English

    Fellowship & Membership

  • International Movement Disorders.
  • Movement disorders society of India.
  • American Academy of Neurology.
  • The Indian Academy of Neurology.
  • Field of Expertise

  • Neurology
  • Pediatric Neurology
  • Stroke
  • Epilepsy
  • Movement Disorders
  • Cognitive Disorders
  • Neuroimmunology
  • Languages Spoken

  • English
  • Telugu
  • Hindi
  • Kannada
  • Awards & Achievements

  • Poster presentation at International Pediatric Neurology conference Mumbai and Neuropedicon 2018 (Topic: Evaluation of hyperandrogenism in children with Autism spectrum disorder and age- sex-matched controls).
  • Poster presentation in Association of Child Neurology (AOCN) 2020 (Topic: CSF1R mutation - rare childhood presentation of an autosomal dominant microgliopathy).
  • Second prize in Quiz conducted at AOCN 2020.
  • First Prize for Poster presentation at MS conference, Bengaluru 2020 (Topic: Aquaporin antibody associated myelitis mimicking as spinal cord tumor – Case series).
  • Poster presentation at MS conference, Bengaluru 2020 (Topic: Sinus Bradycardia as an unreported side effect of Alemtuzumab infusion in MS).
  • Poster presentation at MDSI 2020 (Topic- Episodic ataxia- is it always genetic?).
  • First prize in Torrent Young Scholar Award 2022 (TYSA 2022).
  • Platform presentation in MDSI 2022 (Topic – Clinical, radiological, the genetic profile of a large series of patients with Neuronal Brain Iron accumulation [NBIA] spectrum disorders – 116 cases).
  • Guided poster presentation at international movement disorder society conference, Madrid 2022 (Case series of patients with Neuronal Brain Iron accumulation (NBIA) spectrum disorders).
  • Dr. Anisya Vasanth Memorial award for the best outgoing resident in DM neurology, NIMHANS 2022.
  • Talks & Publications

  • Sriram Neeharika, Madaan P, Malhi P, Sachdeva N, Negi S, Das J, et al. Evaluation of yperandrogenism in Children with Autism Spectrum Disorder. Indian J Pediatr. 2022 Jul;89(7):717–9.
  • Sriram Neeharika, Padmanabha H, Chandra S, Mahale R, Nandeesh B, Bhat M, et al. CSF1R related leukoencephalopathy - Rare childhood presentation of an autosomal dominant microgliopathy! Ann Indian Acad Neurol. 2021;0(0):0.
  • Sriram Neeharika, Srinivas D, Mahadevan A, Netravathi M. Unravelling Diagnostic Dilemma: AQP4-Positive Transverse Myelitis Mimics Spinal Intramedullary Tumor. Ann Indian Acad Neurol. 2021 Jun;24(3):436–9.
  • Shah R, Mahale R, Babu K, Shah D, Vincent M, Nanda S, Sriram Neeharika et al. Granulomatous panuveitis in multiple sclerosis: A rare occurrence. Ann Indian Acad Neurol. 2022;0(0):0.
  • Dr. Snigdha Bellapukonda, Dr. Vikas Kumar, Dr. Rajeev Chauhan, Dr. Sunder Lal Negi, Dr. Neeharika Sriram, et al. Seizures in a Child Sedated with Ketamine: A Rare Presentation. J Med Sci Clin Resp. 2019 Mar 18 [cited 2022 Jul 4];7(3).
  • Kumari, R., Holla, V.V., Phulpagar, P., Sriram, N., Hegde, A.G., Vengalil, S., Kamble, N., Saini, J., Yadav, R., Pal, P.K. and Muthusamy, B. (2022), Whole exome sequencing and transcript analysis discover a novel pathogenic splice site mutation in DCAF17 gene underlying Woodhouse-Sakati syndrome. J Neuroendocrinol. Accepted Author Manuscript e13185. https://doi.org/10.1111/jne.13185.
  • "A rare case of ophthalmoplegia with ataxia in genetically proven abetalipoproteinemia" by Gurram, Sandeep; Holla, Vikram; Sharma, Praveen; Phulpagar, Prashant; Jha, Shreyashi; Sriram, Neeharika; Mallitha, S; Kamble, Nitish; Netravathi, M; Yadav, Ravi; Muthusamy, Babylakshmi; Pal, Pramod. Movement Disorders Clinical Practice.

