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Items: 1 to 50 of 104

1.

Huppke-Brendel Syndrome.

Bindu PS, Chiplunkar S, Vandana VP, Nagappa M, Govindaraj P, Taly A.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019.
2019 Jun 13.

2.

Genetic analysis of ATP7B in 102 south Indian families with Wilson disease.

Singh N, Kallollimath P, Shah MH, Kapoor S, Bhat VK, Viswanathan LG, Nagappa M, Bindu PS, Taly AB, Sinha S, Kumar A.

PLoS One. 2019 May 6;14(5):e0215779. doi: 10.1371/journal.pone.0215779. eCollection 2019.

3.

Autoantibodies in acquired myasthenia gravis: Clinical phenotype and immunological correlation.

Nagappa M, Mahadevan A, Gangadhar Y, Patil SA, Bokolia S, Bindu PS, Sinha S, Taly AB.

Acta Neurol Scand. 2019 May;139(5):428-437. doi: 10.1111/ane.13071. Epub 2019 Feb 19.

PMID:
30693486
4.

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 D, Mundlamuri RC, Satishchandra P, Prathyusha PV, Nagappa M, Bindu PS, Raghavendra K, Saini J, Bharath RD, Thennarasu K, Taly AB, Sinha S.

Seizure. 2019 Feb;65:111-117. doi: 10.1016/j.seizure.2019.01.015. Epub 2019 Jan 15.

PMID:
30682680
5.

Comparison of Cheiloscopy and Rugoscopy in Karnataka, Kerala, and Manipuri Population.

Manikya S, Sureka V, Prasanna MD, Ealla K, Reddy S, Bindu PS.

J Int Soc Prev Community Dent. 2018 Sep-Oct;8(5):439-445. doi: 10.4103/jispcd.JISPCD_223_18. Epub 2018 Oct 8.

6.

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

Bindu PS, Nagappa M, Chiplunkar S, Govindaraj P, Mathuranath PS, Sinha S, Taly AB.

Neurology. 2018 Oct 23;91(17):e1652-e1656. doi: 10.1212/WNL.0000000000006381. No abstract available.

PMID:
30348860
7.

Pediatric opsoclonus-myoclonus-ataxia syndrome: Experience from a tertiary care university hospital.

Huddar A, Bindu PS, Nagappa M, Bharath RD, Sinha S, Mathuranath PS, Taly AB.

Neurol India. 2018 Sep-Oct;66(5):1332-1337. doi: 10.4103/0028-3886.241404.

8.

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

Nagappa M, Bindu PS, Sinha S, Mathuranath PS, Taly AB.

Clin Neurol Neurosurg. 2018 Nov;174:48-56. doi: 10.1016/j.clineuro.2018.09.012. Epub 2018 Sep 7.

PMID:
30212743
9.

Th17 pathway signatures in a large Indian cohort of Guillain Barré syndrome.

Debnath M, Nagappa M, Subbanna M, Sundaravadivel P, Talukdar PM, Shivakumar V, Wahatule R, Dutta D, Binukumar B, Sinha S, Bindu PS, Periyavan S, Umamaheswara Rao GS, Taly AB.

J Neuroimmunol. 2018 Oct 15;323:125-130. doi: 10.1016/j.jneuroim.2018.08.001. Epub 2018 Aug 3.

PMID:
30196825
10.

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

Debnath M, Nagappa M, Talukdar PM, Subbanna M, Sundaravadivel P, Shivakumar V, Dutta D, Wahatule R, Sinha S, Bindu PS, Periyavan S, Umamaheswara Rao GS, Taly AB.

Cytokine. 2018 Oct;110:58-62. doi: 10.1016/j.cyto.2018.04.026. Epub 2018 Apr 25.

PMID:
29704819
11.

Mitochondrial dysfunction in human skeletal muscle biopsies of lipid storage disorder.

Debashree B, Kumar M, Keshava Prasad TS, Natarajan A, Christopher R, Nalini A, Bindu PS, Gayathri N, Srinivas Bharath MM.

J Neurochem. 2018 May;145(4):323-341. doi: 10.1111/jnc.14318. Epub 2018 Apr 19.

12.

