A. Nalini

T. Raju, A. Nalini, K. Shobha, 2007, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Astroglia acquires a toxic neuroinflammatory role in response to the cerebrospinal fluid from amyotrophic lateral sclerosis patients

T. Raju, T. Sathyaprabha, A. Nalini, 2016, Journal of Neuroinflammation.

VEGF alleviates ALS-CSF induced cytoplasmic accumulations of TDP-43 and FUS/TLS in NSC-34 cells

T. Raju, T. Sathyaprabha, A. Nalini, 2017, Journal of Chemical Neuroanatomy.

Pulmonary function tests and diaphragmatic compound muscle action potential in patients with sporadic amyotrophic lateral sclerosis

T. Raju, T. Sathyaprabha, A. Nalini, 2010, Acta neurologica Scandinavica.

Flail arm–like syndrome associated with HIV-1 infection

A. Nalini, A. Desai, S. Mahato, 2009, Annals of Indian Academy of Neurology.

Assessment of pulmonary function in amyotrophic lateral sclerosis.

T. Raju, A. Nalini, C. Pradhan, 2009, The Indian journal of chest diseases & allied sciences.

Reverse split hand syndrome: Dissociated intrinsic hand muscle atrophy pattern in Hirayama disease/brachial monomelic amyotrophy

A. Nalini, K. Polavarapu, C. Prasad, 2017, Amyotrophic lateral sclerosis & frontotemporal degeneration.

(‐)‐Deprenyl alleviates the degenerative changes induced in the neonatal rat spinal cord by CSF from amyotrophic lateral sclerosis patients

T. Raju, A. Nalini, N. Shahani, 2004, Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases.

Distal bimelic amyotrophy (DBMA): Phenotypically distinct but identical on cervical spine MR imaging with brachial monomelic amyotrophy/Hirayama disease

K. Thennarasu, A. Nalini, J. Saini, 2015, Amyotrophic lateral sclerosis & frontotemporal degeneration.

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.

Cerebral Glycolipidoses: Clinical Characteristics of 41 Pediatric Patients

A. Nalini, R. Christopher, 2004, Journal of child neurology.

Cerebral Lipidoses in Patients with Progressive Neurodegeneration: A Study from South India

A. Nalini, R. Christopher, 2002, Public Health Genomics.

Down regulation of trophic factors in neonatal rat spinal cord after administration of cerebrospinal fluid from sporadic amyotrophic lateral sclerosis patients

T. Raju, T. Sathyaprabha, A. Nalini, 2011, Journal of Neural Transmission.

Source and Vocal Tract Cues for Speech-Based Classification of Patients with Parkinson's Disease and Healthy Subjects

A. Nalini, P. Ghosh, R. Yadav, 2021, Interspeech.

Deletion analysis of spinal muscular atrophy in southern Indian population.

A. Nalini, A. Taly, B. Swaminathan, 2008, Neurology India.

Myelin oligodendrocyte glycoprotein-antibody-associated disorder: a new inflammatory CNS demyelinating disorder

A. Mahadevan, A. Nalini, P. Pal, 2020, Journal of Neurology.

Congenital myasthenic syndrome with mild intellectual disability caused by a recurrent SLC25A1 variant

Robert W. Taylor, H. Lochmüller, R. Horvath, 2019, European Journal of Human Genetics.

Perilesional gliosis around solitary cerebral parenchymal cysticerci and long‐term seizure outcome: A prospective study using serial magnetization transfer imaging

K. Thennarasu, A. Nalini, A. de Souza, 2011, Epilepsia.

Prospective Quantitative Imaging Study by Magnetisation Transfer for Appearance of Perilesional Gliosis in Solitary Cerebral Cysticercal Lesion

K. Thennarasu, A. Nalini, A. de Souza, 2010, The neuroradiology journal.

A founder mutation in the GMPPB gene [c.1000G > A (p.Asp334Asn)] causes a mild form of limb-girdle muscular dystrophy/congenital myasthenic syndrome (LGMD/CMS) in South Indian patients

H. Lochmüller, R. Horvath, M. Faruq, 2021, neurogenetics.

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.