    Languages Spoken

  • English
  • Telugu
  • Hindi
  • Kannada
  • Fellowship & Membership

  • International Movement Disorders.
  • Movement disorders society of India.
  • American Academy of Neurology.
  • The Indian Academy of Neurology.
  • Field of Expertise

  • Neurology
  • Pediatric Neurology
  • Stroke
  • Epilepsy
  • Movement Disorders
  • Cognitive Disorders
  • Neuroimmunology
  • Awards & Achievements

  • Poster presentation at International Pediatric Neurology conference Mumbai and Neuropedicon 2018 (Topic: Evaluation of hyperandrogenism in children with Autism spectrum disorder and age- sex-matched controls).
  • Poster presentation in Association of Child Neurology (AOCN) 2020 (Topic: CSF1R mutation - rare childhood presentation of an autosomal dominant microgliopathy).
  • Second prize in Quiz conducted at AOCN 2020.
  • First Prize for Poster presentation at MS conference, Bengaluru 2020 (Topic: Aquaporin antibody associated myelitis mimicking as spinal cord tumor – Case series).
  • Poster presentation at MS conference, Bengaluru 2020 (Topic: Sinus Bradycardia as an unreported side effect of Alemtuzumab infusion in MS).
  • Poster presentation at MDSI 2020 (Topic- Episodic ataxia- is it always genetic?).
  • First prize in Torrent Young Scholar Award 2022 (TYSA 2022).
  • Platform presentation in MDSI 2022 (Topic – Clinical, radiological, the genetic profile of a large series of patients with Neuronal Brain Iron accumulation [NBIA] spectrum disorders – 116 cases).
  • Guided poster presentation at international movement disorder society conference, Madrid 2022 (Case series of patients with Neuronal Brain Iron accumulation (NBIA) spectrum disorders).
  • Dr. Anisya Vasanth Memorial award for the best outgoing resident in DM neurology, NIMHANS 2022.
  • Talks & Publications

  • Sriram Neeharika, Madaan P, Malhi P, Sachdeva N, Negi S, Das J, et al. Evaluation of yperandrogenism in Children with Autism Spectrum Disorder. Indian J Pediatr. 2022 Jul;89(7):717–9.
  • Sriram Neeharika, Padmanabha H, Chandra S, Mahale R, Nandeesh B, Bhat M, et al. CSF1R related leukoencephalopathy - Rare childhood presentation of an autosomal dominant microgliopathy! Ann Indian Acad Neurol. 2021;0(0):0.
  • Sriram Neeharika, Srinivas D, Mahadevan A, Netravathi M. Unravelling Diagnostic Dilemma: AQP4-Positive Transverse Myelitis Mimics Spinal Intramedullary Tumor. Ann Indian Acad Neurol. 2021 Jun;24(3):436–9.
  • Shah R, Mahale R, Babu K, Shah D, Vincent M, Nanda S, Sriram Neeharika et al. Granulomatous panuveitis in multiple sclerosis: A rare occurrence. Ann Indian Acad Neurol. 2022;0(0):0.
  • Dr. Snigdha Bellapukonda, Dr. Vikas Kumar, Dr. Rajeev Chauhan, Dr. Sunder Lal Negi, Dr. Neeharika Sriram, et al. Seizures in a Child Sedated with Ketamine: A Rare Presentation. J Med Sci Clin Resp. 2019 Mar 18 [cited 2022 Jul 4];7(3).
  • Kumari, R., Holla, V.V., Phulpagar, P., Sriram, N., Hegde, A.G., Vengalil, S., Kamble, N., Saini, J., Yadav, R., Pal, P.K. and Muthusamy, B. (2022), Whole exome sequencing and transcript analysis discover a novel pathogenic splice site mutation in DCAF17 gene underlying Woodhouse-Sakati syndrome. J Neuroendocrinol. Accepted Author Manuscript e13185. https://doi.org/10.1111/jne.13185.
  • "A rare case of ophthalmoplegia with ataxia in genetically proven abetalipoproteinemia" by Gurram, Sandeep; Holla, Vikram; Sharma, Praveen; Phulpagar, Prashant; Jha, Shreyashi; Sriram, Neeharika; Mallitha, S; Kamble, Nitish; Netravathi, M; Yadav, Ravi; Muthusamy, Babylakshmi; Pal, Pramod. Movement Disorders Clinical Practice.

