Dad R - Search Results

1

Structural and functional annotation of PR/SET Domain (PRDM) protein family: In-silico study elaborating role of PRDM12 mutation in congenital insensitivity to pain.

Mehmood S, Dad R, Ahmad A, Ullah MI, John P, Ali A, Hubner CA, Mohyuddin A, Hassan MJ. Mehmood S, et al. Among authors: dad r. Comput Biol Chem. 2020 Dec;89:107382. doi: 10.1016/j.compbiolchem.2020.107382. Epub 2020 Sep 24. Comput Biol Chem. 2020. PMID: 33010785

2

Clinical and genetic studies in patients with Lafora disease from Pakistan.

Ahmad A, Dad R, Ullah MI, Baig TA, Ahmad IN, Nasir A, Hübner CA, Hassan MJ. Ahmad A, et al. Among authors: dad r. J Neurol Sci. 2017 Feb 15;373:263-267. doi: 10.1016/j.jns.2017.01.010. Epub 2017 Jan 4. J Neurol Sci. 2017. PMID: 28131202

3

Corrigendum to "Clinical and genetic studies in patients with Lafora disease from Pakistan"[J. Neurol. Sci. 373 (2017) 263-267].

Ahmad A, Dad R, Ullah MI, Baig TA, Ahmad IN, Nasir A, Hübner CA, Hassan MJ. Ahmad A, et al. Among authors: dad r. J Neurol Sci. 2017 Apr 15;375:281. doi: 10.1016/j.jns.2017.02.010. Epub 2017 Feb 12. J Neurol Sci. 2017. PMID: 28320149 No abstract available.

4

Structural annotation of Beta-1,4-N-acetyl galactosaminyltransferase 1 (B4GALNT1) causing Hereditary Spastic Paraplegia 26.

Dad R, Malik U, Javed A, Minassian BA, Hassan MJ. Dad R, et al. Gene. 2017 Aug 30;626:258-263. doi: 10.1016/j.gene.2017.05.041. Epub 2017 May 20. Gene. 2017. PMID: 28536081

5

Chorea-acanthocytosis: Homozygous 1-kb deletion in VPS13A detected by whole-genome sequencing.

Walker S, Dad R, Thiruvahindrapuram B, Ullah MI, Ahmad A, Hassan MJ, Scherer SW, Minassian BA. Walker S, et al. Among authors: dad r. Neurol Genet. 2018 May 18;4(3):e242. doi: 10.1212/NXG.0000000000000242. eCollection 2018 Jun. Neurol Genet. 2018. PMID: 29845114 Free PMC article.

6

Hyperventilation-athetosis in ASXL3 deficiency (Bainbridge-Ropers) syndrome.

Dad R, Walker S, Scherer SW, Hassan MJ, Kang SY, Minassian BA. Dad R, et al. Neurol Genet. 2017 Sep 22;3(5):e189. doi: 10.1212/NXG.0000000000000189. eCollection 2017 Oct. Neurol Genet. 2017. PMID: 28955728 Free PMC article. No abstract available.

7

Febrile ataxia and myokymia broaden the SPG26 hereditary spastic paraplegia phenotype.

Dad R, Walker S, Scherer SW, Hassan MJ, Alghamdi MD, Minassian BA, Alkhater RA. Dad R, et al. Neurol Genet. 2017 May 23;3(3):e156. doi: 10.1212/NXG.0000000000000156. eCollection 2017 Jun. Neurol Genet. 2017. PMID: 28626794 Free PMC article. No abstract available.

8

Biallelic truncating SCN9A mutation identified in four families with congenital insensitivity to pain from Pakistan.

Sawal HA, Harripaul R, Mikhailov A, Dad R, Ayub M, Jawad Hassan M, Vincent JB. Sawal HA, et al. Among authors: dad r. Clin Genet. 2016 Dec;90(6):563-565. doi: 10.1111/cge.12860. Epub 2016 Oct 17. Clin Genet. 2016. PMID: 27747863

9

Identification and Functional Characterization of Mutation in FYCO1 in Families with Congenital Cataract.

Ullah MI, Rehman Z, Dad R, Alsrhani A, Shakil M, Ghanem HB, Alameen AAM, Elsadek MF, Eltayeb LB, Ullah S, Atif M. Ullah MI, et al. Among authors: dad r. Life (Basel). 2023 Aug 21;13(8):1788. doi: 10.3390/life13081788. Life (Basel). 2023. PMID: 37629644 Free PMC article.

10

Evaluation of humoral immunological response of newly prepared bovine multidrug-resistant Staphylococcus aureus mastitis vaccines in rabbits.

Dad RK, Avais M, Khan JA, Anjum AA. Dad RK, et al. Pak J Pharm Sci. 2022 Jul;35(4(Special)):1223-1228. Pak J Pharm Sci. 2022. PMID: 36218101

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

18 results

Search Page

Filters