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1

Comparing the efficacy of sodium valproate and levetiracetam following initial lorazepam in elderly patients with generalized convulsive status epilepticus (GCSE): A prospective randomized controlled pilot study

Nene, Devavrat, Chowdary Mundlamuri, Ravindranadh, Satishchandra, Parthasarathy, Vasuki Prathyusha, Parthipulli, Nagappa, Madhu, Sankaran Bindu, Parayil, Raghavendra, Kenchaiah, Saini, Jitender, Bhara

Journal:

Year:

2019

Language:

english

File:

PDF, 410 KB

english, 2019

2

Mitochondrial Leukoencephalopathies: A Border Zone between Acquired and Inherited White matter Disorders in Children?

Bindu, Parayil Sankaran, Sonam, Kothari, Chiplunkar, Shwetha, Govindaraj, Periyasamy, Nagappa, Madhu, Vekhande, Chetan Chandrakanth, Aravinda, Hanumanthapura R, Ponmalar, JN Jessiena, Mahadevan, Anita

Journal:

Multiple Sclerosis and Related Disorders

Year:

2018

Language:

english

File:

PDF, 1.41 MB

english, 2018

3

Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutations

Sonam, Kothari, Khan, Nahid Akthar, Bindu, Parayil Sankaran, Taly, Arun B., Gayathri, N., Bharath, M.M. Srinivas, Govindaraju, C., Arvinda, H.R., Nagappa, Madhu, Sinha, Sanjib, Thangaraj, K.

Journal:

Brain and Development

Year:

2014

Language:

english

File:

PDF, 224 KB

english, 2014

4

Electro-clinical features and magnetic resonance imaging correlates in Menkes disease

Bindu, Parayil Sankaran, Taly, Arun B., Kothari, Sonam, Christopher, Rita, Gayathri, Narayanappa, Sinha, Sanjib, Nagappa, Madhu, Bhatt, Maya, Bharath, Rose Dawn

Journal:

Brain and Development

Year:

2013

Language:

english

File:

PDF, 901 KB

english, 2013

5

Unusual Imaging Findings in Brain and Spinal Cord in Two Siblings With Maple Syrup Urine Disease

Bhat, Maya, Prasad, Chandrajit, Bindu, Parayil Sankaran, Aziz, Zarina, Christopher, Rita, Saini, Jitender

Journal:

Journal of Neuroimaging

Year:

2013

Language:

english

File:

PDF, 311 KB

english, 2013

6

Therapeutic Strategies for Mitochondrial Disorders

Finsterer, Josef, Bindu, Parayil Sankaran

Journal:

Pediatric Neurology

Year:

2015

Language:

english

File:

PDF, 406 KB

english, 2015

7

A Variant Form of Mucolipidosis IV: Report on 4 Patients From the Indian Subcontinent

Parayil Sankaran Bindu,, Gayathri, N., Yasha, T. C., Kovoor, J. M. E., Subasree, R., Rao, S., Panda, S., Pramod Kumar Pal,

Journal:

Journal of Child Neurology

Year:

2008

Language:

english

File:

PDF, 100 KB

english, 2008

8

Mitochondrial Myopathy, Cardiomyopathy, and Pontine Signal Changes in an Adult Patient With Isolated Complex II Deficiency

Sonam, Kothari, Bindu, Parayil Sankaran, Taly, Arun B., Nalini, Atchayaram, Govindaraju, Chikkanna, Aravinda, Hanumanthapura R., Khan, Nahid Akthar, Thangaraj, Kumaraswamy, Gayathri, Narayanappa

Journal:

Journal of Clinical Neuromuscular Disease

Year:

2014

Language:

english

File:

PDF, 294 KB

english, 2014

9

Oculomotor Apraxia in Gaucher Disease

Nagappa, Madhu, Bindu, Parayil Sankaran, Taly, Arun B., Sinha, Sanjib

Journal:

Pediatric Neurology

Year:

2015

Language:

english

File:

PDF, 354 KB

english, 2015

10

Audiological findings in Infantile Refsum disease

Vandana, V.P., Bindu, Parayil Sankaran, Nagappa, Madhu, Sinha, Sanjib, Taly, Arun B.

