N. Gayathri

发表

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

K. Thangaraj, P. Govindaraj, A. Taly, 2018, Clinical Neurology and Neurosurgery.

Hereditary inclusion body myopathy: A myopathy with unique topography of weakness, yet frequently misdiagnosed: Case series and review of literature

M. Goyal, B. Radotra, V. Lal, 2016, Annals of Indian Academy of Neurology.

Manganese‐ and 1‐methyl‐4‐phenylpyridinium‐induced neurotoxicity display differences in morphological, electrophysiological and genome‐wide alterations: implications for idiopathic Parkinson's disease

T. R. Laxmi, M. Sule, P. Alladi, 2017, Journal of neurochemistry.

Mitochondrial Alterations and Oxidative Stress in an Acute Transient Mouse Model of Muscle Degeneration

Yashwanth Subbannayya, A. Nalini, N. Gayathri, 2013, The Journal of Biological Chemistry.

Novel TCAP Mutation c.32C>A Causing Limb Girdle Muscular Dystrophy 2G

K. Thangaraj, A. Nalini, N. Gayathri, 2014, PloS one.

Mapping the protein phosphorylation sites in human mitochondrial complex I (NADH: Ubiquinone oxidoreductase): A bioinformatics study with implications for brain aging and neurodegeneration

Manish Kumar, T. Prasad, N. Gayathri, 2019, Journal of Chemical Neuroanatomy.

Oxidative Damage in Muscular Dystrophy Correlates with the Severity of the Pathology: Role of Glutathione Metabolism

A. Nalini, N. Gayathri, M. M. Srinivas Bharath, 2012, Neurochemical Research.

Secretory activity of mandibular organ fluctuates in response to reproductive season of the field crab Paratelphusa sp. (Brachyura; Decapoda): an ultrastructural study

N. Gayathri, Anilkumar Gopinathan, S. Sarika, 2014, Zoological Studies.

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

Manish Kumar, A. Nalini, T. S. Keshava Prasad, 2016, Journal of neurochemistry.

Efficacy and Limitations of Pulse Cyclophosphamide Therapy in Polymyositis and Dermatomyositis

A. Mahadevan, A. Taly, S. Sinha, 2013, Journal of clinical neuromuscular disease.

Acute thyrotoxic neuropathy—Basedow's paraplegia revisited

S. Shankar, N. Gayathri, L. Pandit, 1998, Journal of Neurological Sciences.

Epilepsia partialis continua in mitochondrial dysfunction: Interesting phenotypic and MRI observations

M. Goyal, A. Taly, S. Sinha, 2008, Annals of Indian Academy of Neurology.

Mitochondrial changes and oxidative stress in muscle pathology

Yashwanth Subbannayya, A. Nalini, N. Gayathri, 2013 .

Pattern recognition on brain magnetic resonance imaging in alpha dystroglycanopathies.

A. Mahadevan, R. Bharath, A. Taly, 2010, Neurology India.

Analysis of calpain-3 protein in muscle biopsies of different muscular dystrophies from India

A. Nalini, N. Gayathri, M. Bharath, 2012, The Indian journal of medical research.

Ethylmalonic encephalopathy ETHE1 p. D165H mutation alters the mitochondrial function in human skeletal muscle proteome.

A. Pandey, G. Sathe, P. Govindaraj, 2021, Mitochondrion.

A comparative study of mPCR, MLPA, and muscle biopsy results in a cohort of children with Duchenne muscular dystrophy: a first study.

A. Nalini, N. Gayathri, P. Kiran, 2015, Neurology India.

Giant Axonal Neuropathy

A. Mahadevan, R. Bharath, A. Taly, 2015, Journal of child neurology.

Progressive myoclonic epilepsy: A clinical, electrophysiological and pathological study from South India

S. Shankar, S. Sinha, P. Satishchandra, 2007, Journal of the Neurological Sciences.

Detection of Dysferlin Gene Pathogenic Variants in the Indian Population in Patients Predicted to have a Dysferlinopathy Using a Blood-based Monocyte Assay and Clinical Algorithm: A Model for Accurate and Cost-effective Diagnosis

M. Hegde, A. Ankala, S. Khadilkar, 2017, Annals of Indian Academy of Neurology.

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

N. Gayathri, S. Panda, J. Kovoor, 2008, Journal of child neurology.

Duchenne muscular dystrophy: a clinical, histopathological and genetic study at a neurology tertiary care center in Southern India.