Mitochondrial leukoencephalopathies: A border zone between acquired and inherited white matter disorders in children?

Bindu PS, Sonam K, Chiplunkar S, Govindaraj P, Nagappa M, Vekhande CC, Aravinda HR, Ponmalar JJ, Mahadevan A, Gayathri N, Bharath MS, Sinha S, Taly AB.

Mult Scler Relat Disord. 2018 Feb;20:84-92. doi: 10.1016/j.msard.2018.01.003. Epub 2018 Jan 6.

PMID:
29353736
13.

Author Response: Penetrance of the LHON Mutation m.11778G>A May Depend on Factors Other Than Haplotype or Heteroplasmy Rate.

Khan NA, Govindaraj P, Soumittra N, Sharma S, Srilekha S, Ambika S, Vanniarajan A, Meena AK, Uppin MS, Sundaram C, Bindu PS, Gayathri N, Taly AB, Thangaraj K.

Invest Ophthalmol Vis Sci. 2018 Jan 1;59(1):382. doi: 10.1167/iovs.17-23468. No abstract available.

PMID:
29346803
14.

Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations.

Bindu PS, Sonam K, Govindaraj P, Govindaraju C, Chiplunkar S, Nagappa M, Kumar R, Vekhande CC, Arvinda HR, Gayathri N, Srinivas Bharath MM, Ponmalar JNJ, Philip M, Vandana VP, Khan NA, Nunia V, Paramasivam A, Sinha S, Thangaraj K, Taly AB.

Clin Neurol Neurosurg. 2018 Jan;164:182-189. doi: 10.1016/j.clineuro.2017.12.010. Epub 2017 Dec 9.

PMID:
29272804
15.

Palatal Tremor Revisited: Disorder with Nosological Diversity and Etiological Heterogeneity.

Nagappa M, Bindu PS, Sinha S, Bharath RD, Sandhya M, Saini J, Mathuranath PS, Taly AB.

Can J Neurol Sci. 2018 Mar;45(2):243-247. doi: 10.1017/cjn.2017.273. Epub 2017 Dec 18.

PMID:
29249217
16.

Isolated Sulfite Oxidase Deficiency.

Bindu PS, Nagappa M, Bharath RD, Taly AB.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019.
2017 Sep 21.

17.

Guillain Barre Syndrome in the elderly: Experience from a tertiary-care hospital in India.

Nagappa M, Rahul W, Sinha S, Bindu PS, Mathuranath PS, Rao S, Periyavan S, Umamaheshwara Rao GS, Taly AB.

J Clin Neurosci. 2017 Dec;46:45-49. doi: 10.1016/j.jocn.2017.08.048. Epub 2017 Sep 7.

PMID:
28890042
18.

Neuropsychiatric Manifestations of Pediatric NMDA Receptor Autoimmune Encephalitis: A Case Series From a Tertiary Care Center in India.

Basheer S, Nagappa M, Mahadevan A, Bindu PS, Taly AB, Girimaji SC.

Prim Care Companion CNS Disord. 2017 Aug 17;19(4). pii: 17m02110. doi: 10.4088/PCC.17m02110.

19.

Leber's Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India.

Khan NA, Govindaraj P, Soumittra N, Sharma S, Srilekha S, Ambika S, Vanniarajan A, Meena AK, Uppin MS, Sundaram C, Bindu PS, Gayathri N, Taly AB, Thangaraj K.

Invest Ophthalmol Vis Sci. 2017 Aug 1;58(10):3923-3930. doi: 10.1167/iovs.16-20695.

PMID:
28768321
20.

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

Chiplunkar S, Bindu PS, Nagappa M, Panikulam BB, Arvinda HR, Govindaraj P, Srinivas Bharath MM, Gayathri N, Jessiena Ponmalar JN, Mathuranath PS, Sinha S, Taly AB.

Metab Brain Dis. 2017 Aug;32(4):971. doi: 10.1007/s11011-017-0018-0. No abstract available.

PMID:
28466389
21.

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

Chiplunkar S, Bindu PS, Nagappa M, Panikulam BB, Arvinda HR, Govindaraj P, Srinivas Bharath MM, Gayathri N, Jessiena Ponmalar JN, Mathuranath PS, Sinha S, Taly AB.

