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9 results on '"Oommen, Abel"'

1. Classical Hirayama disease presenting as progressive spastic quadriparesis

Author

Oommen, Abel, Vengalil, Seena, Baskar, Dipti, Thomas, Aneesha, Kulanthaivelu, Karthik, Bardhan, Mainak, Bhargava, Sanka, and Nalini, Atchayaram

Subjects
Quadriplegia -- Case studies -- Diagnosis, Monomelic amyotrophy -- Case studies -- Diagnosis, Paralysis, Spastic -- Case studies -- Diagnosis, Health
Abstract

Byline: Abel. Oommen, Seena. Vengalil, Dipti. Baskar, Aneesha. Thomas, Karthik. Kulanthaivelu, Mainak. Bardhan, Sanka. Bhargava, Atchayaram. Nalini Dear Sir, Hirayama disease (HD) is a rare cervical flexion-induced myelopathy predominantly seen [...]

Published
2023

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

Author

Seshagiri, Doniparthi Venkata, Huddar, Akshata, Nashi, Saraswati, Ray, Somdattaa, Ramaswamy, Palanyswamy, Oommen, Abel Thomas, Chawla, Tanushree, Yadav, Srikanth, Annapureddy, Jagadish, Jankar, Rahul, Polavarapu, Kiran, Vengalil, Seena, Preethish-Kumar, Veeramani, Warrier, Manjusha, Thomas, Priya Treesa, Shingavi, Leena, Arunachal, Gautham, Yadav, Ravi, and Nalini, Atchayaram

Published
2021
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4. Clinico-radiological comparison between different subgroups of inflammatory myositis

Author

Sridhar, S., primary, Nashi, Saraswati, additional, Kulanthaivelu, Karthik, additional, Vengalil, Seena, additional, Menon, Deepak, additional, Oommen, Abel, additional, Baskar, Dipti, additional, Thomas, Aneesha, additional, Kumar, Vijay, additional, Huddar, Akshata, additional, Unnikrishnan, Gopikrishan, additional, Prathyusha, P.V., additional, and Nalini, Atchayaram, additional

Published
2023
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6. Biotin-Responsive Basal Ganglia Disease: Treatable Metabolic Disorder with SLC19A3 Mutation Presenting as Rapidly Progressive Dementia

Author

Oommen, Abel, Polavarapu, K., Christopher, R., and Netravathi, M.

Subjects
Dementia -- Case studies -- Diagnosis, Gene mutations -- Case studies, Biotin -- Case studies -- Usage, Extrapyramidal disorders -- Diagnosis -- Drug therapy -- Case studies, Metabolic diseases -- Case studies -- Diagnosis -- Drug therapy, Health
Abstract

Byline: Abel. Oommen, K. Polavarapu, R. Christopher, M. Netravathi Background and Aims: Biotin-thiamine-responsive basal ganglia disease (BTBGD) is an autosomal recessive disorder due to mutations in the SLC19A3-gene, typically seen [...]

Published
2022

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

Author

Netravathi, Manjunath, primary, Holla, Vikram Venkappayya, additional, Nalini, Atchayaram, additional, Yadav, Ravi, additional, Vengalil, Seena, additional, Oommen, Abel Thomas, additional, Reshma, Sultana Shaik, additional, Kamble, Nitish, additional, Thomas, Priya Treesa, additional, Maya, Bhat, additional, Pal, Pramod Kumar, additional, and Mahadevan, Anita, additional

Published
2020
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