Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

15 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Detection of Dysferlin Gene Pathogenic Variants in the Indian Population in Patients Predicted to have a Dysferlinopathy Using a Blood-based Monocyte Assay and Clinical Algorithm: A Model for Accurate and Cost-effective Diagnosis.
Dastur RS, Gaitonde PS, Kachwala M, Nallamilli BRR, Ankala A, Khadilkar SV, Atchayaram N, Gayathri N, Meena AK, Rufibach L, Shira S, Hegde M. Dastur RS, et al. Among authors: atchayaram n. Ann Indian Acad Neurol. 2017 Jul-Sep;20(3):302-308. doi: 10.4103/aian.AIAN_129_17. Ann Indian Acad Neurol. 2017. PMID: 28904466 Free PMC article.
Cryptococal Meningitis Presenting as Acute Cerebellar Syndrome.
Koshy KG, Mundlamuri RC, Vengalil S, Yadav R, Nagarathna S, Bharath RD, Atchayaram N. Koshy KG, et al. Among authors: atchayaram n. Ann Indian Acad Neurol. 2021 Nov-Dec;24(6):983-984. doi: 10.4103/aian.AIAN_733_20. Epub 2021 Jan 11. Ann Indian Acad Neurol. 2021. PMID: 35359532 Free PMC article. No abstract available.
Clinical spectrum, biochemical profile and disease progression of Kennedy disease in an Indian cohort.
Baskar D, Veeramani-Kumar P, Polavarapu K, Nashi S, Vengalil S, Menon D, Thomas A, Bhargava Sanka S, Muddasu Suhasini K, Huddar A, Unnikrishnan G, Bardhan M, Thomas PT, Manjunath N, Atchayaram N. Baskar D, et al. Among authors: atchayaram n. Intern Med J. 2024 Mar;54(3):455-460. doi: 10.1111/imj.16205. Epub 2023 Aug 14. Intern Med J. 2024. PMID: 37578398
Central motor conduction in brachial monomelic amyotrophy.
Pal PK, Atchayaram N, Goel G, Beulah E. Pal PK, et al. Among authors: atchayaram n. Neurol India. 2008 Oct-Dec;56(4):438-43. doi: 10.4103/0028-3886.44820. Neurol India. 2008. PMID: 19127039 Free article.
Tubular aggregate myopathy: a phenotypic spectrum and morphological study.
Ghosh A, Narayanappa G, Taly AB, Chickbasavaiya YT, Mahadevan A, Vani S, Atchayaram N, Mohapatra I, Susarala KS. Ghosh A, et al. Among authors: atchayaram n. Neurol India. 2010 Sep-Oct;58(5):747-51. doi: 10.4103/0028-3886.72166. Neurol India. 2010. PMID: 21045502 Free article.
A Dominant C150Y Mutation in FHL1 Induces Structural Alterations in LIM2 Domain Causing Protein Aggregation In Human and Drosophila Indirect Flight Muscles.
Santhoshkumar R, Preethish-Kumar V, Mangalaparthi KK, Unni S, Padmanabhan B, T S KP, Nongthomba U, Atchayaram N, Narayanappa G. Santhoshkumar R, et al. Among authors: atchayaram n. J Mol Neurosci. 2021 Nov;71(11):2324-2335. doi: 10.1007/s12031-020-01777-4. Epub 2021 Jan 30. J Mol Neurosci. 2021. PMID: 33515430
Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome.
Bardhan M, Polavarapu K, Bevinahalli NN, Veeramani PK, Anjanappa RM, Arunachal G, Shingavi L, Vengalil S, Nashi S, Chawla T, Nagabushana D, Mohan D, Horvath R, Nishino I, Atchayaram N. Bardhan M, et al. Among authors: atchayaram n. J Hum Genet. 2021 Aug;66(8):813-823. doi: 10.1038/s10038-021-00913-1. Epub 2021 Mar 12. J Hum Genet. 2021. PMID: 33712684
15 results