Narayanappa Gayathri

Narayanappa Gayathri

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Narayanappa Gayathri

Narayanappa Gayathri

Publications by authors named "Narayanappa Gayathri"

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60Publications

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

Neuropathology 2020 Feb 5;40(1):93-98. Epub 2019 Dec 5.

Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bangalore, India.

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http://dx.doi.org/10.1111/neup.12607DOI Listing
February 2020

Human muscle pathology is associated with altered phosphoprotein profile of mitochondrial proteins in the skeletal muscle.

J Proteomics 2020 Jan 23;211:103556. Epub 2019 Oct 23.

Department of Clinical Psychopharmacology and Neurotoxicology, NIMHANS, Bangalore 560029, Karnataka, India. Electronic address:

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http://dx.doi.org/10.1016/j.jprot.2019.103556DOI Listing
January 2020

X-Linked Myopathy with Excessive Autophagy; A Case Report.

Neurol India 2019 Sep-Oct;67(5):1344-1346

Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.

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http://dx.doi.org/10.4103/0028-3886.271280DOI Listing
November 2019

Young onset Parkinsonism in a patient with familial central core disease.

Neurol India 2017 Mar-Apr;65(2):386-388

Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram, Kerala, India.

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http://dx.doi.org/10.4103/neuroindia.NI_746_15DOI Listing
July 2019

Chikungunya Virus Interacts with Heat Shock Cognate 70 Protein to Facilitate Its Entry into Mosquito Cell Line.

Intervirology 2017 28;60(6):247-262. Epub 2018 Jun 28.

Centre for Research in Medical Entomology, Madurai, India.

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http://dx.doi.org/10.1159/000489308DOI Listing
June 2018

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

J Neurochem 2018 05 19;145(4):323-341. Epub 2018 Apr 19.

Department of Neurochemistry, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India.

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http://dx.doi.org/10.1111/jnc.14318DOI Listing
May 2018

Sporadic amyotrophic lateral sclerosis (SALS) - skeletal muscle response to cerebrospinal fluid from SALS patients in a rat model.

Dis Model Mech 2018 04 16;11(4). Epub 2018 Apr 16.

Department of Neurophysiology, National Institute of Mental Health and Neurosciences, Hosur Road, Bangalore 560 029, India

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http://dx.doi.org/10.1242/dmm.031997DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5963857PMC
April 2018

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

Mult Scler Relat Disord 2018 Feb 6;20:84-92. Epub 2018 Jan 6.

Departments of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India; Neuromuscular Lab, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India. Electronic address:

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http://dx.doi.org/10.1016/j.msard.2018.01.003DOI Listing
February 2018

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

Clin Neurol Neurosurg 2018 01 9;164:182-189. Epub 2017 Dec 9.

Dept. of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India; Neuromuscular lab-Neurobiology Research Centre, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India. Electronic address:

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http://dx.doi.org/10.1016/j.clineuro.2017.12.010DOI Listing
January 2018

Fatty acid oxidation defects presenting as primary myopathy and prominent dropped head syndrome.

Neuromuscul Disord 2017 Nov 24;27(11):986-996. Epub 2017 Aug 24.

Department of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India. Electronic address:

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http://dx.doi.org/10.1016/j.nmd.2017.08.004DOI Listing
November 2017

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

Metab Brain Dis 2017 08 3;32(4):967-970. Epub 2017 Apr 3.

Neuromuscular Laboratory-Neurobiology Research Centre, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India.

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http://dx.doi.org/10.1007/s11011-017-0005-5DOI Listing
August 2017

MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India.

BMC Med Genet 2017 06 13;18(1):67. Epub 2017 Jun 13.

Molecular Genetics Laboratory, Neurobiology Research Centre, Department of Psychiatry, National Institute of Mental Health and Neurosciences, Hosur Road, Bangalore, 560029, Karnataka, India.

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http://dx.doi.org/10.1186/s12881-017-0431-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470271PMC
June 2017

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

Brain Dev 2017 Feb 3;39(2):161-165. Epub 2016 Sep 3.

Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore 560029, India; Neuromuscular Laboratory, Neurobiology Research Centre, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore 560029, India.

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http://dx.doi.org/10.1016/j.braindev.2016.08.005DOI Listing
February 2017

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

Mitochondrion 2017 Jan 5;32:42-49. Epub 2016 Nov 5.

Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India; Neuromuscular Laboratory, Neurobiology Research Centre, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India.

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http://dx.doi.org/10.1016/j.mito.2016.11.002DOI Listing
January 2017

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

Clin Neurol Neurosurg 2016 Nov 31;150:198-199. Epub 2016 Aug 31.

Department of Neurology, National Institute of Mental Health and Neurosciences(NIMHANS), Bangalore, India; Neuromuscular lab-Neurobiology Research Center,National Institute of Mental Health and Neurosciences(NIMHANS), Bangalore, India.

