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Achal Kumar Srivastava

Showing results (1-10 of 175) with videos related to

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Neurology India|July 25, 2018
Not to forget: Seizures in acute strokeAchal Kumar Srivastava, Anand R Warrier
Postgraduate Medical Journal|May 27, 2021
Symmetrical white matter lesions in a patient with systemic lupus erythematosusPedapati Radhakrishna, Animesh Das, Achal Kumar Srivastava
Neurology India|March 13, 2019
Primary angiitis of the central nervous system - An Indian experienceAchal Kumar Srivastava, Pradeep K Reddy Sura
Movement Disorders Clinical Practice|April 5, 2024
Sensory Trick in Cervical Dystonia with Subacute Sclerosing PanencephalitisDivyani Garg, Ayush Agarwal, Achal Kumar Srivastava
Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2025
Focused Ultrasound versus Radiofrequency Ablation for Pallidothalamic Tractotomy: Looking beyond the Bilateral EffectsArchita Makharia, Divya M Radhakrishnan, Achal Kumar Srivastava
Journal of Clinical Neuromuscular Disease|March 5, 2024
Flail Leg Phenotype in Familial Amyotrophic Lateral Sclerosis: Think of a Cause With Something to OfferSaranya B Gomathy, Animesh Das, Achal Kumar Srivastava
Movement Disorders Clinical Practice|October 27, 2018
Spinocerebellar Ataxia 2 and 12 Mutations in an Indian Family with Cerebellar Ataxia and Slow SaccadesMohammed Faruq, Sunil Shakya, Ajay Garg, et al.
Annals of Indian Academy of Neurology|March 18, 2024
Adult-onset Leukodystrophy due to <i>TMEM63A</i> Variant Presenting with Rapidly Progressive Dementia with ParkinsonismDivyani 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 geneIstaq 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 geneIstaq Ahmad, Himanshi Kapoor, Achal Kumar Srivastava, et al.
Pageof 18

Showing results (1-10 of 175) with videos related to

Sort By:
Pageof 18
Neurology India|July 25, 2018
Not to forget: Seizures in acute strokeAchal Kumar Srivastava, Anand R Warrier
Postgraduate Medical Journal|May 27, 2021
Symmetrical white matter lesions in a patient with systemic lupus erythematosusPedapati Radhakrishna, Animesh Das, Achal Kumar Srivastava
Neurology India|March 13, 2019
Primary angiitis of the central nervous system - An Indian experienceAchal Kumar Srivastava, Pradeep K Reddy Sura
Movement Disorders Clinical Practice|April 5, 2024
Sensory Trick in Cervical Dystonia with Subacute Sclerosing PanencephalitisDivyani Garg, Ayush Agarwal, Achal Kumar Srivastava
Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2025
Focused Ultrasound versus Radiofrequency Ablation for Pallidothalamic Tractotomy: Looking beyond the Bilateral EffectsArchita Makharia, Divya M Radhakrishnan, Achal Kumar Srivastava
Journal of Clinical Neuromuscular Disease|March 5, 2024
Flail Leg Phenotype in Familial Amyotrophic Lateral Sclerosis: Think of a Cause With Something to OfferSaranya B Gomathy, Animesh Das, Achal Kumar Srivastava
Movement Disorders Clinical Practice|October 27, 2018
Spinocerebellar Ataxia 2 and 12 Mutations in an Indian Family with Cerebellar Ataxia and Slow SaccadesMohammed Faruq, Sunil Shakya, Ajay Garg, et al.
Annals of Indian Academy of Neurology|March 18, 2024
Adult-onset Leukodystrophy due to <i>TMEM63A</i> Variant Presenting with Rapidly Progressive Dementia with ParkinsonismDivyani 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 geneIstaq 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 geneIstaq Ahmad, Himanshi Kapoor, Achal Kumar Srivastava, et al.
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