Comparison of The Carrier Frequency of Pathogenic Variants of DMD Gene in an Indian Cohort.

A. Nalini, D. Nagabushana, K. Polavarapu, 2021, Journal of neuromuscular diseases.

Marchiafava-Bignami disease: Two cases with magnetic resonance imaging and positron emission tomography scan findings.

A. Nalini, R. Dawn, J. Kovoor, 2009, Neurology India.

PET-MRI in idiopathic inflammatory myositis: a comparative study of clinical and immunological markers with imaging findings

A. Nalini, K. Polavarapu, B. Nandeesh, 2022, Neurological Research and Practice.

RESPIRATORY DYSFUNCTIONS IN CHILDREN WITH DUCHENNE MUSCULAR DYSTROPHY

T. Raju, T. Sathyaprabha, A. Nalini, 2016 .

Altered REM sleep architecture in patients with Myotonic dystrophy type 1: is related to sleep apnea?

A. Nalini, R. Yadav, K. Polavarapu, 2021, Sleep medicine.

Novel CSF1R variant in adult-onset leukoencephalopathy masquerading as frontotemporal dementia: a follow-up study

A. Nalini, R. Yadav, Silambarasan Maskomani, 2021, Neurocase.

Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia.

J. Ragoussis, R. Schüle, L. Schöls, 2022, The New England journal of medicine.

Mutation pattern in 606 Duchenne muscular dystrophy children with a comparison between familial and non-familial forms: a study in an Indian large single-center cohort

T. Delhaas, T. Sathyaprabha, A. Nalini, 2019, Journal of Neurology.

Chitotriosidase - a putative biomarker for sporadic amyotrophic lateral sclerosis

T. Raju, A. Varghese, T. Sathyaprabha, 2013, Clinical Proteomics.

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

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

Rosai Dorfman disease: Case with extensive dural involvement and cerebrospinal fluid pleocytosis

A. Nalini, V. Santosh, S. Jitender, 2012, Journal of the Neurological Sciences.

Cerebrospinal Fluid from Patients with Sporadic Amyotrophic Lateral Sclerosis Induces Degeneration of Motor Neurons Derived from Human Embryonic Stem Cells

T. Raju, R. Sumitha, T. Sathyaprabha, 2018, Molecular Neurobiology.

Cerebrospinal Fluid from Sporadic Amyotrophic Lateral Sclerosis Patients Induces Mitochondrial and Lysosomal Dysfunction

K. Datta, H. Gowda, T. Raju, 2016, Neurochemical Research.

Vascular Endothelial Growth Factor Attenuates Neurodegenerative Changes in the NSC-34 Motor Neuron Cell Line Induced by Cerebrospinal Fluid of Sporadic Amyotrophic Lateral Sclerosis Patients

T. Raju, T. Sathyaprabha, A. Nalini, 2011, Neurodegenerative Diseases.

Thymic Lesions in Myasthenia Gravis: A Clinicopathological Study from India.

A. Nalini, K. Polavarapu, B. Nandeesh, 2022, Journal of neuromuscular diseases.

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

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

Psychosocial challenges in family caregiving with children suffering from Duchenne muscular dystrophy.

A. Nalini, P. Thomas, P. Rajaram, 2014, Health & social work.

Biotin-Responsive Basal Ganglia Disease: A Treatable and Reversible Neurological Disorder of Childhood

U. Muthane, A. Nalini, P. Bindu, 2009, Journal of child neurology.

Clinicopathological profile of polyneuropathy, organomegaly, endocrinopathy, M protein and skin changes (POEMS) syndrome

A. Mahadevan, S. Shankar, A. Nalini, 2011, Journal of Clinical Neuroscience.

Magnetic resonance neurography identifies involvement of plexuses in leprous neuropathy.

A. Mahadevan, A. Nalini, J. Saini, 2015, Neurology India.

Case Report: Neurobrucellosis with Plastered Spinal Arachnoiditis: A Magnetic Resonance Imaging-Based Report.

A. Nalini, J. Saini, K. Bhattacharya, 2018, The American journal of tropical medicine and hygiene.

Brain and Spinal Cord Lesions in Leprosy: A Magnetic Resonance Imaging-Based Study.