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http://dx.doi.org/10.1016/j.clineuro.2016.08.030DOI Listing
November 2016

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

Metab Brain Dis 2016 10 15;31(5):1195-8. Epub 2016 Jun 15.

Neuromuscular Lab-Neurobiology Research Center, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India.

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http://dx.doi.org/10.1007/s11011-016-9854-6DOI Listing
October 2016

Muscle biopsies from human muscle diseases with myopathic pathology reveal common alterations in mitochondrial function.

J Neurochem 2016 07 16;138(1):174-91. Epub 2016 May 16.

Department of Neurochemistry, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, Karnataka, India.

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http://dx.doi.org/10.1111/jnc.13626DOI Listing
July 2016

Coexistence of central nucleus, cores, and rods: Diagnostic relevance.

Ann Indian Acad Neurol 2016 Apr-Jun;19(2):201-4

Department of Neuropathology, National Institute of Mental Health and Neuroscience (NIMHANS), Bangalore, Karnataka, India.

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http://dx.doi.org/10.4103/0972-2327.176861DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4888682PMC
June 2016

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

Ann Indian Acad Neurol 2015 Oct-Dec;18(4):445-8

Department of Neurology, National Institute of Mental Health and Neurosciences, Bangalore, Karnataka, India.

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http://dx.doi.org/10.4103/0972-2327.169641DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683886PMC
December 2015

Palatal Tremor in -Associated Ataxia.

Mov Disord Clin Pract 2015 Sep 30;2(3):318-320. Epub 2015 Jun 30.

Center for Scientific and Industrial Research-Center for Cellular and Molecular Biology (CSIR-CCMB) Hyderabad India.

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http://dx.doi.org/10.1002/mdc3.12195DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6178733PMC
September 2015

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

Neuropediatrics 2015 Aug 14;46(4):277-81. Epub 2015 May 14.

Centre for Scientific and Industrial Research, Centre for Cellular and Molecular Biology (CSIR-CCMB), Hyderabad, Andhra Pradesh, India.

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http://dx.doi.org/10.1055/s-0035-1550149DOI Listing
August 2015

Giant axonal neuropathy.

J Child Neurol 2015 Jun 11;30(7):912-5. Epub 2014 Sep 11.

Department of Neurology, National Institute of Mental Health and Neurosciences, Bangalore, Karnataka, India.

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http://journals.sagepub.com/doi/10.1177/0883073814547721
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http://dx.doi.org/10.1177/0883073814547721DOI Listing
June 2015

Raman spectroscopic studies on screening of myopathies.

Anal Chem 2015 Feb 27;87(4):2187-94. Epub 2015 Jan 27.

Department of Inorganic and Physical Chemistry, ‡Department of Molecular Reproduction, Development and Genetics, and ∥Department of Instrumentation and Applied Physics, Indian Institute of Science , Bangalore, 560012, India.

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http://dx.doi.org/10.1021/ac503647xDOI Listing
February 2015

Mitochondrial myopathy, cardiomyopathy, and pontine signal changes in an adult patient with isolated complex II deficiency.

J Clin Neuromuscul Dis 2014 Dec;16(2):69-73

Departments of *Neurology, and †Neuroimaging & Interventional Radiology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India; ‡Department of Evolutionary and Medical Genetics, Centre for Cellular and Molecular Biology, Hyderabad, India; and §Department of Neuropathology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, India.

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http://dx.doi.org/10.1097/CND.0000000000000046DOI Listing
December 2014

The "double panda" sign in Leigh disease.

J Child Neurol 2014 Jul 18;29(7):980-2. Epub 2013 Apr 18.

Department of Neurology, National Institute of Mental Health and Neurosciences, Bangalore, India.

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http://dx.doi.org/10.1177/0883073813484968DOI Listing
July 2014

Major histocompatibility complex and inflammatory cell subtype expression in inflammatory myopathies and muscular dystrophies.

Neurol India 2013 Nov-Dec;61(6):614-21

Department of Neurology, National Institute of Mental Health and Neurosciences, Bangalore, Karnataka, India.

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http://dx.doi.org/10.4103/0028-3886.125264DOI Listing
March 2014

New mutation of the desmin gene identified in an extended Indian pedigree presenting with distal myopathy and cardiac disease.

Neurol India 2013 Nov-Dec;61(6):622-6

Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.

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http://dx.doi.org/10.4103/0028-3886.125269DOI Listing
March 2014

GNE myopathy in India.

Neurol India 2013 Jul-Aug;61(4):371-4

Department of Neurology, National Institute of Mental Health and Neurosciences, Bangalore, Karnataka, India.

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http://www.neurologyindia.com/text.asp?2013/61/4/371/117609
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http://dx.doi.org/10.4103/0028-3886.117609DOI Listing
February 2014

A large series of immunohistochemically confirmed cases of congenital muscular dystrophy seen over a period of one decade.

