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103 results for Nalini,+Atchayaram

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Myelin oligodendrocyte glycoprotein-antibody-associated disorder: a new inflammatory CNS demyelinating disorder
Author / Creator:Manjunath, Netravathi ; Holla Vikram Venkappayya ; Atchayaram, Nalini ; Yadav, Ravi ; Vengalil Seena ; Oommen Abel Thomas ; Reshma Sultana Shaik ; Kamble Nitish ; Thomas Priya Treesa ; Bhat, Maya ; Pal, Pramod Kumar ; Mahadevan, Anita
Publisher:Heidelberg: Springer Nature B.V
Journal title:Journal of neurology, 2021-04, Vol.268 (4), p.1419-1433
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Status Dystonicus in Subacute Sclerosing Panencephalitis-A Rare Presentation in Emergency
Author / Creator:Harikrishna, Ganaraja Valakunja ; Chowdary, Mundlamuri Ravindranadh ; Vengalil, Seena ; Nalini, Atchayaram ; Yadav, Ravi
Publisher:Mumbai: Medknow Publications and Media Pvt. Ltd
Journal title:Neurology India, 2023-09, Vol.71 (5), p.994-997
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Myotonic Dystrophy Type 1 (DM1): Clinical Characteristics and Disease Progression in a Large Cohort
Author / Creator:Chawla, Tanushree ; Reddy, Nishanth ; Jankar, Rahul ; Vengalil, Seena ; Polavarapu, Kiran ; Arunachal, Gautham ; Preethish-Kumar, Veeramani ; Nashi, Saraswati ; Bardhan, Mainak ; Rajeshwaran, Jamuna ; Afsar, Mohammad ; Warrier, Manjusha ; Thomas, Priya T ; Thennarasu, Kandavel ; Nalini, Atchayaram
Publisher:India: Wolters Kluwer - Medknow
Journal title:Neurology India, 2024, Vol.72 (1), p.83-89
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Telehealth Services for an Adolescent with Duchenne Muscular Dystrophy (DMD) During the COVID-19 Pandemic
Author / Creator:Sadasivan, Arun ; Warrier, Manjusha G. ; Vengalil, Seena ; Thomas, Priya Treesa ; Nalini, Atchayaram
Publisher:United Kingdom: Routledge
Journal title:Australian social work, 2025-01, Vol.78 (1), p.108-114
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Lymphoma Masquerading as Radiculoneuropathy: A Rare Presentation of Neurolymphomatosis
Author / Creator:Dasari, Nikitha ; Mundlamuri, Ravindranadh Chowdary ; Vengaleel, Seena ; Raja, Pritam ; Yadav, Ravi ; Sadashiva, Nishanth ; Karthick, K ; Nandeesh, BN ; Atchayaram, Nalini
Publisher:India: Wolters Kluwer - Medknow
Journal title:Annals of the Indian Academy of Neurology, 2024-11, Vol.27 (6), p.734-736
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Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome
Author / Creator:Bardhan, Mainak ; Polavarapu, Kiran ; Bevinahalli, Nandeesh N. ; Veeramani, Preethish-Kumar ; Anjanappa, Ram Murthy ; Arunachal, Gautham ; Shingavi, Leena ; Vengalil, Seena ; Nashi, Saraswati ; Chawla, Tanushree ; Nagabushana, Divya ; Mohan, Dhaarini ; Horvath, Rita ; Nishino, Ichizo ; Atchayaram, Nalini
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2021-08, Vol.66 (8), p.813-823
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Respiratory shoulder synkinesis: A rare case report
Author / Creator:Baskar, Dipti ; Vengalil, Seena ; Nashi, Saraswati ; Kamble, Nitish ; Nalini, Atchayaram
Publisher:Mumbai: Wolters Kluwer India Pvt. Ltd
Journal title:Annals of the Indian Academy of Neurology, 2023-07, Vol.26 (4), p.610-611
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Muscle MRI Pattern in Dysferlinopathy and its Correlation with Dysferlin Gait
Author / Creator:Chawla, Tanushree ; Baskar, Dipti ; Polavarapu, Kiran ; Preethish-Kumar, Veeramani ; Nashi, Saraswati ; Vengalil, Seena ; Kulanthaivelu, Karthik ; Saini, Jitender ; Huddar, Akshata ; Unnikrishnan, Gopikrishnan ; Nandeesh, Bevinahalli Nanjegowda ; Nalini, Atchayaram
Publisher:India: Wolters Kluwer - Medknow
Journal title:Annals of the Indian Academy of Neurology, 2025-03, Vol.28 (2), p.182-188
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Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathy
Author / Creator:Sanga, Shamita ; Chakraborty, Sudipta ; Bardhan, Mainak ; Polavarapu, Kiran ; Kumar, Veeramani Preethish ; Bhattacharya, Chandrika ; Nashi, Saraswati ; Vengalil, Seena ; Geetha, Thenral S. ; Ramprasad, Vedam ; Nalini, Atchayaram ; Basu, Analabha ; Acharya, Moulinath
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2023-09, Vol.13 (1), p.15095-10, Article 15095
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Disrupted structural connectome and neurocognitive functions in Duchenne muscular dystrophy: classifying and subtyping based on Dp140 dystrophin isoform
Author / Creator:Preethish-Kumar Veeramani ; Shah, Apurva ; Polavarapu Kiran ; Kumar, Manoj ; Safai Apoorva ; Vengalil Seena ; Nashi Saraswati ; Sekar, Deepha ; Govindaraj Periyasamy ; Afsar Mohammad ; Rajeswaran Jamuna ; Atchayaram, Nalini ; Saini Jitender ; Ingalhalikar Madhura
Publisher:Heidelberg: Springer Nature B.V
Journal title:Journal of neurology, 2022-04, Vol.269 (4), p.2113-2125
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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
Author / Creator:Polavarapu Kiran ; Mathur Aradhna ; Joshi, Aditi ; Nashi Saraswati ; Preethish-Kumar Veeramani ; Bardhan Mainak ; Sharma, Pooja ; Parveen Shaista ; Seth Malika ; Vengalil Seena ; Chawla Tanushree ; Shingavi Leena ; Shamim Uzma ; Nayak Sushmita ; Vivekanand, A ; Töpf Ana ; Roos, Andreas ; Horvath, Rita ; Lochmüller Hanns ; Bevinahalli, Nandeesh ; Arunachal Gautham ; Atchayaram, Nalini ; Faruq Mohammed