G. Parry, A. Mahadevan, A. Nalini, 2019, The American journal of tropical medicine and hygiene.

Appropriately Selected Nerve in Suspected Leprous Neuropathy Yields High Positive Results for Mycobacterium leprae DNA by Polymerase Chain Reaction Method.

G. Parry, A. Mahadevan, A. Nalini, 2020, The American journal of tropical medicine and hygiene.

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.

Mutation Spectrum of Primary Lipid Storage Myopathies

I. Nishino, A. Nalini, M. Faruq, 2022, Annals of Indian Academy of Neurology.

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

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

Muscle MRI in Duchenne muscular dystrophy: Evidence of a distinctive pattern

T. Sathyaprabha, A. Nalini, R. Bharath, 2016, 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.

Clinical, genetic profile and disease progression of sarcoglycanopathies in a large cohort from India: high prevalence of SGCB c.544A > C

A. Nalini, K. Polavarapu, S. Vengalil, 2022, neurogenetics.

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.

Early or late appearance of “dropped head syndrome” in amyotrophic lateral sclerosis

A Nalini, A. Nalini, M Gourie-Devi, 2003, Journal of neurology, neurosurgery, and psychiatry.

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.

Spectrum of magnetic resonance imaging findings in a family with giant axonal neuropathy confirmed by genetic studies.

A. Nalini, G. Goel, S. Ravishankar, 2009, Neurology India.

Sotos syndrome: An interesting disorder with gigantism

A. Nalini, A. Biswas, 2008, Annals of Indian Academy of Neurology.

Chronic eosinophilic meningitis as a manifestation of isolated spinal neurocysticercosis: A rare case and a review of literature

A. Nalini, Y. Chickabasaviah, M. Netravathi, 2018, Neurology India.

Natural history of solitary cerebral cysticercosis on serial magnetic resonance imaging and the effect of albendazole therapy on its evolution

K. Thennarasu, A. Nalini, J. Kovoor, 2009, Journal of the Neurological Sciences.

Solitary cerebral parenchymal cysticercosis: a prospective comparative study with computed tomography and magnetic resonance imaging.

A. Nalini, A. Souza, S. G. Srikanth, 2013, Neurology India.

Severe form of radiculo - myelo - neuropathy with meningo - encephalitis secondary to Angiostrongylus cantonensis infection: unusual corpus callosal lesions and serial magnetic resonance imaging findings.

A. Nalini, J. Saini, Vinay S Hegde, 2013, Neurology India.

Anti-AChR, MuSK, and LRP4 antibodies coexistence: A rare and distinct subtype of myasthenia gravis from Indian subcontinent.

A. Nalini, S. Patil, K. Polavarapu, 2018, Clinica chimica acta; international journal of clinical chemistry.

Comparison of Speech Tasks for Automatic Classification of Patients with Amyotrophic Lateral Sclerosis and Healthy Subjects

Prasanta Kumar Ghosh, Aravind Illa, B. K. Yamini, 2018, 2018 IEEE International Conference on Acoustics, Speech and Signal Processing (ICASSP).

Ventral longitudinal intraspinal fluid collection: Rare presentation as brachial amyotrophy and intracranial hypotension

A. Nalini, M. Netravathi, K. Polavarapu, 2019, The journal of spinal cord medicine.

Monomelic amyotrophy: Clinical profile and natural history of 279 cases seen over 35 years (1976–2010)

K. Thennarasu, A. Nalini, M. Gourie‐Devi, 2014, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Mitochondrial dysfunction in human skeletal muscle biopsies of lipid storage disorder

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

Missing genetic variations in GNE myopathy: rearrangement hotspots encompassing 5′UTR and founder allele

I. Nishino, T. Yonekawa, A. Nalini, 2016, Journal of Human Genetics.

Neuropsychological Profile of Duchenne Muscular Dystrophy

A. Nalini, J. Rajeswaran, Anna Roshini Perumal, 2015, Applied neuropsychology. Child.

Amide proton transfer imaging for differentiation of tuberculomas from high-grade gliomas: Preliminary experience