Neurol India 2013 Sep-Oct;61(5):481-7

Department of Neurology, National Institute of Mental Health and Neurosciences, Bangalore, Karnataka, India.

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http://www.neurologyindia.com/text.asp?2013/61/5/481/121913
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http://dx.doi.org/10.4103/0028-3886.121913DOI Listing
January 2014

Mucolipidosis and progressive myoclonus epilepsy: a distinctive phenotype.

Neurol India 2013 Sep-Oct;61(5):537-9

Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, Kerala, India.

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http://dx.doi.org/10.4103/0028-3886.121943DOI Listing
January 2014

Bethlem myopathy: An autosomal dominant myopathy with flexion contractures, keloids, and follicular hyperkeratosis.

Ann Indian Acad Neurol 2013 Oct;16(4):712-5

Department of Neurology, KLE University's Jawaharlal Nehru Medical College and KLES Dr. Prabhakar Kore Hospital and MRC, Belgaum, India.

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http://dx.doi.org/10.4103/0972-2327.120453DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841639PMC
October 2013

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

Brain Dev 2013 May 24;35(5):398-405. Epub 2012 Aug 24.

Department of Neurology, National Institute of Mental Health And Neurosciences, Bangalore, India.

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http://dx.doi.org/10.1016/j.braindev.2012.07.016DOI Listing
May 2013

Genetic analysis of an Indian family with members affected with Waardenburg syndrome and Duchenne muscular dystrophy.

Mol Vis 2012 20;18:2022-32. Epub 2012 Jul 20.

Department of Molecular Reproduction, Development and Genetics, Indian Institute of Science, Bangalore, India.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3413420PMC
December 2012

Lipid storage myopathy with clinical markers of Marfan syndrome: A rare association.

Ann Indian Acad Neurol 2012 Oct;15(4):332-5

Department of Neurology, National Institute of Mental Health and Neurosciences, Bangalore, India.

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http://dx.doi.org/10.4103/0972-2327.104352DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3548382PMC
October 2012

Mitochondrial neurogastrointestinal encephalopathy in an Indian family with possible manifesting carriers of heterozygous TYMP mutation.

J Neurol Sci 2011 Oct 26;309(1-2):131-5. Epub 2011 Jul 26.

Department of Neurology, National Institute of Mental health and Neurosciences, Bangalore, India.

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http://linkinghub.elsevier.com/retrieve/pii/S0022510X1100387
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http://dx.doi.org/10.1016/j.jns.2011.06.052DOI Listing
October 2011

Tubular aggregate myopathy: a phenotypic spectrum and morphological study.

Neurol India 2010 Sep-Oct;58(5):747-51

Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bangalore, India.

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http://dx.doi.org/10.4103/0028-3886.72166DOI Listing
May 2011

Pattern recognition on brain magnetic resonance imaging in alpha dystroglycanopathies.

Neurol India 2010 May-Jun;58(3):460-5

Department of Neurology, National Institute of Mental Health And Neurosciences (NIMHANS), Bangalore, India.

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http://dx.doi.org/10.4103/0028-3886.65925DOI Listing
October 2010

Autosomal recessive tubular aggregate myopathy in an Indian family.

Eur J Paediatr Neurol 2009 Jul 6;13(4):373-5. Epub 2008 Aug 6.

Department of Neurology, KS Hegde Medical Academy, Deralakatte, Mangalore, Karnataka, India.

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http://dx.doi.org/10.1016/j.ejpn.2008.06.008DOI Listing
July 2009

Congenital myopathy with tubular aggregates: report on two siblings from India.

J Child Neurol 2009 Jul 23;24(7):874-8. Epub 2009 Feb 23.

Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bangalore, India.

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http://dx.doi.org/10.1177/0883073808331352DOI Listing
July 2009

A variant form of mucolipidosis IV: report on 4 patients from the Indian subcontinent.

J Child Neurol 2008 Dec;23(12):1443-6

Department of Neurology, National Institute of Mental Health and Neurosciences, Bangalore, India.

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http://journals.sagepub.com/doi/10.1177/0883073808318537
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http://dx.doi.org/10.1177/0883073808318537DOI Listing
December 2008

Clinical features of adult GM1 gangliosidosis: report of three Indian patients and review of 40 cases.

Mov Disord 2004 Nov;19(11):1334-41

Department of Neurology, National Institute of Mental Health and Neurosciences, Bangalore, India.

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http://dx.doi.org/10.1002/mds.20193DOI Listing
November 2004

Myopic strabismus fixus: a mitochondrial myopathy?

Am J Ophthalmol 2003 May;135(5):720-2

Vittala International Institute of Ophthalmology, Bangalore, India.

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http://dx.doi.org/10.1016/s0002-9394(02)02086-xDOI Listing
May 2003