Journal:

International Journal of Pediatric Otorhinolaryngology

Year:

2015

Language:

english

File:

PDF, 833 KB

english, 2015

11

Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: A study from south India

Bindu, Parayil Sankaran, Arvinda, Hamumanthapura R., Taly, Arun B., Govindaraju, C., Sonam, Kothari, Chiplunkur, Shwetha, Kumar, Rakesh, Gayathri, Narayanappa, Bharath, Srinivas, Nagappa, Madhu, Sinha

Journal:

Year:

2015

Language:

english

File:

PDF, 1.03 MB

english, 2015

12

Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south India

Bindu, Parayil Sankaran, Govindaraju, C., Sonam, Kothari, Nagappa, Madhu, Shwetha, Chiplunkar, Kumar, Rakesh, Gayathri, N., Srinivas Bharath, M.M., Arvinda, Hanumanthapura R., Sinha, Sanjib, Khan, Nah

Journal:

Year:

2016

Language:

english

File:

PDF, 436 KB

english, 2016

13

Audiological Manifestations in Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke like Episodes (MELAS) Syndrome

Vandana, V.P., Bindu, Parayil Sankaran, Sonam, Kothari, Govindaraj, Periyasamy, Taly, Arun B., Gayathri, Narayanappa, Chiplunkar, Shwetha, Govindraju, Chikkanna, Arvinda, H.R., Nagappa, Madhu, Sinha,

Journal:

Clinical Neurology and Neurosurgery

Year:

2016

Language:

english

File:

PDF, 588 KB

english, 2016

14

Palatal Tremor in POLG -Associated Ataxia

Nagappa, Madhu, Bindu, Parayil Sankaran, Taly, Arun B., Sonam, Kothari, Shwetha, Chiplunkar, Kumar, Rakesh, Gayathri, Narayanappa, Srinivas-Bharath, M.M., Arvinda, Hanumanthapura R., Sinha, Sanjib, Pa

Journal:

Movement Disorders Clinical Practice

Year:

2015

Language:

english

File:

PDF, 247 KB

english, 2015

15

Huppke-Brendel syndrome in a seven months old boy with a novel 2-bp deletion inSLC33A1

Chiplunkar, Shwetha, Bindu, Parayil Sankaran, Nagappa, Madhu, Bineesh, Cheminikara, Govindaraj, Periyasamy, Gayathri, Narayanappa, Bharath, M. M. Srinivas, Arvinda, Hanumanthapura R., Mathuranath, Pav

Journal:

Metabolic Brain Disease

Year:

2016

Language:

english

File:

PDF, 559 KB

english, 2016

16

Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) gene

Nagappa, Madhu, Bindu, Parayil Sankaran, Chiplunkar, Shwetha, Govindaraj, Periasamy, Narayanappa, Gayathri, Krishnan, Ayyappan, Bharath, M.M. Srinivas, Swaminathan, Aarthi, Saini, Jitender, Arvinda, H

Journal:

Brain and Development

Year:

2016

Language:

english

File:

PDF, 952 KB

english, 2016

17

Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India

Sonam, Kothari, Bindu, Parayil Sankaran, Srinivas Bharath, MM, Govindaraj, Periyasamy, Gayathri, Narayanappa, Arvinda, Hanumanthapura R, Chiplunkar, Shwetha, Nagappa, Madhu, Sinha, Sanjib, Khan, Nahid

Journal:

Year:

2017

Language:

english

File:

PDF, 746 KB

english, 2017

18

Erratum to: Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiency

Chiplunkar, Shwetha, Bindu, Parayil Sankaran, Nagappa, Madhu, Panikulam, Bobby Baby, Arvinda, Hanumanthapura R, Govindaraj, Periyasamy, Srinivas Bharath, MM, Gayathri, Narayanappa, Jessiena Ponmalar,

Journal:

Metabolic Brain Disease

Year:

2017

Language:

english

File:

PDF, 210 KB

english, 2017

19

Novel magnetic resonance imaging findings in a patient with short chain acyl CoA dehydrogenase deficiency

Chiplunkar, Shwetha, Bindu, Parayil Sankaran, Nagappa, Madhu, Panikulam, Bobby Baby, Arvinda, Hanumanthapura R, Govindaraj, Periyasamy, Srinivas Bharath, MM, Gayathri, Narayanappa, Jessiena Ponmalar,

Journal:

Metabolic Brain Disease

Year:

2017

Language:

english

File:

PDF, 1.82 MB

english, 2017

20

Outcome of Epilepsy in patients with Mitochondrial Disorders: Phenotype Genotype and Magnetic Resonance Imaging Correlations

Bindu, Parayil Sankaran, Sonam, Kothari, Govindaraj, Periyasamy, Govindaraju, Chikkanna, Chiplunkar, Shwetha, Nagappa, Madhu, Kumar, Rakesh, Vekhande, Chetan Chandrakanth, Arvinda, Hanumanthapura R.,

Journal:

Clinical Neurology and Neurosurgery

Year:

2017

Language:

english

File:

PDF, 352 KB

english, 2017

21

Comprehensive cytokine profiling provides evidence for a multi-lineage Th responses in Guillain Barré Syndrome

Debnath, Monojit, Nagappa, Madhu, Talukdar, Pinku Mani, Subbanna, Manjula, Sundaravadivel, P., Shivakumar, Venkataram, Dutta, Debprasad, Wahatule, Rahul, Sinha, Sanjib, Bindu, Parayil Sankaran, Periya

Journal:

Year:

2018

Language:

english

File:

PDF, 529 KB

english, 2018

22

Exome sequencing in adult neurology practice: challenges and rewards in a mixed resource setting

Nagappa, Madhu, Bindu, Parayil Sankaran, Sinha, Sanjib, Mathuranath, Pavagada S., Taly, Arun B.

Journal:

Clinical Neurology and Neurosurgery

Year:

2018

Language:

english

File:

PDF, 501 KB

english, 2018

23

Clinical Reasoning: West syndrome, pontocerebellar hypoplasia, and hypomyelination in a 6-month-old boy

Bindu, Parayil Sankaran, Nagappa, Madhu, Chiplunkar, Shwetha, Govindaraj, Periyasamy, Mathuranath, Pavagada S., Sinha, Sanjib, Taly, Arun B.

Journal:

Year:

2018

Language:

english

File:

PDF, 532 KB

english, 2018

24

Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report

Nandeesh, Bevinahalli N., Bindu, Parayil Sankaran, Narayanappa, Gayathri, Chickabasaviah Yasha, T., Mahadevan, Anita, Kulanthaivelu, Karthik, Santosh, Vani

Journal:

Year:

2019

File:

PDF, 3.88 MB

2019

25

Sjogren-Larsson Syndrome: Mechanisms and Management

Bindu, Parayil Sankaran

Journal:

The Application of Clinical Genetics

Year:

2020

File:

PDF, 2.47 MB

2020

26

Child Neurology: Ethylmalonic encephalopathy

Govindaraj, Periyasamy, Parayil Sankaran, Bindu, Nagappa, Madhu, Arvinda, Hanumanthapura R., Deepha, Sekar, Jessiena Ponmalar, J.N., Sinha, Sanjib, Gayathri, Narayanappa, Taly, Arun B.

Journal:

Year:

2020

File:

PDF, 459 KB

2020

27

Leukodystrophies and Genetic Leukoencephalopathies in Children Specified by Exome Sequencing in an Expanded Gene Panel

Sankaran, Bindu Parayil, Nagappa, Madhu, Chiplunkar, Shwetha, Kothari, Sonam, Govindaraj, Periyasamy, Sinha, Sanjib, Taly, Arun B.

Journal:

Journal of Child Neurology

Year:

2020

Language:

english

File:

PDF, 392 KB

english, 2020

28

Evidence of altered Th17 pathway signatures in the cerebrospinal fluid of patients with Guillain BarrÃ© Syndrome

Debnath, Monojit, Nagappa, Madhu, Dutta, Debprasad, Talukdar, Pinku Mani, Subbanna, Manjula, Shivakumar, Venkataram, Wahatule, Rahul, Sinha, Sanjib, Bindu, Parayil Sankaran, Periyavan, Sundar, Umamahe

Journal:

Journal of Clinical Neuroscience

Year:

2020

File:

PDF, 274 KB

2020

29

Variable treatment response in a patient with pyridoxal N phosphate oxidase (PNPO) deficiency- understanding the paradox

Mohanlal, Smilu, Bindu, Parayil Sankaran, Sureshbabu, Sachin, Kumar, Suresh

Journal:

Epilepsy & Behavior Reports

Year:

2020

File:

PDF, 1.27 MB

2020