Dickson PI - Search Results

1

Postmortem diagnosis of very long chain acyl-CoA dehydrogenase (VLCAD) deficiency in a neonate with sudden cardiac death.

Singh P, Amaro D, Obi O, Kiran F, Hediger E, Toler TL, Dickson PI, Grange DK. Singh P, et al. Among authors: dickson pi. JIMD Rep. 2023 Apr 30;64(4):261-264. doi: 10.1002/jmd2.12365. eCollection 2023 Jul. JIMD Rep. 2023. PMID: 37404675 Free PMC article.

2

Entering the playing field: Therapy for multiple sulfatase deficiency.

Dickson P. Dickson P. Mol Ther. 2024 Nov 6;32(11):3756-3757. doi: 10.1016/j.ymthe.2024.10.008. Epub 2024 Oct 30. Mol Ther. 2024. PMID: 39481371 No abstract available.

3

Characterization of early markers of disease in the mouse model of mucopolysaccharidosis IIIB.

McCullough KB, Titus A, Reardon K, Conyers S, Dougherty JD, Ge X, Garbow JR, Dickson P, Yuede CM, Maloney SE. McCullough KB, et al. J Neurodev Disord. 2024 Apr 17;16(1):16. doi: 10.1186/s11689-024-09534-z. J Neurodev Disord. 2024. PMID: 38632525 Free PMC article.

4

Genetics is Scary.

Dickson PI. Dickson PI. Mo Med. 2024 Jul-Aug;121(4):276. Mo Med. 2024. PMID: 39575072 Free PMC article. No abstract available.

5

D-mannose as a new therapy for fucokinase deficiency-related congenital disorder of glycosylation (FCSK-CDG).

Starosta RT, Lee AJ, Toolan ER, He M, Wongkittichote P, Daniel EJP, Radenkovic S, Budhraja R, Pandey A, Sharma J, Morava E, Nguyen H, Dickson PI. Starosta RT, et al. Among authors: dickson pi. Mol Genet Metab. 2024 Jun;142(2):108488. doi: 10.1016/j.ymgme.2024.108488. Epub 2024 May 9. Mol Genet Metab. 2024. PMID: 38735264

6

GABAergic interneurons contribute to the fatal seizure phenotype of CLN2 disease mice.

Takahashi K, Rensing NR, Eultgen EM, Wang SH, Nelvagal HR, Le SQ, Roberts MS, Doray B, Han EB, Dickson PI, Wong M, Sands MS, Cooper JD. Takahashi K, et al. Among authors: dickson pi. bioRxiv [Preprint]. 2024 Mar 30:2024.03.29.587276. doi: 10.1101/2024.03.29.587276. bioRxiv. 2024. PMID: 38585903 Free PMC article. Preprint.

7

Combining angiotensin receptor blockade and enzyme replacement therapy for vascular disease in mucopolysaccharidosis type I.

Hurt SC, Vera MU, Le SQ, Kan SH, Bui Q, Dickson PI. Hurt SC, et al. Among authors: dickson pi. Mol Genet Metab Rep. 2023 Dec 14;38:101036. doi: 10.1016/j.ymgmr.2023.101036. eCollection 2024 Mar. Mol Genet Metab Rep. 2023. PMID: 38173710 Free PMC article.

8

Whole-Genome and Long-Read Sequencing Identify a Novel Mechanism in RFC1 Resulting in CANVAS Syndrome.

King KA, Wegner DJ, Bucelli RC, Shapiro J, Paul AJ, Dickson PI, Wambach JA; Undiagnosed Disease Network (UDN). King KA, et al. Among authors: dickson pi. Neurol Genet. 2022 Nov 1;8(6):e200036. doi: 10.1212/NXG.0000000000200036. eCollection 2022 Dec. Neurol Genet. 2022. PMID: 36524104 Free PMC article.

9

Brain transplantation of genetically corrected Sanfilippo type B neural stem cells induces partial cross-correction of the disease.

Pearse Y, Clarke D, Kan SH, Le SQ, Sanghez V, Luzzi A, Pham I, Nih LR, Cooper JD, Dickson PI, Iacovino M. Pearse Y, et al. Among authors: dickson pi. Mol Ther Methods Clin Dev. 2022 Oct 27;27:452-463. doi: 10.1016/j.omtm.2022.10.013. eCollection 2022 Dec 8. Mol Ther Methods Clin Dev. 2022. PMID: 36419468 Free PMC article.

10

Infantile-onset Pompe disease complicated by sickle cell anemia: Case report and management considerations.

Starosta RT, Hou YC, Leestma K, Singh P, Viehl L, Manwaring L, Granadillo JL, Schroeder MC, Colombo JN, Whitehead H, Dickson PI, Hulbert ML, Nguyen HT. Starosta RT, et al. Among authors: dickson pi. Front Pediatr. 2022 Sep 28;10:944178. doi: 10.3389/fped.2022.944178. eCollection 2022. Front Pediatr. 2022. PMID: 36245745 Free PMC article.

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