    Field of Expertise

  • Neurology
  • Pediatric Neurology
  • Stroke
  • Epilepsy
  • Movement Disorders
  • Cognitive Disorders
  • Neuroimmunology
  • Fellowship & Membership

  • International Movement Disorders.
  • Movement disorders society of India.
  • American Academy of Neurology.
  • The Indian Academy of Neurology.
  • Languages Spoken

  • English
  • Telugu
  • Hindi
  • Kannada
  • Awards & Achievements

  • Poster presentation at International Pediatric Neurology conference Mumbai and Neuropedicon 2018 (Topic: Evaluation of hyperandrogenism in children with Autism spectrum disorder and age- sex-matched controls).
  • Poster presentation in Association of Child Neurology (AOCN) 2020 (Topic: CSF1R mutation - rare childhood presentation of an autosomal dominant microgliopathy).
  • Second prize in Quiz conducted at AOCN 2020.
  • First Prize for Poster presentation at MS conference, Bengaluru 2020 (Topic: Aquaporin antibody associated myelitis mimicking as spinal cord tumor – Case series).
  • Poster presentation at MS conference, Bengaluru 2020 (Topic: Sinus Bradycardia as an unreported side effect of Alemtuzumab infusion in MS).
  • Poster presentation at MDSI 2020 (Topic- Episodic ataxia- is it always genetic?).
  • First prize in Torrent Young Scholar Award 2022 (TYSA 2022).
  • Platform presentation in MDSI 2022 (Topic – Clinical, radiological, the genetic profile of a large series of patients with Neuronal Brain Iron accumulation [NBIA] spectrum disorders – 116 cases).
  • Guided poster presentation at international movement disorder society conference, Madrid 2022 (Case series of patients with Neuronal Brain Iron accumulation (NBIA) spectrum disorders).
  • Dr. Anisya Vasanth Memorial award for the best outgoing resident in DM neurology, NIMHANS 2022.
  • Talks & Publications

  • Sriram Neeharika, Madaan P, Malhi P, Sachdeva N, Negi S, Das J, et al. Evaluation of yperandrogenism in Children with Autism Spectrum Disorder. Indian J Pediatr. 2022 Jul;89(7):717–9.
  • Sriram Neeharika, Padmanabha H, Chandra S, Mahale R, Nandeesh B, Bhat M, et al. CSF1R related leukoencephalopathy - Rare childhood presentation of an autosomal dominant microgliopathy! Ann Indian Acad Neurol. 2021;0(0):0.
  • Sriram Neeharika, Srinivas D, Mahadevan A, Netravathi M. Unravelling Diagnostic Dilemma: AQP4-Positive Transverse Myelitis Mimics Spinal Intramedullary Tumor. Ann Indian Acad Neurol. 2021 Jun;24(3):436–9.
  • Shah R, Mahale R, Babu K, Shah D, Vincent M, Nanda S, Sriram Neeharika et al. Granulomatous panuveitis in multiple sclerosis: A rare occurrence. Ann Indian Acad Neurol. 2022;0(0):0.
  • Dr. Snigdha Bellapukonda, Dr. Vikas Kumar, Dr. Rajeev Chauhan, Dr. Sunder Lal Negi, Dr. Neeharika Sriram, et al. Seizures in a Child Sedated with Ketamine: A Rare Presentation. J Med Sci Clin Resp. 2019 Mar 18 [cited 2022 Jul 4];7(3).
  • Kumari, R., Holla, V.V., Phulpagar, P., Sriram, N., Hegde, A.G., Vengalil, S., Kamble, N., Saini, J., Yadav, R., Pal, P.K. and Muthusamy, B. (2022), Whole exome sequencing and transcript analysis discover a novel pathogenic splice site mutation in DCAF17 gene underlying Woodhouse-Sakati syndrome. J Neuroendocrinol. Accepted Author Manuscript e13185. https://doi.org/10.1111/jne.13185.
  • "A rare case of ophthalmoplegia with ataxia in genetically proven abetalipoproteinemia" by Gurram, Sandeep; Holla, Vikram; Sharma, Praveen; Phulpagar, Prashant; Jha, Shreyashi; Sriram, Neeharika; Mallitha, S; Kamble, Nitish; Netravathi, M; Yadav, Ravi; Muthusamy, Babylakshmi; Pal, Pramod. Movement Disorders Clinical Practice.