Publisher:Heidelberg: Springer Nature B.V
Journal title:Neurogenetics, 2021-10, Vol.22 (4), p.271-285
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Chitotriosidase, a biomarker of amyotrophic lateral sclerosis, accentuates neurodegeneration in spinal motor neurons through neuroinflammation
Author / Creator:Varghese, Anu Mary ; Ghosh, Mausam ; Bhagat, Savita Kumari ; Vijayalakshmi, K. ; Preethish-Kumar, Veeramani ; Vengalil, Seena ; Chevula, Pradeep-Chandra-Reddy ; Nashi, Saraswati ; Polavarapu, Kiran ; Sharma, Meenakshi ; Dhaliwal, Rupinder Singh ; Philip, Mariamma ; Nalini, Atchayaram ; Alladi, Phalguni Anand ; Sathyaprabha, Talakad N. ; Raju, Trichur R.
Publisher:England: BioMed Central Ltd
Journal title:Journal of neuroinflammation, 2020-08, Vol.17 (1), p.232-15, Article 232
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Congenital myasthenic syndrome with mild intellectual disability caused by a recurrent SLC25A1 variant
Author / Creator:Balaraju Sunitha ; Töpf Ana ; McMacken Grace ; Kumar Veeramani Preethish ; Pechmann Astrid ; Roper, Helen ; Vengalil Seena ; Polavarapu Kiran ; Nashi Saraswati ; Mahajan, Niranjan Prakash ; Barbosa, Ines A ; Deshpande Charu ; Taylor, Robert W ; Cossins, Judith ; Beeson, David ; Laurie, Steven ; Kirschner Janbernd ; Horvath, Rita ; McFarland, Robert ; Atchayaram, Nalini ; Lochmüller Hanns
Publisher:Leiden: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2020-03, Vol.28 (3), p.373-377
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Inflammatory myofibroblastic tumors: A short series with an emphasis on the diagnostic and therapeutic challenges
Author / Creator:Nishadham, Vikas ; Rao, Shilpa ; Saravanan, Akshaya ; Kulanthaivelu, Karthik ; Vengalil, Seena ; Venkatappa, Hema A. ; Valasani, Ravi Kiran ; Bardhan, Mainak ; Pruti, Nupur ; Nalini, Atchayaram ; Mahadevan, Anita
Publisher:Germany: Dustri - Verlag Dr. Karl Feistle GmbH & Co. KG
Journal title:Clinical neuropathology, 2023-05, Vol.42 (5), p.100-111
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Late-Onset Presentation of Spastic Paraplegia 3A (ATL1-HSP) and Its Rare Occurrence with Multiple Spinal Neurofibromas
Author / Creator:Davuluri, Anudeep DS ; Ananthasubramanian, Sangeeth T ; Nashi, Saraswati ; Arshad, Faheem ; Padmanabha, Hansashree ; Vengalil, Seena ; Mahale, Rohan ; Mailankody, Pooja ; Srijithesh, PR ; Kulkarni, Girish B ; Pavagada, Mathuranath S ; Alladi, Suvarna ; Nalini, Atchayaram
Publisher:India: Wolters Kluwer - Medknow
Journal title:Annals of the Indian Academy of Neurology, 2024-11, Vol.27 (6), p.727-729
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Novel Variant of the Desert Hedgehog Gene in an Indian Patient of 46, XY Gonadal Dysgenesis with Peripheral Neuropathy
Author / Creator:Srivastava, Kosha ; Baskar, Dipti ; Vengalil, Seena ; Nashi, Saraswati ; Menon, Deepak ; Ganji, Suma R. ; Sanka, Sai B. ; Polavarapu, Kiran ; Rao, Bhoomika M ; Arunachal, Gautham ; Nalini, Atchayaram
Publisher:India: Wolters Kluwer - Medknow
Journal title:Neurology India, 2025-03, Vol.73 (2), p.352-355
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A Novel L1 Linker Mutation in DES Resulted in Total Absence of Protein
Author / Creator:Santhoshkumar Rashmi ; Preethish-Kumar Veeramani ; Polavarapu Kiran ; Reghunathan Dinesh ; Chaudhari Sima ; Satyamoorthy Kapaettu ; Vengalil Seena ; Nashi Saraswati ; Faruq Muhammed ; Joshi, Aditi ; Atchayaram Nalini ; Narayanappa Gayathri
Publisher:Totowa: Springer Nature B.V
Journal title:Journal of molecular neuroscience, 2021-12, Vol.71 (12), p.2468-2473
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Morvan's Syndrome with Myasthenia Gravis: An Autoimmune or Paraneoplastic Association?
Author / Creator:Menon, Deepak ; Chakkera, Priyanka ; Jha, Shreyashi ; Kumar, B Pradeep ; Anjusha, JSS ; Sena, M Chandra ; Rao, Shilpa ; Arshad, Faheem ; Nashi, Saraswati ; Vengalil, Seena ; Alladi, Suvarna ; Nalini, Atchayaram
Publisher:India: Wolters Kluwer - Medknow
Journal title:Annals of the Indian Academy of Neurology, 2024-09, Vol.27 (5), p.612-615
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Cardiac MRI in Duchenne and Becker Muscular Dystrophy
Author / Creator:Girija, Manu Santhappan ; Menon, Deepak ; Polavarapu, Kiran ; Preethish-Kumar, Veeramani ; Vengalil, Seena ; Nashi, Saraswati ; Keertipriya, Madassu ; Bardhan, Mainak ; Thomas, Priya Treesa ; Kiran, Valasani Ravi ; Nishadham, Vikas ; Sadasivan, Arun ; Huddar, Akshata ; Unnikrishnan, Gopi Krishnan ; Barthur, Ashita ; Nalini, Atchayaram
Publisher:India: Wolters Kluwer - Medknow
Journal title:Annals of the Indian Academy of Neurology, 2024-09, Vol.27 (5), p.552-557
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Outpatient Neuropalliative Care Services in a Tertiary Hospital Setting
Author / Creator:Thomas, Priya T. ; Kumar, Gargi S. ; Baby, Priya ; Vengalil, Seena ; Srijithesh, P. R. ; Yamini, B. K. ; Netravathi, M ; Yadav, Ravi ; Pandian, R. Dhanasekhara ; Gupta, Anupam ; Alladi, Suvarna ; Nalini, Atchayaram
Publisher:India: Medknow Publications & Media Pvt. Ltd
Journal title:Annals of the Indian Academy of Neurology, 2024-05, Vol.27 (3), p.332-334
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Myelin oligodendrocyte glycoprotein-antibody-associated disorder: a new inflammatory CNS demyelinating disorder

