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Govindaraj, Periyasamy
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1

A unique case of hyperammonemia due to CA5A deficiency: Imp..:

Mathew, Rohan Peter ; Ranya Raghavendra, Prashanth ; Disha, Biradar..
American Journal of Medical Genetics Part A.  , 2024
Link: https://doi.org/10.1002/..
 
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2

Mitochondria in biology and medicine – 2023:

Disha, B. ; Mathew, Rohan Peter ; Dalal, Ashwin B....
Mitochondrion.  76 (2024)  - p. 101853 , 2024
Link: https://doi.org/10.1016/..
 
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3

Signatures of high altitude adaptation in Tibeto‐Burman tri..:

De, Saptaparni ; Rai, Divya ; Tamang, Shishir...
American Journal of Human Biology.  35 (2023)  5 - p. , 2023
Link: https://doi.org/10.1002/..
 
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4

A proteomic study to unveil lead toxicity-induced memory im..:

Mohanraj, Nivedha ; Joshi, Neha S. ; Poulose, Roshni...
Toxicology Reports.  9 (2022)  - p. 1501-1513 , 2022
Link: https://doi.org/10.1016/..
 
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5

Genetic spectrum of inherited neuropathies in India:

Nagappa, Madhu ; Sharma, Shivani ; Govindaraj, Periyasamy...
Annals of Indian Academy of Neurology.  25 (2022)  3 - p. 407 , 2022
Link: https://doi.org/10.4103/..
 
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6

Child Neurology: Hereditary Folate Malabsorption:

Huddar, Akshata ; Chiplunkar, Shwetha ; Nagappa, Madhu...
Neurology.  97 (2021)  1 - p. 40-43 , 2021
Link: https://doi.org/10.1212/..
 
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7

Whole exome sequencing reveals a homozygous C1QBP deletion ..:

Guo, Le ; Govindaraj, Periyasamy ; Kievit, Mariëlle...
Neuromuscular Disorders.  31 (2021)  9 - p. 859-864 , 2021
Link: https://doi.org/10.1016/..
 
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8

Clinico-pathological and Molecular Spectrum of Mitochondria..:

Deepha, Sekar ; Govindaraj, Periyasamy ; Sankaran, Bindu Parayil...
Journal of Molecular Neuroscience.  71 (2021)  11 - p. 2219-2228 , 2021
Link: https://doi.org/10.1007/..
 
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9

Contribution of nuclear and mitochondrial gene mutations in..:

Chakrabarty, Sanjiban ; Govindaraj, Periyasamy ; Sankaran, Bindu Parayil...
Journal of Neurology.  268 (2021)  6 - p. 2192-2207 , 2021
Link: https://doi.org/10.1007/..
 
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10

Serum fibroblast growth factor 21 and growth differentiatio..:

Huddar, Akshata ; Govindaraj, Periyasamy ; Chiplunkar, Shwetha...
Mitochondrion.  60 (2021)  - p. 170-177 , 2021
Link: https://doi.org/10.1016/..
 
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11

Ethylmalonic encephalopathy ETHE1 p. D165H mutation alters ..:

Sathe, Gajanan ; Deepha, Sekar ; Gayathri, Narayanappa...
Mitochondrion.  58 (2021)  - p. 64-71 , 2021
Link: https://doi.org/10.1016/..
 
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12

Leukodystrophy Due to eIF2B Mutations in Adults:

Shivaram, Sumanth ; Nagappa, Madhu ; Seshagiri, Doniparthi Venkata...
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.  49 (2021)  5 - p. 708-712 , 2021
Link: https://doi.org/10.1017/..
 
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13

Disrupted structural connectome and neurocognitive function..:

Preethish-Kumar, Veeramani ; Shah, Apurva ; Polavarapu, Kiran...
Journal of Neurology.  269 (2021)  4 - p. 2113-2125 , 2021
Link: https://doi.org/10.1007/..
 
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14

PMP22 Gene–Associated Neuropathies: Phenotypic Spectrum in ..:

Nagappa, Madhu ; Sharma, Shivani ; Govindaraj, Periyasamy...
Journal of Molecular Neuroscience.  70 (2020)  5 - p. 778-789 , 2020
Link: https://doi.org/10.1007/..
 
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15

Leukodystrophies and Genetic Leukoencephalopathies in Child..:

Parayil Sankaran, Bindu ; Nagappa, Madhu ; Chiplunkar, Shwetha...
Journal of Child Neurology.  35 (2020)  7 - p. 433-441 , 2020
Link: https://doi.org/10.1177/..
 
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