Sanjeev Jain, A. Nalini, B. Swaminathan, 2009, Neurology India.

Schwartz–Jampel syndrome

T. Issac, N. Gayathri, S. Chandra, 2015, Journal of pediatric neurosciences.

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

P. S. Mathuranath, P. Govindaraj, A. Taly, 2016, Metabolic Brain Disease.

Ullrich congenital muscular dystrophy: report of nine cases from India.

A. Nalini, V. Santosh, N. Gayathri, 2009, Neurology India.

Beevor's sign: a potential clinical marker for GNE myopathy

I. Nishino, Hanns Lochmüller, A. Nalini, 2016, European journal of neurology.

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

K. Thangaraj, S. Ambika, P. Govindaraj, 2017, Investigative ophthalmology & visual science.

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

G. Chandak, Saketh Kapoor, A. Taly, 2012, Molecular vision.

The Y-organ secretory activity fluctuates in relation to seasons of molt and reproduction in the brachyuran crab, Metopograpsus messor (Grapsidae): Ultrastructural and immunohistochemical study.

N. Gayathri, G. Anilkumar, K. Sudha, 2014, General and comparative endocrinology.

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

A. Nalini, N. Gayathri, 2011, Journal of the Neurological Sciences.

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

A. Nalini, R. Christopher, N. Gayathri, 2017, Neuromuscular Disorders.

Dysferlinopathy: spectrum of pathological changes in skeletal muscle tissue.

S. Shankar, A. Nalini, V. Santosh, 2011, Indian journal of pathology & microbiology.

Dysferlinopathy: a clinical and histopathological study of 28 patients from India.

A. Nalini, N. Gayathri, 2008, Neurology India.

A prospective study on the immunophenotypic characterization of limb girdle muscular dystrophies 2 in India.

A. Nalini, N. Gayathri, K. Polavarapu, 2015, Neurology India.

GNE myopathy in India.

Y. Hayashi, A. Nalini, N. Gayathri, 2013, Neurology India.

Sarcoglycanopathy: clinical and histochemical characteristics in 66 patients.

A. Nalini, N. Gayathri, Sarala Das, 2010, Neurology India.

Distal myopathy with rimmed vacuoles: report on clinical characteristics in 23 cases.

A. Nalini, N. Gayathri, R. Dawn, 2010, Neurology India.

Whole‐exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations

S. Chakrabarti, Sudipto Roy, A. Nalini, 2020, European journal of neurology.

Congenital myopathies: clinical and immunohistochemical study.

N. Gayathri, Fazil Thaha, A. Nalini, 2011, Neurology India.

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

K. Thangaraj, P. Govindaraj, A. Taly, 2017, Mitochondrion.

Diagnosis of primary mitochondrial disorders -emphasis on myopathological aspects.

N. Gayathri, Shivani Sharma, S. Deepha, 2021, Mitochondrion.

Clinical, electrophysiological, imaging, and ultrastructural description in 68 patients with neuronal ceroid lipofuscinoses and its subtypes.

Sanjib Sinha, Shobini L. Rao, P. Satishchandra, 2014, Pediatric neurology.

Leber ’ s Hereditary Optic Neuropathy – Specific Mutation

K. Thangaraj, S. Ambika, P. Govindaraj, 2017 .

Haplogroup heterogeneity of LHON patients carrying the m.14484T>C mutation in India.

K. Thangaraj, S. Ambika, P. Govindaraj, 2013, Investigative ophthalmology & visual science.

Genetics Haplogroup Heterogeneity of LHON Patients Carrying the m . 14484 T > C Mutation in India

K. Thangaraj, S. Ambika, P. Govindaraj, 2013 .

Clinical, pathological and molecular findings in two siblings with giant axonal neuropathy (GAN): report from India.

