaq Ahmad, Himanshi Kapoor, Achal Kumar Srivastava, et al.
Nepalese Journal of Ophthalmology : a Biannual Peer-Reviewed Academic Journal of the Nepal Ophthalmic Society : NEPJOPH
|
September 17, 2019
An Unusual case of neurocysticercosis leading to blindness in a young Indian male
Meenakshi Wadhwani, Ananya Panda, Rajpal Vohra, et al.
Stem Cell Research
|
December 23, 2023
Generation and characterization of two human iPSC lines, IGIBi014-A and IGIBi015-A, from Friedreich's ataxia (FRDA) patients with pathogenic (GAA/TTC)n repeat expansion in first intron of the Frataxin (FXN) gene
Istaq Ahmad, Himanshi Kapoor, Achal Kumar Srivastava, et al.
Journal of Movement Disorders
|
February 29, 2024
The First Indian Patient With Benign Hereditary Chorea due to a De Novo Mutation in the NKX2-1 Gene
Divyani Garg, Ayush Agarwal, Mohammed Faruq, et al.
Acta Neurologica Belgica
|
July 24, 2025
Neck muscle hypertrophy in paramyotonia congenita caused by a missense variant in the SCN4A gene (p.Val445Met)
Farsana Mustafa, Divyani Garg, Ayush Agarwal, et al.
Acta Neurologica Belgica
|
December 5, 2024
Examination of the autonomic nervous system at the bedside
Baikuntha Panigrahi, Achal Kumar Srivastava, Divyani Garg, et al.
Neurology
|
April 5, 2022
Teaching NeuroImage: Drug Refractory Epilepsy With Developmental Dysarthria Due to Bilateral Perisylvian Polymicrogyria
Manda Goveen, Ayush Agarwal, Ajay Garg, et al.
Annals of Indian Academy of Neurology
|
August 8, 2022
Genetic Testing in Neurology: What Every Neurologist Must Know
Manish Salunkhe, Ayush Agarwal, Mohd Faruq, et al.
Page
of 19