A. Nalini, J. Saini, Shilpa Rao, 2021, The neuroradiology journal.

Recessive variants of MuSK are associated with late onset CMS and predominant limb girdle weakness

M. Gut, I. Gut, S. Beltran, 2018, American journal of medical genetics. Part A.

Hoffmann's syndrome with unusually long duration: Report on clinical, laboratory and muscle imaging findings in two cases

A. Nalini, P. Kalra, C. Govindaraju, 2014, Annals of Indian Academy of Neurology.

Hoffmann’s syndrome with unusually long duration: Report on clinical, laboratory and muscle imaging ﬁ ndings in two cases Case Report

A. Nalini, C. Govindaraju, P. Kalra, 2022 .

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.

Expanding the Phenotypic Spectrum of ECEL1-Associated Distal Arthrogryposis

Hanns Lochmüller, A. Nalini, K. Polavarapu, 2021, Children.

Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome

I. Nishino, R. Horvath, A. Nalini, 2021, Journal of Human Genetics.

Genomics of rare genetic diseases—experiences from India

V. R. Rajendran, K. M. Cherian, Sruthi S. Nair, 2019, Human Genomics.

A. Nalini, Y. Nishimoto, I. Mizuta, 2020, Frontiers in Neurology.

CARASIL families from India with 3 novel null mutations in the HTRA1 gene

A. Nalini, O. Onodera, J. Saini, 2017, Neurology.

Astroglia acquires a toxic neuroinflammatory role in response to the cerebrospinal fluid from amyotrophic lateral sclerosis patients

T. Raju, T. Sathyaprabha, A. Nalini, 2016, Journal of Neuroinflammation.

Clinical, Biochemical, Radiological, and Genetic Profile of Patients with Homocysteine Remethylation Pathway Defect and Spastic Paraplegia

P. S. Mathuranath, P. Mathuranath, A. Nalini, 2021, Annals of Indian Academy of Neurology.

Disrupted structural connectome and neurocognitive functions in Duchenne muscular dystrophy: classifying and subtyping based on Dp140 dystrophin isoform

M. Ingalhalikar, A. Nalini, P. Govindaraj, 2021, Journal of Neurology.

Identification of a shared, common haplotype cosegregating with an SGCB c.544A>C mutation in Indian patients affected with sarcoglycanopathy

A. Nalini, S. Chakraborty, M. Bardhan, 2021, medRxiv.

Ankle-Foot Orthosis in Duchenne Muscular Dystrophy: A 4 year Experience in a Multidisciplinary Neuromuscular Disorders Clinic

A. Nalini, A. Taly, Anupam Gupta, 2017, The Indian Journal of Pediatrics.

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.

Congenital Myopathy With Tubular Aggregates: Report on Two Siblings From India

A. Nalini, G. Narayanappa, Fazil Thaha, 2009, Journal of child neurology.

Neurofilament phosphorylation is enhanced in cultured chick spinal cord neurons exposed to cerebrospinal fluid from amyotrophic lateral sclerosis patients

T. Raju, A. Nalini, T. Nagaraja, 2004, Acta Neuropathologica.

Co-VAN study: COVID-19 vaccine associated neurological diseases- an experience from an apex neurosciences centre and review of the literature

A. Nalini, P. Pal, Vishal Patel, 2022, Journal of Clinical Neuroscience.

HARLEQUIN FOETUS - CONGENITAL ICHTHYOSIS - A CASE REPORT

A. Nalini, R. Thirumal, Shery Angel Rajakumar, 2013 .

Neuroimaging in leprosy: The nerves and beyond

A. Mahadevan, A. Nalini, J. Saini, 2020 .

Influence of hydrotherapy on clinical and cardiac autonomic function in migraine patients

T. Raju, T. Sathyaprabha, A. Nalini, 2016, Journal of neurosciences in rural practice.

Cross-Sectional Area Reference Values of Nerves in the Upper and Lower Extremities using Ultrasonography in the Indian Population

A. Nalini, L. Visser, T. Kandavel, 2021, Clinical Neurophysiology.

Sympathetic skin response in monomelic amyotrophy

A. Nalini, M. Gourie‐Devi, 2001, Acta neurologica Scandinavica.

Assessment of cardiac autonomic function in patients with Duchenne muscular dystrophy using short term heart rate variability measures.