    Awards & Achievements

  • Poster presentation at International Pediatric Neurology conference Mumbai and Neuropedicon 2018 (Topic: Evaluation of hyperandrogenism in children with Autism spectrum disorder and age- sex-matched controls).
  • Poster presentation in Association of Child Neurology (AOCN) 2020 (Topic: CSF1R mutation - rare childhood presentation of an autosomal dominant microgliopathy).
  • Second prize in Quiz conducted at AOCN 2020.
  • First Prize for Poster presentation at MS conference, Bengaluru 2020 (Topic: Aquaporin antibody associated myelitis mimicking as spinal cord tumor – Case series).
  • Poster presentation at MS conference, Bengaluru 2020 (Topic: Sinus Bradycardia as an unreported side effect of Alemtuzumab infusion in MS).
  • Poster presentation at MDSI 2020 (Topic- Episodic ataxia- is it always genetic?).
  • First prize in Torrent Young Scholar Award 2022 (TYSA 2022).
  • Platform presentation in MDSI 2022 (Topic – Clinical, radiological, the genetic profile of a large series of patients with Neuronal Brain Iron accumulation [NBIA] spectrum disorders – 116 cases).
  • Guided poster presentation at international movement disorder society conference, Madrid 2022 (Case series of patients with Neuronal Brain Iron accumulation (NBIA) spectrum disorders).
  • Dr. Anisya Vasanth Memorial award for the best outgoing resident in DM neurology, NIMHANS 2022.
  • Fellowship & Membership

  • International Movement Disorders.
  • Movement disorders society of India.
  • American Academy of Neurology.
  • The Indian Academy of Neurology.
  • Field of Expertise

  • Neurology
  • Pediatric Neurology
  • Stroke
  • Epilepsy
  • Movement Disorders
  • Cognitive Disorders
  • Neuroimmunology
  • Languages Spoken

  • English
  • Telugu
  • Hindi
  • Kannada
  • Talks & Publications

  • Sriram Neeharika, Madaan P, Malhi P, Sachdeva N, Negi S, Das J, et al. Evaluation of yperandrogenism in Children with Autism Spectrum Disorder. Indian J Pediatr. 2022 Jul;89(7):717–9.
  • Sriram Neeharika, Padmanabha H, Chandra S, Mahale R, Nandeesh B, Bhat M, et al. CSF1R related leukoencephalopathy - Rare childhood presentation of an autosomal dominant microgliopathy! Ann Indian Acad Neurol. 2021;0(0):0.
  • Sriram Neeharika, Srinivas D, Mahadevan A, Netravathi M. Unravelling Diagnostic Dilemma: AQP4-Positive Transverse Myelitis Mimics Spinal Intramedullary Tumor. Ann Indian Acad Neurol. 2021 Jun;24(3):436–9.
  • Shah R, Mahale R, Babu K, Shah D, Vincent M, Nanda S, Sriram Neeharika et al. Granulomatous panuveitis in multiple sclerosis: A rare occurrence. Ann Indian Acad Neurol. 2022;0(0):0.
  • Dr. Snigdha Bellapukonda, Dr. Vikas Kumar, Dr. Rajeev Chauhan, Dr. Sunder Lal Negi, Dr. Neeharika Sriram, et al. Seizures in a Child Sedated with Ketamine: A Rare Presentation. J Med Sci Clin Resp. 2019 Mar 18 [cited 2022 Jul 4];7(3).
  • Kumari, R., Holla, V.V., Phulpagar, P., Sriram, N., Hegde, A.G., Vengalil, S., Kamble, N., Saini, J., Yadav, R., Pal, P.K. and Muthusamy, B. (2022), Whole exome sequencing and transcript analysis discover a novel pathogenic splice site mutation in DCAF17 gene underlying Woodhouse-Sakati syndrome. J Neuroendocrinol. Accepted Author Manuscript e13185. https://doi.org/10.1111/jne.13185.
  • "A rare case of ophthalmoplegia with ataxia in genetically proven abetalipoproteinemia" by Gurram, Sandeep; Holla, Vikram; Sharma, Praveen; Phulpagar, Prashant; Jha, Shreyashi; Sriram, Neeharika; Mallitha, S; Kamble, Nitish; Netravathi, M; Yadav, Ravi; Muthusamy, Babylakshmi; Pal, Pramod. Movement Disorders Clinical Practice.

