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Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Ravouf Asimi

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Neurology India|March 5, 2024

Cerebrotendinous Xanthomatosis, a Treatable Disorder Often Missed: Case Series of Three Patients Confirmed by Genetic TestingArjimand Yaqoob, Waseem R Dar, Adnan Raina, et al.

Surgical Neurology International|March 23, 2012

Decompressive hemicraniectomy in supra-tentorial malignant infarctsFurqan A Nizami, Altaf U Ramzan, Abrar A Wani, et al.

Journal of Family Medicine and Primary Care|November 17, 2022

Miller Fisher syndrome associated with COVID 19Arjimand Yaqoob, Waseem Dar, Zubair Khuja, et al.

Annals of Indian Academy of Neurology|March 25, 2016

Association of ACE Gene I/D polymorphism with migraine in Kashmiri populationIrfan Yousuf Wani, Saleem Sheikh, Zafar Amin Shah, et al.

Gene|February 8, 2022

Interleukin 32 gene promoter polymorphism: A genetic risk factor for multiple sclerosis in Kashmiri populationZahoor Parray, Mahrukh H Zargar, Ravouf Asimi, et al.

The Lancet Regional Health. Southeast Asia|April 21, 2026

Patient profiles and disease characteristics of the IMSRN cohort: a multicentre study (2021-2025)Rohit Bhatia, Dheeraj Khurana, Madakasira Vasantha Padma Srivastava, et al.

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Search research articles

Showing results (11-20 of 16) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 16 results.

Neurology India|March 5, 2024

Cerebrotendinous Xanthomatosis, a Treatable Disorder Often Missed: Case Series of Three Patients Confirmed by Genetic TestingArjimand Yaqoob, Waseem R Dar, Adnan Raina, et al.

Surgical Neurology International|March 23, 2012

Decompressive hemicraniectomy in supra-tentorial malignant infarctsFurqan A Nizami, Altaf U Ramzan, Abrar A Wani, et al.

Journal of Family Medicine and Primary Care|November 17, 2022

Miller Fisher syndrome associated with COVID 19Arjimand Yaqoob, Waseem Dar, Zubair Khuja, et al.

Annals of Indian Academy of Neurology|March 25, 2016

Association of ACE Gene I/D polymorphism with migraine in Kashmiri populationIrfan Yousuf Wani, Saleem Sheikh, Zafar Amin Shah, et al.

Gene|February 8, 2022

Interleukin 32 gene promoter polymorphism: A genetic risk factor for multiple sclerosis in Kashmiri populationZahoor Parray, Mahrukh H Zargar, Ravouf Asimi, et al.

The Lancet Regional Health. Southeast Asia|April 21, 2026

Patient profiles and disease characteristics of the IMSRN cohort: a multicentre study (2021-2025)Rohit Bhatia, Dheeraj Khurana, Madakasira Vasantha Padma Srivastava, et al.

Pageof 2