T. Raju, T. Sathyaprabha, A. Nalini, 2014, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Madras motor neuron disease (MMND): Clinical description and survival pattern of 116 patients from Southern India seen over 36 years (1971–2007)

K. Thennarasu, A. Nalini, N. Krishna, 2008, Journal of the Neurological Sciences.

Sural nerve biopsy in chronic inflammatory demyelinating polyneuropathy: are supportive pathologic criteria useful in diagnosis?

A. Mahadevan, S. Shankar, A. Nalini, 2010, Neurology India.

C9orf72 hexanucleotide repeat expansion in Indian patients with ALS: a common founder and its geographical predilection

A. Srivastava, M. Faruq, A. Nalini, 2020, Neurobiology of Aging.

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.

Multichannel somato sensory evoked potential study demonstrated abnormalities in cervical cord function in brachial monomelic amyotrophy.

A. Nalini, S. Praveen-kumar, D. Subbakrishna, 2008, Neurology India.

Intrafamilial phenotypic variations in familial cases of cervical flexion induced myelopathy/Hirayama disease

A. Nalini, K. Bhattacharya, N. Pruthi, 2018, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Familial monomelic amyotrophy: a case report from India

A. Nalini, E. Ratnavalli, L. Lokesh, 2004, Journal of the Neurological Sciences.

Neuro-Cardio-Autonomic Modulations in Children with Duchenne Muscular Dystrophy.

T. Raju, T. Sathyaprabha, A. Nalini, 2023, Journal of neuromuscular diseases.

Multiparametric magnetic resonance imaging features of giant intracranial tuberculomas

A. Nalini, M. Netravathi, J. Saini, 2021, Clinical Neurology and Neurosurgery.

Clinical characteristics and survival pattern of 1153 patients with amyotrophic lateral sclerosis: Experience over 30 years from India

K. Thennarasu, A. Nalini, D. Kulshreshtha, 2008, Journal of the Neurological Sciences.

New-onset seizures among HIV infected drug naïve patients from south India

S. Shankar, A. Nalini, V. Ravi, 2005 .

Case Report: Post-Chikungunya-Associated Myeloneuropathy.

A. Nalini, R. Yadav, A. Patwardhan, 2021, The American journal of tropical medicine and hygiene.

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.

T2 relaxometry helps prognosticate seizure outcome in patients with solitary cerebral cysticercosis

K. Thennarasu, A. Nalini, J. Saini, 2017, Journal of the Neurological Sciences.

Quantitative Serial T2 Relaxometry: A Prospective Evaluation in Solitary Cerebral Cysticercosis

K. Thennarasu, A. Nalini, J. Saini, 2014, The neuroradiology journal.

Randomized controlled trial of albendazole in new onset epilepsy and MRI confirmed solitary cerebral cysticercal lesion: Effect on long-term seizure outcome

K. Thennarasu, A. Nalini, A. Souza, 2009, Journal of the Neurological Sciences.

Etiogenic factors present in the cerebrospinal fluid from amyotrophic lateral sclerosis patients induce predominantly pro-inflammatory responses in microglia

T. Raju, T. Sathyaprabha, A. Nalini, 2017, Journal of Neuroinflammation.

Palliative Care in Duchenne Muscular Dystrophy: A Study on Parents' Understanding

A. Nalini, K. Polavarapu, S. Vengalil, 2021, Indian journal of palliative care.

Role of VEGF and VEGFR2 Receptor in Reversal of ALS-CSF Induced Degeneration of NSC-34 Motor Neuron Cell Line

T. Raju, R. Sumitha, A. Varghese, 2014, Molecular Neurobiology.

Phenotype Genotype Characterization of FKRP-related Muscular Dystrophy among Indian Patients

A. Nalini, K. Polavarapu, B. Nandeesh, 2023, Journal of neuromuscular diseases.

Large Region of Homozygous (ROH) Identified in Indian Patients with Autosomal Recessive Limb-Girdle Muscular Dystrophy with p.Thr182Pro Variant in SGCB Gene