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Status Dystonicus in Subacute Sclerosing Panencephalitis-A Rare Presentation in Emergency

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Myotonic Dystrophy Type 1 (DM1): Clinical Characteristics and Disease Progression in a Large Cohort

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Telehealth Services for an Adolescent with Duchenne Muscular Dystrophy (DMD) During the COVID-19 Pandemic

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Lymphoma Masquerading as Radiculoneuropathy: A Rare Presentation of Neurolymphomatosis

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

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Respiratory shoulder synkinesis: A rare case report

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Muscle MRI Pattern in Dysferlinopathy and its Correlation with Dysferlin Gait

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Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathy

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

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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

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Chitotriosidase, a biomarker of amyotrophic lateral sclerosis, accentuates neurodegeneration in spinal motor neurons through neuroinflammation

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

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Inflammatory myofibroblastic tumors: A short series with an emphasis on the diagnostic and therapeutic challenges

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Late-Onset Presentation of Spastic Paraplegia 3A (ATL1-HSP) and Its Rare Occurrence with Multiple Spinal Neurofibromas

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Novel Variant of the Desert Hedgehog Gene in an Indian Patient of 46, XY Gonadal Dysgenesis with Peripheral Neuropathy

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A Novel L1 Linker Mutation in DES Resulted in Total Absence of Protein

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Morvan's Syndrome with Myasthenia Gravis: An Autoimmune or Paraneoplastic Association?

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Cardiac MRI in Duchenne and Becker Muscular Dystrophy

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Outpatient Neuropalliative Care Services in a Tertiary Hospital Setting

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