Ministry of Education
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Dr Shalesh Rohatgi

vidwan id: 135221
Male

Professor, Neurology (Medical College, Hospital and Research Centre)
Dr D Y Patil Vidyapeeth, Pune

Orchid Icon 0000-0001-6652-5342 Google Scholar Icon vnRmXFwAAAAJ

Expertise

  • Clinical Neurology

Publications

Total Articles 29
Books 0
Proceedings 0

Publications

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Scopus

Citations 6
h-index 1

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Bio

Clinical Neurology

Personal Details

  • Male
  • Professor , Dr D Y Patil Vidyapeeth, Pune
  • Dr D Y Patil Vidyapeeth, Sant Tukaram Nagar, Pimpri
DM
Other Institute 1994
Professor Nov 2016 – Present
Dr D Y Patil Vidyapeeth, Pune | Neurology (Medical College, Hospital and Research Centre)

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Co-Authors (3)

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Satish P

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Dr D Y Patil Vidyapeeth, Pune

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Scholarly Work

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Scholarly Publications

A Study of Clinical, Radiological \& Thrombophilia Profile in Cerebral Venous Thrombosis

Open Access
inproceedings
Year: 2020. Volume: 27 , Pages: 559--559 .
Authors: Dave, D and Khan, FM and Rohatgi, S and Nirhale, S and Rao, P and Naphade, P

Atypical multiple sclerosis with antibody to MOG

Open Access
Article
Neurology India. Year: 2020. Volume: 68 , Issue: 5 , Pages: 1235-1237 .
Authors: Dave D.;Khan F.;Rohatgi S.;Nirhale S.;Rao P.;Naphade P.
DOI 10.4103/0028-3886.299157
5

Myelin Oligodendrocyte Glycoprotein Antibody-associated Neuromyelitis optica spectrum disorders (NMOSD)

Open Access
inproceedings
Year: 2020. Volume: 27 , Pages: 924--924 .
Authors: Khan, FM and Dave, D and Nirhale, S and Rohatgi, S and Rao, P and Naphade, P

A study of clinical, radiological and thrombophilia profile in cerebral venous sinus thrombosis

Open Access
article
Journal of the Neurological Sciences. Year: 2019. Volume: 405 , Pages: 172--173 .
Authors: Dave, D and Khan, F and Rohatgi, S and Nirhale, S and Rao, P and Naphade, P

Charot-marie-tooth disease type 2O: First case report from India

Open Access
article
Journal of the Neurological Sciences. Year: 2019. Volume: 405 , Pages: 89 .
Authors: Khan, FMA and Dave, D and Rohatgi, S and Nirhale, S and Rao, P and Naphade, P

Study of spectrum of inflammatory demyelinating disease of central nervous system

Open Access
article
Journal of the Neurological Sciences. Year: 2019. Volume: 405 , Pages: 324--325 .
Authors: Khan, FMA and Dave, D and Rohatgi, S and Nirhale, S and Rao, P and Naphade, P

Severe 5, 10-Methylenetetrahydrofolate reductase deficiency: A rare, treatable cause of complicated hereditary spastic paraplegia

Open Access
article
Journal of the Neurological Sciences. Year: 2019. Volume: 405 , Pages: 89 .
Authors: Dave, D and Khan, F and Rohatgi, S and Nirhale, S and Rao, P and Naphade, P

MTHFR mutation-A rare potentially treatable cause of adult-onset complicated hereditary spastic paraplegia

Open Access
article
Journal of the Neurological Sciences. Year: 2019. Volume: 405 , Pages: 325 .
Authors: Khan, FMA and Dave, D and Rohatgi, S and Nirhale, S and Rao, P and Naphade, P