Author

Taly AB

Fromerly Senior Professor of Neurology (NIMHANS) and Emeritus Medical Scientist ( ICMR) - Cited by 8,616 - Clinical research Neurology

Biography

Departments of Neurology and Biostatistics, National Institute of Mental Health and NeuroSciences (NIMHANS), Bangalore. Sleep Abnormalities in Guillain Barre Syndrome: A Clinical and Polysomnographic Study. Guillain Barre Syndrome Mitochondrial disease Inherited Neuropathies Wilson's Disease
Title
Cited by
Year
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome
S Chakrabarty, P Govindaraj, BP Sankaran, M Nagappa, SP Kabekkodu, ...Journal of neurology 268, 2192-2207, 2021202
18
2021
Child neurology: ethylmalonic encephalopathy
P Govindaraj, BP Sankaran, M Nagappa, HR Arvinda, S Deepha, ...Neurology 94 (12), e1336-e1339, 2020202
14
2020
Leukodystrophies and genetic leukoencephalopathies in children specified by exome sequencing in an expanded gene panel
B Parayil Sankaran, M Nagappa, S Chiplunkar, S Kothari, P Govindaraj, ...Journal of Child Neurology 35 (7), 433-441, 2020202
12
2020
Antecedent infections in Guillain‐Barré syndrome patients from south India
D Dutta, M Debnath, M Nagappa, SK Das, R Wahatule, S Sinha, AB Taly, ...Journal of the Peripheral Nervous System 26 (3), 298-306, 2021202
10
2021
Sleep profile and Polysomnography in patients with drug-resistant temporal lobe epilepsy (TLE) due to hippocampal sclerosis (HS) and the effect of epilepsy surgery on sleep-a …
SD Yaranagula, A Asranna, M Nagappa, CS Nayak, PV Pratyusha, ...Sleep Medicine 80, 176-183, 2021202
10
2021
Clinical profile and treatment response in patients with CASPR2 antibody-associated neurological disease
S Shivaram, M Nagappa, DV Seshagiri, A Mahadevan, Y Gangadhar, ...Annals of Indian Academy of Neurology 24 (2), 178, 2021202
9
2021
Ganglioside complex antibodies in an Indian cohort of Guillain‐Barré syndrome
R Wahatule, D Dutta, M Debnath, M Nagappa, A Mahadevan, S Sinha, ...Muscle & Nerve 62 (6), 28-34, 2020202
7
2020
PMP22 Gene–Associated Neuropathies: Phenotypic Spectrum in a Cohort from India
M Nagappa, S Sharma, P Govindaraj, YT Chickabasaviah, R Siram, ...Journal of Molecular Neuroscience 0, 8-89, 2020202
7
2020
Evidence of altered Th17 pathway signatures in the cerebrospinal fluid of patients with Guillain Barré syndrome
Evidence of altered Th1 pathway signatures in the cerebrospinal fluid of patients with Guillain Barré syndromeM Debnath, M Nagappa, D Dutta, PM Talukdar, M Subbanna, ...Journal of Clinical Neuroscience 5, 16-180, 2020202
7
2020
Genetically established familial amyloidotic polyneuropathy from India: Narrating the diagnostic “Odyssey” and a mini review
M Nagappa, S Sinha, A Mahadevan, PS Bindu, KA Krishnan, S Ray, ...Neurology India 68 (5), 1084, 2020202
7
2020
Variations within Toll‐like receptor (TLR) and TLR signaling pathway‐related genes and their synergistic effects on the risk of Guillain‐Barré syndrome
D Dutta, M Nagappa, BV Sreekumaran Nair, SK Das, R Wahatule, ...Journal of the Peripheral Nervous System 27 (2), 131-143, 2022202
5
2022
Case report: chronic fungal meningitis masquerading as tubercular meningitis
N Hesarur, DV Seshagiri, M Nagappa, S Rao, V Santosh, ...The American Journal of Tropical Medicine and Hygiene 103 (4), 1473, 2020202
5
2020
Serum fibroblast growth factor 21 and growth differentiation factor 15: Two sensitive biomarkers in the diagnosis of mitochondrial disorders
Serum fibroblast growth factor 21 and growth differentiation factor 1: Two sensitive biomarkers in the diagnosis of mitochondrial disordersA Huddar, P Govindaraj, S Chiplunkar, S Deepha, JNJ Ponmalar, M Philip, ...Mitochondrion 60, 170-177, 2021202
5
2021
Role of altered IL‐33/ST2 immune axis in the immunobiology of Guillain‐Barré syndrome
PP Sharma, DV Seshagiri, M Nagappa, T Mullapudi, N Sreenivas, S Dey, ...European Journal of Neurology 29 (7), 2074-2083, 2022202
5
2022
Role of pulse methylprednisolone in epileptic encephalopathy: a retrospective observational analysis
A Chatterjee, RC Mundlamuri, R Kenchaiah, A Asranna, M Nagappa, ...Epilepsy Research 173, 106611, 2021202
4
2021
Child neurology: hereditary folate malabsorption
A Huddar, S Chiplunkar, M Nagappa, P Govindaraj, S Sinha, AB Taly, ...Neurology 97 (1), 0-3, 2021202
4
2021
Sequential Nerve Conduction Studies in Guillain-Barre Syndrome: Is it Worth the Efforts?
M Nagappa, AB TalyNeurology India 69 (2), 376, 2021202
4
2021
Spectrum and evolution of EEG changes in anti-NMDAR encephalitis
LG Viswanathan, SA Siddappa, M Nagappa, A Mahadevan, S Duble, ...Annals of Indian Academy of Neurology 24 (), 96, 2021202
3
2021
Clinico-pathological and molecular spectrum of mitochondrial polymerase γ mutations in a cohort from India
S Deepha, P Govindaraj, BP Sankaran, S Chiplunkar, C Kashinkunti, ...Journal of Molecular Neuroscience, 1-10, 2021202
3
2021
Genetic spectrum of inherited neuropathies in India
S Sharma, P Govindaraj, YT Chickabasaviah, R Siram, A Shroti, ...Annals of Indian Academy of Neurology 25 (), 407, 2022202
3
2022

Referred From: https://scholar.google.co.in/citations?user=gSD_qeEAAAAJ&hl=en

Cited by
Citations 8616
h-index 49
i10-index 202
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