Metab Brain Dis. 2017 Aug;32(4):967-970. doi: 10.1007/s11011-017-0005-5. Epub 2017 Apr 3. Erratum in: Metab Brain Dis. 2017 May 2;:.

PMID:
28374236
22.

Child Neurology: Sjögren-Larsson syndrome.

Nagappa M, Bindu PS, Chiplunkar S, Gupta N, Sinha S, Mathuranath PS, Bharath RD, Taly AB.

Neurology. 2017 Jan 3;88(1):e1-e4. doi: 10.1212/WNL.0000000000003456. No abstract available.

PMID:
28025403
23.

Fatal Morvan Syndrome Associated With Myasthenia Gravis.

Nagappa M, Mahadevan A, Sinha S, Bindu PS, Mathuranath PS, Bineesh C, Bharath RD, Taly AB.

Neurologist. 2017 Jan;22(1):29-33. doi: 10.1097/NRL.0000000000000097.

PMID:
28009770
24.

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

Sonam K, Bindu PS, Srinivas Bharath MM, Govindaraj P, Gayathri N, Arvinda HR, Chiplunkar S, Nagappa M, Sinha S, Khan NA, Nunia V, Paramasivam A, Thangaraj K, Taly AB.

Mitochondrion. 2017 Jan;32:42-49. doi: 10.1016/j.mito.2016.11.002. Epub 2016 Nov 5.

PMID:
27826120
25.

Reply to Letter to the Editor: Hearing impairment in m.3243A>G carriers requires comprehensive work- and follow-up.

Vandana VP, Bindu PS, Sonam K, Govindaraj P, Chiplunkar S, Gayathri N, Govindaraj C, Arvinda HR, Nagappa M, Sinha S, Thangaraj K, Taly AB.

Clin Neurol Neurosurg. 2016 Nov;150:198-199. doi: 10.1016/j.clineuro.2016.08.030. Epub 2016 Aug 31. No abstract available.

PMID:
27600858
26.

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

Nagappa M, Bindu PS, Chiplunkar S, Govindaraj P, Narayanappa G, Krishnan A, Bharath MM, Swaminathan A, Saini J, Arvinda HR, Sinha S, Mathuranath PS, Taly AB.

Brain Dev. 2017 Feb;39(2):161-165. doi: 10.1016/j.braindev.2016.08.005. Epub 2016 Sep 3.

PMID:
27596361
27.

Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery.

Scott EM, Halees A, Itan Y, Spencer EG, He Y, Azab MA, Gabriel SB, Belkadi A, Boisson B, Abel L, Clark AG; Greater Middle East Variome Consortium, Alkuraya FS, Casanova JL, Gleeson JG.

Nat Genet. 2016 Sep;48(9):1071-6. doi: 10.1038/ng.3592. Epub 2016 Jul 18.

28.

Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome.

Vandana VP, Bindu PS, Sonam K, Govindaraj P, Taly AB, Gayathri N, Chiplunkar S, Govindaraju C, Arvinda HR, Nagappa M, Sinha S, Thangaraj K.

Clin Neurol Neurosurg. 2016 Sep;148:17-21. doi: 10.1016/j.clineuro.2016.04.024. Epub 2016 Jun 14.

PMID:
27359089
29.

Huppke-Brendel syndrome in a seven months old boy with a novel 2-bp deletion in SLC33A1.

Chiplunkar S, Bindu PS, Nagappa M, Bineesh C, Govindaraj P, Gayathri N, Bharath MM, Arvinda HR, Mathuranath PS, Sinha S, Taly AB.

Metab Brain Dis. 2016 Oct;31(5):1195-8. doi: 10.1007/s11011-016-9854-6. Epub 2016 Jun 15.

PMID:
27306358
30.

Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex.

Kapoor S, Shah MH, Singh N, Rather MI, Bhat V, Gopinath S, Bindu PS, Taly AB, Sinha S, Nagappa M, Bharath RD, Mahadevan A, Narayanappa G, Chickabasaviah YT, Kumar A.

PLoS One. 2016 May 19;11(5):e0155605. doi: 10.1371/journal.pone.0155605. eCollection 2016.

