Dahl N - Search Results

1

Genetic Investigation of Consanguineous Pakistani Families Segregating Rare Spinocerebellar Disorders.

Saadi SM, Cali E, Khalid LB, Yousaf H, Zafar G, Khan HN, Sher M, Vona B, Abdullah U, Malik NA, Klar J, Efthymiou S, Dahl N, Houlden H, Toft M, Baig SM, Fatima A, Iqbal Z. Saadi SM, et al. Among authors: dahl n. Genes (Basel). 2023 Jul 6;14(7):1404. doi: 10.3390/genes14071404. Genes (Basel). 2023. PMID: 37510308 Free PMC article.

2

ZEB2 haploinsufficient Mowat-Wilson syndrome induced pluripotent stem cells show disrupted GABAergic transcriptional regulation and function.

Schuster J, Klar J, Khalfallah A, Laan L, Hoeber J, Fatima A, Sequeira VM, Jin Z, Korol SV, Huss M, Nordgren A, Anderlid BM, Gallant C, Birnir B, Dahl N. Schuster J, et al. Among authors: dahl n. Front Mol Neurosci. 2022 Oct 24;15:988993. doi: 10.3389/fnmol.2022.988993. eCollection 2022. Front Mol Neurosci. 2022. PMID: 36353360 Free PMC article.

3

Palmoplantar keratoderma and digital clubbing in 2 sisters with hypertrophic osteoarthropathy.

Eriksson D, Gyll D, Virtanen M, Dahl N, Klar J, Stattin EL. Eriksson D, et al. Among authors: dahl n. JAAD Case Rep. 2022 Dec 1;31:133-136. doi: 10.1016/j.jdcr.2022.11.025. eCollection 2023 Jan. JAAD Case Rep. 2022. PMID: 36583142 Free PMC article. No abstract available.

4

Early-onset hereditary isolated non-neurogenic orthostatic hypotension in a Swedish family.

Fagius J, Klar J, Dahl N. Fagius J, et al. Among authors: dahl n. Clin Auton Res. 2023 Aug;33(4):421-432. doi: 10.1007/s10286-023-00963-9. Epub 2023 Jul 17. Clin Auton Res. 2023. PMID: 37460866 Free PMC article.

5

Novel PNKP mutations associated with reduced DNA single-strand break repair and severe microcephaly, seizures, and developmental delay.

Thuresson AC, Brazina J, Akram T, Albrecht J, Dahl N, Soussi Zander C, Caldecott KW. Thuresson AC, et al. Among authors: dahl n. Mol Genet Genomic Med. 2024 Jan;12(1):e2295. doi: 10.1002/mgg3.2295. Epub 2023 Nov 2. Mol Genet Genomic Med. 2024. PMID: 37916443 Free PMC article.

6

Heredity of pregnancy-related pelvic girdle pain in Sweden.

Kristiansson P, Zöller B, Dahl N, Kalliokoski P, Hallqvist J, Li X. Kristiansson P, et al. Among authors: dahl n. Acta Obstet Gynecol Scand. 2023 Oct;102(10):1250-1258. doi: 10.1111/aogs.14646. Epub 2023 Jul 20. Acta Obstet Gynecol Scand. 2023. PMID: 37470484 Free PMC article.

7

Mutations in human DNA methyltransferase DNMT1 induce specific genome-wide epigenomic and transcriptomic changes in neurodevelopment.

Davis KN, Qu PP, Ma S, Lin L, Plastini M, Dahl N, Plazzi G, Pizza F, O'Hara R, Wong WH, Hallmayer J, Mignot E, Zhang X, Urban AE. Davis KN, et al. Among authors: dahl n. Hum Mol Genet. 2023 Oct 17;32(21):3105-3120. doi: 10.1093/hmg/ddad123. Hum Mol Genet. 2023. PMID: 37584462

8

Rapid P-TEFb-dependent transcriptional reorganization underpins the glioma adaptive response to radiotherapy.

Walker FM, Sobral LM, Danis E, Sanford B, Donthula S, Balakrishnan I, Wang D, Pierce A, Karam SD, Kargar S, Serkova NJ, Foreman NK, Venkataraman S, Dowell R, Vibhakar R, Dahl NA. Walker FM, et al. Among authors: dahl na. Nat Commun. 2024 May 30;15(1):4616. doi: 10.1038/s41467-024-48214-3. Nat Commun. 2024. PMID: 38816355 Free PMC article.

9

What is the Appropriate Dose of Tolvaptan in ADPKD?

Dahl NK, Torres VE. Dahl NK, et al. Kidney Int Rep. 2024 Feb 1;9(4):737-739. doi: 10.1016/j.ekir.2024.01.049. eCollection 2024 Apr. Kidney Int Rep. 2024. PMID: 38765581 Free PMC article. No abstract available.

10

Pain and Health-Related Quality of Life in Autosomal Dominant Polycystic Kidney Disease: Results from a National Patient-Powered Registry.

Hoover E, Holliday V, Merullo N, Oberdhan D, Perrone RD, Rusconi C, Park M, Phadnis MA, Thewarapperuma N, Dahl NK. Hoover E, et al. Among authors: dahl nk. Kidney Med. 2024 Mar 24;6(5):100813. doi: 10.1016/j.xkme.2024.100813. eCollection 2024 May. Kidney Med. 2024. PMID: 38689835 Free PMC article.

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