    Talks & Publications

  • Sriram Neeharika, Madaan P, Malhi P, Sachdeva N, Negi S, Das J, et al. Evaluation of yperandrogenism in Children with Autism Spectrum Disorder. Indian J Pediatr. 2022 Jul;89(7):717–9.
  • Sriram Neeharika, Padmanabha H, Chandra S, Mahale R, Nandeesh B, Bhat M, et al. CSF1R related leukoencephalopathy - Rare childhood presentation of an autosomal dominant microgliopathy! Ann Indian Acad Neurol. 2021;0(0):0.
  • Sriram Neeharika, Srinivas D, Mahadevan A, Netravathi M. Unravelling Diagnostic Dilemma: AQP4-Positive Transverse Myelitis Mimics Spinal Intramedullary Tumor. Ann Indian Acad Neurol. 2021 Jun;24(3):436–9.
  • Shah R, Mahale R, Babu K, Shah D, Vincent M, Nanda S, Sriram Neeharika et al. Granulomatous panuveitis in multiple sclerosis: A rare occurrence. Ann Indian Acad Neurol. 2022;0(0):0.
  • Dr. Snigdha Bellapukonda, Dr. Vikas Kumar, Dr. Rajeev Chauhan, Dr. Sunder Lal Negi, Dr. Neeharika Sriram, et al. Seizures in a Child Sedated with Ketamine: A Rare Presentation. J Med Sci Clin Resp. 2019 Mar 18 [cited 2022 Jul 4];7(3).
  • Kumari, R., Holla, V.V., Phulpagar, P., Sriram, N., Hegde, A.G., Vengalil, S., Kamble, N., Saini, J., Yadav, R., Pal, P.K. and Muthusamy, B. (2022), Whole exome sequencing and transcript analysis discover a novel pathogenic splice site mutation in DCAF17 gene underlying Woodhouse-Sakati syndrome. J Neuroendocrinol. Accepted Author Manuscript e13185. https://doi.org/10.1111/jne.13185.
  • "A rare case of ophthalmoplegia with ataxia in genetically proven abetalipoproteinemia" by Gurram, Sandeep; Holla, Vikram; Sharma, Praveen; Phulpagar, Prashant; Jha, Shreyashi; Sriram, Neeharika; Mallitha, S; Kamble, Nitish; Netravathi, M; Yadav, Ravi; Muthusamy, Babylakshmi; Pal, Pramod. Movement Disorders Clinical Practice.
  • Fellowship & Membership

  • International Movement Disorders.
  • Movement disorders society of India.
  • American Academy of Neurology.
  • The Indian Academy of Neurology.
  • Field of Expertise

  • Neurology
  • Pediatric Neurology
  • Stroke
  • Epilepsy
  • Movement Disorders
  • Cognitive Disorders
  • Neuroimmunology
  • Languages Spoken

  • English
  • Telugu
  • Hindi
  • Kannada
  • Awards & Achievements

  • Poster presentation at International Pediatric Neurology conference Mumbai and Neuropedicon 2018 (Topic: Evaluation of hyperandrogenism in children with Autism spectrum disorder and age- sex-matched controls).
  • Poster presentation in Association of Child Neurology (AOCN) 2020 (Topic: CSF1R mutation - rare childhood presentation of an autosomal dominant microgliopathy).
  • Second prize in Quiz conducted at AOCN 2020.
  • First Prize for Poster presentation at MS conference, Bengaluru 2020 (Topic: Aquaporin antibody associated myelitis mimicking as spinal cord tumor – Case series).
  • Poster presentation at MS conference, Bengaluru 2020 (Topic: Sinus Bradycardia as an unreported side effect of Alemtuzumab infusion in MS).
  • Poster presentation at MDSI 2020 (Topic- Episodic ataxia- is it always genetic?).
  • First prize in Torrent Young Scholar Award 2022 (TYSA 2022).
  • Platform presentation in MDSI 2022 (Topic – Clinical, radiological, the genetic profile of a large series of patients with Neuronal Brain Iron accumulation [NBIA] spectrum disorders – 116 cases).
  • Guided poster presentation at international movement disorder society conference, Madrid 2022 (Case series of patients with Neuronal Brain Iron accumulation (NBIA) spectrum disorders).
  • Dr. Anisya Vasanth Memorial award for the best outgoing resident in DM neurology, NIMHANS 2022.