31.

Combined MEG-EEG source localisation in patients with sub-acute sclerosing pan-encephalitis.

Velmurugan J, Sinha S, Nagappa M, Mariyappa N, Bindu PS, Ravi GS, Hazra N, Thennarasu K, Ravi V, Taly AB, Satishchandra P.

Neurol Sci. 2016 Aug;37(8):1221-31. doi: 10.1007/s10072-016-2571-4. Epub 2016 Apr 7.

PMID:
27056375
32.

Tangier's disease: An uncommon cause of facial weakness and non-length dependent demyelinating neuropathy.

Nagappa M, Taly AB, Mahadevan A, Pooja M, Bindu PS, Chickabasaviah YT, Gayathri N, Sinha S.

Ann Indian Acad Neurol. 2016 Jan-Mar;19(1):137-9. doi: 10.4103/0972-2327.175436.

33.

Non-Wilsonian hepatolenticular degeneration: Clinical and MRI observations in four families from south India.

Nagappa M, Sinha S, Saini JS, Kallolimath P, Singh N, Kumar A, Bindu PS, Taly AB.

J Clin Neurosci. 2016 May;27:91-4. doi: 10.1016/j.jocn.2015.06.035. Epub 2016 Jan 4.

PMID:
26765764
34.

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

Bindu PS, Govindaraju C, Sonam K, Nagappa M, Chiplunkar S, Kumar R, Gayathri N, Bharath MM, Arvinda HR, Sinha S, Khan NA, Govindaraj P, Nunia V, Paramasivam A, Thangaraj K, Taly AB.

Mitochondrion. 2016 Mar;27:1-5. doi: 10.1016/j.mito.2015.12.009. Epub 2016 Jan 4.

PMID:
26762927
35.

Clinical Features, Therapeutic Response, and Follow-Up in Pediatric Anti-N-Methyl-D-Aspartate Receptor Encephalitis: Experience from a Tertiary Care University Hospital in India.

Nagappa M, Bindu PS, Mahadevan A, Sinha S, Mathuranath PS, Taly AB.

Neuropediatrics. 2016 Jan;47(1):24-32. doi: 10.1055/s-0035-1569464. Epub 2016 Jan 4.

PMID:
26727295
36.

An uncommon cause of bifacial weakness and non-length-dependent demyelinating neuropathy.

Nagappa M, Taly AB, Mahadevan A, Pooja M, Bindu PS, Chickabasaviah YT, Gayathri N, Sinha S.

Ann Indian Acad Neurol. 2015 Oct-Dec;18(4):445-8. doi: 10.4103/0972-2327.169641.

37.

Clinical, electrophysiological, imaging, pathological and therapeutic observations among 18 patients with Rasmussen's encephalitis.

Pradeep K, Sinha S, Mahadevan A, Saini J, Arivazhagan A, Bharath RD, Bindu PS, Jamuna R, Rao MB, Govekar S, Ravikumar BV, Chandramouli BA, Satishchandra P.

J Clin Neurosci. 2016 Mar;25:96-104. doi: 10.1016/j.jocn.2015.05.062. Epub 2015 Dec 7.

PMID:
26675623
38.

Child Neurology: Molybdenum cofactor deficiency.

Nagappa M, Bindu PS, Taly AB, Sinha S, Bharath RD.

Neurology. 2015 Dec 8;85(23):e175-8. doi: 10.1212/WNL.0000000000002194. No abstract available.

PMID:
26644055
39.

Auditory neuropathy spectrum disorder in hypomyelinating leukodystrophy--A case study.

Yuvaraj P, Jayaram M, Abubacker R, Bindu PS.

Int J Pediatr Otorhinolaryngol. 2015 Dec;79(12):2479-83. doi: 10.1016/j.ijporl.2015.10.053. Epub 2015 Nov 9. No abstract available.

PMID:
26611342
40.

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

Bindu PS, Arvinda H, Taly AB, Govindaraju C, Sonam K, Chiplunkar S, Kumar R, Gayathri N, Bharath Mm S, Nagappa M, Sinha S, Khan NA, Govindaraj P, Nunia V, Paramasivam A, Thangaraj K.