K. Huehne, B. Rautenstrauss, A. Nalini, 2008, European journal of medical genetics.

Giant Axonal Neuropathy: A Pictorial Essay and Review of Literature

R. Bharath, H. Arvinda, N. Gayathri, 2010, The neuroradiology journal.

RETROSPECTIVE ANALYSIS OF OPHTHALMIC AILMENTS IN CHILDREN ATTENDING THE CHILD DEVELOPMENT UNIT IN A TERTIARY CARE HOSPITAL IN SOUTH INDIA

N. Gayathri, R. Vaishnavi, Mary Thomas, 2016 .

Emery dreifuss muscular dystrophy: a clinico-pathological study.

A. Taly, S. Sinha, N. Gayathri, 2006, Neurology India.

Mitochondrial dysfunction in human skeletal muscle biopsies of lipid storage disorder

Manish Kumar, A. Nalini, R. Christopher, 2018, Journal of neurochemistry.

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

A. Nalini, M. Purushottam, N. Gayathri, 2017, BMC Medical Genetics.

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

A. Nalini, P. Richard, J. Urtizberea, 2013, Neurology India.

Cholesterol Ester Storage Disease With Unusual Neurological Manifestations in Two Siblings: A Report From South India

A. Mahadevan, R. Christopher, A. Taly, 2007, Journal of child neurology.

Vasculitic neuropathy in HIV infection: a clinicopathological study.

A. Mahadevan, S. Shankar, V. Santosh, 2001, Neurology India.

Inhibition of mitochondrial complex II in neuronal cells triggers unique pathways culminating in autophagy with implications for neurodegeneration

N. Jamshidi, B. Padmanabhan, N. Gayathri, 2021, Scientific Reports.

Novel Insights into Neuroprotective Strategies Employing NQO1 and DCLK1 in Parkinson’s Disease

N. Gayathri, K. Kanchana, Kandage, 2021 .

Paternal inheritance or a de novo mutation in a Duchenne Muscular Dystrophy pedigree from South India

A. Nalini, M. Purushottam, N. Gayathri, 2008, Journal of the Neurological Sciences.

Neurocytoma/rhabdomyoma (myoneurocytoma) of the cerebellum

S. Shankar, V. Santosh, L. Pal, 1998, Acta Neuropathologica.

Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome

K. Thangaraj, K. Satyamoorthy, P. Govindaraj, 2021, Journal of Neurology.

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

K. Thangaraj, P. Govindaraj, A. Taly, 2015, Mitochondrion.

Myopic strabismus fixus: a mitochondrial myopathy?

N. Gayathri, K. Murthy, Canjeevaram P Venkatesh, 2003, American journal of ophthalmology.

The “Double Panda” Sign in Leigh Disease

A. Taly, S. Sinha, P. Bindu, 2014, Journal of child neurology.

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

K. Thangaraj, A. Taly, S. Sinha, 2014, Brain and Development.

Bilateral hypertrophic olivary nucleus degeneration on magnetic resonance imaging in children with Leigh and Leigh-like syndrome.

K. Thangaraj, A. Taly, S. Sinha, 2014, The British journal of radiology.

BJRD13478 1..8

K. Thangaraj, A. Taly, S. Sinha, 2014 .

Clinico-pathological and Molecular Spectrum of Mitochondrial Polymerase γ Mutations in a Cohort from India

K. Thangaraj, P. Govindaraj, A. Taly, 2021, Journal of Molecular Neuroscience.

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

K. Thangaraj, P. Govindaraj, A. Taly, 2016, Mitochondrion.

Palatal Tremor in POLG‐Associated Ataxia

K. Thangaraj, A. Taly, C. Shwetha, 2015, Movement disorders clinical practice.

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

Manish Kumar, A. Nalini, T. S. Keshava Prasad, 2020, Journal of proteomics.

