Bellad A - Search Results

1

PLA2G6-associated neurodegeneration in four different populations-case series and literature review.

Hanna Al-Shaikh R, Milanowski LM, Holla VV, Kurihara K, Yadav R, Kamble N, Muthusamy B, Bellad A, Koziorowski D, Szlufik S, Hoffman-Zacharska D, Fujioka S, Tsuboi Y, Ross OA, Wierenga K, Uitti RJ, Wszolek Z, Pal PK. Hanna Al-Shaikh R, et al. Among authors: bellad a. Parkinsonism Relat Disord. 2022 Aug;101:66-74. doi: 10.1016/j.parkreldis.2022.06.016. Epub 2022 Jun 30. Parkinsonism Relat Disord. 2022. PMID: 35803092 Review.

2

A Novel Missense Variant in PHF6 Gene Causing Börjeson-Forssman-Lehman Syndrome.

Bellad A, Bandari AK, Pandey A, Girimaji SC, Muthusamy B. Bellad A, et al. J Mol Neurosci. 2020 Sep;70(9):1403-1409. doi: 10.1007/s12031-020-01560-5. Epub 2020 May 12. J Mol Neurosci. 2020. PMID: 32399860

3

A Novel LINS1 Truncating Mutation in Autosomal Recessive Nonsyndromic Intellectual Disability.

Muthusamy B, Bellad A, Prasad P, Bandari AK, Bhuvanalakshmi G, Kiragasur RM, Girimaj SC, Pandey A. Muthusamy B, et al. Among authors: bellad a. Front Psychiatry. 2020;11:354. doi: 10.3389/fpsyt.2020.00354. Epub 2020 May 18. Front Psychiatry. 2020. PMID: 32499722 Free PMC article.

4

KIAA1109 gene mutation in surviving patients with Alkuraya-Kučinskas syndrome: a review of literature.

Kumar K, Bellad A, Prasad P, Girimaji SC, Muthusamy B. Kumar K, et al. Among authors: bellad a. BMC Med Genet. 2020 Jun 26;21(1):136. doi: 10.1186/s12881-020-01074-2. BMC Med Genet. 2020. PMID: 32590954 Free PMC article. Review.

5

Shukla-Vernon Syndrome: A Second Family with a Novel Variant in the BCORL1 Gene.

Muthusamy B, Bellad A, Girimaji SC, Pandey A. Muthusamy B, et al. Among authors: bellad a. Genes (Basel). 2021 Mar 22;12(3):452. doi: 10.3390/genes12030452. Genes (Basel). 2021. PMID: 33810051 Free PMC article.

6

A novel loss of function mutation in adaptor protein complex 4, subunit mu-1 causing autosomal recessive spastic paraplegia 50.

Bellad A, Girimaji SC, Muthusamy B. Bellad A, et al. Neurol Sci. 2021 Dec;42(12):5311-5319. doi: 10.1007/s10072-021-05262-7. Epub 2021 Apr 21. Neurol Sci. 2021. PMID: 33884525

7

Loss of function variants in L2HGDH gene causing L-2-hydroxyglutaric aciduria.

Bellad A, Holla VV, Kumari R, Kamble N, Yadav R, Pandey A, Pal PK, Muthusamy B. Bellad A, et al. Acta Neurol Belg. 2023 Dec;123(6):2315-2323. doi: 10.1007/s13760-023-02318-7. Epub 2023 Jun 28. Acta Neurol Belg. 2023. PMID: 37378753

8

Urinary Proteomics for Discovery of Gastric Cancer Biomarkers to Enable Precision Clinical Oncology.

Joshi N, Bhat F, Bellad A, Sathe G, Jain A, Chavan S, Sirdeshmukh R, Pandey A. Joshi N, et al. Among authors: bellad a. OMICS. 2023 Aug;27(8):361-371. doi: 10.1089/omi.2023.0077. Epub 2023 Aug 9. OMICS. 2023. PMID: 37579183 Free PMC article.

9

Conotruncal Heart Defects: A Narrative Review of Molecular Genetics, Genomics Research and Innovation.

Viswanathan S, Sandeep Oza P, Bellad A, Uttarilli A. Viswanathan S, et al. Among authors: bellad a. OMICS. 2024 Jul;28(7):324-346. doi: 10.1089/omi.2024.0097. OMICS. 2024. PMID: 38986083 Review.

10

Dysregulated Cerebrospinal Fluid Proteome of Spinocerebellar Ataxia Type 2 and its Clinical Implications.

Stezin A, Sathe GJ, Gajbhiye A, Bharadwaj S, Ghose V, Bellad A, Malo PK, Holla V, Hegde S, Bharath RD, Saini J, Jain S, Yadav R, Pandey A, Pal PK. Stezin A, et al. Among authors: bellad a. Mov Disord. 2024 Aug;39(8):1418-1423. doi: 10.1002/mds.29834. Epub 2024 May 20. Mov Disord. 2024. PMID: 38769639

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