A. Nalini, V. Pai, Rikita Gupta, 2023, Human Mutation.

Symposium 3: Motor neuron disease SY3.1. Monomelic amyotrophy – Experience from a large cohort

A. Nalini, K. Polavarapu, D. Bhat, 2021, Clinical Neurophysiology.

Madras motor neuron disease (MMND) is distinct from the riboflavin transporter genetic defects that cause Brown–Vialetto–Van Laere syndrome

H. Houlden, A. Pandraud, A. Nalini, 2013, Journal of the Neurological Sciences.

Familial Madras motor neuron disease (FMMND): Study of 15 families from southern India

K. Thennarasu, A. Nalini, R. Gope, 2006, Journal of the Neurological Sciences.

Madras motor neuron disease variant, clinical features of seven patients

A. Nalini, M. Gourie‐Devi, 2003, Journal of the Neurological Sciences.

Oligodendroglia Confer Neuroprotection to NSC-34 Motor Neuronal Cells Against the Toxic Insults of Cerebrospinal Fluid from Sporadic Amyotrophic Lateral Sclerosis Patients

T. Raju, A. Varghese, T. Sathyaprabha, 2023, Molecular Neurobiology.

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

T. Raju, A. Nalini, P. Alladi, 2018, Disease Models & Mechanisms.

Exposure to cerebrospinal fluid of sporadic Amyotrophic Lateral Sclerosis patients alters Nav1.6 and Kv1.6 channel expression in rat spinal motor neurons

T. Raju, T. Sathyaprabha, A. Nalini, 2009, Brain Research.

Acoustic-to-Articulatory Inversion for Dysarthric Speech by Using Cross-Corpus Acoustic-Articulatory Data

Prasanta Kumar Ghosh, Sarthak Kumar Maharana, Aravind Illa, 2021, ICASSP 2021 - 2021 IEEE International Conference on Acoustics, Speech and Signal Processing (ICASSP).

Social Cognition Deficits Are Pervasive across Both Classical and Overlap Frontotemporal Dementia Syndromes

A. Nalini, P. Pal, S. Alladi, 2020, Dementia and Geriatric Cognitive Disorders Extra.

Raw Speech Waveform Based Classification of Patients with ALS, Parkinson's Disease and Healthy Controls Using CNN-BLSTM

Prasanta Kumar Ghosh, Dipanjan Gope, Pradeep Reddy, 2020, INTERSPEECH.

Analysis of Cymbopogon Citratus, Pinus sylvestris and Syzygium cumini biodiesel feedstocks for its fatty acid composition

A. Nalini, M. Prabhahar, S. Sendilvelan, 2020 .

A meta-ethnographic synthesis of lived experience of spouse caregivers in chronic illness

A. Nalini, S. Vengalil, S. Nashi, 2021, Qualitative Social Work.

Resistance Heated Catalytic Converter (RHCC) with copper oxide catalyst for reducing HC/CO emission from automobile

A. Nalini, M. Prabhahar, S. Sendilvelan, 2020 .

Reactive Astrogliosis in Neonatal Rat Spinal Cord after Exposure to Cerebrospinal Fluid from Patients with Amyotrophic Lateral Sclerosis

T. Raju, A. Nalini, N. Shahani, 1998, Experimental Neurology.

BRIEF COMMUNICATION Reactive Astrogliosis in Neonatal Rat Spinal Cord after Exposure to Cerebrospinal Fluid from Patients with Amyotrophic Lateral Sclerosis

T. Raju, A. Nalini, N. Shahani, 1998 .

Cribriform Appearance of White Matter in Canavan Disease Associated with Novel Mutations of ASPA Gene

R. Kumari, M. Faruq, A. Nalini, 2021, Journal of Pediatric Genetics.

Genotype–phenotype correlation and natural history study of dysferlinopathy: a single-centre experience from India

K. Thangaraj, M. Faruq, A. Nalini, 2022, neurogenetics.

Mutation Spectrum of GNE Myopathy in the Indian Sub-Continent.

P. Majumder, A. Nalini, A. Bhattacharya, 2018, Journal of neuromuscular diseases.

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.

