Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Shankar Tejwani"'
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 2, Pp 229-234 (2022)
Background: Recanalization rates in cerebral venous thrombosis (CVT) and its effect on neurological outcome have been debated worldwide and are inadequately addressed in studies from India. Our objective was to study the clinical profile of CVT and d
Externí odkaz:
https://doaj.org/article/004c80d9c25d439eba27c4b283a714dd
Autor:
Rajendra Singh Jain, Deepak Jain, Sourabh Murarka, Arvind Vyas, Bhawna Sharma, Trilochan Srivastava, Kamlesh Kumar, Yavnika Jain, Kavya Rao, Jitesh Agrawal, Shankar Tejwani
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 2, Pp 246-255 (2022)
Background: More and more cases of myelin oligodendrocyte glycoprotein (MOG) antibody are being diagnosed with the availability of laboratory tests helping us to know the differing patterns from AQP-4 antibody disease and we need to understand the na
Externí odkaz:
https://doaj.org/article/099209fc383b42fcbcc401c06a4aef17
Autor:
Trilochan Srivastava, Raghavendra Bakki Sannegowda, R. S Mittal, R. S Jain, Shankar Tejwani, Rahul Jain
Publikováno v:
Annals of Indian Academy of Neurology, Vol 17, Iss 2, Pp 182-186 (2014)
Aim: Moyamoya disease (MMD) is a slowly progressive bilateral stenocclusive process of the distal internal carotid and proximal portions of the anterior and middle cerebral arteries and the formation of an abnormal vascular network at the base of the
Externí odkaz:
https://doaj.org/article/315509738eb14e7a9d9c239d4b9bf73a
Autor:
RajendraSingh Jain, Deepak Jain, Sourabh Murarka, Arvind Vyas, Bhawna Sharma, Trilochan Srivastava, Kamlesh Kumar, Yavnika Jain, Kavya Rao, Jitesh Agrawal, Shankar Tejwani
Publikováno v:
Annals of Indian Academy of Neurology. 25(2)
More and more cases of myelin oligodendrocyte glycoprotein (MOG) antibody are being diagnosed with the availability of laboratory tests helping us to know the differing patterns from AQP-4 antibody disease and we need to understand the natural course
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23f72802dd40fe072927ed4932b5e171
https://pubmed.ncbi.nlm.nih.gov/35693673
https://pubmed.ncbi.nlm.nih.gov/35693673
Publikováno v:
Annals of Indian Academy of Neurology. 25(2)
Recanalization rates in cerebral venous thrombosis (CVT) and its effect on neurological outcome have been debated worldwide and are inadequately addressed in studies from India. Our objective was to study the clinical profile of CVT and determine rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6919bf2a3532efa2081105ca85805120
https://pubmed.ncbi.nlm.nih.gov/35693659
https://pubmed.ncbi.nlm.nih.gov/35693659
Publikováno v:
Journal of Medical Imaging and Radiation Sciences. 47:113-115
Multiple-system atrophy (MSA) is a progressive neurodegenerative disorder. It is characterized by dysfunction of multiple systems including autonomic, extrapyramidal, pyramidal and cerebellar. Pontine hot-cross bun (HCB) sign in MSA is a well-documen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94e21db482e5d3295af7e457d6ca8c10
https://doi.org/10.1016/j.jmir.2015.10.001
https://doi.org/10.1016/j.jmir.2015.10.001
Autor:
Raghavendra Bakki Sannegowda, Rahul Jain, Shankar Tejwani, Trilochan Srivastava, R. S Mittal, Rajendra Singh Jain
Publikováno v:
Annals of Indian Academy of Neurology, Vol 17, Iss 2, Pp 182-186 (2014)
Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology
Aim: Moyamoya disease (MMD) is a slowly progressive bilateral stenocclusive process of the distal internal carotid and proximal portions of the anterior and middle cerebral arteries and the formation of an abnormal vascular network at the base of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f9ecb6b1b5963609237a1c3e23749c3
http://www.annalsofian.org/article.asp?issn=0972-2327
http://www.annalsofian.org/article.asp?issn=0972-2327
Publikováno v:
Oxford Medical Case Reports
Longitudinally extensive transverse myelitis (LETM) is an unusual manifestation of systemic malignancy. It has been mainly reported with lung cancers and lymphoproliferative malignancy. LETM in systemic malignancy can be caused by either intramedulla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f71b0172cdf98501ffc40fb82dc863e1
https://doi.org/10.1093/omcr/omv011
https://doi.org/10.1093/omcr/omv011
Publikováno v:
Clinical neurology and neurosurgery. 148
Objectives To evaluate the demographic profile, clinical presentations, laboratory parameters and etiologies of longitudinally extensive transverse myelitis (LETM) patients in Indian population. Patients and methods LETM is characterized by contiguou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f23fa1bb59ab00c6651032ad3b124381
https://pubmed.ncbi.nlm.nih.gov/27348743
https://pubmed.ncbi.nlm.nih.gov/27348743
Publikováno v:
SpringerPlus
Introduction Friedreich’s ataxia (FRDA) is the most common autosomal recessive inherited ataxia. It is characterized by onset before the age of 25 year, progressive limb and truncal ataxia, lower limb areflexia, extensor plantars, dysarthria and im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49014824f6b30f32d5daf613f6a33c6f
https://doi.org/10.1186/s40064-015-1121-5
https://doi.org/10.1186/s40064-015-1121-5