Mitochondrion. 2015 Nov;25:6-16. doi: 10.1016/j.mito.2015.08.002. Epub 2015 Sep 1.

PMID:
26341968
41.

Mucopolysaccharidosis type I with craniosynostosis.

Sadashiva N, Bindu PS, Santosh V, Devi BI, Shukla D.

Neurol India. 2015 Jul-Aug;63(4):612-5. doi: 10.4103/0028-3886.162088. No abstract available.

42.

Improvement of Diffusion Tensor Imaging (DTI) Parameters with Decoppering Treatment in Wilson's Disease.

Lawrence A, Saini J, Sinha S, Rao S, Naggappa M, Bindu PS, Taly AB.

JIMD Rep. 2016;25:31-37. Epub 2015 Jun 30.

43.

Palatal Tremor in POLG-Associated Ataxia.

Nagappa M, Bindu PS, Taly AB, Sonam K, Shwetha C, Kumar R, Gayathri N, Srinivas-Bharath MM, Arvinda HR, Sinha S, Paramasivam A, Thangaraj K.

Mov Disord Clin Pract. 2015 Jun 30;2(3):318-320. doi: 10.1002/mdc3.12195. eCollection 2015 Sep. No abstract available.

44.

Management of generalised convulsive status epilepticus (SE): A prospective randomised controlled study of combined treatment with intravenous lorazepam with either phenytoin, sodium valproate or levetiracetam--Pilot study.

Mundlamuri RC, Sinha S, Subbakrishna DK, Prathyusha PV, Nagappa M, Bindu PS, Taly AB, Umamaheswara Rao GS, Satishchandra P.

Epilepsy Res. 2015 Aug;114:52-8. doi: 10.1016/j.eplepsyres.2015.04.013. Epub 2015 May 1.

PMID:
26088885
45.

Audiological findings in Infantile Refsum disease.

Vandana VP, Bindu PS, Nagappa M, Sinha S, Taly AB.

Int J Pediatr Otorhinolaryngol. 2015 Aug;79(8):1366-9. doi: 10.1016/j.ijporl.2015.05.023. Epub 2015 May 30.

PMID:
26055198
46.

Novel imaging findings in two cases of biotinidase deficiency-a treatable metabolic disorder.

Bhat MD, Bindu PS, Christopher R, Prasad C, Verma A.

Metab Brain Dis. 2015 Oct;30(5):1291-4. doi: 10.1007/s11011-015-9690-0. Epub 2015 Jun 4.

PMID:
26037171
47.

Clinical and Neuroimaging Features in Two Children with Mutations in the Mitochondrial ND5 Gene.

Sonam K, Bindu PS, Taly AB, Govindaraju C, Gayathri N, Arvinda HR, Nagappa M, Sinha S, Khan NA, Govindaraj P, Thangaraj K.

Neuropediatrics. 2015 Aug;46(4):277-81. doi: 10.1055/s-0035-1550149. Epub 2015 May 14.

PMID:
25974876
48.

Speech-Language and swallowing manifestations and rehabilitation in an 11-year-old girl with MELAS syndrome.

Vandana VP, Bindu PS, Sonam K, Taly AB, Gayathri N, Madhu N, Sinha S.

J Pediatr Neurosci. 2015 Jan-Mar;10(1):31-4. doi: 10.4103/1817-1745.154326.

49.

Ictal Generalized EEG Attenuation (IGEA) and hypopnea in a child with occipital type 1 cortical dysplasia - Is it a biomarker for SUDEP?

Chaitanya G, Santosh NS, Velmurugan J, Arivazhagan A, Bharath RD, Mahadevan A, Nagappa M, Bindu PS, Rao MB, Taly AB, Satishchandra P, Sinha S.

Ann Indian Acad Neurol. 2015 Jan-Mar;18(1):103-7. doi: 10.4103/0972-2327.144279.

50.

Therapeutic strategies for mitochondrial disorders.

Finsterer J, Bindu PS.

Pediatr Neurol. 2015 Mar;52(3):302-13. doi: 10.1016/j.pediatrneurol.2014.06.023. Epub 2014 Nov 15. Review.

PMID:
25701186

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