Development of Guidelines for Spouses Engaged in Home-Based Care of Persons With Motor Neuron Disease From Indian Context

A. Nalini, S. Vengalil, S. Nashi, 2022, Journal of patient experience.

Caregiver burden and quality of life of patients with amyotrophic lateral sclerosis in India

A. Nalini, K. Polavarapu, S. Vengalil, 2018, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Clinical and imaging characteristics of 16 patients with autoimmune neuronal synaptic encephalitis.

A. Mahadevan, A. Nalini, P. Pal, 2015, Neurology India.

Familial amyotrophic lateral sclerosis: first report from India.

A. Nalini, M. Veerendrakumar, G. Yeshraj, 2006, Neurology India.

Speech task based automatic classification of ALS and Parkinson’s Disease and their severity using log Mel spectrograms

Prasanta Kumar Ghosh, Dipanjan Gope, Aravind Illa, 2020, 2020 International Conference on Signal Processing and Communications (SPCOM).

Integrated Home-Based Palliative Care in Motor Neuron Disease: A Case Report from Low- Middle Income Country

A. Nalini, S. Vengalil, P. Thomas, 2021, Journal of social work in end-of-life & palliative care.

Resting heart rate variability as a diagnostic marker of cardiovascular dysautonomia in postural tachycardia syndrome

T. Sathyaprabha, A. Nalini, K. Udupa, 2022, Journal of basic and clinical physiology and pharmacology.

Altered neuronal activities in the motor cortex with impaired motor performance in adult rats observed after infusion of cerebrospinal fluid from amyotrophic lateral sclerosis patients

T. Raju, A. Nalini, T. Laxmi, 2010, Behavioural Brain Research.

Effect of Yoga as an Add-on Therapy in the Modulation of Heart Rate Variability in Children with Duchenne Muscular Dystrophy

T. Raju, T. Sathyaprabha, A. Nalini, 2019, International journal of yoga.

Neurofilament phosphorylation is increased in ventral horn neurons of neonatal rat spinal cord exposed to cerebrospinal fluid from patients with amyotrophic lateral sclerosis.

T. Raju, A. Nalini, N. Shahani, 1995, Neurodegeneration : a journal for neurodegenerative disorders, neuroprotection, and neuroregeneration.

Reach task-associated excitatory overdrive of motor cortical neurons following infusion with ALS-CSF

T. Raju, A. Nalini, M. Raghavan, 2013, Journal of Neural Transmission.

Distinct and Recognisable Muscle MRI Pattern in a Series of Adults Harbouring an Identical GMPPB Gene Mutation.

H. Lochmüller, M. Faruq, A. Nalini, 2021, Journal of neuromuscular diseases.

Mutations causing congenital myasthenia reveal principal coupling pathway in the acetylcholine receptor ε-subunit.

S. Sine, A. Engel, A. Nalini, 2018, JCI insight.

Evaluation of Cardiac, Autonomic Functions in Ambulant Patients with Duchenne Muscular Dystrophy

T. Sathyaprabha, A. Nalini, K. Udupa, 2023, SN Comprehensive Clinical Medicine.

A. Nalini, D. Baskar, H. Padmanabha, 2023, Journal of neuromuscular diseases.

Mitochondrial DNA variations in Madras motor neuron disease.

R. Tamang, K. Thangaraj, A. Nalini, 2013, Mitochondrion.

Lived Experience of Spouses of Persons with Motor Neuron Disease: Preliminary Findings through Interpretative Phenomenological Analysis

A. Nalini, K. Polavarapu, S. Vengalil, 2020, Indian journal of palliative care.

Differential expression of microRNA-206 in the gastrocnemius and biceps brachii in response to CSF from sporadic amyotrophic lateral sclerosis patients

T. Raju, R. Sumitha, T. Sathyaprabha, 2014, Journal of the Neurological Sciences.

TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease

Pedro Rebelo-Guiomar, L. Van Haute, M. Minczuk, 2023, Nature Communications.

Hemiplegia: an initial manifestation of Japanese encephalitis.

A. Nalini, G. Arunodaya, A. Taly, 2003, Neurology India.

Recessive VAMP1 mutations associated with severe congenital myasthenic syndromes - A recognizable clinical phenotype.