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

A. Mahadevan, Y. Chickabasaviah, A. Taly, 2015, Annals of Indian Academy of Neurology.

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

A. Mahadevan, Y. Chickabasaviah, A. Taly, 2016, Annals of Indian Academy of Neurology.

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

K. Thangaraj, P. Govindaraj, A. Taly, 2015, Neuropediatrics.

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

A. Nalini, A. Taly, P. Bindu, 2014, Journal of clinical neuromuscular disease.

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

A. Mahadevan, P. Govindaraj, A. Taly, 2018, Multiple sclerosis and related disorders.

Exposure to the neurotoxin 3-nitropropionic acid in neuronal cells induces unique histone acetylation pattern: Implications for neurodegeneration

P. Govindaraj, N. Gayathri, M. M. Srinivas Bharath, 2020, Neurochemistry International.

Characterization of age-dependent changes in the striatum: Response to the mitochondrial toxin 3-nitropropionic acid

Muralidhara, H. Gowda, N. Gayathri, 2017, Mechanisms of Ageing and Development.

Raman spectroscopic studies on screening of myopathies.

U. Nongthomba, S. Vanga, S. Umapathy, 2015, Analytical chemistry.

Variable histomorphology of muscle in congenital muscular dystrophy

N. Gayathri, M. Gourie‐Devi, Sarala Das, 1997, Journal of the Neurological Sciences.

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

K. Thangaraj, P. Govindaraj, A. Taly, 2016, Clinical Neurology and Neurosurgery.

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

P. Mathuranath, P. Govindaraj, A. Taly, 2017, Metabolic Brain Disease.

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

P. Mathuranath, P. Govindaraj, A. Taly, 2017, Metabolic Brain Disease.

Reversible Neuropathy in Chronic Renal Failure

U. Misra, J. Kalita, N. Gayathri, 1998, Nephron.

Oxidative Damage in Muscular Dystrophy Correlates with the Severity of the Pathology: Role of Glutathione Metabolism

A. Nalini, N. Gayathri, M. M. Srinivas Bharath, 2012, Neurochemical Research.

Peripheral neuropathy in metachromatic leucodystrophy. A study of 40 cases from south India

A. Mahadevan, S. Shankar, R. Christopher, 2005, Journal of Neurology, Neurosurgery & Psychiatry.

Menkes Syndrome Presenting as Myoclonic Seizures: Neuroimaging and EEG Observations

G. Arunodaya, S. Sinha, A. Taly, 2007, Journal of child neurology.

Prospective study on sonographic measurement of umbilical cord thickness, foetal fat layer, interventricular septal thickness as predictors of macrosomia in fetus of women with gestational diabetes mellitus

N. Gayathri, N. Janani, D. Vimala., 2018 .

Infantile Onset Encephalomyopathy, Heart Block, and Sensorineural Hearing Loss: RMND1-Associated Mitochondrial Disease

P. Govindaraj, A. Taly, S. Sinha, 2020, Journal of Pediatric Neurology.

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

R. Bharath, R. Christopher, A. Taly, 2013, Brain and Development.

Fabry's disease: An ultrastructural study of nerve biopsy

S. Shankar, V. Santosh, S. Agarwal, 2008, Annals of Indian Academy of Neurology.

Whole exome sequencing reveals a homozygous C1QBP deletion as the cause of progressive external ophthalmoplegia and multiple mtDNA deletions

H. Smeets, P. Govindaraj, A. Taly, 2021, Neuromuscular Disorders.

Natural history of a cohort of Duchenne muscular dystrophy children seen between 1998 and 2014: An observational study from South India

K. Thennarasu, A. Nalini, N. Gayathri, 2018, Neurology India.

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

N. Gayathri, A. Saroja, K. Naik, 2013, Annals of Indian Academy of Neurology.

Metabolic Disorders Presenting as Vacuolar Myopathy

S. Shankar, V. Santosh, N. Gayathri, 1999 .

Disabilities in children with Duchenne muscular dystrophy: a profile.

A. Taly, N. Gayathri, M. Gourie‐Devi, 2001, Journal of rehabilitation medicine.

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

K. Thangaraj, P. Govindaraj, A. Taly, 2016, Mitochondrion.