H. Lochmüller, A. Nalini, Vykuntaraju K Gowda, 2021, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Effect of posture on levels of arousal and awareness in vegetative and minimally conscious state patients: a

A. Nalini, S. Ravishankar, 2004 .

Vitamin B-12 , serum folate , and cognitive change between 11 and 79 years

A. Nalini, S. Ravishankar, 2022 .

Evidence for Mycobacterium leprae Drug Resistance in a Large Cohort of Leprous Neuropathy Patients from India.

G. Parry, A. Mahadevan, A. Nalini, 2020, The American journal of tropical medicine and hygiene.

Voice based classification of patients with Amyotrophic Lateral Sclerosis, Parkinson’s Disease and Healthy Controls with CNN-LSTM using transfer learning

Prasanta Kumar Ghosh, Dipanjan Gope, N. SuhasB., 2020, ICASSP 2020 - 2020 IEEE International Conference on Acoustics, Speech and Signal Processing (ICASSP).

Letter regarding “Detection of cerebral cortical vein thrombosis with high-resolution susceptibility weighted imaging — a comparison with MR venography and standard MR sequences”, a case demonstrating shortcoming of SWI in detecting clots in the late subacute phase

A. Nalini, J. Saini, Sabhan Ahmed, 2023, Neuroradiology.

Genomics of rare genetic diseases—experiences from India

V. R. Rajendran, K. M. Cherian, Sruthi S. Nair, 2019, Human Genomics.

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.

Effect of Yoga and Physiotherapy on Pulmonary Functions in Children with Duchenne Muscular Dystrophy – A Comparative Study

T. Raju, T. Sathyaprabha, A. Nalini, 2021, International Journal of Yoga.

Obstructive Hydrocephalus as the Solitary Manifestation of Young Onset Erdheim–Chester Disease

A. Nalini, D. Baskar, S. Vengalil, 2023, Annals of Indian Academy of Neurology.

Distal bimelic amyotrophy (DBMA): Phenotypically distinct but identical on cervical spine MR imaging with brachial monomelic amyotrophy/Hirayama disease

K. Thennarasu, A. Nalini, J. Saini, 2015, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Experimental Setup for Investigating the PV Cells with Distinctive Aspects - I

S. Bhuvaneswari, A. Nalini, S. Rama, 2018, 2018 4th International Conference on Electrical Energy Systems (ICEES).

Cerebrospinal Fluid from Sporadic Amyotrophic Lateral Sclerosis Patients Induces Mitochondrial and Lysosomal Dysfunction

K. Datta, H. Gowda, T. Raju, 2015, Neurochemical Research.

Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies

David L. Bennett, T. Hornemann, S. Züchner, 2023, Brain : a journal of neurology.

Neuromuscular disease genetics in under-represented populations: increasing data diversity

K. Thangaraj, P. Chinnery, S. Efthymiou, 2023, Brain : a journal of neurology.

Inflammatory Myositis in a Child due to Anti-NXP2 Antibody, First Case Report from India

A. Nalini, S. Alladi, G. Kulkarni, 2022, Neurology India.

Respiratory Shoulder Synkinesis: A Rare Case Report

A. Nalini, N. Kamble, D. Baskar, 2023, Annals of Indian Academy of Neurology.

Family with Ehlers–Danlos syndrome (combined classic and vascular type) with rare presentation of progressive myopathy and unusual association of severe facial and trigeminal motor weakness

A. Nalini, N. Gayathri, K. Polavarapu, 2017, Neurology India.

Static and Dynamic Source and Filter Cues for Classification of Amyotrophic Lateral Sclerosis Patients and Healthy Subjects

A. Nalini, P. Ghosh, Tanuka Bhattacharjee, 2023, ICASSP 2023 - 2023 IEEE International Conference on Acoustics, Speech and Signal Processing (ICASSP).

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

A. Nalini, M. Nagappa, G. Narayanappa, 2013, Neurology India.

Disseminated Cysticercosis in Indian Scenario – Experience from a Teaching University Hospital

P. Satishchandra, A. Nalini, P. Pal, 2022, Neurology India.